Evidence-Based Complementary and Alternative Medicine

Evidence-Based Complementary and Alternative Medicine / 2016 / Article

Review Article | Open Access

Volume 2016 |Article ID 7279361 | 10 pages | https://doi.org/10.1155/2016/7279361

Synergism of Chinese Herbal Medicine: Illustrated by Danshen Compound

Academic Editor: Avni Sali
Received19 Aug 2015
Revised05 Jan 2016
Accepted16 Feb 2016
Published13 Apr 2016


The primary therapeutic effects of Chinese herbal medicine (CHM) are based on the properties of each herb and the strategic combination of herbs in formulae. The herbal formulae are constructed according to Chinese medicine theory: the “Traditional Principles for Constructing Chinese Herbal Medicinal Formulae” and the “Principles of Combining Medicinal Substances.” These principles of formulation detail how and why multiple medicinal herbs with different properties are combined together into a single formula. However, the concept of herbal synergism in CHM still remains a mystery due to lack of scientific data and modern assessment methods. The Compound Danshen Formula (CDF) is a validated formula that has been used to treat a variety of diseases for hundreds of years in China and other countries. The CDF will be employed to illustrate the theory and principle of Chinese herbal medicine formulation. The aim of this review is to describe how Chinese herbal medicinal formulae are constructed according to Chinese medicine theory and to illustrate with scientific evidence how Chinese herbs work synergistically within a formula, thereby supporting Chinese medicine theory and practice.

1. Introduction

Traditional Chinese Medicine (TCM) encompasses a variety of therapies including Chinese herbal medicine (CHM), acupuncture, Qigong, and physical therapy such as massage and Gua Sha (scraping). Due to its unique philosophy and treatment characteristics, TCM was identified as one of the advanced medical sciences until the 17th century [1, 2]. CHM, as the most important part of TCM, has been used to treat disease for over 4,000 years [1, 3]. Even though Western medicine is widely accepted by modern Chinese culture, CHM still plays a very important role in daily medical practice; about 46% of patients were prescribed CHM in hospitals or outpatient clinics. CHM is popularly used for the treatment of variety of diseases such as the common cold, hepatitis, nephrotic syndrome, diabetes, cardiovascular disease, and cancer [49]. Worldwide, increasing numbers of Westerners are recognizing the importance of CHM and seeking it as part of their healthcare.

Medical science has long realized that the pathogenesis and progression of diseases are too complex for single drug treatment. For example, cardiovascular disease is the primary killer worldwide [10, 11], with coronary artery disease (CAD) as the most common cause of cardiovascular morbidity and mortality. The pathophysiology of CAD is very complex and warrants multifaceted treatment [12, 13]. The strategies include treatment of the primary disease as well as intervention in risk factors and comorbid conditions such as high cholesterol, hypertension, obesity, and diabetes [14, 15]. The treatment regimen is a combination of pharmaceutical drugs that target the different organs and systems involved in the pathophysiological processes of the primary and secondary conditions. These medications include but are not limited to aspirin, nitrates, Angiotensin II receptor blocker (ARB), statins, diuretics, and metformin [1517]. Interestingly, to achieve better therapeutic outcomes and diminish side effects, multiherb therapy is an essential component of traditional Chinese herbal medicine and has been utilized in China for thousands of years [3, 18].

Originally, practitioners of Chinese herbal medicine used just single herbs for disease treatment. But, over time, Chinese herbalists gained more experience from clinical practice and learned that the causes of diseases were imbalances among different systems in the body. To restore the dynamic balance among body systems and get the best curative effect with the least toxicological effect, Chinese herbalists chose a combination of several herbs based on the distinct disease presentations. Through this process, the theory of herbal synergism in CHM was developed and refined by herbalists over thousands of years of clinical practice. Single herbal medicines and herbal formulae compose the Chinese herbal medicine system [19]. There are 8980 herbs compiled into Zhong Hua Ben Cao (Chinese Materia Medica 1999) and 1444 Chinese herbal formulae collected in 2010 edition of the Chinese Pharmacopoeia. CHM combines two or more herbs with different properties synergistically to form a compound formula named “方 (fù fānɡ)” or “方 (fānɡ jì)” based on the Principles of Combining Medicinal Substances [20].

When two or more Chinese herbal medicines (CHMs) are combined, they become a named formula. Over 2,000 years of practice, CHM has accumulated over 100,000 formulae that are constructed according to specific TCM principles [18, 21]. Based on empirical evidence gathered over many centuries, CHM providers learned that particular herbal combinations work synergistically or antagonistically [3]. Herbal formulae are constructed based on this synergism, outlined as theories in Materia Medica. With the rise of scientific research methods, the synergism between herbs is being investigated pharmacologically. This research substantiates Chinese medicine theory and elucidates correct dosage combinations [22]. Through the example of a cardiovascular herbal formula, this paper will explain how Chinese herbs are combined into formulae, the seven traditional types of herbal combinations, and how scientific research contributes additional knowledge.

2. Traditional Principles for Constructing Chinese Herbal Medicinal Formulae: Seven Types of Herbal Combinations

Traditionally, there are seven types of Chinese herbal combinations, differentiated by their physiologic effects (seven emotions, Chinese name 七 qīqínɡ). Seven emotions have two different definitions in TCM. The first one emphasizes the relation between diseases and mental activities, the main pathogenic factors of endogenous diseases [23]. Emotional mental activities are categorized as the seven emotional factors: joy, anger, melancholy, worry, grief, fear, and fright. This is beyond the scope of our topic.

The second one is used in herbal medicine to elucidate the seven possible outcomes that could be yielded if multiple herbs with different pharmacological properties are used in combination. It was first recorded in Shennong Bencao Jing, a classic book systemically describing CHM that was written approximately 2000 years ago between the Qin and Han dynasties. From a modern pharmacology perspective, this is a theory about herb-herb interactions [24, 25]. These were described in the Grand Materia Medica.

(1) Single Effect (单 dān xínɡ). Single effect (行 dān xínɡ) is the use of one medicinal substance to treat a patient. An example is the Du Shen Tang decoction, which consists of only one herbal medicine, Panax ginseng (Asian ginseng). It was historically prescribed to patients with “Qi and Xue deficiency” states such as postpartum hemorrhage [26], acute myocardial infarction [27], cirrhosis [28], upper gastrointestinal bleeding [29], and congestive heart failure [30].

(2) Mutual Accentuation (須 xiāng xū). Mutual accentuation (相 xiāng xū) means that the combination of two herbal substances with similar functions will accentuate their therapeutic actions, also called “mutual necessity.” For instance, herbal decoction of Da Huang (Rheum palmatum, rhubarb) and Mang Xiao (natrii sulfas, mirabilite) is used to treat constipation. Pharmacological research showed that Da Huang is able to stimulate the colon by increasing the intensity and frequency of contractions, which subsequently improves bowel motility. The Mang Xiao contains sodium sulfate, which when absorbed in colon creates a hyperosmotic environment, bringing water into the colon and softening the stool. When Da Huang and Mang Xiao are used together in combination they have a better laxative effect compared to each used alone [25, 31].

(3) Mutual Enhancement (使 xiāng shǐ). Mutual enhancement (相使 xiāng shǐ) is the combination of two or more substances with different actions in which one of the substances enhances the effect of the other in a specific clinical situation, also called “mutual employment.” For example, Huang Lian (rhizoma coptidis, coptis root) and Mu Xiang (vladimiriae radix, costus root) are herbs often prescribed as a pair for the treatment of dysentery. Modern pharmacological study has demonstrated that Huang Lian has antimicrobial effect against Shigella spp. both in vivo and in vitro. Mu Xiang has been proven to increase the serum concentration of berberine, the major active antimicrobial component of Huang Lian. When used with Mu Xiang, Huang Lian has a greater efficacy for patients with dysentery [25, 32].

(4) Mutual Counteraction (畏 xiāng wèi). Mutual counteraction (相 xiāng wèi) literally translates to “mutual fear” and means a combination in which the toxicity or side effects of one substance are reduced or eliminated by another substance. For instance, Fu Zi (Aconitum carmichaelii, aconite root) is a toxic herb where the primary component is harmful to cardiac and nerve cells. When it is prepared with Gan Cao (radix glycyrrhizae, licorice root), the toxicity of Fu Zi is diminished [25, 33]. The emphasis in mutual counteraction is on the toxic herb that is being counteracted in the formulation.

(5) Mutual Suppression (杀 xiāng shā). Mutual suppression (相 xiāng shā) literally translates to “mutual killing” and is the reverse of mutual counteraction. With mutual suppression, one substance also reduces the undesirable side effects of another but the emphasis is on the herb that performs the beneficial suppressive action. For example, Sheng Jiang (Zingiber officinale, ginger root), which was commonly prescribed for cold prevention, as antiemetic, and for detoxication, suppresses or literally “kills” the toxicity of Ban Xia (Pinellia ternata, pinellia root) commonly used to relieve cough and to stop vomiting and it is toxic when used alone. In short, mutual counteraction and mutual suppression describe the same herb-herb interaction, but from differing viewpoints [25, 33].

(6) Mutual Antagonism (恶 xiāng wù). Mutual antagonism (相 xiāng wù) literally translates to “mutual aversion” and means the ability of two substances to minimize each herb’s positive effects. Traditionally, there are eight pairs and one trio of substances that have mutually antagonistic effects on each other. Together they are referred to as the “nineteen antagonisms (十九畏 shí jiǔ wèi) [34].” Ren Shen (radix ginseng, Chinese ginseng) is capable of replenishing Qi, which increases the overall function of the body. This beneficial function can be reduced or abolished if combined with the herb Lai Fu Zi (semen raphani, radish seed) [25, 33].

(7) Mutual Incompatibility (反 xiāng fǎn). Mutual incompatibility (相 xiāng fǎn) translates literally to “mutual opposition” and occurs when the combination of two substances causes side effects or toxicity which would not be caused by any one of the substances if used alone. Traditionally there are three sets or a total of eighteen substances called the “eighteen incompatibilities’ (十八反 shí bā fǎn) [35].” For example, it is prohibited in CHM to use Danshen (Salvia miltiorrhiza, red sage) and Li Lu (Veratrum nigrum, black false hellebore) together. A toxicological study showed that when Danshen was combined with Li Lu, the Danshen increased the concentration of harmful Veratrum alkaloids that can produce serious adverse effects such as nausea, vomiting, dizziness, hypotension, and tachycardia. Thus, such a mutually incompatible pair of herbs should not be used in clinical practice according to the principles of CHM [25, 35].

3. The Principles of Combining Medicinal Substances: King, Ministers, Adjutants, and Messengers (君臣佐使 jūn chén zuǒ shǐ)

The Principles of Combining Medicinal Substances provide guidelines for the composition of Chinese herbal prescriptions. Traditionally described in terms of a feudal hierarchy, a formula is usually composed of several medicinal herbs [22, 25]. The chief (also called king, sovereign, or lord, in Chinese jūn) is the principal herbal ingredient in modern texts and is the substance that provides the main therapeutic effect in the prescription. The deputies (also called ministers or associates, in Chinese chén) enhance or assist the therapeutic actions of the chief. The assistants (also called adjutants, in Chinese zuǒ) provide one or more of the following functions: treating accompanying symptoms, moderating the harshness or toxicity of the primary substances, assisting the chief and deputies in accomplishing their main objectives, or providing assistance from another therapeutic direction, such as the addition of cooling substance to a warming prescription or vice versa. The envoys (also called messengers or couriers, in Chinese 使 shǐ) either guide the other herbs in the formula to a specific channel or organ or exert a harmonizing influence. A common herb used as a messenger is glycyrrhizae root (甘草 gān cǎo). Not all principles need to be used in every herbal prescription. There are many simple prescriptions that contain only a chief and deputies, and there are prescriptions in which one substance serves more than one function. For instance, there may be multiple adjutants and messengers in one formula, and one herb may act both as an adjutant and as a messenger [36, 37].

A good example to illustrate the different roles of herbs in formulation is the Compound Danshen Formula (Figure 1), a commonly used formula for treating coronary artery disease including angina and acute myocardial infarction [9]. In this formula, Danshen (Salvia miltiorrhiza, red sage) serves as the chief herb. Pharmacological research shows that Danshen causes relaxation of the coronary arteries which is one of the herb’s major physiologic, cardioprotective effects. Another herb, Sanqi (Panax notoginseng, notoginseng), serves as the deputy herb in the formulation because it has its cardiomyocyte protective and antiplatelet functions. A third herb, Bingpian (Dryobalanops aromitaca, borneol), serves as assistant and envoy by increasing the blood concentration of Danshen and Sanqi [38, 39].

4. Pharmacological Research on the Synergism among Danshen, Sanqi, and Bingpian

Compound Danshen Formula (CDF), composed of Danshen, Sanqi, and Bingpian, has been widely used in the treatment of cardiovascular diseases in China and other countries for over thirty years [4042]. CDF has been employed by over 600 Chinese pharmaceutical companies and many different products were produced from CDF in China [43].

The dried root of plant Danshen is a popular herbal medicine in China and Japan, used alone or in combination with other herbs [44, 45]. It was first recorded in the Shennong’s Classic Materia Medica, Shennong Bencao Jing, which is the oldest medicine monograph in China. One of the most widely used traditional medicines, Danshen, is used in the treatment of coronary heart disease [46], cerebrovascular disease [47], Alzheimer’s disease [48], Parkinson’s disease [49], renal deficiency [50], liver cirrhosis [51], cancer [52], and bone loss [53]. The composition of Danshen has been analyzed and found to contain 49 diterpenoid quinones, 36 hydrophilic phenolic acids, and 23 essential oil constituents. The diterpenoid quinones and hydrophilic phenolic acids are the principal bioactive components in Danshen [54].

The dry root of Sanqi has been traditionally used in CHM for thousands of years as a hemostatic medicine to control internal and external bleeding [55]. Currently, Sanqi is a commonly used herb to treat cardiovascular disease by stopping bleeding, as well as invigorating and supplementing blood [56]. Moreover, it has function of protecting myocardium, specifically for improving ischemia/reperfusion (I/R) induced injury after percutaneous coronary interventional therapy [54, 57]. It has been reported to have antihypertensive, antithrombotic, antiatherosclerotic, and neuroprotective activities [57]. Various chemical constituents in Sangi have been identified, including ginsenosides, notoginsenosides, flavonoids, volatile oils, amino acids, and polysaccharides [58].

Bingpian contains monoterpenoid constituents and is included in 63 CHM prescriptions according to the Chinese Pharmacopoeia. Its wide use as an assistant in CHM is due to its ability to improve percutaneous absorption, enhance oral bioavailability, and facilitate passage of herbal formulation through the blood brain barrier [5961].

It has been demonstrated through years of clinical use that Danshen and Sanqi have a synergistic effect when combined but the molecular mechanisms underlying their synergism have yet to be clearly elucidated [41, 62]. Cardiovascular disease is the number one cause of death in Europe and in the United States according to the Centers for Disease Control in 2013 [10, 63]. Compound Danshen Formula (CDF) has been widely accepted and used in the treatment of cardiovascular diseases in China and other countries for decades with beneficial outcomes confirmed by clinical trials [9, 64]. There are three preparations compiled in the Chinese Pharmacopoeia 2010 edition: Compound Danshen Tablet (CDT), Compound Danshen Granule (CDG), and Compound Danshen Dripping Pill (CDDP). In 1997 the United States Food and Drug Administration (FDA) accepted the Chinese medicinal product CDDP as an investigational new drug (IND number 56956) [9, 64]. In 2010, a phase II clinical study on CDDP was completed and now a phase III clinical trial is underway (ClinicalTrials.gov Identifier: NCT01659580), which is an important milestone in the incorporation of CHM into the Western medical system.

Effects of Danshen and Sanqi on the cardiovascular system are summarized as follows: (1) antioxidant and cardiac protection [65, 66]; (2) inhibition of platelet aggregation and adhesion [67, 68]; (3) vasorelaxation [69]; and (4) prevention of arthrosclerosis [70]. Sanqi prevents arthrosclerosis [41, 71] and protects cardiac myocytes [65, 72]. Danshen contains both hydrophobic and hydrophilic bioactive components such as danshensu, salvianolic acid B, and tanshinone [7375]. Sanqi contains abundant saponins such as ginsenosides and notoginsenosides [76]. When the two herbs are decocted together in a combination formula, studies have shown that the interaction between the herbs results in a compound with stronger pharmacological properties compared to each herb alone [62].

4.1. Synergistic Effect of Danshen and Sanqi Demonstrated by Chemistry and Pharmacokinetic Studies

Zeng et al. [77] performed an in vitro comparative study on the influence of Danshen and Sanqi on the dissolution of active components from Danshen when the two herbs were decocted in different mass ratios. The ethanol extracts from Danshen and Sanqi were decocted in different mass ratio and HPLC was employed to quantitate the active components from Danshen. The result demonstrated that the main active ingredients from Danshen is higher in all codecocted groups than in the Danshen only group with highest extraction rate at ratio of 5 : 3, Danshen to Sanqi, which is the ratio in classic CDF. In contrast, the effect of mixture or single decoction of Danshen and Sanqi on the dissolution of active components from Sanqi differs from that of Danshen. The effect of Danshen and Sanqi on the extraction of active components from Sanqi was studied by using HPLC combined with UV-visible spectroscopy, infrared spectroscopy, and time-of-flight mass spectrometry [78]. The results demonstrated that codecoction of Danshen and Sanqi inhibited the dissolution of the active components from Sanqi.

A recent in vivo study on Guinea pigs extended these findings using three experimental groups [79]. Danshen extracts (salvianolic acid B and tanshinone IIA), Sanqi extracts (panax notoginseng saponins), and a combination of the two extracts were given to three groups of Guinea pigs for a pharmacokinetic study. Parameters analyzed included maximum blood concentration () and area under curve [(AUC) (0–t)]. The result demonstrated that the pharmacokinetic levels of active constituents salvianolic acid B (SalB), tanshinone IIA (Ts IIA), notoginsenoside R1 (R1), ginsenoside Rg1 (Rg1), and ginsenoside Rb1 (Rb1) were markedly different in the Danshen-Sanqi combination group compared to the groups that took Danshen and Sanqi alone. of R1, Rb1, and Rg1 were significantly decreased while of Ts IIA and SalB were increased in both cerebrospinal fluid (CSF) and plasma. These effects are most likely achieved by increased absorption and distribution of the compound in the body, a result of coadministration of Danshen and Sanqi. This study shows the significant pharmacokinetic changes that can result from the herb-herb interactions. Another study that showed similar results administered oral Danshen alone, Sanqi alone, or Danshen and Sanqi combination suspension to beagle dogs [80]. After administration, the plasma concentration-time profiles of danshensu, tanshinone IIA, cryptotanshinone, notoginsenoside R1, ginsenoside Rg1, and ginsenoside Rb1 were analyzed by LC-MS/MS. The results showed that both and AUC of Danshensu, notoginsenoside R1, ginsenoside Rg1, and ginsenoside Rb1 in the Danshen and Sanqi combination group decreased in comparison with those in either the Danshen alone or Sanqi alone groups.

4.2. Synergistic Interaction and Cardiac Protection of Danshen and Sanqi in an Acute Myocardial Infarction Animal Model

Pharmacological studies indicate that the coadministration of Danshen and Sanqi has a cardiac protective effect of improving coronary circulation and improving symptoms of myocardial ischemia, while individual administration of Danshen expands blood vessels and individual administration of Sanqi targets cardiac myocytes. Specifically, the herb pair exerts the best cardiac protective effects when the mass ratio of Danshen to Sanqi is between 10 : 3 and 10 : 7 [41, 81]. A preclinical study [82] comparing the cardioprotective effect of salvianolic acid (SAL) and tanshinone (TAN) was performed in a rat model of acute myocardial infarction (MI). Rats were randomly assigned to four groups: sham group (the ligation suture was placed in the heart, but without ligation), myocardial infarction (MI) group, SAL treatment group, or TAN treatment group (SAL + MI, TAN + MI, resp.). The MI was produced by occlusion of the left anterior descending coronary artery and SAL (120 mg/kg) and TA (120 mg/kg) were given once daily after MI by oral administration. The cardiac functional parameters were measured at 3, 7, 14, and 28 days after surgery. The data demonstrated that both the SAL and TAN treatment groups delayed the development of ischemia by decreasing infarct size and improving systolic function after MI. Gene chip analysis indicated different kinetics and gene expression profiles presented after the administration of SAL and TAN. SAL acted in a later period after ischemia, and its effect was likely mediated by downregulation of genes involved in oxidative stress, specific G-protein coupled receptor activities, and apoptosis [82]. Meanwhile TAN acted relatively early after ischemic injury and its effect was mediated by the inhibition of intracellular calcium, cell adhesion, and alternative complement pathway. Although both SAL and TAN contributed to the cardioprotective effect of Danshen, there were significant mechanistic and temporal differences between the two constituents. To test the effects of the major components from Danshen and Sanqi on cardiac function in a myocardial infarction (MI) rat model, salvianolic B (SalB) from Danshen and ginsenosides Rg1 (GRg1) and Rb1 (GRb1) from Sanqi were administered alone or in combination intragastrically [83]. Fifty rats were randomized into six groups: Sham operation, MI + saline, MI + SalB, MI + GRg1, MI + GRe, MI + SalB + GRg1 (mass ratio of SalB to GRg1 is 2 : 5), and MI + SalB + GRe (mass ratio of SalB to GRe is 2 : 5). The medication was administered in a 60 mg/kg dose twice. The first dose was given one hour before MI generation and the second dose was given at 23rd hour after MI. The group who received the combination of SalB and GRg1 at the mass ratio of 2 : 5 significantly improved cardiac function in this MI model, illustrated by increased left ventricular contractility (+dp/dt) parameter without negative effects on heart rate or blood pressure. No significant improvement in +dp/dt was noted in rats administrated with SalB, GRg1, or GRb1 alone. Nor was improvement seen in the group with coadministration of SalB and GRb1. This result demonstrated that SalB from Danshen and GRg1 from Sanqi worked synergistically to improve cardiac function in a myocardial infarction rat model with mass ratio of 2 : 5.

Lu et al. [84] compared the cardioprotective effects of tanshinone IIA (T), salvianolic acid B (S), ginsenoside Rb1 (G), and Compound Danshen Formula (CDF) on acute myocardial ischemia in rats. The T, S, G, TSG (combination of T, S, and G), and CDF were administered to the MI rats. The cardioprotective effect was evaluated by measuring MI associated parameters including ECG and cardiac enzymes. The result indicated that the combination administration of TSG, and not the administration of the single components alone, had a similar beneficial cardiac effect on MI rats as the CDF group. Other cell biology studies confirmed these findings. Zeng et al. [85] reported that combinational use of Danshen and Sanqi had protective effects on human umbilical vein endothelial cells (HUVEC) that underwent hypoxia-reoxygenation induced cell injury. Measurement of LDH leakage, an index of cell injury, in a culture medium from cells treated by the mixture of Danshen and Sanqi prepared in different ratios demonstrated that Danshen and Sanqi had protective effects on HUVEC at the ratios of 10 : 1, 5 : 3, 1 : 1, and 0 : 10, with best benefit effect at ratios of 5 : 3 and 1 : 1, Danshen to Sanqi.

4.3. Combination of Danshen and Sanqi in the Modulation of Platelet Function

Herbal combination of Danshen and Sanqi in different mass ratios (10 : 0, 10 : 1, 10 : 3, 10 : 6, and 1 : 10, Danshen to Sanqi) significantly inhibited ADP-induced platelet aggregation with the best inhibitory action at 10 : 3, although Sanqi alone did inhibit platelet aggregation [86]. Three combinations at ratios of 10 : 3, 10 : 6, and 0 : 10 had the ability of inhibiting platelet adhesion with the best result at 0 : 10, that is, Sanqi alone. Interestingly, the mass combination of Danshen and Sanqi at ratios of 10 : 0, 10 : 1, and 1 : 10 did not affect platelet adhesion. Another in vivo study showed that administration of total salvianolic acids (TSA) extracted from Danshen and total notoginsenosides (TNG) from Sanqi at a dose of 550 mg/kg/day for five days could significantly inhibit ADP-induced platelet aggregation [87]. Moreover, even though the use of TSA or TNG alone and the combination of TSA and TNG at mass ratios of 1 : 1, 1 : 5, and 5 : 1 all showed significant inhibition of platelet aggregation, the combination of TSA and TNG at a ratio of 5 : 1 had the best synergistic effect on platelet aggregation. However, there is no synergistic effect on platelet aggregation of the combination of Danshen and Sanqi in vitro [84]. High performance liquid chromatography analysis of the plasma of rats that received TSA, TNG, or combination of TSA and TNG showed that coadministration of TNG caused change in the plasma distribution profile of TSA. The influence of combination on the absorption and/or metabolism of SA may be one of the reasons for the synergism of TSA and TNG in vivo.

The above-mentioned research results suggest that Danshen-Sanqi herb pair exerts multitarget and multifunction effects that single herb usage could not achieve. Additionally the research shows that a specific herbal combination ratio is critical for maximum synergetic action of Danshen and Sanqi.

4.4. The Role of Bingpian in Compound Danshen Formula

To define the role of Bingpian in Compound Danshen Formula (CDF), a pharmacokinetic study was conducted in rats [38]. After oral administration of extract from Danshen alone or Danshen extracts combined with Bingpian, plasma concentrations of rosmarinic acid (RA), salvianolic acid A (SAA), and salvianolic acid B (SAB) were assessed at different time points. In comparison with Danshen extracts alone, significant changes in pharmacokinetic parameters of RA, SAA, and SAB were observed in the Danshen-Bingpian group. The bioavailability of all three salvianolic acids increased when the Danshen extracts and Bingpian were administrated together. These results indicated that Bingpian could enhance intestinal absorption, decrease distribution in the body, and inhibit the metabolism of salvianolic acids. Coadministration of salvianolic acid B, saponins, and Bingpian upregulated mRNA of vascular endothelial growth factor (VEGF) in a rat model with focal cerebral ischemia/reperfusion injury [39]. In comparison with rabbits given Sanqi extract alone, animals simultaneously taking Sanqi extract and Bingpian exhibited significant differences in pharmacokinetic parameters of notoginsenosides R1 (NGR1), ginsenosides Rg1 (GRg1), and Re (GRe), which are three major active components of Sanqi. The plasma concentration of NGR1, GRg1, and GRe is increased significantly in rabbits given simultaneously Sanqi extract and Bingpian via improvements in their absorption and bioavailability. For Bingpian combined with Sanqi extract, the three saponin levels were all increased markedly in heart, lung, liver, and brain tissues with peak levels at one hour after the administration of Sanqi extract [88].

This data indicates that, in the Compound Danshen Formula, Bingpian acts as adjutant and messenger herb and can increase the blood concentration of Danshen and Sanqi.

4.5. Bioactive Equivalent Combinatorial Components (BECCs) Study: The Example of Synergistic Interaction of Multiple Components in CDF

Even though more than 100 components have been isolated and identified in Danshen and Sanqi to date [84], only a small fraction of these components have been studied to confirm their pharmacological effects. The following study provided a new method for the evaluation of CHM synergism. A bioactive equivalent oriented feedback screening method was developed and applied to discover the bioactive equivalence of combinatorial components (BECCs) from a cardiotonic pill (CP, a CDDP formula) [89]. To obtain the components of candidate BECCs, the real-time components trapping and combining system was employed. Eighteen components were identified as BECCs by HPLC-UV chromatography including ten phenolic acids, four saponins, and four tanshinone. The subsequent in vitro study showed that only the combination of 18 components had the bioequivalent protective activity as the CP in cultured HUVEC. None of the combinations (phenolic acids + saponins, phenolic acids + tanshinone, or tanshinone + saponins) exerted similar cell protective effect as the CP. In an in vivo evaluation test, the combination of 18 components of BECCs was identified to be as effective as the CP in improving the ischemic parameters of cardiac enzymes and left ventricular function in a rat model with myocardial infarction.

4.6. Herb-Drug Interaction Explored by Coadministration of CDDP and Warfarin

Due to high healthcare costs, easy access to over-the-counter herbal products, and an interest in natural approaches to disease treatment, increasing numbers of patients in the USA are turning to alternative and complementary medicines [90]. In parallel, the rate of consumption of herbal products in conjunction with conventional medications has increased and with it the potential for adverse herb-drug interactions increased [9193]. Due to Compound Danshen Formula’s wide clinical use, a recent concern has been raised about interactions between various herbal products and warfarin [91]. A study was conducted to evaluate whether CDDP interacted with warfarin when administered concomitantly: the results demonstrated that CDDP in rats did not significantly alter the pharmacodynamics of warfarin [94]. It was speculated that the interactions between CDDP and warfarin was likely to be negligible [95].

5. Conclusion

Chinese herbal medicine (CHM) is a major part of Traditional Chinese Medicine (TCM) and the use of synergistic compound formulae (方 fù fānɡ) is a main therapeutic tool that is customarily composed of multiple medicinal herbs with different pharmacological properties. The combinational use of herbal medicines is at the heart of CHM and continues to play a very important role in the treatment of disease. The synergism of herbs is based on the Traditional Principles for Constructing Chinese Herbal Medicinal Formulae and the Principles of Combining Medicinal Substances. The principles are evidenced by an example formula, Compound Danshen Formula, and recent research has unveiled pharmacological and pharmacokinetic properties of the formula. This review provides preliminary explanation of CHM theory, which helps to better understand the rationale and the principal mechanism of herbal synergism and the clinical application of the formulae. However, further investigation is needed to provide more evidence of the molecular and cellular mechanisms of the synergism of CHM formulae.

Competing Interests

The authors declare that there is no conflict of interests regarding the publication of this paper. All authors are employed by Tasly Pharmaceuticals Inc., in USA, a subsidiary of Tasly (Tasly Holding Group) in China. Tasly China does manufacture, together with other hundreds (more than 600) of companies in China, the Compound Danshen Formula. However, Tasly Pharmaceuticals Inc., USA, does not manufacture nor distribute this compound in USA.

Authors’ Contributions

All authors reviewed and approved the paper.


The authors acknowledge and thank Carrie Runde, ND, from Casey Health Institute for her perspicacious review and editing of this paper.


  1. Y. D. Yi and I. M. Chang, “An overview of traditional Chinese herbal formulae and a proposal of a new code system for expressing the formula titles,” Evidence-Based Complementary and Alternative Medicine, vol. 1, no. 2, pp. 125–132, 2004. View at: Publisher Site | Google Scholar
  2. N. J. Sucher, “The application of Chinese medicine to novel drug discovery,” Expert Opinion on Drug Discovery, vol. 8, no. 1, pp. 21–34, 2013. View at: Publisher Site | Google Scholar
  3. S. Xutian, J. Zhang, and W. Louise, “New exploration and understanding of traditional Chinese medicine,” The American Journal of Chinese Medicine, vol. 37, no. 3, pp. 411–426, 2009. View at: Publisher Site | Google Scholar
  4. X. Zhang, T. Wu, J. Zhang, Q. Yan, L. Xie, and G. J. Liu, “Chinese medicinal herbs for the common cold,” Cochrane Database of Systematic Reviews, no. 1, Article ID CD004782, 2007. View at: Publisher Site | Google Scholar
  5. L. Zhang, G. Wang, W. Hou, P. Li, A. Dulin, and H. L. Bonkovsky, “Contemporary clinical research of traditional Chinese medicines for chronic hepatitis B in china: an analytical review,” Hepatology, vol. 51, no. 2, pp. 690–698, 2010. View at: Publisher Site | Google Scholar
  6. P. Chen, Y. Wan, C. Wang et al., “Mechanisms and effects of Abelmoschus manihot preparations in treating chronic kidney disease,” Zhongguo Zhong Yao Za Zhi, vol. 37, no. 15, pp. 2252–2256, 2012. View at: Publisher Site | Google Scholar
  7. X. Xu, L. Guo, and G. Tian, “Diabetes cognitive impairments and the effect of traditional Chinese herbs,” Evidence-Based Complementary and Alternative Medicine, vol. 2013, Article ID 649396, 10 pages, 2013. View at: Publisher Site | Google Scholar
  8. T. Wu, X. Yang, X. Zeng, and G. D. Eslick, “Traditional Chinese medicinal herbs in the treatment of patients with esophageal cancer, a systematic review,” Gastroenterology Clinics of North America, vol. 38, no. 1, pp. 153–167, 2009. View at: Publisher Site | Google Scholar
  9. Y. Jia, F. Huang, S. Zhang, and S.-W. Leung, “Is danshen (Salvia miltiorrhiza) dripping pill more effective than isosorbide dinitrate in treating angina pectoris? A systematic review of randomized controlled trials,” International Journal of Cardiology, vol. 157, no. 3, pp. 330–340, 2012. View at: Publisher Site | Google Scholar
  10. CDC and NCHS, “Underlying Cause of Death 1999–2013 on CDC WONDER Online Database,” August 2015, http://wonder.cdc.gov/ucd-icd10.html. View at: Google Scholar
  11. Z. Sun, “Atherosclerosis and atheroma plaque rupture: normal anatomy of vasa vasorum and their role associated with atherosclerosis,” The Scientific World Journal, vol. 2014, Article ID 285058, 6 pages, 2014. View at: Publisher Site | Google Scholar
  12. M. Rafieian-Kopaei, M. Setorki, M. Doudi, A. Baradaran, and H. Nasri, “Atherosclerosis: process, indicators, risk factors and new hopes,” International Journal of Preventive Medicine, vol. 5, no. 8, pp. 927–946, 2014. View at: Google Scholar
  13. P. Libby, “Inflammation in atherosclerosis,” Arteriosclerosis, Thrombosis, and Vascular Biology, vol. 32, no. 9, pp. 2045–2051, 2012. View at: Publisher Site | Google Scholar
  14. A. Gupta and D. A. Smith, “The 2013 American College of Cardiology/American Heart Association guidelines on treating blood cholesterol and assessing cardiovascular risk: a busy practitioner's guide,” Endocrinology and Metabolism Clinics of North America, vol. 43, no. 4, pp. 869–892, 2014. View at: Publisher Site | Google Scholar
  15. D. K. Arnett, R. A. Goodman, J. L. Halperin, J. L. Anderson, A. K. Parekh, and W. A. Zoghbi, “AHA/ACC/HHS strategies to enhance application of clinical practice guidelines in patients with cardiovascular disease and comorbid conditions: from the American Heart Association, American College of Cardiology, and US Department of Health and Human Services,” Circulation, vol. 130, no. 18, pp. 1662–1667, 2014. View at: Publisher Site | Google Scholar
  16. J. R. N. Nansseu and J. J. N. Noubiap, “Aspirin for primary prevention of cardiovascular disease,” Thrombosis Journal, vol. 13, no. 1, article 38, 2015. View at: Publisher Site | Google Scholar
  17. G. L. Jennings, “A new guideline on treatment of hypertension in those with coronary artery disease: scientific statement from the American Heart Association, American College of Cardiology, and American Society of Hypertension about treatment of hypertension in patients with coronary artery disease,” Heart, Lung & Circulation, vol. 24, no. 11, pp. 1037–1040, 2015. View at: Google Scholar
  18. Y. Liu, N. Ai, J. Liao, and X. Fan, “Transcriptomics: a sword to cut the Gordian knot of traditional Chinese medicine,” Biomarkers in Medicine, vol. 9, no. 11, pp. 1201–1213, 2015. View at: Publisher Site | Google Scholar
  19. S. Li, “Network systems underlying traditional Chinese medicine syndrome and herb formula,” Current Bioinformatics, vol. 4, no. 3, pp. 188–196, 2009. View at: Publisher Site | Google Scholar
  20. Z. Ma and M. Liang, “Review of reducing toxicity and increasing beneficial effects of TCM,” Journal of Liaoning University of Traditional Chinese Medicine, no. 6, pp. 187–190, 2011. View at: Google Scholar
  21. J. Qiu, “Traditional medicine: a culture in the balance,” Nature, vol. 448, no. 7150, pp. 126–128, 2007. View at: Publisher Site | Google Scholar
  22. S. Xutian, D. Cao, J. Wozniak, J. Junion, and J. Boisvert, “Comprehension of the unique characteristics of traditional Chinese medicine,” The American Journal of Chinese Medicine, vol. 40, no. 2, pp. 231–244, 2012. View at: Publisher Site | Google Scholar
  23. Y. C. Liu, The Essential Book of Traditional Chinese Medicine, Vol. 1: Theory, Columbia University Press, New York, NY, USA, 1988.
  24. Z. X. Zhou and X. Q. Ke, “Discussion of the seven features of compatibility of Chinese herb medicine,” Journal of Hubei Traditional Chinese Medicine, vol. 17, no. 118, pp. 24–25, 1995. View at: Google Scholar
  25. D. Bensky, S. Clavey, and E. Stoger, Chinese Herbal Medicine Materia Medica, Eastland Press, Seattle, Wash, USA, 3rd edition, 2004.
  26. Y. Chen, F. Lin, X. Liang, and R. Tan, “Application of Du Shen Tang, powder of Panax notoginseng, and cold compress in treatment of 30 cases of postpartum hemorrhage,” Journal of Emergency in Traditional Chinese Medicine, vol. 20, pp. 1523–1524, 2011. View at: Google Scholar
  27. X. Gong, “Thrombolytic therapy along with Du Shen Tang in the treatment of acute myocardial infarction,” Chinese Journal of Integrated Traditional and Western Medicine in Intensive and Critical Care, vol. 11, no. 2, pp. 126–127, 2004. View at: Google Scholar
  28. Z. Zhao, G. Cai, S. Xie, X. Zhou, and X. Hu, “Naval compression with root of Kansui plus intake of Du Shen Tang in treatment of cirrhosis with ascites,” Journal of Emergency in Traditional Chinese Medicine, vol. 19, no. 3, pp. 388–389, 2010. View at: Google Scholar
  29. W. Yang, “Effect of treating 67 cases of upper gastrointestinal bleeding with Du Shen Tang,” Gansu Journal of Traditional Chinese Medicine, vol. 7, no. 5, pp. 9–10, 1995. View at: Google Scholar
  30. D. Qin, “Si Ni Tang combining Du Shen Tang in treatment of 30 cases of congestive heart failure,” Henan Journal of Traditional Chinese Medicine, no. 8, pp. 1510–1511, 2014. View at: Google Scholar
  31. Y. Mao and G. Zhou, “Effects of compatibility of Rhubarb and Glauber on anthraquinone glycosides content in different proportions,” Journal of Jiangxi TCM, vol. 42, no. 2, pp. 60–61, 2011. View at: Google Scholar
  32. L. Wan, Z. Z. Lin, W. Liu, and Z. Liu, “Pharmacokinetic study on berberine in the extract of rhizoma coptidis-radix aucklandiae drug-pair in rats,” Chinese Journal of Modern Applied Pharmacy, vol. 26, no. 6, pp. 443–446, 2009. View at: Google Scholar
  33. M. Shong, J. Yu, and Z. Bao, “Compatibility of traditional Chinese medicine to reduce the toxicity and modern research progress,” Pharmacy and Clinics of Chinese Materia Medica, vol. 3, no. 2, pp. 51–53, 2012. View at: Google Scholar
  34. W. Long, X.-D. Zhang, H.-Y. Wu et al., “Study on incompatibility of traditional Chinese medicine: evidence from formula network, chemical space, and metabolism room,” Evidence-Based Complementary and Alternative Medicine, vol. 2013, Article ID 352145, 8 pages, 2013. View at: Publisher Site | Google Scholar
  35. J. J. Zhang, X. S. Fan, H. Yang, C. X. Jiang, Y. Li, and Z. H. Qi, “Review of eighteen incompatibility pairs of Veratrum nigrum and its drug incompatibility in TCM,” Journal of Traditional Chinese Medicine and Pharmacy, vol. 29, no. 9, pp. 2870–2873, 2014. View at: Google Scholar
  36. J. Dong and Y. Fan, “Compatibility of Chinese herb medicine and its connection with effects and toxicity,” Chinese Medical Pharmacy Journal, vol. 26, no. 3, pp. 618–619, 2008. View at: Google Scholar
  37. L. Wang, G.-B. Zhou, P. Liu et al., “Dissection of mechanisms of Chinese medicinal formula Realgar-Indigo naturalis as an effective treatment for promyelocytic leukemia,” Proceedings of the National Academy of Sciences of the United States of America, vol. 105, no. 12, pp. 4826–4831, 2008. View at: Publisher Site | Google Scholar
  38. X.-J. Lai, L. Z. Zhang, J.-S. Li et al., “Comparative pharmacokinetic and bioavailability studies of three salvianolic acids after the administration of Salviae miltiorrhizae alone or with synthetical borneol in rats,” Fitoterapia, vol. 82, no. 6, pp. 883–888, 2011. View at: Publisher Site | Google Scholar
  39. M. Li, Y. Z. Zhang, W. Wang et al., “Influence of borneol when combined with salvianolic acid B and saponins of panax notoginseng on the expression of vascular endothelial growth factor (VEGF) mRNA in brain tissue of rats with cerebral ischemia/reperfusion,” Chinese Journal of TCM WM Critical Care, vol. 12, no. 5, pp. 263–266, 2005. View at: Google Scholar
  40. C. Z. Liang, “Focus on the theory of precaution of disease in Tradition Chinese Medicine from the function of compound Danshen dripping pill to the heart and blood vessel's illness,” Chinese Archives of Traditional Chinese Medicine, vol. 26, no. 3, Article ID 643644, 2008. View at: Google Scholar
  41. Q. Zheng, C. C. Peng, M. L. Shen, and M. Yang, “Study on compatibility of Radix et Rhizoma Salviae miltiorrhizae and Radix et Rhizoma Notoginseng,” Chinese Journal of Experimental Traditional Medical Formulae, vol. 15, no. 2, pp. 83–86, 2009. View at: Google Scholar
  42. T. O. Cheng, “Cardiovascular effects of Danshen,” International Journal of Cardiology, vol. 121, no. 1, pp. 9–22, 2007. View at: Publisher Site | Google Scholar
  43. Y.-K. Li and L.-D. Li, “Urgency and necessity of standardisation of Chinese medicine with confusions of compound Danshen preparations,” Chinese Journal of Chinese Materia Medica, vol. 33, no. 4, pp. 349–352, 2008. View at: Google Scholar
  44. L. Zhou, Z. Zuo, and M. S. S. Chow, “Danshen: an overview of its chemistry, pharmacology, pharmacokinetics, and clinical use,” Journal of Clinical Pharmacology, vol. 45, no. 12, pp. 1345–1359, 2005. View at: Publisher Site | Google Scholar
  45. J. H.-C. Ho and C.-Y. Hong, “Salvianolic acids: small compounds with multiple mechanisms for cardiovascular protection,” Journal of Biomedical Science, vol. 18, article 30, 2011. View at: Publisher Site | Google Scholar
  46. C.-S. Zheng, X.-J. Xu, H.-Z. Ye et al., “Computational pharmacological comparison of Salvia miltiorrhiza and Panax notoginseng used in the therapy of cardiovascular diseases,” Experimental and Therapeutic Medicine, vol. 6, no. 5, pp. 1163–1168, 2013. View at: Publisher Site | Google Scholar
  47. X. D. Song, W. L. Zhu, R. An, Y. Li, and Z. Du, “Protective effect of Daming capsule against chronic cerebral ischemia,” BMC Complementary and Alternative Medicine, vol. 15, article 149, 2015. View at: Publisher Site | Google Scholar
  48. K. K.-K. Wong, M. T.-W. Ho, H. Q. Lin et al., “Cryptotanshinone, an acetylcholinesterase inhibitor from salvia miltiorrhiza, ameliorates scopolamine-induced amnesia in morris water maze task,” Planta Medica, vol. 76, no. 3, pp. 228–234, 2010. View at: Publisher Site | Google Scholar
  49. J. Zhou, X.-D. Qu, Z.-Y. Li et al., “Salvianolic acid B attenuates toxin-induced neuronal damage via Nrf2-dependent glial cells-mediated protective activity in Parkinson's disease models,” PLoS ONE, vol. 9, no. 7, Article ID e101668, 2014. View at: Publisher Site | Google Scholar
  50. X. H. Tian, W. J. Xue, and X. M. Ding, “Application of Danshen injection on early stage of renal transplantation,” Chinese Journal of Integrative Medicine, vol. 25, no. 5, pp. 404–407, 2005. View at: Google Scholar
  51. L. Gao, K. Yan, Y. Cui, G. Fan, and Y. Wang, “Protective effect of Salvia miltiorrhiza and Carthamus tinctorius extract against lipopolysaccharide-induced liver injury,” World Journal of Gastroenterology, vol. 21, no. 30, pp. 9079–9092, 2015. View at: Google Scholar
  52. Y. Zhang, P. X. Jiang, M. Ye, S.-H. Kim, C. Jiang, and J. X. Lü, “Tanshinones: sources, pharmacokinetics and anti-cancer activities,” International Journal of Molecular Sciences, vol. 13, no. 10, pp. 13621–13666, 2012. View at: Publisher Site | Google Scholar
  53. V. Nicolin, F. Dal Piaz, S. L. Nori, P. Narducci, and N. de Tommasi, “Inhibition of bone resorption by Tanshinone VI isolated from Salvia miltiorrhiza Bunge,” European Journal of Histochemistry, vol. 54, no. 2, pp. 104–106, 2010. View at: Google Scholar
  54. S. Gao, Z. Liu, H. Li, P. J. Little, P. Liu, and S. Xu, “Cardiovascular actions and therapeutic potential of tanshinone IIA,” Atherosclerosis, vol. 220, no. 1, pp. 3–10, 2012. View at: Publisher Site | Google Scholar
  55. D. Xu, P. Huang, Z. Yu, D. H. Xing, S. Ouyang, and G. Xing, “Efficacy and safety of panax notoginseng saponin therapy for acute intracerebral hemorrhage, meta-analysis, and mini review of potential mechanisms of action,” Frontiers in Neurology, vol. 5, article 274, 2015. View at: Publisher Site | Google Scholar
  56. Q. H. Shang, H. Xu, Z. L. Liu, K. Chen, and J. P. Liu, “Oral Panax notoginseng preparation for coronary heart disease: a systematic review of randomized controlled trials,” Evidence-Based Complementary and Alternative Medicine, vol. 2013, Article ID 940125, 12 pages, 2013. View at: Publisher Site | Google Scholar
  57. T. B. Ng, “Pharmacological activity of sanchi ginseng (Panax notoginseng),” Journal of Pharmacy and Pharmacology, vol. 58, no. 8, pp. 1007–1019, 2006. View at: Publisher Site | Google Scholar
  58. J. Q. Cao, P. Fu, and Y. Q. Zhao, “Isolation and identification of a new compound from acid hydrolysate of saponinin stems and leaves of Panax notoginseng,” Chinese Traditional and Herbal Drugs, vol. 44, no. 2, pp. 137–140, 2013. View at: Google Scholar
  59. Z. Cai, S. Hou, Y. Li et al., “Effect of borneol on the distribution of gastrodin to the brain in mice via oral administration,” Journal of Drug Targeting, vol. 16, no. 2, pp. 178–184, 2008. View at: Publisher Site | Google Scholar
  60. J.-P. Dai, J. Chen, Y.-F. Bei, B.-X. Han, and S. Wang, “Influence of borneol on primary mice oral fibroblasts: a penetration enhancer may be used in oral submucous fibrosis,” Journal of Oral Pathology and Medicine, vol. 38, no. 3, pp. 276–281, 2009. View at: Publisher Site | Google Scholar
  61. Y.-Y. Xiao, Q.-N. Ping, and Z.-P. Chen, “The enhancing effect of synthetical borneol on the absorption of tetramethylpyrazine phosphate in mouse,” International Journal of Pharmaceutics, vol. 337, no. 1-2, pp. 74–79, 2007. View at: Publisher Site | Google Scholar
  62. Z. Jiang, Y. Wang, X. Gao, H. Shang, and X. Wang, “The pharmacological actions of danshen ThemeD formulas,” in Dan Shen (Salvia miltiorrhiza) in Medicine, X. Yan, Ed., chapter 2, pp. 19–47, Springer, Dordrecht, The Netherlands, 2015. View at: Publisher Site | Google Scholar
  63. M. Nichols, N. Townsend, P. Scarborough, and M. Rayner, “Cardiovascular disease in Europe 2014: epidemiological update,” European Heart Journal, vol. 35, no. 42, pp. 2950–2959, 2014. View at: Publisher Site | Google Scholar
  64. Y. Yao, Y. Feng, and L. Wang, “Systematic review and meta-analysis of randomized controlled trials comparing compound danshen dripping pills and isosorbide dinitrate in treating angina pectoris,” International Journal of Cardiology, vol. 182, pp. 46–47, 2015. View at: Google Scholar
  65. Q.-X. Yue, F.-B. Xie, X.-Y. Song et al., “Proteomic studies on protective effects of salvianolic acids, notoginsengnosides and combination of salvianolic acids and notoginsengnosides against cardiac ischemic-reperfusion injury,” Journal of Ethnopharmacology, vol. 141, no. 2, pp. 659–667, 2012. View at: Publisher Site | Google Scholar
  66. X.-Y. Yang, N. Zhao, Y.-Y. Liu et al., “Inhibition of NADPH oxidase mediates protective effect of cardiotonic pills against rat heart ischemia/reperfusion injury,” Evidence-Based Complementary and Alternative Medicine, vol. 2013, Article ID 728020, 15 pages, 2013. View at: Publisher Site | Google Scholar
  67. H.-Y. Fan, F.-H. Fu, M.-Y. Yang, H. Xu, A.-H. Zhang, and K. Liu, “Antiplatelet and antithrombotic activities of salvianolic acid A,” Thrombosis Research, vol. 126, no. 1, pp. e17–e22, 2010. View at: Publisher Site | Google Scholar
  68. F. Maione, V. De Feo, E. Caiazzo, L. De Martino, C. Cicala, and N. Mascolo, “Tanshinone IIA, a major component of Salvia milthorriza Bunge, inhibits platelet activation via Erk-2 signaling pathway,” Journal of Ethnopharmacology, vol. 155, no. 2, pp. 1236–1242, 2014. View at: Publisher Site | Google Scholar
  69. F. F. Y. Lam, S. Y. Deng, E. S. K. Ng et al., “Mechanisms of the relaxant effect of a Danshen and Gegen formulation on rat isolated cerebral basilar artery,” Journal of Ethnopharmacology, vol. 132, no. 1, pp. 186–192, 2010. View at: Publisher Site | Google Scholar
  70. C. M. Koon, K. S. woo, P. C. Leung, and K. P. Fung, “Salviae Miltiorrhizae Radix and Puerariae Lobatae Radi herb formula mediate anti-arthrosclerosis by modulating key atherogenic events both in vascular smooth muscle cells and endothelial cell,” Journal of Ethnopharmacology, vol. 138, no. 1, pp. 175–183, 2011. View at: Google Scholar
  71. G. Liu, B. Wang, J. Zhang, H. Jiang, and F. Liu, “Total panax notoginsenosides prevent atherosclerosis in apolipoprotein E-knockout mice: role of downregulation of CD40 and MMP-9 expression,” Journal of Ethnopharmacology, vol. 126, no. 2, pp. 350–354, 2009. View at: Publisher Site | Google Scholar
  72. L. Xue, Z. Wu, X.-P. Ji, X.-Q. Gao, and Y.-H. Guo, “Effect and mechanism of salvianolic acid B on the myocardial ischemia-reperfusion injury in rats,” Asian Pacific Journal of Tropical Medicine, vol. 7, no. 4, pp. 280–284, 2014. View at: Publisher Site | Google Scholar
  73. L. Ma, X. Zhang, H. Guo, and Y. Gan, “Determination of four water-soluble compounds in Salvia miltiorrhiza Bunge by high-performance liquid chromatography with a coulometric electrode array system,” Journal of Chromatography B: Analytical Technologies in the Biomedical and Life Sciences, vol. 833, no. 2, pp. 260–263, 2006. View at: Publisher Site | Google Scholar
  74. P. Li, S.-P. Li, F.-Q. Yang, and Y.-T. Wang, “Simultaneous determination of four tanshinones in Salvia miltiorrhiza by pressurized liquid extraction and capillary electrochromatography,” Journal of Separation Science, vol. 30, no. 6, pp. 900–905, 2007. View at: Publisher Site | Google Scholar
  75. P. Li, G. Xu, S.-P. Li et al., “Optimizing ultraperformance liquid chromatographic analysis of 10 diterpenoid compounds in Salvia miltiorrhiza using central composite design,” Journal of Agricultural and Food Chemistry, vol. 56, no. 4, pp. 1164–1171, 2008. View at: Publisher Site | Google Scholar
  76. J.-B. Wan, P. Li, S. Li, Y. Wang, T. T.-X. Dong, and K. W.-K. Tsim, “Simultaneous determination of 11 saponins in Panax notoginseng using HPLC-ELSD and pressurized liquid extraction,” Journal of Separation Science, vol. 29, no. 14, pp. 2190–2196, 2006. View at: Publisher Site | Google Scholar
  77. G. F. Zeng, Q. Xu, H. B. Xiao, and X. M. Liang, “Influence of compatibility ratio of Fufang Danshen on the dissolution of Danshen compositions,” Chinese Journal of Chromatography, vol. 22, no. 2, pp. 141–143, 2004. View at: Google Scholar
  78. S. H. Li, K. L. Xu, and Y. Z. Xu, “The study on the interaction between Danshen and Sanqi in Compound Danshen formula,” Progress in Natural Sciences, vol. 13, no. 2, pp. 186–189, 2003. View at: Google Scholar
  79. W. Long, S.-C. Zhang, L. Wen, L. Mu, F. Yang, and G. Chen, “In vivo distribution and pharmacokinetics of multiple active components from Danshen and Sanqi and their combination via inner ear administration,” Journal of Ethnopharmacology, vol. 156, pp. 199–208, 2014. View at: Publisher Site | Google Scholar
  80. S.-Y. Zhang, M. Song, J.-G. Lu, and T.-J. Hang, “Effects of combination of Salvia miltiorrhiza and Panax notoginseng on the pharmacokinetics of their major bioactive components in Beagle dog,” Acta Pharmaceutica Sinica, vol. 45, no. 11, pp. 1433–1439, 2010. View at: Google Scholar
  81. H. C. Shang, B. L. Zhang, and X. M. Gao, “Characteristics of compatibility Danshen and Sanqi and new drug design accordingly,” Herald of Technology, vol. 5, no. 24, pp. 25–27, 2006. View at: Google Scholar
  82. X. Wang, Y. Wang, M. Jiang et al., “Differential cardioprotective effects of salvianolic acid and tanshinone on acute myocardial infarction are mediated by unique signaling pathways,” Journal of Ethnopharmacology, vol. 135, no. 3, pp. 662–671, 2011. View at: Publisher Site | Google Scholar
  83. Y. Deng, T. Zhang, F. Teng et al., “Ginsenoside Rg1 and Rb1, in combination with salvianolic acid B, play different roles in myocardial infarction in rats,” Journal of the Chinese Medical Association, vol. 78, no. 2, pp. 114–120, 2015. View at: Publisher Site | Google Scholar
  84. Y. L. Lu, X. Liu, X. Liang, L. Xiang, and W. Zhang, “Metabolomic strategy to study therapeutic and synergistic effects of tanshinone IIA, salvianolic acid B and ginsenoside Rb1 in myocardial ischemia rats,” Journal of Ethnopharmacology, vol. 134, no. 1, pp. 45–49, 2011. View at: Publisher Site | Google Scholar
  85. G. F. Zeng, X. Jian, P. Li, S. P. Fu, H. B. Xiao, and X. M. Liang, “Protective effects of different ratios of danshen to sanqi on hypoxia and reoxygenation-induced HUVECs injury,” Fine Chemicals, vol. 23, no. 2, pp. 126–129, 2006. View at: Google Scholar
  86. T. Liu, C. L. Qin, and B. L. Zhang, “Effects of combinatory usage of Danshen and Sanqi on platelet adhesion and aggregation,” Journal of Chinese Herbal Medicines, vol. 27, no. 8, pp. 609–611, 2002. View at: Google Scholar
  87. Y. Yao, W.-Y. Wu, A.-H. Liu et al., “Interaction of salvianolic acids and notoginsengnosides in inhibition of ADP-induced platelet aggregation,” The American Journal of Chinese Medicine, vol. 36, no. 2, pp. 313–328, 2008. View at: Publisher Site | Google Scholar
  88. S. Wang, W. Zang, X. Zhao et al., “Effects of borneol on pharmacokinetics and tissue distribution of notoginsenoside R1 and ginsenosides Rg1 and Re in Panax notoginseng in rabbits,” Journal of Analytical Methods in Chemistry, vol. 2013, Article ID 706723, 11 pages, 2013. View at: Publisher Site | Google Scholar
  89. P. Liu, H. Yang, F. Long et al., “Bioactive equivalence of combinatorial components identified in screening of an herbal medicine,” Pharmaceutical Research, vol. 31, no. 7, pp. 1788–1800, 2014. View at: Publisher Site | Google Scholar
  90. S. Bent, “Herbal medicine in the United States: review of efficacy, safety, and regulation: grand rounds at University of California, San Francisco Medical Center,” Journal of General Internal Medicine, vol. 23, no. 6, pp. 854–859, 2008. View at: Publisher Site | Google Scholar
  91. M. L. Chavez, M. A. Jordan, and P. I. Chavez, “Evidence-based drug-herbal interactions,” Life Sciences, vol. 78, no. 18, pp. 2146–2157, 2006. View at: Publisher Site | Google Scholar
  92. M.-Z. Liu, Y.-L. Zhang, M.-Z. Zeng et al., “Pharmacogenomics and herb-drug interactions: merge of future and tradition,” Evidence-Based Complementary and Alternative Medicine, vol. 2015, Article ID 321091, 8 pages, 2015. View at: Publisher Site | Google Scholar
  93. S. J. Brantley, A. A. Argikar, Y. S. Lin, S. Nagar, and M. F. Paine, “Herb-drug interactions: challenges and opportunities for improved predictions,” Drug Metabolism and Disposition, vol. 42, no. 3, pp. 301–317, 2014. View at: Publisher Site | Google Scholar
  94. Y. Chu, L. Zhang, X.-Y. Wang, J.-H. Guo, Z.-X. Guo, and X.-H. Ma, “The effect of Compound Danshen Dripping Pills, a Chinese herb medicine, on the pharmacokinetics and pharmacodynamics of warfarin in rats,” Journal of Ethnopharmacology, vol. 137, no. 3, pp. 1457–1461, 2011. View at: Publisher Site | Google Scholar
  95. P. Wang, H. Sun, L. Yang et al., “Absence of an effect of t89 on the steady-state pharmacokinetics and pharmacodynamics of warfarin in healthy volunteers,” Journal of Clinical Pharmacology, vol. 54, no. 2, pp. 234–239, 2014. View at: Publisher Site | Google Scholar

Copyright © 2016 Xuefeng Su et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

More related articles

4659 Views | 898 Downloads | 6 Citations
 PDF  Download Citation  Citation
 Download other formatsMore
 Order printed copiesOrder

Related articles

We are committed to sharing findings related to COVID-19 as quickly and safely as possible. Any author submitting a COVID-19 paper should notify us at help@hindawi.com to ensure their research is fast-tracked and made available on a preprint server as soon as possible. We will be providing unlimited waivers of publication charges for accepted articles related to COVID-19. Sign up here as a reviewer to help fast-track new submissions.