Evidence-Based Complementary and Alternative Medicine

Evidence-Based Complementary and Alternative Medicine / 2020 / Article

Research Article | Open Access

Volume 2020 |Article ID 9185707 | 9 pages | https://doi.org/10.1155/2020/9185707

Antiarrhythmic Mechanisms of Chinese Herbal Medicine Dingji Fumai Decoction

Academic Editor: Mario Ledda
Received13 Jun 2019
Revised16 Jan 2020
Accepted29 Jan 2020
Published20 Mar 2020

Abstract

Background. Dingji Fumai decoction (DFD) is used to treat ventricular arrhythmia, and it has provided a very good curative effect. However, its cellular electrophysiological mechanism is unknown. Methods. Electrocardiogram was recorded, and oxidative stress response and ion-channel-related molecules were detected in rats with barium chloride- and aconitine-induced ventricular arrhythmia. Moreover, whole-cell patch-clamp assay was used to investigate the inhibitory effect of DFD on Nav1.5 in Chinese hamster ovary cells. Results. DFD prolonged the occurrence time and shortened the duration of ventricular arrhythmia, decreased the malondialdehyde and increased the superoxide dismutase, and alleviated the activation of Na+-K+-ATPase and connexin-43. DFD suppressed Nav1.5dose-dependently with an IC50 of 24.0 ± 2.4 mg/mL. Conclusions. The clinical antiarrhythmic mechanisms of DFD are based on its antioxidant potential, alleviation of Na+-K+-ATPase and connexin-43, and class I antiarrhythmic properties by suppressing Nav1.5dose-dependently with an IC50 of 24.0 ± 2.4 mg/mL.

1. Introduction

Cardiac arrhythmia is a group of conditions in which the heart beats irregularly [1]. Although some arrhythmias are not serious because many arrhythmic patients have no symptoms, some patients are prone to developing fatal or nonfatal complications, including heart failure, stroke, and cardiac arrest.

A large number of ongoing studies have attempted to gain a better understanding of cardiac arrhythmia [2] and have found solutions to cure it. Pharmaceutical agents that work well and have fewer side effects are also being explored; however, the progress is far from satisfactory [3, 4]. Drug development for ion channels has been relatively mature for nearly half a century, but the results of new drugs are not very encouraging because of the adverse reactions [5].

Dingji Fumai decoction (DFD) is an empirical prescription developed by Professor Luo, a national tutor, according to the basic theory of traditional Chinese medicine for the treatment of palpitation (also known as arrhythmia in modern medicine). DFD, consisting of Chuanxiong Rhizoma (Chuanxiong), Jujubae Fructus (Dazao), Poria cocos (Schw.) Wolf (Fuling), Cinnamomi Ramulus (Guizhi), Silktree Albizia Bark (Hehuanpi), Osdraconis (Fossiliaossiamastodi) (Longgu), Ostrea Gigas Thunberg (Muli), Ziziphi Spinosae Semen (Suanzaoren), Radix Polygalae (Yuanzhi), and Licorice (Gancao), is a multiherbal medicine for ventricular arrhythmia (VA), especially ventricular premature contraction (VPC) [6]. Its co-components with Xinsuning are Poria Cocos (Schw.) Wolf and Licorice, which significantly restrain arrhythmias induced by the chemical reagents [7]. Our previous research showed that DFD combined with metoprolol is more effective than metoprolol alone in the treatment of VPC, and there are no side effects [6]. Here, we report the effect of DFD on the electrocardiogram (ECG) of rats with barium chloride- and aconitine-induced VA, antioxygen free radical, Na+-K+-ATPase and connexin-43 (Cx43), and Nav1.5 sodium channel to elicit the antiarrhythmic mechanisms of DFD to provide counseling for clinicians and clinical researchers. We also hope to make a contribution to the mechanisms study of the clinically safe and effective multicomponent Chinese herbal medicine.

2. Methods

2.1. Reagents and Animals

Chinese herbs that constitute DFD were provided by the Traditional Chinese Medicine Pharmacy, Hospital (T.C.M.) Affiliated to Southwest Medical University (Luzhou, China) and were authenticated by two deputy director pharmacists. Metoprolol was purchased from AstraZeneca (London, England). Aconitine and barium chloride were purchased from Must Biotechnology (Chengdu, China) and Thermo Fisher Scientific (Heysham, England), respectively. All other chemicals were purchased from Sigma-Aldrich (St. Louis, MO, USA). Sprague-Dawley rats (180 g–220 g), obtained from the Animal Experiments Center of Southwest Medical University, were housed under standard conditions. All 40 rats were randomly divided into the following 4 groups: DFD group treated by gavage of 17.6 g/kg DFD [8], metoprolol group treated by gavage of 5.2 mg/kg metoprolol, and blank group and control group treated by gavage of 10 mg/kg normal saline once a day for 14 days. At the end of the experiment, all rats were killed by neck fracture. All experiments were reviewed and approved by the Ethics Committee on Animal Experiments and were carried out under the Guidelines for Animal Experiments at the Animal Experiments Center of Southwest Medical University (SCXK2013-17).

2.2. ECG Recording

The animal model was established based on previous studies [2, 9]. In brief, rats were anesthetized with 1% pentobarbital 30 mg/kg intraperitoneally, and the anesthetized rats were fixed on the plank in a prone position. Acupuncture needles were inserted subcutaneously into the medial part of limbs of rats to connect the electrodes and BL-420F Biological function experiment system (Taimeng, Chengdu, China). The normal II lead ECG was recorded, and the baseline was adjusted to zero. After the ECG was stable, rats in the other three groups, except those in the blank group, were immediately injected with either 0.4% barium chloride 4 mg/kg or 0. 001% aconitine 30 ug/kg through the caudal vein, and the same volume of 0.9% normal saline was injected into rats in the blank group. Finally, ECGs were recorded for 20 minutes. The following parameters were measured: types, occurrence, and duration of various VAs.

2.3. Detection of Molecules

Abdominal aorta blood samples were taken and freeze-thawed; and heart tissues were mixed with 10-fold volume PBS, freeze-thawed thrice, and crushed by a homogenizer. Then all specimens were centrifuged at 10 000 g for 8 min, and detection of malondialdehyde (MDA, one of the most important products of membrane lipid peroxidation) and superoxide dismutase (SOD, the natural enemy of oxygen free radicals) in the supernatant of blood samples and Na+-K+-ATPase in the supernatant of heart tissues was performed using the corresponding assay kit (Jiancheng, Nanjing, China).

2.4. Immunohistochemistry Assays

Before immersion in 0.05 mol/L PBS containing 30% sucrose for cryoprotection, heart tissues were fixed with 4% paraformaldehyde for 24 h. Then, the frozen tissues were cut into 25 μm sections for immunohistochemical staining using a Cx43 polyclonal antibody (Abcam, Cambridge, UK). Positive cells were observed with an Olympus microscope (Tokyo, Japan), and six fields were randomly selected to record the number of positive cells in each group.

2.5. Cell Culture

The Chinese hamster ovary (CHO) cell line stably expressing human cardiac Nav1.5 channel (Haiwei, Qingdao, China) was grown in F-12 Nutrient Mixture (Gibco, California, USA) containing 10% fetal bovine serum (FBS, Gibco) and 600 μg/mL G-418 (Gibco) at 37°C in 5% CO2-enriched air. In each experiment, a coverslip was removed and cleaned twice with bath solution, and then it was placed in an inverted microscope stage. Nav1.5 current was recorded by the whole-cell patch-clamp technique.

2.6. Solutions and Materials

The standard bath solution contained the following (in mmol/L) : NaCl 137, KCl 4, CaCl2 1.8, MgCl2 1, glucose 10, and HEPES 10, while the standard pipette solution contained the following (in mmol/L) : KF 100, KCl 40, MgCl2 2, EGTA 5, and HEPES 10. The pH was adjusted to 7.4 with NaOH and 7.2 with KOH, respectively, and the osmolality was all adjusted to 300 mOsm with sucrose.

Chinese herbs that constituted DFD were soaked in an eightfold volume distilled water at room temperature (20°C–25°C) for 1 h and filtered for 30 min, and then sixfold volume distilled water was added to the filter residue for 30 min filtration. The filtrate obtained after two sessions of decoction before and after merging was concentrated under vacuum, filtered by 0.22 μm filter, and used as a stock solution of 2.4103 mg/mL, which was frozen and stored at –80°C after sterilization. Then, the herbs were diluted with bath solution to obtain the desired concentrations.

Lidocaine (Sigma-Aldrich) was dissolved with dimethyl sulfoxide to obtain 100 mmol/L stock solution, which was stored at –20°C, and then it was diluted with the extracellular solution to achieve 0.1 mmol/L as the positive control. At the final dilution, dimethyl sulfoxide concentration was less than 0.1%, which had no effect on Na+ current [10].

2.7. Patch-Clamp Recording

The experiments were conducted at room temperature and performed as described previously with some modifications [10]. The borosilicate glass microelectrode tip had a resistance of 1–2 MΩ. After whole-cell recordings were achieved, the capacitance and resistance were compensated. The current signal was filtered at 8 kHz and sampled at 10 kHz. After perfusing the cells with bath solution for about 10 min to stabilize Na+ current, the bath solution was transferred to either the control or the compound-containing solution.

2.8. Statistical Analysis

Differences between two groups were analyzed by Student’s two-tailed t-test, and multiple groups were analyzed by one-way analysis of variance (SPSS, Inc., Chicago, IL, USA). values less than 0.05 were considered statistically significant.

3. Results

3.1. DFD Prolonged the Occurrence Time and Shortened the Duration of VA

Firstly, experiments were carried out to test the effect of DFD on ECG after dose conversion from human to animal studies [8]. There were no arrhythmias in the blank group. In rats with barium chloride-induced VA, VPC occurred in all cases (Figures 1(a) and 1(b)). Compared with the control group, DFD and metoprolol prolonged the occurrence and shortened the duration of VA. The time did not show any significant difference between the DFD group and the metoprolol group (Figure 1(c)).

Besides, in rats with aconitine-induced VA, VPC, ventricular tachycardia (VT), and ventricular fibrillation (VF) occurred successively (Figures 1(d) and 1(e)). Compared with the control group, in the same manner, DFD and metoprolol prolonged the occurrence of arrhythmia. The time did not show any significant alteration between the DFD group and the metoprolol group (Figure 1(f)).

3.2. DFD Had the Effect of Antioxygen Free Radicals

The expression levels of oxidative stress response-related molecules, MDA and SOD, in the serum of rats with barium chloride-induced VA were changed 1.7-fold and 0.8-fold, respectively, compared with those in the blank group. The administration of DFD and metoprolol alleviated these changes (Figures 2(a) and 2(b)). Similar results were obtained in rats with aconitine-induced VA (Figures 2(a) and (b)).

3.3. DFD May Have an Effect on Ion Channels

The activity of Na+-K+-ATPase was detected. The activity of Na+-K+-ATPase was decreased 0.8-fold after barium chloride injection, and DFD and metoprolol treatment alleviated the decrease (Figure 2(c)). In addition, the results after aconitine injection were the same (Figure 2(c)). Cx43 was detected by immunohistochemical staining, and histological results were obtained by the pathologists from Southwest Medical University. The quantity of Cx43-positive cells was reduced in the barium chloride control group, the metoprolol group, and the DFD group by 23%, 20%, and 25%, respectively (Figures 2(d) and 2(e)). Moreover, the number of activated Cx43 was decreased by 1% after aconitine injection, and DFD and metoprolol alleviated the activation of Cx43-positive cardiac myocytes by 93% and 83%, respectively (Figures 2(d) and 2(e)).

3.4. DFD Inhibited the Sodium Current Dose-dependently

Different DFD concentrations, ranging from 0.8 to 24.0 mg/mL, inhibited the Nav1.5 current of CHO cells to varying degrees (Figure 3). The inhibition rate of 0.1 mmol/L lidocaine for Nav1.5 was 39.14 ± 3.96% (Figure 4(a)). The higher the concentration, the more obvious the inhibitory effect (Figure 4(b)). DFD suppressed Nav1.5dose-dependently with an IC50 of 24.0 ± 2.4 mg/mL (Figures 4(c) and (d)).

4. Discussion

Over time, the prevention and treatment of arrhythmias are evolving, and early medical therapy and ablation guided by electrophysiology have been replaced by implantable cardioverter defibrillators [11]. However, their relatively high cost limits their use and promotion, and thus, all patients are not benefitted. As the treatment of arrhythmias becomes increasingly diverse, the use of Chinese herbal medicines has spread from home to abroad and they are being widely and frequently used [12, 13]. Wenxin Keli and Shensong Yangxin capsules are commonly used [14], and their antiarrhythmic mechanisms are being discovered [1517]. DFD, as a noninvasive therapy, is widely used in hospitals and has a good curative effect [6]. Herein, we illustrated that DFD protected against the barium chloride- and aconitine-induced VA and oxygen free radicals. Moreover, we showed that the mitigation effects of DFD were mediated by inhibiting Nav1.5 current.

In the ECG study, we found that DFD prolonged the occurrence and shortened the duration of VA in rats with VA induced by barium chloride and aconitine. Therefore, we deduced that DFD may be related to inward rectifier potassium channel, and it can prevent and postpone arrhythmia by promoting K+ outflow and reducing intracellular positive potential and automaticity. It may also be associated with a fast Na+, and it may prevent arrhythmias by inhibiting Na+ influx and reducing the fast response of cellular autonomy. Studies have shown that oxidative stress is one of the causes of arrhythmias [18]. Our results showed that DFD may reduce the content of MDA and increase the activity of SOD in rats with VA, by having the effect of antioxidant free radicals to protect the cardiomyocytes.

Cardiomyocytes are almost entirely dependent on aerobic metabolism. Na+-K+-ATPase is an omnipresent biofilm enzyme system on the cell membrane of the body [19]. Na+-K+-ATPase can regulate the concentration of sodium/potassium ion in cells, thus maintaining the resting potential of cells. Maintaining the activity of Na+-K+-ATPase helps to maintain the normal physiological function of cells. While further exploring the mechanism of DFD in arrhythmia, we found that DFD can protect Na+-K+-ATPase, an important indicator to monitor the occurrence of VAs [20]. Cx43 is the most abundant protein in the formation of gap junction pores in cardiomyocytes, which plays a vital role in the propagation of normal action potentials [21]. The decrease in Cx43 can reduce the coupling between myocytes, and it can also lead to an uneven action potential duration, thus inducing VAs [22]. Both the quantity and distribution of Cx43 are likely to cause abnormal electrical conduction velocity and heterogeneity between ventricular myocytes, which is particularly likely to result in the occurrence of VAs. Moreover, lowering the intracellular redox potential increases the opening of Cx43 [23]. Our results showed that one of the mechanisms of DFD in preventing and postponing VAs may be achieved by increasing the expression of Cx43 protein in left ventricular myocytes. To further explore the electrophysiological mechanism of DFD in arrhythmia, we conducted a whole-cell patch-clamp experiment and found that DFD inhibited the Nav1.5dose-dependently with an IC50 of 24.0 ± 2.4 mg/mL. There is strong evidence that DFD is a clinically effective antiarrhythmic medicine for treating VPC [6]. Thus, we studied the effect of DFD in animal arrhythmia models, which provided valuable laboratory research data. Additionally, absence of Torsade de Pointes or other new types of arrhythmias and the dose-dependent effect indicates the safety property of DFD.

Ion channels are critical for all aspects of cardiac function, including rhythmicity and contractility [24]. Indeed, most antiarrhythmic drugs modulate ion channel conductivity [25]. The structures, voltage sensor movements, and regulation of ion channels have been reported [2628], which may help us to elucidate the disease mechanisms and potential therapeutic targets for future drug development. In this study, we determined the effect of DFD on Nav1.5 current, which generates cardiac action potentials and initiates the heartbeat [26], but we did not investigate the other ion channels, although other ion channels also play a role in arrhythmias. In view of the multicomponent nature of DFD, it may also affect other ion channels, like Xinsuning [7]. In our future report, we aim to show the multi-ion channel mechanism of DFD. In addition, with the development of mass spectrometry, multiple constituents of the components of DFD have been analyzed and characterized in recent years [2934]. Modern pharmacological studies have shown that the components of DFD have anti-inflammatory [3539], antioxidative stress [4042], and myocardial protection [4245] effects. Inflammation and oxidative stress are closely related to arrhythmia [4648]. Moreover, Radix Polygalae plays an antiarrhythmic role by inhibiting the triggered activities in cardiomyocytes [45]. All of these findings suggest the antiarrhythmic mechanisms of DFD. In the future research, we will use ultraperformance liquid chromatography-quadrupole time-of-flight mass spectrometry (UPLC-QTOF-MS) to further clarify and identify the multiple components of DFD.

The results presented in this study improved our understanding of the clinical antiarrhythmic action of DFD, which is harmonized to obtain the therapeutic efficacy without causing any side effects. It is known that arrhythmia is caused by other underlying heart diseases and is a multifactorial disease requiring multicomponent medication. In this study, we found that DFD, a multicomponent medicine, inhibits arrhythmias and displays clear cellular electrophysiological mechanisms that support its clinical efficacy, and the results are similar to the properties shown by antiarrhythmic chemical drugs, although the data present the overall effect of a multicomponent medicine.

5. Conclusions

DFD conclusively showed the mechanism of the class I antiarrhythmic properties and the safety profile. The discovery that DFD mitigates oxidative stress, alleviates the activation of Na+-K+-ATPase and Cx43, and blocks Nav1.5current shows the cellular electrophysiological mechanisms that support the clinical therapeutic effect of DFD.

Data Availability

The raw data used to support the findings of this study were supplied by Hui-Ling Liao under license and so cannot be made freely available. Requests for access to these data should be made to Hui-Ling Liao, liaohl@swmu.edu.cn.

Conflicts of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as potential conflicts of interest.

Acknowledgments

This study is conducted as a dissertation for degree of integrated traditional Chinese and western medicine. The authors thank Xue-Hui Fan from Key Laboratory of Medical Electrophysiology, Ministry of Education, and Institute of Cardiovascular Research, Southwest Medical University, for excellent technical assistance. This work was supported by Sichuan Science and Technology Program (grant no. 2019YJ0694), Joint Project of Southwest Medical University and Hospital (T.C.M.) Affiliated to Southwest Medical University (grant no. 2018XYLH-014), Chongqing Health Commission Program (grant no. ZY201602167), and Luzhou Science and Technology Program (grant no. 2016LZXNYD-J09).

References

  1. B. O’Rourke, T. Liu, and D. B. Foster, “Seeing the forest for the trees,” Circulation Research, vol. 119, no. 11, pp. 1170–1172, 2016. View at: Google Scholar
  2. M.-H. Tian, Y. Xiao, J.-J. Xue et al., “The expression of BNP, ET-1, and TGF-β1 in myocardium of rats with ventricular arrhythmias,” International Journal of Molecular Sciences, vol. 20, no. 23, 2019. View at: Publisher Site | Google Scholar
  3. J. N. Weiss, A. Garfinkel, S. Hrayr et al., “Perspective: a dynamics-based classification of ventricular arrhythmias,” Journal of Molecular and Cellular Cardiology, vol. 82, pp. 136–152, 2015. View at: Publisher Site | Google Scholar
  4. A. John Camm, “Hopes and disappointments with antiarrhythmic drugs,” International Journal of Cardiology, vol. 237, pp. 71–74, 2017. View at: Publisher Site | Google Scholar
  5. G. Frommeyer and L. Eckardt, “Drug-induced proarrhythmia: risk factors and electrophysiological mechanisms,” Nature Reviews Cardiology, vol. 13, no. 1, pp. 36–47, 2016. View at: Publisher Site | Google Scholar
  6. Bo Liang, L. Fu, F.-Hu Zou et al., “The efficacy and safety of Dingji Fumai Decoction combined with metoprolol in premature ventricular contractions: a randomized controlled clinical trial,” Medicine and Medical Sciences, vol. 7, no. 3, pp. 1–5, 2019. View at: Google Scholar
  7. T.-Yi Wang, W.-W. Xie, Yu Jia-Hui et al., “Ion channel targeted mechanisms of anti-arrhythmic Chinese herbal medicine xin su ning,” Front in Pharmacol, vol. 10, p. 70, 2019. View at: Publisher Site | Google Scholar
  8. Ji-H. Huang, X.-H. Huang, Z.-Y. Chen et al., “Dose conversion among different animals and healthy volunteers in pharmacological study,” Chinese Journal of Clinical Pharmacology and Therapeutics, no. 9, pp. 1069–1072, 2004. View at: Google Scholar
  9. B.-X. Liu, S. Li, Y. Su et al., “Comparative study of the protective effects of terfenadine and amiodarone on barium chloride/aconitine-induced ventricular arrhythmias in rats: a potential role of terfenadine,” Molecular Medicine Reports, vol. 10, no. 6, pp. 3217–3226, 2014. View at: Publisher Site | Google Scholar
  10. X. Qiao, G.-C. Sun, J. J. Clare et al., “Properties of human brain sodium channel α-subunits expressed in HEK293 cells and their modulation by carbamazepine, phenytoin and lamotrigine,” British Journal of Pharmacology, vol. 171, no. 4, pp. 1054–1067, 2014. View at: Publisher Site | Google Scholar
  11. W. J. McKenna, N. A. Asaad, and D. L. Jacoby, “Prediction of ventricular arrhythmia and sudden death in arrhythmogenic right ventricular cardiomyopathy,” European Heart Journal, vol. 40, no. 23, pp. 1859–1861, 2019. View at: Google Scholar
  12. X.-Yi Wang, Y. Wang, X.-Y. Feng et al., “Systematic review and meta-analysis of randomized controlled trials on Wenxin keli,” Drug Design Development & Therapy, vol. 10, pp. 3725–3736, 2016. View at: Publisher Site | Google Scholar
  13. Bo Liang, W.-L. Liang, and H.-L. Liao, “Efficacy and safety of Mahuang Fuzi Xixin Decoction on sick sinus syndrome: a meta - analysis,” TMR Integrative Medicine, vol. 2, no. 1, pp. 30–38, 2018. View at: Google Scholar
  14. Bo Liang, M.-T. Jing, and H.-L. Liao, “Research and prospective of traditional Chinese medicine on sodium ion channels,” Drug Combination Therapy, vol. 1, no. 1, pp. 2–8, 2019. View at: Google Scholar
  15. An-T. Luo, Z.-P. Liu, Z.-Z. Cao et al., “Wenxin Keli diminishes Ca2+ overload induced by hypoxia/reoxygenation in cardiomyocytes through inhibiting INaL and ICaL,” Pacing and Clinical Electrophysiology, vol. 40, no. 12, pp. 1412–1425, 2017. View at: Publisher Site | Google Scholar
  16. G. Tian, Y. Sun, S. Liu et al., “Therapeutic effects of wenxin keli in cardiovascular diseases: an experimental and mechanism overview,” Frontiers in Pharmacology, vol. 9, p. 1005, 2018. View at: Publisher Site | Google Scholar
  17. K. Zhang, L. Shi, H.-J. Tang et al., “Effect of shen song yang xin Capsule on myocardial electrophysiology of acute atrial fibrillation in canine model,” Chinese Medical Journal, vol. 130, no. 20, pp. 2513-2514, 2017. View at: Publisher Site | Google Scholar
  18. M. Zakkar, R. Ascione, A. F. James et al., “Inflammation, oxidative stress and postoperative atrial fibrillation in cardiac surgery,” Pharmacology and Therapeutics, vol. 154, pp. 13–20, 2015. View at: Publisher Site | Google Scholar
  19. G. Scheiner-Bobis, “The sodium pump. Its molecular properties and mechanics of ion transport,” European Journal of Biochemistry, vol. 269, no. 10, pp. 2424–2433, 2002. View at: Publisher Site | Google Scholar
  20. D. Noble and P. J. Noble, “Late sodium current in the pathophysiology of cardiovascular disease: consequences of sodium-calcium overload,” Heart., vol. 92, no. 4, pp. iv1–iv5, 2006. View at: Publisher Site | Google Scholar
  21. M. Delmar and N. Makita, “Cardiac connexins, mutations and arrhythmias,” Current Opinion in Cardiology, vol. 27, no. 3, pp. 236–241, 2012. View at: Publisher Site | Google Scholar
  22. X. Ai, W.-W. Zhao, and S. M. Pogwizd, “Connexin43 knockdown or overexpression modulates cell coupling in control and failing rabbit left ventricular myocytes,” Cardiovascular Research, vol. 85, no. 4, pp. 751–762, 2010. View at: Publisher Site | Google Scholar
  23. M. A. Retamal, K. A. Schalper, K. F. Shoji et al., “Opening of connexin 43 hemichannels is increased by lowering intracellular redox potential,” Proceedings of the National Academy of Sciences of the United States of America, vol. 104, no. 20, pp. 8322–8327, 2007. View at: Publisher Site | Google Scholar
  24. B. T. Priest and J. S. McDermott, “Cardiac ion channels,” Channels, vol. 9, no. 6, pp. 352–359, 2015. View at: Publisher Site | Google Scholar
  25. A. N. B. Arne, W. L. McKeithan, D. A. M. Feyen, and M. Mercola, “Using iPSC models to probe regulation of cardiac ion channel function,” Current Cardiology Reports, vol. 20, no. 7, p. 57, 2018. View at: Publisher Site | Google Scholar
  26. D.-H. Jiang, H. Shi, L. Tonggu et al., “Structure of the cardiac sodium channel,” Cell, vol. 180, no. 1, pp. 31326–31321, 2019. View at: Google Scholar
  27. C.-H. Lee and R. MacKinnon, “Voltage sensor movements during hyperpolarization in the HCN channel,” Cell, vol. 179, no. 7, Article ID e1587, pp. 1582–1589, 2019. View at: Publisher Site | Google Scholar
  28. C.-H. Lee and R. MacKinnon, “Structures of the human HCN1 hyperpolarization-activated channel,” Cell, vol. 168, no. 1-2, 2017. View at: Publisher Site | Google Scholar
  29. S. Wu, Li Guo, and F. Qiu, “Anti-migraine effect of the herbal combination of chuanxiong rhizoma and cyperi rhizoma and UPLC-MS/MS method for the simultaneous quantification of the active constituents in rat serum and cerebral cortex,” Molecules, vol. 24, no. 12, p. E2230, 2019. View at: Publisher Site | Google Scholar
  30. Li-X. Zhu, J. Xu, S.-J. Zhang et al., “Qualitatively and quantitatively comparing secondary metabolites in three medicinal parts derived from Poria cocos (Schw.) Wolf using UHPLC-QTOF-MS/MS-based chemical profiling,” Journal of Pharmaceutical and Biomedical Analysis, vol. 150, pp. 278–286, 2018. View at: Publisher Site | Google Scholar
  31. X.-H. Nost, E.-M. Pferschy-Wenzig, S. Nikles et al., “Identification of constituents affecting the secretion of pro-inflammatory cytokines in LPS-induced U937 cells by UHPLC-HRMS-based metabolic profiling of the traditional Chinese medicine formulation huangqi jianzhong tang,” Molecules, vol. 24, no. 17, 2019. View at: Publisher Site | Google Scholar
  32. O. Placide Note, L. Made Simo, J. Ngo Mbing et al., “Structural determination of two new acacic acid-type saponins from the stem barks of Albizia zygia (DC) J. F. Macbr,” Natural Product Research, vol. 33, no. 2, pp. 180–188, 2019. View at: Publisher Site | Google Scholar
  33. X.-C. Zhu, X. Liu, Ke Pei et al., “Development of an analytical strategy to identify and classify the global chemical constituents of Ziziphi Spinosae Semen by using UHPLC with quadrupole time-of-flight mass spectrometry combined with multiple data-processing approaches,” Journal of Separation Science, vol. 41, no. 17, pp. 3389–3396, 2018. View at: Publisher Site | Google Scholar
  34. G.-F. Feng, S. Liu, Zi-F. Pi et al., “Comprehensive characterization of in vivo metabolic profile of Polygalae radix based on ultra-high-performance liquid chromatography-tandem mass spectrometry,” Journal of Pharmaceutical and Biomedical Analysis, vol. 165, pp. 173–181, 2019. View at: Publisher Site | Google Scholar
  35. M. Wang, M.-J. Yao, J.-X. Liu et al., “Ligusticum chuanxiong exerts neuroprotection by promoting adult neurogenesis and inhibiting inflammation in the hippocampus of ME cerebral ischemia rats,” Journal of Ethnopharmacology, vol. 249, p. 112385, 2019. View at: Publisher Site | Google Scholar
  36. J.-Bo Xie, Li Guo, G.-C. Pang et al., “Modulation effect ofSemen Ziziphi Spinosaeextracts on IL-1β, IL-4, IL-6, IL-10, TNF-α and IFN-γ in mouse serum,” Natural Product Research, vol. 25, no. 4, pp. 464–467, 2011. View at: Publisher Site | Google Scholar
  37. N. Prakash Babu, P. Pandikumar, and S. Ignacimuthu, “Anti-inflammatory activity of Albizia lebbeck Benth., an ethnomedicinal plant, in acute and chronic animal models of inflammation,” Journal of Ethnopharmacology, vol. 125, no. 2, pp. 356–360, 2009. View at: Publisher Site | Google Scholar
  38. L. Jia, Q. Zhang, R.-L. Li et al., “The traditional uses, phytochemistry, pharmacology and toxicology of Cinnamomi ramulus: a review,” Journal of Pharmacy and Pharmacology, vol. 72, 2019. View at: Publisher Site | Google Scholar
  39. Wu-X. Zhang, Lu Chen, Li Peng et al., “Antidepressant and immunosuppressive activities of two polysaccharides from Poria cocos (Schw.) Wolf,” International Journal of Biological Macromolecules, vol. 120, no. Pt B, pp. 1696–1704, 2018. View at: Publisher Site | Google Scholar
  40. Y. Zhu, Ya-J. Zhang, X. Huang et al., “Z-Ligustilide protects vascular endothelial cells from oxidative stress and rescues high fat diet-induced atherosclerosis by activating multiple NRF2 downstream genes,” Atherosclerosis, vol. 284, pp. 110–120, 2019. View at: Publisher Site | Google Scholar
  41. H. Umar, D. Kavaz, and N. Rizaner, “Biosynthesis of zinc oxide nanoparticles using Albizia lebbeck stem bark, and evaluation of its antimicrobial, antioxidant, and cytotoxic activities on human breast cancer cell lines,” International Journal of Nanomedicine, vol. 14, pp. 87–100, 2019. View at: Publisher Site | Google Scholar
  42. D. Ahmed, V. Kumar, A. Verma et al., “Antidiabetic, renal/hepatic/pancreas/cardiac protective and antioxidant potential of methanol/dichloromethane extract of Albizzia Lebbeck Benth. stem bark (ALEx) on streptozotocin induced diabetic rats,” BMC Complementary and Alternative Medicine, vol. 14, p. 243, 2014. View at: Publisher Site | Google Scholar
  43. X.-S. Zhang, H.-W. Dong, Y. Liu et al., “Tetramethylpyrazine partially relieves hypoxia-caused damage of cardiomyocytes H9c2 by downregulation of miR-449a,” Journal of Cellular Physiology, vol. 234, 2019. View at: Publisher Site | Google Scholar
  44. Yu Wang, Bo Ding, D. Luo et al., “New triterpene glycosides from Ziziphi Spinosae semen,” Fitoterapia, vol. 90, pp. 185–191, 2013. View at: Publisher Site | Google Scholar
  45. Z.-H. Zhao, M.-F. Fang, D.-D. Xiao et al., “Potential antiarrhythmic effect of methyl 3,4,5-trimethoxycinnamate, a bioactive substance from roots of polygalae radix: suppression of triggered activities in rabbit myocytes,” Biological and Pharmaceutical Bulletin, vol. 36, no. 2, pp. 238–244, 2013. View at: Publisher Site | Google Scholar
  46. J. M. van Opbergen Chantal, M. Noorman, P. Anna et al., “Plakophilin-2 haploinsufficiency causes calcium handling deficits and modulates the cardiac response towards stress,” International Journal of Molecular Sciences, vol. 20, no. 17, p. E4076, 2019. View at: Publisher Site | Google Scholar
  47. P. Enea Lazzerini, P. Leopoldo Capecchi, and F. Laghi-Pasini, “Systemic inflammation and arrhythmic risk: lessons from rheumatoid arthritis,” European Heart Journal, vol. 38, no. 22, pp. 1717–1727, 2017. View at: Publisher Site | Google Scholar
  48. J. Slawik, L. Adrian, M. Hohl et al., “Irregular pacing of ventricular cardiomyocytes induces pro-fibrotic signalling involving paracrine effects of transforming growth factor beta and connective tissue growth factor,” European Journal of Heart Failure, vol. 21, no. 4, pp. 482–491, 2019. View at: Publisher Site | Google Scholar

Copyright © 2020 Bo Liang 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.


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