Bioactive Natural Molecules and Traditional Herbal Medicine in the Treatment of Airways DiseasesView this Special Issue
Research Article | Open Access
Cortex phellodendri Extract Relaxes Airway Smooth Muscle
Cortex phellodendri is used to reduce fever and remove dampness and toxin. Berberine is an active ingredient of C. phellodendri. Berberine from Argemone ochroleuca can relax airway smooth muscle (ASM); however, whether the nonberberine component of C. phellodendri has similar relaxant action was unclear. An n-butyl alcohol extract of C. phellodendri (NBAECP, nonberberine component) was prepared, which completely inhibits high K+- and acetylcholine- (ACH-) induced precontraction of airway smooth muscle in tracheal rings and lung slices from control and asthmatic mice, respectively. The contraction induced by high K+ was also blocked by nifedipine, a selective blocker of L-type Ca2+ channels. The ACH-induced contraction was partially inhibited by nifedipine and pyrazole 3, an inhibitor of TRPC3 and STIM/Orai channels. Taken together, our data demonstrate that NBAECP can relax ASM by inhibiting L-type Ca2+ channels and TRPC3 and/or STIM/Orai channels, suggesting that NBAECP could be developed to a new drug for relieving bronchospasm.
Asthma is a common chronic respiratory disease . Excessive airway obstruction is a cardinal symptom that results from the contraction of airway smooth muscle (ASM). In this study, we attempted to develop an effective and safe drug from bitter Chinese herbs to inhibit ASM contraction.
Cortex phellodendri, called Huang Bai in Chinese, which tasted bitter, is the dried bark of Phellodendron chinense Schneid. or Phellodendron amurense Rupr., which belongs to the group of Rutaceae arbor plants. It is bitter in flavor and cold in nature, categorized in kidney, urinary bladder, and large intestine meridians. The traditional functions are to clear heat, dry dampness, purge fire, and remove toxicity. It is one of fundamental traditional Chinese medicines. Previous study reported that C. phellodendri has many physiological activities, including antioxidant [2, 3], anti-inflammatory [4–6], antiulcer , and immune-stimulating properties , as well as neuroprotection and inhibition of coronavirus replication [9, 10]. Moreover, C. phellodendri combining with other herbs can reduce complications of corticosteroid-resistant asthma . Berberine is one active ingredient of C. phellodendri; berberine from Argemone ochroleuca was demonstrated to have a relaxant effect in guinea-pig ASM . However, whether the nonberberine component has similar relaxant action has not been investigated.
In the present study, we found that an n-butyl alcohol extract of C. phellodendri (NBAECP, nonberberine component) exerted inhibitory action on ASM contraction, and the underlying mechanism was also investigated.
2. Materials and Methods
2.1. C. phellodendri Extraction
C. phellodendri, bark of Phellodendron chinensis Schneid. (Rutaceae), were collected in Sichuan Province, China, and were authenticated by Professor Dr. Ding-Rong Wan of our university. A voucher specimen (SCUN201310010) is deposited at the Herbarium of College of Pharmacy, South-Central University for Nationalities, China.
Air-dried C. phellodendri (1 Kg) was milled into powder and immersed into 70% ethanol (5 L) for 24 h. The components in the mixture were extracted by hot reflux and were centrifuged. The supernatant was collected and evaporated to dryness under reduced pressure using a rotary evaporator to remove ethanol and get residues, which were immersed in a 2% HCl solution (1000 mL). The yellow precipitates (mainly berberine) were removed and the supernatants were consecutively extracted with petroleum ether, chloroform, ethyl acetate, and n-butyl alcohol. The n-butyl alcohol extract was further evaporated under reduced pressure, and the extraction yield was 1.5% of the raw material dry weight. The dried n-butyl alcohol extract of C. phellodendri (NBAECP) was dissolved in 3% DMSO for the experiments.
Nifedipine, acetylcholine chloride (ACH), and pyrazole 3 (Pyr 3) were purchased from Sigma Chemical Co. (St. Louis, MO, USA); DMEM was purchased from Gibco BRL Co. (Invitrogen Life Technologies, Carlsbad, CA, USA). Other chemicals were purchased from Sinopharm Chemical Reagent Co. (Shanghai, China).
Sexually mature male BALB/c mice were purchased from the Hubei Provincial Center for Disease Control and Prevention (Wuhan, China). The mice were housed at room temperature (20–25°C) and constant humidity (50–60%) under a 12 h light-dark cycle in an SPF grade animal facility. The experiments on animals were approved by the Animal Care and Ethics Committee of the South-Central University for Nationalities and conformed to the guidelines of the Institutional Animal Care and Use Committee of the South-Central University for Nationalities (QHL-6, 12-10-2013).
2.4. Experimental Asthma Model in Mice
Asthmatic mice were prepared as described previously . Briefly, mice were sensitized by intraperitoneal injection administration of 0.2 mL of 0.9% saline solution containing 0.6 mg OVA and 0.4 mg of adjuvant aluminum hydroxide on days 1 and 8; then, the mice were challenged from days 15 through 19 by daily intranasal instillation of 50 μL of OVA solution (3 mg/mL). Control mice were sensitized and challenged by identical vehicle media.
2.5. Tracheal ASM Contraction Measurement
Mouse ASM contraction was measured as previously described . Adult male BALB/c mice were sacrificed by an intraperitoneal injection of sodium pentobarbital (150 mg/kg), and their tracheae were isolated and quickly transferred to ice cold PSS (composition in mM: NaCl 135, KCl 5, MgCl2 1, CaCl2 2, HEPES 10, glucose 10, pH 7.4). The connective tissue was removed, and tracheal rings (~5 mm) were cut from the bottom of the tracheae. Each ring was mounted with a preload of 0.5 g in an organ bath with a 10 mL capacity containing PSS bubbled with 95% O2 and 5% CO2 at 37°C. The rings were equilibrated for 60 min, precontracted with high K+ (80 mM) or ACH (10−4 M), washed, and rested for a total of 3 times. The experiments were performed following an additional 30 min rest.
2.6. Bronchial ASM Contraction Measurement
Lung slices were prepared according to a previous report . Lung slices were placed in a chamber and were held with a small nylon mesh. Perfusion was maintained in Hanks’ balanced salt solution (HBSS) at a rate of ~800 μL/min. HBSS was supplemented with 20 mM HEPES buffer (composition in mM: NaCl 137.93, KCl 5.33, NaHCO3 4.17, CaCl2 1.26, MgCl2 0.493, MgSO4 0.407, KH2PO 0.4414, Na2HPO4 0.338, and D-glucose 5.56) and adjusted to a pH of 7.4. Images of lung slices under 10x objective were acquired at the rate of 30 frames/min using an LSM 700 laser confocal microscope (Carl Zeiss, Goettingen, Germany). The cross-sectional area of the bronchial lumen was measured using Zen 2010 software (Carl Zeiss, Goettingen, Germany). The experiments were performed at room temperature.
2.7. Data Analysis
The results are expressed as the mean ± SEM. Comparisons of 2 groups were performed using Student’s t-test. Differences with were considered significant.
3.1. NBAECP Inhibits High K+-Induced Tracheal Smooth Muscle Contraction
To observe the effect of NBAECP on the contraction of airway smooth muscle (ASM), the tracheal rings (TRs) from healthy mice (i.e., controls) were contracted using high K+. Following the increase in the K+ concentration from 10 to 80 mM, the TRs exhibited dose-dependent contraction (Figure 1(a)). Upon the contraction reaching the maximum (at 80 mM K+), NBAECP was added. The contraction was inhibited in a dose-dependent manner. An identical experiment was also performed in a TR from an asthmatic model mouse, and similar results were observed (Figure 1(b)). NBAECP-induced relaxation in both control and asthmatic TRs was analyzed, and the values of half maximal inhibitory concentration (IC50) were calculated (Figure 1(c)). There were no significant differences between the two traces and the values of IC50. These results indicated that NBAECP could inhibit agonist-induced sustained contraction of control and asthmatic ASM.
3.2. NBAECP Blocks ACH-Induced Tracheal Smooth Muscle Contraction
To know whether NBAECP is capable of inhibiting another agonist-induced precontraction in ASM, healthy TRs were contracted using ACH. Upon the contraction reaching the maximum, NBAECP was added (Figure 2(a)). Similar dose-dependent relaxation responses occurred. Moreover, these responses existed in asthmatic TRs (Figure 2(b)). The dose-relaxation relationships and IC50 values of NBAECP were analyzed (Figure 2(c)), and they did not show differences between the control and asthmatic TRs. These experiments demonstrated that NBAECP could also inhibit ACH-induced precontraction in control and asthmatic ASM.
Were these relaxation responses also mediated by L-type Ca2+ channels? To answer this question, TRs from healthy and asthmatic mice were precontracted with ACH, and 10 μM nifedipine, a selective blocker of voltage-dependent L-type Ca2+ channels (VDCCs), was then added (Figures 3(a) and 3(b)). Following the addition of nifedipine, the contractions were partially inhibited. The resistant components were further blocked by NBAECP. The inhibitions induced by nifedipine and NBAECP were not different between the control and asthmatic TRs (Figure 3(c)).
To further investigate the underlying mechanism of NBAECP-induced relaxation of the nifedipine-resistant component, TRs were incubated with 10 μM nifedipine for 10 min and contracted using ACH, and we then observed the action of Pyr 3 (an inhibitor of TRPC3 and STIM/Orai channels). The results showed that Pyr 3 induced partial relaxation, and the remaining contractions were completely blocked by NBAECP (Figures 4(a) and 4(b)); however, Pyr 3-induced relaxation in asthmatic TRs was markedly greater than in the controls (Figure 4(c)).
Taken together, these results indicated that NBAECP-induced relaxation responses were mediated by L-type Ca2+, TRPC3, and/or STIM/Orai channels.
3.3. NBAECP Inhibits Bronchial Smooth Muscle Contraction
To define whether NBAECP has similar relaxant action on bronchial smooth muscle, lung slices were cut, and the cross-sectional area of the airway lumen was measured. The area of the airway lumen from healthy mice markedly decreased following application of 100 μM ACH; however, it was restored upon addition of 3.16 mg/mL NBAECP (Figure 5(a)). Identical experiments were conducted in lung slices from asthmatic mice, and similar phenomena were observed (Figure 5(b)). The summary data are shown in Figure 5(c). These results indicated that NBAECP had similar relaxant action on bronchial smooth muscle.
In the present study, our data demonstrate that NBAECP can inhibit L-type Ca2+ channels, blocking high K+-induced contractions in healthy and asthmatic airway smooth muscle and additionally inhibiting TRPC3 and/or STIM/Orai channels to reduce ACH-induced contractions in both types of airway smooth muscle. These results indicate that NBAECP could be a new bronchodilator for the treatment of asthma.
The purpose of this study was to find bronchodilators among Chinese medicines. We extracted a component (NBAECP, nonberberine active ingredient) from C. phellodendri. To investigate whether NBAECP has relaxant action, we used high K+ and ACH to contract airway smooth muscle and then observed the effect of NBAECP. NBAECP totally relaxed high K+-induced precontractions (Figure 1). High K+ could induce membrane depolarization, resulting in the activation of voltage-dependent L-type Ca2+ channels (VDCCs) . The channels then mediated Ca2+ influx, resulting in intracellular Ca2+ concentration increases, leading to muscle contraction. Nifedipine, a selective blocker of VDCCs, completely blocked high K+-induced contractions. This phenomenon was observed in our previous study [14, 17]. These results indicated that high K+-induced contractions completely depended on L-type Ca2+ channel-mediated Ca2+ influx. Thus, NBAECP-induced complete inhibition of high K+-induced contraction due to NBAECP resulted in the inhibition of L-type Ca2+ channels, thus terminating Ca2+ influx. However, the inhibitory mechanism of NBAECP on L-type Ca2+ channels must be further investigated.
Airway smooth muscle expresses the muscarinic (M) receptor family, which includes 5 subtypes (M1–M5) . Among them, G protein-coupled M3 plays a more important role in the contraction of airway smooth muscle . Stimulation of M3 by agonists results in intracellular Ca2+ release from the sarcoplasmic reticulum (SR) via the PLC-IP3-IP3R pathway . This leads to intracellular Ca2+ concentrations increasing and further triggering airway smooth muscle contraction. However, this pathway only mediates transient contractions , while the sustained contraction depends on Ca2+ influx from the extracellular side and/or Ca2+ sensitization [22, 23]. Hence, the M3 agonist ACH-induced sustained contraction in airway smooth muscle (Figure 2) was probably due to Ca2+ influx. Previous reports have demonstrated that L-type Ca2+ channels play roles in ACH-induced airway smooth muscle contraction . These findings were further confirmed in this study, in which nifedipine partially inhibited ACH-induced contraction in TRs (Figure 3).
Moreover, TRPC3 and/or STIM/Orai channels also play roles in ACH-induced contractions [14, 25]. TRPC3 and STIM/Orai channels are nonselective cation channels (NSCCs) that can mediate Ca2+ influx, resulting in intracellular Ca2+ increase to trigger airway smooth muscle contraction and contributing to ACH-induced contractions . In our data, following the addition of Pyr 3 (blocker of TRPC3 and STIM/Orai channels), ACH-induced contractions were partly inhibited (Figure 3). In addition to L-type Ca2+ channels and two types of NSCCs, there are still other mechanisms that mediate ACH-induced contraction on the basis of nifedipine-resistant and Pyr 3-resistant contractions being further blocked by NBAECP (Figure 4). These unknown mechanisms must be further determined in the future.
Taken together, the above results indicate that ACH-induced sustained contraction results from L-type Ca2+ channels- and TRPC3 and/or STIM/Orai channels-mediated Ca2+ influx and unknown mechanisms. Thus, NBAECP-induced inhibition could be partially due to NBAECP inhibiting these channels. However, the detailed inhibitory mechanism requires further investigation.
Although the above data showed that NBAECP could inhibit agonist-induced precontractions in tracheal smooth muscle, whether it has similar inhibitory functions on bronchial smooth muscle is uncertain. Our experiments conducted in lung slices showed that NBAECP was also able to inhibit precontraction in small bronchial smooth muscle (Figure 5), indicating that NBAECP could inhibit whole airway smooth muscle contraction.
In addition, in this study, all of the experiments were performed in both healthy and asthmatic smooth muscles, and similar responses were observed. This finding indicates that NBAECP has similar inhibitory roles in both types of ASM, suggesting that NBAECP could be a potent bronchodilator for asthmatics.
NBAECP can inhibit agonist-induced sustained contractions of healthy and asthmatic airway smooth muscle by inhibiting several types of ion channels. These findings indicate that NBAECP could be a new inhibitor of asthma attacks.
The authors declare no conflict of interests.
Qiu-Ju Jiang, Weiwei Chen, and Hong Dan contributed equally to this work.
This work was supported by the National Natural Science Foundation of China (31571200, 31140087, and 30971514 to Qing-Hua Liu and 81400015 to Weiwei Chen), the Natural Science Foundation of State Ethnic Affairs Commission of China (14ZNZ021 to Liqun Ma), the Open Foundation of Hubei Provincial Key Laboratory for Protection and Application of Special Plants in Wuling Area of China, and the Fundamental Research Funds for the Central Universities, South-Central University for Nationalities (CZW15012 and CZW15025).
- D. J. Jackson, A. Sykes, P. Mallia, and S. L. Johnston, “Asthma exacerbations: origin, effect, and prevention,” The Journal of Allergy and Clinical Immunology, vol. 128, no. 6, pp. 1165–1174, 2011.
- S. Li, C. Liu, L. Guo et al., “Ultrafiltration liquid chromatography combined with high-speed countercurrent chromatography for screening and isolating potential α-glucosidase and xanthine oxidase inhibitors from Cortex Phellodendri,” Journal of Separation Science, vol. 37, no. 18, pp. 2504–2512, 2014.
- Y.-M. Lee, H. Kim, E.-K. Hong, B.-H. Kang, and S.-J. Kim, “Water extract of 1:1 mixture of Phellodendron cortex and Aralia cortex has inhibitory effects on oxidative stress in kidney of diabetic rats,” Journal of Ethnopharmacology, vol. 73, no. 3, pp. 429–436, 2000.
- Y.-F. Mao, Y.-Q. Li, L. Zong, X.-M. You, F.-Q. Lin, and L. Jiang, “Methanol extract of Phellodendri cortex alleviates lipopolysaccharide-induced acute airway inflammation in mice,” Immunopharmacology and Immunotoxicology, vol. 32, no. 1, pp. 110–115, 2010.
- Y.-F. Xian, Q.-Q. Mao, S.-P. Ip, Z.-X. Lin, and C.-T. Che, “Comparison on the anti-inflammatory effect of Cortex Phellodendri Chinensis and Cortex Phellodendri Amurensis in 12-O-tetradecanoyl-phorbol-13-acetate- induced ear edema in mice,” Journal of Ethnopharmacology, vol. 137, no. 3, pp. 1425–1430, 2011.
- G. Chen, K.-K. Li, C.-H. Fung et al., “Er-Miao-San, a traditional herbal formula containing Rhizoma Atractylodis and Cortex Phellodendri inhibits inflammatory mediators in LPS-stimulated RAW264.7 macrophages through inhibition of NF-κB pathway and MAPKs activation,” Journal of Ethnopharmacology, vol. 154, no. 3, pp. 711–718, 2014.
- T. Uchiyama, H. Kamikawa, and Z. Ogita, “Anti-ulcer effect of extract from phellodendri cortex,” Yakugaku Zasshi, vol. 109, no. 9, pp. 672–676, 1989.
- J.-I. Park, J.-K. Shim, J.-W. Do et al., “Immune-stimulating properties of polysaccharides from Phellodendri cortex (Hwangbek),” Glycoconjugate Journal, vol. 16, no. 3, pp. 247–252, 1999.
- H. W. Jung, G.-Z. Jin, S. Y. Kim, Y. S. Kim, and Y.-K. Park, “Neuroprotective effect of methanol extract of Phellodendri Cortex against 1-methyl-4-phenylpyridinium (MPP+)-induced apoptosis in PC-12 cells,” Cell Biology International, vol. 33, no. 9, pp. 957–963, 2009.
- H.-Y. Kim, H.-S. Shin, H. Park et al., “In vitro inhibition of coronavirus replications by the traditionally used medicinal herbal extracts, Cimicifuga rhizoma, Meliae cortex, Coptidis rhizoma, and Phellodendron cortex,” Journal of Clinical Virology, vol. 41, no. 2, pp. 122–128, 2008.
- Z. Xie, C. Wen, J. Sun, and Y. Fan, “Clinical retrospective study on the characteristics of pattern of syndromes and traditional Chinese medicines in different using phases of glucocorticoid in treating bronchial asthma,” Journal of Zhejiang University of Traditional Chinese Medicine, vol. 35, no. 1, pp. 21–22, 30, 2011.
- M. E. Sánchez-Mendoza, C. Castillo-Henkel, and A. Navarrete, “Relaxant action mechanism of berberine identified as the active principle of Argemone ochroleuca Sweet in guinea-pig tracheal smooth muscle,” Journal of Pharmacy and Pharmacology, vol. 60, no. 2, pp. 229–236, 2008.
- Q.-R. Tuo, Y.-F. Ma, W. Chen et al., “Reactive oxygen species induce a Ca2+-spark increase in sensitized murine airway smooth muscle cells,” Biochemical and Biophysical Research Communications, vol. 434, no. 3, pp. 498–502, 2013.
- L. Tan, W. Chen, M.-Y. Wei et al., “Relaxant action of Plumula Nelumbinis extract on mouse airway smooth muscle,” Evidence-Based Complementary and Alternative Medicine, vol. 2015, Article ID 523640, 10 pages, 2015.
- Y. Bai and M. J. Sanderson, “Airway smooth muscle relaxation results from a reduction in the frequency of Ca2+ oscillations induced by a cAMP-mediated inhibition of the IP3 receptor,” Respiratory Research, vol. 7, article 34, 2006.
- T. Kirschstein, M. Rehberg, R. Bajorat, T. Tokay, K. Porath, and R. Köhling, “High K+-induced contraction requires depolarization-induced Ca2+ release from internal stores in rat gut smooth muscle,” Acta Pharmacologica Sinica, vol. 30, no. 8, pp. 1123–1131, 2009.
- W.-B. Sai, M.-F. Yu, M.-Y. Wei et al., “Bitter tastants induce relaxation of rat thoracic aorta precontracted with high K+,” Clinical and Experimental Pharmacology and Physiology, vol. 41, no. 4, pp. 301–308, 2014.
- M. Ishii and Y. Kurachi, “Muscarinic acetylcholine receptors,” Current Pharmaceutical Design, vol. 12, no. 28, pp. 3573–3581, 2006.
- A. F. Roffel, C. R. S. Elzinga, and J. Zaagsma, “Muscarinic M3 receptors mediate contraction of human central and peripheral airway smooth muscle,” Pulmonary Pharmacology, vol. 3, no. 1, pp. 47–51, 1990.
- Y.-H. Liu, S.-Z. Wu, G. Wang, N.-W. Huang, and C.-T. Liu, “A long-acting β2-adrenergic agonist increases the expression of muscarine cholinergic subtype-3 receptors by activating the β2-adrenoceptor cyclic adenosine monophosphate signaling pathway in airway smooth muscle cells,” Molecular Medicine Reports, vol. 11, no. 6, pp. 4121–4128, 2015.
- S. Mukherjee, J. Trice, P. Shinde, R. E. Willis, T. A. Pressley, and J. F. Perez-Zoghbi, “Ca2+ oscillations, Ca2+ sensitization, and contraction activated by protein kinase C in small airway smooth muscle,” The Journal of General Physiology, vol. 141, no. 2, pp. 165–178, 2013.
- L. Tang, T. M. Gamal El-Din, J. Payandeh et al., “Structural basis for Ca2+ selectivity of a voltage-gated calcium channel,” Nature, vol. 505, no. 7481, pp. 56–61, 2014.
- S. H. Young, O. Rey, and E. Rozengurt, “Intracellular Ca2+ oscillations generated via the extracellular Ca2+-sensing receptor (CaSR) in response to extracellular Ca2+ or l-phenylalanine: impact of the highly conservative mutation Ser170Thr,” Biochemical and Biophysical Research Communications, vol. 467, no. 1, pp. 1–6, 2015.
- M.-Y. Wei, L. Xue, L. Tan et al., “Involvement of large-conductance Ca2+-activated K+ channels in chloroquine-induced force alterations in pre-contracted airway smooth muscle,” PLoS ONE, vol. 10, no. 3, Article ID e0121566, 2015.
- T. Zhang, X.-J. Luo, W.-B. Sai et al., “Non-selective cation channels mediate chloroquine-induced relaxation in precontracted mouse airway smooth muscle,” PLoS ONE, vol. 9, no. 7, Article ID e101578, 2014.
- T. Song, Q. Hao, Y. M. Zheng, Q. H. Liu, and Y. X. Wang, “Inositol 1,4,5-trisphosphate activates TRPC3 channels to cause extracellular Ca2+ influx in airway smooth muscle cells,” American Journal of Physiology—Lung Cellular and Molecular Physiology, vol. 309, no. 12, pp. L1455–L1466, 2015.
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