Astragaloside IV inhibits isoprenaline‑induced cardiac fibrosis by targeting the reactive oxygen species/mitogen‑activated protein kinase signaling axis

  • Authors:
    • Hongliang Dai
    • Guizhi Jia
    • Meili Lu
    • Chunguang Liang
    • Yue Wang
    • Hongxin Wang
  • View Affiliations

  • Published online on: February 17, 2017     https://doi.org/10.3892/mmr.2017.6220
  • Pages: 1765-1770
Metrics: Total Views: 0 (Spandidos Publications: | PMC Statistics: )
Total PDF Downloads: 0 (Spandidos Publications: | PMC Statistics: )


Abstract

Cardiac fibrosis is considered an important pathological mechanism in the progression of cardiac remodeling and heart failure. Astragaloside IV (AsIV) is a major active ingredient in Astragalus membranaceus. In a preliminary experiment, it was demonstrated that this naturally occurring substance exhibited cardioprotective effects via preventing cardiomyocyte hypertrophy and apoptosis. The present study aimed to investigate the effects of AsIV on β‑adrenergic receptor (β‑AR)‑mediated cardiac fibrosis, and the associated mechanism. Cell Counting Kit‑8 (CCK‑8) assay was used to examine the proliferation of rat cardiac fibroblast (CF) cultures. Collagen I secretion was detected by ELISA. Dihydroethidium was used to determine intracellular ROS levels. Western blotting was used to examine the expression level of total and phosphorylated mitogen‑activated protein kinases (MAPKs). In the present study, the effects of AsIV on β‑adrenergic receptor (β‑AR) ‑mediated cardiac fibrosis were investigated, and the associated mechanism was revealed. Isoprenaline (ISO) is a selective β‑AR agonist, and treatment with AsIV significantly inhibited (ISO)‑triggered cardiac fibroblast proliferation and type I collagen synthesis. In addition, ISO resulted in a significant elevation of reactive oxygen species (ROS) levels and phosphorylation of the three profibrotic MAPKs, namely extracellular signal‑regulated kinase, p38MAPK and c‑Jun N‑terminal kinase. AsIV effectively reversed the aforementioned ISO‑induced alterations. In addition, N‑acetylcysteine, a typical ROS scavenger, mimicked the inhibitory effects of AsIV on MAPK activation. The present study demonstrated that AsIV may inhibit ISO‑induced cardiac fibrosis by suppressing ROS‑mediated MAPK activation.

Introduction

Cardiac hypertrophy and fibrosis are two important pathological alterations that occur during the progressive development of heart failure (1,2). Cardiac fibrosis refers to the excessive accumulation of extracellular matrix (ECM) and fibroblast deposition in the heart (3). Cardiac fibrosis is important in pathological cardiac remodeling and correlates with the occurrence of several fatal heart diseases, including heart failure, severe arrhythmia and sudden cardiac death (3,4). It has previously been demonstrated that isoprenaline (ISO) is important in cardiac fibrosis via increasing and/or activating several effector molecules, including reactive oxygen species (ROS), p38 mitogen-activated protein kinase (p38MAPK) and extracellular signal-regulated kinase (ERK) (3,5).

Astragaloside IV (AsIV) is one of the major active ingredients of the plant Astragalus membranaceus, which is referred to as HuangQi in Chinese. As an important Qi-invigorating medicinal herb, A. membranaceus is extensively used in traditional Chinese medicine for the treatment of cardiovascular diseases, hepatitis, and kidney and skin diseases (2,6,7). Chemically, AsIV is a cycloartane triterpene saponin with a well-defined molecular formula, the chemical structure of which is presented in Fig. 1. It has previously been demonstrated that AsIV exhibits cardioprotective effects via its antioxidative and anti-inflammatory properties (8,9). In addition, AsIV has been reported to improve cardiac function via the inhibition of cardiomyocyte hypertrophy and apoptosis (6,8). However, the function of AsIV in cardiac fibrosis remains to be fully elucidated, with only one previous study, to the best of our knowledge, currently available reporting its anti-fibrotic effect in coxsackievirus-induced cardiomyopathy (10). Therefore, the present study aimed to examine whether AsIV possesses antifibrotic activity under ISO stimulation and aimed to elucidate the associated underlying molecular mechanism.

Materials and methods

Animals

A total of 80 Sprague Dawley rat pups (age, 1–3 days; weight, 7±2 g, 40 male, 40 female), provided by the Animal Center of Jinzhou Medical University, were used for the current study. Rat pups, together with their mothers, were maintained at standard conditions with temperature at 25±1°C, and relative humidity at 70±10%. Animals were given free access to food and water and maintained under a 12/12 h light/dark cycle. The experiments were performed in accordance with the U.S. National Institute of Health guidelines for the Use of Laboratory Animals and ethical approval was granted by the Jinzhou Medical University Committee on Animal Care.

Cardiac fibroblast (CF) culture

The rats were anesthetized by ether inhalation and euthanized by cervical dislocation. Primary cultures of CFs were prepared as previously described, following the method for culture of cardiomyocytes (2), with the exception that pre-attached CFs rather than cardiomyocytes were collected for use. CFs were identified by their specific marker vimentin. Dispersed CFs were cultured in Dulbecco's modified Eagle's medium (DMEM; Corning Incorporated, Corning, NY, USA) supplemented with 10% fetal bovine serum (GE Healthcare Life Sciences, Logan, UT, USA) in a humidified atmosphere of 5% CO2, at 37°C.

CF proliferation assay

CFs were digested with 0.25% trypsin and ethylene diamine tetraacetic acid, then cultured in 96-well plates in the presence and absence of 100 µM AsIV (>98% purity; Nanjing Jingzhu Bio-Technology Co., Ltd., Nanjing, China) or the specific inhibitor of JNK, SP600125 (10 µΜ, Sigma-Aldrich, Merck KGaA, Darmstadt, Germany) for 30 min prior to treatment with 10 µM ISO (Sigma-Aldrich; Merck KGaA). Following incubation for 24 h in a humidified atmosphere of 5% CO2, at 37°C, the supernatant was removed, and 100 µl DMEM containing 10 µl Cell Counting Kit-8 (Dojindo Molecular Technologies, Inc., Kumamoto, Japan) was added to each well for a further 4 h at 37°C. The optical density was measured at a wavelength of 450 nm using an automated ELISA plate reader (Thermo Fisher Scientific, Inc., Waltham, MA, USA).

ELISA

The secretion of collagen type I by CFs was measured using a commercial ELISA kit (catalog no. CSB-E 12732r; Cusabio Biotech Co., Ltd., Wuhan, China) according to the manufacturer's protocol.

Measurement of intracellular ROS

Dihydroethidium (DHE; Molecular Probes; Thermo Fisher Scientific, Inc.) was used to determine intracellular ROS levels in cultured CFs. Briefly, CFs were incubated with 10 µM DHE for 30 min at 37°C in the dark. Cells were then washed 3 times with phosphate-buffered saline (PBS) to remove unincorporated dye. CFs loaded with DHE were then treated with 100 µM AsIV for 30 min, followed by treatment with 10 µM ISO for an additional 30 min. ROS levels were subsequently analyzed using an inverted fluorescence microscope (Leica Microsystems GmbH, Wetzlar, Germany).

Western blotting

Primary cultures of cardiac fibroblasts were pretreated with 100 µM AsIV or 10 mM N-acetylcysteine (NAC, Sigma-Aldrich; Merck KGaA) for 30 min, then treated with 10 µM ISO for a further 24 h in a humidified atmosphere of 5% CO2 at 37°C. Cells were washed with cold PBS and harvested with freshly prepared lysis buffer [150 mM NaCl, 50 mM Tris-HCl, pH 8.0, 0.1% sodium dodecyl sulfate, 1% Triton X-100 and 1% proteinase inhibitors (Sigma-Aldrich, Merck KGaA)]. Following quantification of total protein by Lowry's method, equal amounts of protein (50 µg) were subjected to 10% sodium dodecyl sulfate-polyacrylamide gel electrolysis and blotted onto a polyvinylidene fluoride membrane. The membrane was blocked with 1% bovine serum albumin (Sigma-Aldrich; Merck KGaA) for 1 h and then incubated overnight at 4°C with the primary rabbit anti-rat polyclonal antibodies against ERK (1:1,000; catalog no. sc-292838; Santa Cruz Biotechnology, Inc., Dallas, TX, USA), phosphorylated (p)-ERK (1:1,000; catalog no. sc-101760; Santa Cruz Biotechnology, Inc.), p38MAPK, (1:800; catalog no. 21683; Signalway Antibody LLC, College Park, ML, USA), p-p38MAPK (1:800; catalog no. 11581; Signalway Antibody LLC), c-Jun N-terminal kinase (JNK; 1:800; catalog no. 21241; Signalway Antibody LLC) and p-JNK, (1:800; catalog no. sc-135642; Santa Cruz Biotechnology, Inc.). Following 2 h incubation at room temperature with the polyclonal horseradish peroxidase-conjugated secondary goat anti-rabbit antibody (1:2,500; catalog no. sc-2004; Santa Cruz Biotechnology, Inc.), the bands were visualized by an enhanced chemiluminescence reagent (Thermo Fisher Scientific, Inc.). Optical density for each band was assessed using Quantity One software, version 4.6.9 (Bio-Rad Laboratories, Inc., Hercules, CA, USA).

Statistical analysis

Data are presented as the mean ± standard error of the mean, from at least three independent experiments. One-way analysis of variance followed by Fisher's least significant difference test was used to compare groups by use of SPSS version 17.0 software (SPSS, Inc., Chicago, IL, USA). P<0.05 was considered to indicate a statistically significant difference.

Results

AsIV attenuates ISO-induced CF proliferation and type I collagen synthesis

To evaluate the effects of AsIV on ISO-induced cardiac fibrosis, CF proliferation and type I collagen levels were examined. As presented in Fig. 2A, CF proliferation was significantly increased upon ISO stimulation for 24 h. Treatment with AsIV (100 µM) inhibited ISO-triggered CF proliferation. Increased collagen synthesis in ISO-treated cultured CFs was also significantly decreased with application of AsIV (Fig. 2B).

JNK mediates ISO-induced CF proliferation and type I collagen synthesis

The MAPK signaling pathway is composed of ERK, p38MAPK and JNK. Previous studies have demonstrated that ERK and p38MAPK are required for β-adrenergic activation of CF proliferation (3,5,11). However, it remains to be elucidated whether JNK is involved in this process. To investigate this, CF proliferation and type I collagen synthesis were measured following 24 h treatment with ISO in the absence or presence of the JNK inhibitor, SP600125. As presented in Fig. 3A and B, ISO-induced CF proliferation and collagen synthesis were significantly decreased by pretreatment with SP600125, indicative of a key role of JNK in ISO-induced cardiac fibrosis.

AsIV decreases ISO-induced ROS generation in CFs

AsIV is a potent antioxidant (12,13). Furthermore, ROS is important in ISO-induced cardiac fibrosis (3,14). The present study therefore examined the effects of AsIV on ROS production in CFs. As presented in Fig. 4, ISO-induced ROS production was effectively decreased by pretreatment with 100 µM AsIV.

AsIV and NAC attenuate ISO-induced phosphorylation of MAPK family members

In view of the important role of MAPK molecules in ISO-induced cardiac fibrosis, the present study investigated the effects of AsIV on MAPK activation. As presented in Fig. 5, ISO activated the three MAPKs, ERK, p38MAPK and JNK. Conversely, AsIV inhibited the activation of these three MAPKs. In addition, NAC, which is a typical ROS scavenger, exhibited similar inhibitory effects to those demonstrated by AsIV on MAPK activation.

Discussion

The present study demonstrated that AsIV may protect against ISO-induced CF proliferation and type I collagen synthesis. The underlying mechanism involved inhibition of ROS production and the resultant downregulation of MAPK signaling. To the best of our knowledge, this study is the first to reveal the antifibrotic effect, and associated mechanism, of AsIV in response to ISO stimulation.

Cardiac fibrosis is characterized by enhanced CF proliferation and excessive production and deposition of the ECM, of which ~85% is composed of type I collagen (15,16). This consequently results in myocardial stiffness, impaired diastolic function and cardiac failure (17,18). Antifibrotic mechanisms are therefore regarded as effective therapeutic strategies for the treatment of various cardiovascular diseases. It has previously been demonstrated that AsIV exerts therapeutic effects on fibrosis in several disorders, including chronic kidney disease (19), systemic sclerosis (20), liver fibrosis (21), and coxsackievirus B3-induced cardiomyopathy (10). However, its effect on β-adrenergic receptor-induced cardiac fibrosis remains to be fully elucidated. The present study therefore investigated the effects of AsIV on ISO-mediated cardiac fibrosis and the associated signaling transduction. The results demonstrated that pretreatment with AsIV significantly inhibited ISO-induced CF proliferation and type I collagen synthesis, thus suggesting that AsIV is a promising agent for the prevention and treatment of cardiac fibrosis under increased sympathetic drive.

Oxidative stress is important in the development and progression of diverse cardiac disorders, including cardiac fibrosis (14), hypertrophy (22), apoptosis (23), inflammation (24) and resultant heart failure (25,26). It has previously been demonstrated that ROS may modulate ECM remodeling by mediating CF function and stimulating collagen turnover (26). Antioxidative mechanisms may prevent numerous adverse cardiovascular events, including cardiac fibrosis. GKT137831 (14), oleanolic acid (27), 3,3′-diindolymethane (28) and magnolol (29), have been demonstrated to attenuate cardiac fibrosis via antioxidative bioactivity. The antioxidative capacity of AsIV has increasingly been identified by previous studies (12,13). Data from the present study revealed that application of AsIV effectively suppressed ROS accumulation. It was therefore concluded that the antifibrotic effects of AsIV may depend on its antioxidative activity.

One important consequence of oxidative stress is the phosphorylation of MAPK proteins, including ERK, p38MAPK and JNK. MAPK activation has been observed in cardiac fibrosis in response to oxidative stress triggered by angiotensin II (3033). In addition, it has been suggested that ISO induces cardiac fibrosis via activation of p38MAPK and ERK (3,5). To elucidate the involvement of JNK in ISO-induced cardiac fibrosis, the effect of SP600125, a selective inhibitor of JNK, was investigated. The results indicated that SP600125 inhibited CF proliferation and type I collagen synthesis, suggesting a similarly indispensible role of JNK in ISO-triggered cardiac fibrosis, as that observed of ERK and p38MAPK. Furthermore, data from the present study revealed that the phosphorylation of the three pro-fibrotic MAPK molecules was abrogated by application of AsIV. In addition, the inhibitory effects of AsIV on MAPK signaling were mimicked by the selective ROS inhibitor, NAC; thus, indicating that AsIV inhibits MAPK signaling in a ROS-dependent manner.

In conclusion, the present study demonstrated that AsIV effectively inhibited ISO-induced CF proliferation and type I collagen synthesis via attenuation of ROS-mediated MAPK signaling activation. These findings may aid to further elucidate the protective role and underlying molecular mechanism of AsIV in the cardiovascular system.

Acknowledgements

The present study was supported by the National Natural Science Foundation of China (grant no. 81374008), the Natural Science Foundation of Liaoning Province (grant no. 2015020360) and the President Foundation, Aohongboze Foundation of Liaoning Medical University (grant no. XZJJ20140111). The authors would like to thank Dr Guannan Wang (Jinzhou Medical University, Jinzhou, China) for his assistance in drawing the chemical structure of AsIV.

References

1 

Yu LM and Xu Y: Epigenetic regulation in cardiac fibrosis. World J Cardiol. 7:784–791. 2015. View Article : Google Scholar : PubMed/NCBI

2 

Dai H, Jia G, Liu X, Liu Z and Wang H: Astragalus polysaccharide inhibits isoprenaline-induced cardiac hypertrophy via suppressing Ca2+-mediated calcineurin/NFATc3 and CaMKII signaling cascades. Environ Toxicol Pharmacol. 38:263–271. 2014. View Article : Google Scholar : PubMed/NCBI

3 

Lu H, Tian A, Wu J, Yang C, Xing R, Jia P, Yang L, Zhang Y, Zheng X and Li Z: Danshensu inhibits β-adrenergic receptors-mediated cardiac fibrosis by ROS/p38 MAPK axis. Biol Pharm Bull. 37:961–967. 2014. View Article : Google Scholar : PubMed/NCBI

4 

Morita N, Mandel WJ, Kobayashi Y and Karagueuzian HS: Cardiac fibrosis as a determinant of ventricular tachyarrhythmias. J Arrhythm. 30:389–394. 2014. View Article : Google Scholar : PubMed/NCBI

5 

Kim J, Eckhart AD, Eguchi S and Koch WJ: Beta-adrenergic receptor-mediated DNA synthesis in cardiac fibroblasts is dependent on transactivation of the epidermal growth factor receptor and subsequent activation of extracellular signal-regulated kinases. J Biol Chem. 277:32116–32123. 2002. View Article : Google Scholar : PubMed/NCBI

6 

Yang J, Wang HX, Zhang YJ, Yang YH, Lu ML, Zhang J, Li ST, Zhang SP and Li G: Astragaloside IV attenuates inflammatory cytokines by inhibiting TLR4/NF-кB signaling pathway in isoproterenol-induced myocardial hypertrophy. J Ethnopharmacol. 150:1062–1070. 2013. View Article : Google Scholar : PubMed/NCBI

7 

Jiang X, Cao X, Huang Y, Chen J, Yao X, Zhao M, Liu Y, Meng J, Li P, Li Z, et al: Effects of treatment with Astragalus Membranaceus on function of rat leydig cells. BMC Complement Altern Med. 15:2612015. View Article : Google Scholar : PubMed/NCBI

8 

Mei M, Tang F, Lu M, He X, Wang H, Hou X, Hu J, Xu C and Han R: Astragaloside IV attenuates apoptosis of hypertrophic cardiomyocyte through inhibiting oxidative stress and calpain-1 activation. Environ Toxicol Pharmacol. 40:764–773. 2015. View Article : Google Scholar : PubMed/NCBI

9 

Zhao P, Wang Y, Zeng S, Lu J, Jiang TM and Li YM: Protective effect of astragaloside IV on lipopolysaccharide-induced cardiac dysfunction via downregulation of inflammatory signaling in mice. Immunopharmacol Immunotoxicol. 37:428–433. 2015. View Article : Google Scholar : PubMed/NCBI

10 

Chen P, Xie Y, Shen E, Li GG, Yu Y, Zhang CB, Yang Y, Zou Y, Ge J, Chen R and Chen H: Astragaloside IV attenuates myocardial fibrosis by inhibiting TGF-β1 signaling in coxsackievirus B3-induced cardiomyopathy. Eur J Pharmacol. 658:168–174. 2011. View Article : Google Scholar : PubMed/NCBI

11 

Liu N, Xing R, Yang C, Tian A, Lv Z, Sun N, Gao X, Zhang Y and Li Z: HIP-55/DBNL-dependent regulation of adrenergic receptor mediates the ERK1/2 proliferative pathway. Mol Biosyst. 10:1932–1939. 2014. View Article : Google Scholar : PubMed/NCBI

12 

Lu Y, Li S, Wu H, Bian Z, Xu J, Gu C, Chen X and Yang D: Beneficial effects of astragaloside IV against angiotensin II-induced mitochondrial dysfunction in rat vascular smooth muscle cells. Int J Mol Med. 36:1223–1232. 2015.PubMed/NCBI

13 

Wang SG, Xu Y, Xie H, Wang W and Chen XH: Astragaloside IV prevents lipopolysaccharide-induced injury in H9C2 cardiomyocytes. Chin J Nat Med. 13:127–132. 2015.PubMed/NCBI

14 

Somanna NK, Valente AJ, Krenz M, Fay WP, Delafontaine P and Chandrasekar B: The Nox1/4 dual inhibitor GKT137831 or Nox4 knockdown Inhibits Angiotensin-II-Induced adult mouse cardiac fibroblast proliferation and migration. AT1 physically associates with Nox4. J Cell Physiol. 231:1130–1141. 2016. View Article : Google Scholar : PubMed/NCBI

15 

Porter KE and Turner NA: Cardiac fibroblasts: At the heart of myocardial remodeling. Pharmacol Ther. 123:255–278. 2009. View Article : Google Scholar : PubMed/NCBI

16 

Ye Y, Lv X, Wang MH, Zhu J, Chen SQ, Jiang CY and Fu GS: Alendronate prevents angiotensin II-induced collagen I production through geranylgeranylation-dependent RhoA/Rho kinase activation in cardiac fibroblasts. J Pharmacol Sci. 129:205–209. 2015. View Article : Google Scholar : PubMed/NCBI

17 

Segura AM, Frazier OH and Buja LM: Fibrosis and heart failure. Heart Fail Rev. 19:173–185. 2014. View Article : Google Scholar : PubMed/NCBI

18 

Tao H, Yang JJ, Shi KH, Deng ZY and Li J: DNA methylation in cardiac fibrosis: New advances and perspectives. Toxicology. 323:125–129. 2014. View Article : Google Scholar : PubMed/NCBI

19 

Che X, Wang Q, Xie Y, Xu W, Shao X, Mou S and Ni Z: Astragaloside IV suppresses transforming growth factor-β1 induced fibrosis of cultured mouse renal fibroblasts via inhibition of the MAPK and NF-B signaling pathways. Biochem Biophys Res Commun. 464:1260–1266. 2015. View Article : Google Scholar : PubMed/NCBI

20 

Qi Q, Mao Y, Yi J, Li D, Zhu K and Cha X: Anti-fibrotic effects of Astragaloside IV in systemic sclerosis. Cell Physiol Biochem. 34:2105–2116. 2014. View Article : Google Scholar : PubMed/NCBI

21 

Li X, Wang X, Han C, Wang X, Xing G, Zhou L, Li G and Niu Y: Astragaloside IV suppresses collagen production of activated hepatic stellate cells via oxidative stress-mediated p38 MAPK pathway. Free Radic Biol Med. 60:168–176. 2013. View Article : Google Scholar : PubMed/NCBI

22 

Zhang C, Wang F, Zhang Y, Kang Y, Wang H, Si M, Su L, Xin X, Xue F, Hao F, et al: Celecoxib prevents pressure overload-induced cardiac hypertrophy and dysfunction by inhibiting inflammation, apoptosis and oxidative stress. J Cell Mol Med. 20:116–127. 2016. View Article : Google Scholar : PubMed/NCBI

23 

Liu B, Zhang J, Liu W, Liu N, Fu X, Kwan H and Liu S, Liu B, Zhang S, Yu Z and Liu S: Calycosin inhibits oxidative stress-induced cardiomyocyte apoptosis via activating estrogen receptor-α/β. Bioorg Med Chem Lett. 26:181–185. 2016. View Article : Google Scholar : PubMed/NCBI

24 

Kayama Y, Raaz U, Jagger A, Adam M, Schellinger IN, Sakamoto M, Suzuki H, Toyama K, Spin JM and Tsao PS: Diabetic cardiovascular disease induced by oxidative stress. Int J Mol Sci. 16:25234–25263. 2015. View Article : Google Scholar : PubMed/NCBI

25 

Fournier P, Fourcade J, Roncalli J, Salvayre R, Galinier M and Causse E: Homocysteine in chronic heart failure. Clin Lab. 61:1137–1145. 2015. View Article : Google Scholar : PubMed/NCBI

26 

Murdoch CE, Zhang M, Cave AC and Shah AM: NADPH oxidase-dependent redox signalling in cardiac hypertrophy, remodelling and failure. Cardiovasc Res. 71:208–215. 2006. View Article : Google Scholar : PubMed/NCBI

27 

Liao HH, Zhang N, Feng H, Zhang N, Ma ZG, Yang Z, Yuan Y, Bian ZY and Tang QZ: Oleanolic acid alleviated pressure overload-induced cardiac remodeling. Mol Cell Biochem. 409:145–154. 2015. View Article : Google Scholar : PubMed/NCBI

28 

Yao Z, Hu W, Yin S, Huang Z, Zhu Q, Chen J, Zang Y, Dong L and Zhang J: 3,3′-Diindolymethane ameliorates adriamycin-induced cardiac fibrosis via activation of a BRCA1-dependent anti-oxidant pathway. Pharmacol Res. 70:139–146. 2013. View Article : Google Scholar : PubMed/NCBI

29 

Liou JY, Chen YL, Loh SH, Chen PY, Hong CY, Chen JJ, Cheng TH and Liu JC: Magnolol depresses urotensin-II-induced cell proliferation in rat cardiac fibroblasts. Clin Exp Pharmacol Physiol. 36:711–716. 2009. View Article : Google Scholar : PubMed/NCBI

30 

Chan P, Liu JC, Lin LJ, Chen PY, Cheng TH, Lin JG and Hong HJ: Tanshinone IIA inhibits angiotensin II-induced cell proliferation in rat cardiac fibroblasts. Am J Chin Med. 39:381–394. 2011. View Article : Google Scholar : PubMed/NCBI

31 

Zhang W, Chen XF, Huang YJ, Chen QQ, Bao YJ and Zhu W: 2,3,4′, 5-Tetrahydroxystilbene-2-O-β-D-glucoside inhibits angiotensin II-induced cardiac fibroblast proliferation via suppression of the reactive oxygen species-extracellular signal-regulated kinase 1/2 pathway. Clin Exp Pharmacol Physiol. 39:429–437. 2012. View Article : Google Scholar : PubMed/NCBI

32 

Yu M, Zheng Y, Sun HX and Yu DJ: Inhibitory effects of enalaprilat on rat cardiac fibroblast proliferation via ROS/P38MAPK/TGF-β1 signaling pathway. Molecules. 17:2738–2751. 2012. View Article : Google Scholar : PubMed/NCBI

33 

Shyu KG, Wang BW, Chen WJ, Kuan P and Lin CM: Angiotensin II mediates urotensin II expression by hypoxia in cultured cardiac fibroblast. Eur J Clin Invest. 42:17–26. 2012. View Article : Google Scholar : PubMed/NCBI

Related Articles

Journal Cover

April-2017
Volume 15 Issue 4

Print ISSN: 1791-2997
Online ISSN:1791-3004

Sign up for eToc alerts

Recommend to Library

Copy and paste a formatted citation
x
Spandidos Publications style
Dai H, Jia G, Lu M, Liang C, Wang Y and Wang H: Astragaloside IV inhibits isoprenaline‑induced cardiac fibrosis by targeting the reactive oxygen species/mitogen‑activated protein kinase signaling axis. Mol Med Rep 15: 1765-1770, 2017
APA
Dai, H., Jia, G., Lu, M., Liang, C., Wang, Y., & Wang, H. (2017). Astragaloside IV inhibits isoprenaline‑induced cardiac fibrosis by targeting the reactive oxygen species/mitogen‑activated protein kinase signaling axis. Molecular Medicine Reports, 15, 1765-1770. https://doi.org/10.3892/mmr.2017.6220
MLA
Dai, H., Jia, G., Lu, M., Liang, C., Wang, Y., Wang, H."Astragaloside IV inhibits isoprenaline‑induced cardiac fibrosis by targeting the reactive oxygen species/mitogen‑activated protein kinase signaling axis". Molecular Medicine Reports 15.4 (2017): 1765-1770.
Chicago
Dai, H., Jia, G., Lu, M., Liang, C., Wang, Y., Wang, H."Astragaloside IV inhibits isoprenaline‑induced cardiac fibrosis by targeting the reactive oxygen species/mitogen‑activated protein kinase signaling axis". Molecular Medicine Reports 15, no. 4 (2017): 1765-1770. https://doi.org/10.3892/mmr.2017.6220