机构:[1]School of Basic Medicine, Hebei University of Chinese Medicine, 6 Xingyuan Road, Shijiazhuang 050200, Hebei, People’s Republic of China[2]School of Pharmacy, Hebei University of Chinese Medicine, 6 Xingyuan Road, Shijiazhuang 050200, Hebei, People’s Republic of China[3]Affiliated Hospital, Hebei University of Chinese Medicine, Shijiazhuang 050011, Hebei, China[4]Department of Pharmacy, The Fourth Hospital of Hebei Medical University, Hebei Medical University, Shijiazhuang 050011, Hebei, China药学部药学部河北医科大学第四医院[5]Hebei Key Laboratory of Integrative Medicine on Liver-Kidney Patterns, Hebei University of Chinese Medicine, Shijiazhuang 050200, Hebei, China
Crocin is isolated from saffron and has multiple activities. There are many reports on its beneficial effects for cardiovascular disease, but crocin's effects on anti-myocardial fibrosis have not yet been reported. This study investigated crocin's effects and potential mechanisms on isoproterenol (ISO)-induced myocardial fibrosis (MF) in mice. Mice were infused intraperitoneally with crocin with concurrent ISO subcutaneous injections over 2 weeks. Electrocardiography, cardiac weight index (CWI), hydroxyproline content, and heart morphology changes were observed. Administration of crocin markedly decreased heart rate, J-point elevation, QRS interval, CWI, and hydroxyproline content in the myocardial tissues, and improved heart pathologic morphology. Versus the control group, the ISO group showed an increase in lactate dehydrogenase and creatine kinase activities and malondialdehyde content. Meanwhile, superoxide dismutase, catalase, and glutathione contents decreased in the ISO group; crocin caused a significant reduction in oxidative stress levels in ISO-induced MF. ISO led to a significant increase in interleukin-1 and -6 and tumor necrosis factor-a in addition to nuclear factor kappa B (NF-kappa B) (p65) and toll-like receptor (TLR) 4 expressions. Crocin treatment suppressed these inflammatory cytokine expressions. Moreover, crocin treatment caused a significant decrease in connective tissue growth factor and transforming growth factor-beta 1 mRNA levels in addition to a decrease in B cell lymphoma-2, Bcl-2-associated X protein, caspase-3, and cleaved caspase-3 expressions. Crocin has a protective effect on ISO-induced MF, which may be associated with the TLR4/NF-kappa B (p65) signal transduction pathway.
基金:
This work was supported by the Research
Foundation of Administration of Traditional Chinese Medicine of Hebei
Province, China (No. 2015030 and 2019081), Natural Science Fund of
Education Department of Hebei Province (ZD 2018038 and ZD
2016091).
第一作者机构:[1]School of Basic Medicine, Hebei University of Chinese Medicine, 6 Xingyuan Road, Shijiazhuang 050200, Hebei, People’s Republic of China
通讯作者:
通讯机构:[1]School of Basic Medicine, Hebei University of Chinese Medicine, 6 Xingyuan Road, Shijiazhuang 050200, Hebei, People’s Republic of China[2]School of Pharmacy, Hebei University of Chinese Medicine, 6 Xingyuan Road, Shijiazhuang 050200, Hebei, People’s Republic of China[3]Affiliated Hospital, Hebei University of Chinese Medicine, Shijiazhuang 050011, Hebei, China[5]Hebei Key Laboratory of Integrative Medicine on Liver-Kidney Patterns, Hebei University of Chinese Medicine, Shijiazhuang 050200, Hebei, China
推荐引用方式(GB/T 7714):
Jin Weiyue,Zhang Yuanyuan,Xue Yurun,et al.Crocin attenuates isoprenaline-induced myocardial fibrosis by targeting TLR4/NF-kappa B signaling: connecting oxidative stress, inflammation, and apoptosis[J].NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY.2020,393(1):13-23.doi:10.1007/s00210-019-01704-4.
APA:
Jin, Weiyue,Zhang, Yuanyuan,Xue, Yurun,Han, Xue,Zhang, Xuan...&Chu, Li.(2020).Crocin attenuates isoprenaline-induced myocardial fibrosis by targeting TLR4/NF-kappa B signaling: connecting oxidative stress, inflammation, and apoptosis.NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY,393,(1)
MLA:
Jin, Weiyue,et al."Crocin attenuates isoprenaline-induced myocardial fibrosis by targeting TLR4/NF-kappa B signaling: connecting oxidative stress, inflammation, and apoptosis".NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY 393..1(2020):13-23