麝香保心丸可能通过抑制CaV1.2钙通道电流缓解异丙肾上腺素所致心力衰竭。

IF 3.4 Q2 BIOCHEMICAL RESEARCH METHODS Biochemistry Research International Pub Date : 2022-11-09 eCollection Date: 2022-01-01 DOI:10.1155/2022/5498023
Jianwei Wu, Juan Yu, Jianyong Qi, Minzhou Zhang
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摘要

心力衰竭(HF)影响着全世界数百万患者。麝香保心丸(SXB)在我国医院广泛应用于治疗冠心病和心衰。然而,对于为什么SXB可以防止HF,仍然没有解释。为了评估其保护作用,我们采用异丙肾上腺素(ISO)皮下注射,每公斤体重85毫克,连续7天建立大鼠HF模型。分为CON组(对照组)、ISO组(HF疾病组)、CAP组(卡托普利阳性药物治疗)和SXB组。采用超声心动图评价大鼠体内HF。采用膜片钳技术检测tsA-201细胞中人CaV1.2 (hCaV1.2)通道电流。本研究选择5种不同浓度的SXB(5、10、30、50和100 mg/L)。结果表明,SXB能增强心脏收缩功能,抑制ISO诱导的大鼠心肌肥厚和心肌纤维化。随后发现,SXB受到hCaV1.2通道电流峰值幅值的抑制(P < 0.01)。SXB半抑制剂量为9.09 mg/L。稳态激活曲线为22.8 mV退极化位移;而失活曲线和失活后的恢复无明显影响。综上所述,SXB对iso诱导的大鼠HF有抑制作用,对hCaV1.2通道电流有抑制作用。目前的研究为SXB保护自身免受HF的影响铺平了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Shexiang Baoxin Pills Could Alleviate Isoproterenol-Induced Heart Failure Probably through its Inhibition of CaV1.2 Calcium Channel Currents.

Heart failure (HF) affects millions of patients in the world. Shexiang Baoxin Pills (SXB) are extensively applied to treat coronary artery diseases and HF in Chinese hospitals. However, there are still no explanations for why SXB protects against HF. To assess the protective role, we created the HF model in rats by isoproterenol (ISO) subcutaneous injection, 85 milligrams per kilogram body weight for seven days. Four groups were implemented: CON (control), ISO (HF disease group), CAP (captopril, positive drug treatment), and SXB groups. Echocardiography was used to evaluate rats' HF in vivo. The human CaV1.2 (hCaV1.2) channel currents were detected in tsA-201 cells by patch clamp technique. Five different concentrations of SXB (5, 10, 30, 50, and 100 mg/L) were chosen in this study. The results showed that SXB increased cardiac systolic function and inhibited rats' cardiac hypertrophy and myocardial fibrosis induced by ISO. Subsequently, it was found that SXB was inhibited by the peak amplitudes of hCaV1.2 channel current (P < 0.01). The SXB half inhibitory dosage was 9.09 mg/L. The steady-state activation curve was 22.8 mV depolarization shifted; while the inactivation curve and the recovery from inactivation were not affected significantly. In conclusion, these results indicated that SXB inhibited ISO-induced HF in rats and inhibited the hCaV1.2 channel current. The present study paved the way for SXB to protect itself from HF.

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来源期刊
Biochemistry Research International
Biochemistry Research International BIOCHEMICAL RESEARCH METHODS-
CiteScore
6.30
自引率
0.00%
发文量
27
审稿时长
14 weeks
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