[心通颗粒通过调节肠道菌群改善大鼠心肌缺血再灌注损伤的作用及机制]。

Q3 Pharmacology, Toxicology and Pharmaceutics
Yun-Jia Wang, Ji-Dong Zhou, Qiu-Yu Su, Jing-Chun Yao, Rui-Qiang Su, Guo-Fei Qin, Gui-Min Zhang, Hong-Bao Liang, Shuai Feng, Jia-Cheng Zhang
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引用次数: 0

摘要

本研究探讨心通颗粒通过调节肠道菌群及其代谢产物,特别是短链脂肪酸(SCFAs)改善心肌缺血再灌注损伤(MIRI)的机制。将大鼠按体重随机分为假手术组、模型组、心通颗粒低剂量组(1.43 g·kg~(-1)·d~(-1))、中剂量组(2.86 g·kg~(-1)·d~(-1))、高剂量组(5.72 g·kg~(-1)·d~(-1))、美托洛尔组(10 mg·kg~(-1)·d~(-1))。预给药14天后,结扎左冠状动脉前降支,建立MIRI大鼠模型。采用2,3,5-三苯基四氮唑(TTC)染色法测定心肌梗死面积。采用末端脱氧核苷酸转移酶介导的dUTP镍端标记(TUNEL)法检测组织细胞凋亡。苏木精-伊红(HE)染色观察心肌细胞和结肠组织的病理变化。采用酶联免疫吸附试验(ELISA)试剂盒定量测定大鼠血清中肿瘤坏死因子-α(TNF-α)、白细胞介素-1β(IL-1β)、白细胞介素-6(IL-6)、肌酸激酶MB同工酶(CK-MB)、心肌肌钙蛋白T(cTnT)水平。用比色法测定心肌组织乳酸脱氢酶(LDH)、肌酸激酶(CK)和超氧化物歧化酶(SOD)的活性以及丙二醛(MDA)的水平。采用16S rDNA测序分析肠道菌群组成,采用气相色谱-质谱联用(GC-MS)测定粪便SCFAs含量。结果表明,心通颗粒可显著减少心肌梗死面积,抑制心肌细胞凋亡,降低血清促炎因子(TNF-α、IL-1β、IL-6)、心肌损伤标志物(CK- mb、cTnT、LDH、CK)和氧化应激标志物MDA水平。此外,心通颗粒可显著改善MIRI大鼠的肠道炎症,调节肠道菌群组成和多样性,提高SCFAs(醋酸酯、丙酸酯、异丁酸酯等)水平。综上所述,心通颗粒能有效缓解MIRI症状。本研究初步证实心通颗粒通过调节肠道菌群失衡和提高SCFA水平发挥抑制MIRI的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Effect and mechanism of Xintong Granules in ameliorating myocardial ischemia-reperfusion injury in rats by regulating gut microbiota].

This study investigates the mechanism by which Xintong Granules improve myocardial ischemia-reperfusion injury(MIRI) through the regulation of gut microbiota and their metabolites, specifically short-chain fatty acids(SCFAs). Rats were randomly divided based on body weight into the sham operation group, model group, low-dose Xintong Granules group(1.43 g·kg~(-1)·d~(-1)), medium-dose Xintong Granules group(2.86 g·kg~(-1)·d~(-1)), high-dose Xintong Granules group(5.72 g·kg~(-1)·d~(-1)), and metoprolol group(10 mg·kg~(-1)·d~(-1)). After 14 days of pre-administration, the MIRI rat model was established by ligating the left anterior descending coronary artery. The myocardial infarction area was assessed using the 2,3,5-triphenyltetrazolium chloride(TTC) staining method. Apoptosis in tissue cells was detected by the terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling(TUNEL) assay. Pathological changes in myocardial cells and colonic tissue were observed using hematoxylin-eosin(HE) staining. The levels of tumor necrosis factor-α(TNF-α), interleukin-1β(IL-1β), interleukin-6(IL-6), creatine kinase MB isoenzyme(CK-MB), and cardiac troponin T(cTnT) in rat serum were quantitatively measured using enzyme-linked immunosorbent assay(ELISA) kits. The activities of lactate dehydrogenase(LDH), creatine kinase(CK), and superoxide dismutase(SOD) in myocardial tissue, as well as the level of malondialdehyde(MDA), were determined using colorimetric assays. Gut microbiota composition was analyzed by 16S rDNA sequencing, and fecal SCFAs were quantified using gas chromatography-mass spectrometry(GC-MS). The results show that Xintong Granules significantly reduced the myocardial infarction area, suppressed cardiomyocyte apoptosis, and decreased serum levels of pro-inflammatory cytokines(TNF-α, IL-1β, and IL-6), myocardial injury markers(CK-MB, cTnT, LDH, and CK), and oxidative stress marker MDA. Additionally, Xintong Granules significantly improved intestinal inflammation in MIRI rats, regulated gut microbiota composition and diversity, and increased the levels of SCFAs(acetate, propionate, isobutyrate, etc.). In summary, Xintong Granules effectively alleviate MIRI symptoms. This study preliminarily confirms that Xintong Granules exert their inhibitory effects on MIRI by regulating gut microbiota imbalance and increasing SCFA levels.

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来源期刊
Zhongguo Zhongyao Zazhi
Zhongguo Zhongyao Zazhi Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
1.50
自引率
0.00%
发文量
581
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