Shenxiang Suhe pill improves cardiac function through modulating gut microbiota and serum metabolites in rats after acute myocardial infarction-Reference-Cited by-同舟云学术

Shenxiang Suhe pill improves cardiac function through modulating gut microbiota and serum metabolites in rats after acute myocardial infarction

Published:2023-12-12 Issue:1 Volume:62 Page:1-12
ISSN:1388-0209
Container-title:Pharmaceutical Biology
language:en
Short-container-title:Pharmaceutical Biology

Author:

Zhong Xinqin¹²,Yan Junyuan¹²,Wei Xing¹²,Xie Tian¹²,Zhang Zhaojian¹²,Wang Kaiyue¹²,Sun Congying¹²,Chen Wei³,Zhu Jiaming³,Zhao Xin¹²,Wang Xiaoying¹²⁴

Affiliation:

1. Ministry of Education Key Laboratory of Pharmacology of Traditional Chinese Medical Formulae, Tianjin University of Traditional Chinese Medicine, Tianjin, China

2. State Key Laboratory of Component-based Chinese Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin, China

3. Hangzhou Hu Qing Yu Tang Pharmaceutical Co., Ltd, Hangzhou, China

4. School of Chinese Materia Medica, Tianjin University of Traditional Chinese Medicine, Tianjin, China

Funder

Innovation Team and Talents Cultivation Program of National Administration of Traditional Chinese Medicine

Publisher

Informa UK Limited

Subject

Complementary and alternative medicine,Drug Discovery,Pharmaceutical Science,Pharmacology,Molecular Medicine,General Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1080/13880209.2023.2289577

Reference46 articles.

1. Rebalancing of the gut flora and microbial metabolism is responsible for the anti-arthritis effect of kaempferol

2. Effects of Gallic Acid and Cyclosporine A on Antioxidant Capacity and Cardiac Markers of Rat Isolated Heart After Ischemia/Reperfusion

3. Effect of Shenxiang Suhe pill on rats with myocardial ischemia;Chen D;Tradi Chinese Drug Res Clin Pharmacol,2000

4. The Integrated Analysis of Transcriptomics and Metabolomics Unveils the Therapeutical Effect of Asiatic Acid on Alcoholic Hepatitis in Rats

5. Prevotellaceae produces butyrate to alleviate PD-1/PD-L1 inhibitor-related cardiotoxicity via PPARα-CYP4X1 axis in colonic macrophages

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