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糖脂清改善高脂血症合并心肌缺血小鼠心脏功能的作用及机制

Effect and mechanism of Tangzhiqing in improving cardiac function in mice with hyperlipidaemia complicated with myocardial ischaemia.

作者信息

Song Zhihui, Chen Rui, Wang Caijun, Pan Guiyun, Yan An, Xie Guinan, Yang Zhihua, Feng Wanying, Wang Yi

机构信息

Institute of Traditional Chinese Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin, 301617, China.

College of Traditional Chinese Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin, 300193, China.

出版信息

Heliyon. 2023 Apr 20;9(5):e15645. doi: 10.1016/j.heliyon.2023.e15645. eCollection 2023 May.

Abstract

PURPOSE

Tangzhiqing formula (TZQ) is a traditional Chinese medicine prescribed to treat lipid metabolism disorders, atherosclerosis, diabetes and diabetic cardiomyopathy. However, some challenges and hurdles remain. TZQ showed promising results in treating diabetes and hyperlipidaemia. However, its effect on and mechanism of action in hyperlipidaemia complicated with myocardial ischaemia (HL-MI) remain unknown.

METHODS

In this study, a network pharmacology-based strategy integrating target prediction was adopted to predict the targets of TZQ relevant to the treatment of HL-MI and to further explore the involved pharmacological mechanisms.

RESULTS

A total of 104 potential therapeutic targets were obtained, including MMP9, Bcl-2, and Bax, which may be related to the apoptosis and PI3K/AKT signalling pathways. Then, we confirmed these potential targets and pathways with animal experimentation. TZQ reduced lipid levels, increased the expression levels of Bcl-2, decreased Bax, caspase-3 and caspase-9 expression levels, and activated the PI3K/AKT signalling pathway.

CONCLUSION

In conclusion, this study provides new insights into the protective mechanisms of TZQ against HL-MI through network pharmacology and pharmacological approaches.

摘要

目的

糖脂清方(TZQ)是一种用于治疗脂质代谢紊乱、动脉粥样硬化、糖尿病及糖尿病心肌病的中药。然而,仍存在一些挑战和障碍。TZQ在治疗糖尿病和高脂血症方面显示出了有前景的结果。然而,其对合并心肌缺血的高脂血症(HL-MI)的作用及作用机制仍不清楚。

方法

在本研究中,采用基于网络药理学并整合靶点预测的策略,来预测与HL-MI治疗相关的TZQ靶点,并进一步探究其涉及的药理机制。

结果

共获得104个潜在治疗靶点,包括基质金属蛋白酶9(MMP9)、B细胞淋巴瘤-2(Bcl-2)和Bax,这些靶点可能与细胞凋亡及磷脂酰肌醇-3激酶/蛋白激酶B(PI3K/AKT)信号通路相关。随后,我们通过动物实验证实了这些潜在靶点和通路。TZQ降低了血脂水平,增加了Bcl-2的表达水平,降低了Bax、半胱天冬酶-3(caspase-3)和半胱天冬酶-9(caspase-9)的表达水平,并激活了PI3K/AKT信号通路。

结论

总之,本研究通过网络药理学和药理学方法,为TZQ对HL-MI的保护机制提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8d7/10163619/0e47c20094e9/gr1.jpg

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