4.7 Article

Gentiopicroside alleviates cardiac inflammation and fibrosis in T2DM rats through targeting Smad3 phosphorylation

期刊

PHYTOMEDICINE
卷 106, 期 -, 页码 -

出版社

ELSEVIER GMBH
DOI: 10.1016/j.phymed.2022.154389

关键词

T2DM; Gentiopicroside; Heart failure; Cardiac fibrosis; Inflammation; Smad3

资金

  1. Special project of Hospital Pharmacy of Zhejiang Pharmaceutical Society [2020ZYY06]
  2. Zhejiang pro- vincial ten thousand program of Leading talents of science and tech- nology innovation [2020R52029]
  3. Chinese Medicine Research Program of Zhejiang Province [2022ZB037]

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This study investigated the cardioprotective role of Gentiopicroside (GPS) in rats with type 2 diabetes mellitus (T2DM) and its underlying mechanism. The results showed that GPS improved cardiac function in T2DM rats and attenuated inflammation and fibrosis by inhibiting the phosphorylation of Smad3.
Background: Cardiac fibrosis is a major structural change observed in the heart of patients with type 2 diabetes mellitus (T2DM), ultimately resulting in heart failure (HF). Suppression of inflammation is an effective therapeutic strategy for treating cardiac fibrosis and HF. Gentiopicroside (GPS), the primary component of Gentiana manshurica Kitagawa, possess potent anti-inflammatory activity. However, its cardioprotective role remains elusive. Purpose: We explored the potential cardioprotective role of GPS in T2DM rats and its underlying mechanisms. Methods: T2DM rats built by high-fat diet and streptozotocin were orally administered 25, 50, or 100 mg/kg GPS, daily for 8 weeks. The positive control drug was Metformin (200 mg/kg/day). Primary cardiac fibroblasts (CFs) were induced by high glucose (30 mM) and subsequently treated with GPS (100 mu M). Cardiac function and pathological changes were analyzed using echocardiography and histological staining. Potential targets of GPS were predicted using Molecular docking. Real-time PCR as well as western blotting were applied to verify the expression of objective genes. Results: All three doses reduced fasting blood glucose levels, but only 50 and 100 mg/kg GPS improved cardiac function and alleviated inflammation and fibrosis in T2DM rats. GPS (100 mg/kg) exhibited a better effect, similar to that of metformin. Mechanistically, binding between GPS and the MH2 domain of Smad3 blocked high glucose-induced Smad3 phosphorylation, thus attenuating inflammation, oxidative stress, and activation in CFs. Conclusion: We, for the first time, demonstrated that GPS improved cardiac function in T2DM rats and elucidated the underlying mechanism through which GPS targeted Smad3 phosphorylation to suppress inflammation and activation in CFs, thereby revealing the potential application of GPS in HF therapy.

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