Goreisan suppresses cardiac remodeling and dysfunction in a new mouse model with diabetic cardiomyopathy

IF 3 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Masafumi Funamoto , Shunji Hirose , Mizuho Yamamoto , Hai Du Ly-Nguyen , Masaki Imanishi , Fuka Ebi , Mai Ito , Hirokazu Ohminami , Koichiro Tsuchiya , Yasumasa Ikeda
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引用次数: 0

Abstract

Background

The global increase in diabetes, driven by aging populations and lifestyle changes, has led to an increase in the incidence of diabetic cardiomyopathy (DCM). DCM is characterized by metabolic abnormalities, oxidative stress, and inflammation, leading to cardiac remodeling and dysfunction. Goreisan (GRS), a traditional Japanese Kampo medicine, is commonly used to treat fluid control such as edema, due to its diuretic effect. In this study, we examined the effects of GRS on DCM.

Methods

We first established a new mouse model of DCM and then evaluated the effects of GRS on DCM using a recently developed model.

Results

The DCM mouse model developed cardiac hypertrophy, fibrosis, and dysfunction by nine weeks, which was ameliorated by GRS administration. GRS suppressed apoptosis and protein degradation by inhibiting Akt dephosphorylation and oxidative stress in DCM mice. In contrast, no differences in inflammatory cytokine levels were observed, regardless of GRS administration.

Conclusion

GRS has potential efficacy in preventing DCM onset and development.
Goreisan抑制糖尿病性心肌病小鼠模型的心脏重塑和功能障碍。
背景:在人口老龄化和生活方式改变的推动下,全球糖尿病患者增加,导致糖尿病性心肌病(DCM)的发病率增加。DCM的特点是代谢异常、氧化应激和炎症,导致心脏重塑和功能障碍。高丽散(GRS)是一种传统的日本汉布药,由于其利尿作用,通常用于治疗水肿等液体控制。在本研究中,我们研究了GRS对DCM的影响。方法:首先建立小鼠DCM模型,然后利用新建立的模型评价GRS对DCM的影响。结果:DCM小鼠模型在9周时出现心肌肥厚、纤维化和功能障碍,GRS给药后心肌肥厚、纤维化和功能障碍得到改善。GRS通过抑制Akt去磷酸化和氧化应激抑制DCM小鼠细胞凋亡和蛋白降解。相比之下,无论给药与否,炎症细胞因子水平均无差异。结论:GRS具有预防DCM发生发展的潜在疗效。
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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来源期刊
CiteScore
6.20
自引率
2.90%
发文量
104
审稿时长
31 days
期刊介绍: Journal of Pharmacological Sciences (JPS) is an international open access journal intended for the advancement of pharmacological sciences in the world. The Journal welcomes submissions in all fields of experimental and clinical pharmacology, including neuroscience, and biochemical, cellular, and molecular pharmacology for publication as Reviews, Full Papers or Short Communications. Short Communications are short research article intended to provide novel and exciting pharmacological findings. Manuscripts concerning descriptive case reports, pharmacokinetic and pharmacodynamic studies without pharmacological mechanism and dose-response determinations are not acceptable and will be rejected without peer review. The ethnopharmacological studies are also out of the scope of this journal. Furthermore, JPS does not publish work on the actions of biological extracts unknown chemical composition.
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