Abstract

Diabetic cardiomyopathy (DCM) is one of the main causes of mortality among diabetic patients, with oxidative stress and inflammation major contributors to its development. Dietary flavonoids show strong antioxidant and anti-inflammatory activities, although their potential additive outcomes in combination with antidiabetic drugs have been scarcely explored. The present study investigates the cardioprotective effects of a cocoa–carob blend (CCB) diet, rich in flavonoids, alone or in combination with metformin, in the development of DCM. Zucker diabetic fatty rats (ZDF) were fed with a CCB rich-diet or a control diet, with or without metformin for 12 weeks. Glucose homeostasis, cardiac structure and function, and oxidative and inflammatory biomarkers were analysed. CCB improved glucose homeostasis, and mitigated cardiac dysfunction, hypertrophy, and fibrosis in ZDF rats. Mechanistically, CCB counteracted oxidative stress in diabetic hearts by down-regulating NADPH oxidases, reducing reactive oxygen species (ROS) generation and modulating the sirtuin-1 (SIRT1)/ nuclear factor E2-related factor 2 (Nrf2) signalling pathway, overall improving antioxidant defence. Moreover, CCB suppressed inflammatory and fibrotic reactions by inhibiting nuclear factor kappa B (NFκB) and pro-inflammatory and pro-fibrotic cytokines. Noteworthy, several of these effects were further improved in combination with metformin. Our results demonstrate that CCB strongly prevents the cardiac remodelling and dysfunction observed in diabetic animals, highlighting its potential, alone or in adjuvant therapy, for treating DCM.

Highlights

  • Type 2 diabetes (T2D) represents a major worldwide health problem because of its high prevalence and associated cardiovascular complications [1]

  • The total food intake during the 12 weeks of the study was higher in all Zucker diabetic fatty rats (ZDF) groups as compared to Zucker lean (ZL) animals; the food efficiency was significantly decreased in ZDF animals

  • Zucker lean (ZL), Zucker Diabetic rats (ZDF), Zucker Diabetic rats treated with metformin (ZDF (M)), Zucker Diabetic rats fed with a cocoa–carob blend (CCB) rich-diet (ZDF (CCB)), and Zucker Diabetic rats treated with metformin and fed with a CCB rich-diet (ZDF (CCB + M))

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Summary

Introduction

Type 2 diabetes (T2D) represents a major worldwide health problem because of its high prevalence and associated cardiovascular complications [1]. Diabetic cardiomyopathy (DCM) is one of the main causes of diabetes-associated morbidity and mortality [2]. There are many glucose-lowering drugs available for the treatment of T2D. Some of them may reduce the cardiovascular mortality but the risk of cardiovascular 4.0/). Antioxidants 2022, 11, 432 death is still very high in this population. Development of novel preventive or therapeutic strategies is needed to treat diabetic cardiomyopathy

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