Abstract

Type 2 diabetes mellitus, which an outcome of impaired insulin action and its secretion, is concomitantly associated with lipid abnormalities. The study was designed to evaluate the combinational effect of omega-3 fatty acids (flax and fish oil) and glibenclamide on abnormal lipid profiles, increased blood glucose, and impaired liver and kidney functions in a high fat diet with low streptozotocin (STZ)-induced diabetic rats, including its probable mechanism of action. The male Wistar rats (n = 48) were distributed into eight groups. All animal groups except the healthy received a high fat diet (HFD) for 90 days. Further, diabetes was developed by low dose STZ (35 mg/kg). Diabetic animals received, omega-3 fatty acids (500 mg/kg), along with glibenclamide (0.25 mg/kg). Both flax and fish oil intervention decreased (p ≤ 0.001) serum triglycerides and very low density lipoprotein and elevated (p ≤ 0.001) high density lipoprotein levels in diabetic rats. Total cholesterol and low-density lipoprotein level was decreased (p ≤ 0.001) in fish oil-treated rats. However, it remained unaffected in the flax oil treatment group. Both flax and fish oil intervention downregulate the expression of fatty acid metabolism genes, transcription factors (sterol regulatory element-binding proteins-1c and nuclear factor-κβ), and their regulatory genes i.e., acetyl-coA carboxylase alpha, fatty acid synthase, and tumor necrosis factors-α. The peroxisome proliferator-activated receptor gamma gene expression was upregulated (p ≤ 0.001) in the fish oil treatment group. Whereas, carnitine palmitoyltransferase 1 and fatty acid binding protein gene expression were upregulated (p ≤ 0.001) in both flax and fish oil intervention group.

Highlights

  • Type 2 diabetes mellitus (T2DM) is a metabolic disorder characterized by an increase in blood glucose due to impaired insulin secretion and its action [1]

  • We investigated the effect of omega-3 fatty acids i.e., flax and fish oil, along with glibenclamide, against diabetic dyslipidemia by using a high fat diet with low dose streptozotocin-induced diabetic rat model

  • The serum level found toareberepresented comparable among each group). ** p ≤ 0.01 and *** p ≤ 0.001, when compared with the diet control; group III (DC) group

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Summary

Introduction

Type 2 diabetes mellitus (T2DM) is a metabolic disorder characterized by an increase in blood glucose due to impaired insulin secretion and its action [1]. The consistent hyperglycemia, insulin resistance, and insulin deficiency contribute to lipid abnormalities in T2DM [2]. The lipid abnormality is an independent risk factor for cardiovascular disease (CVD) development and commonly found in T2DM individuals [3]. Diabetic dyslipidemia is significantly associated with mortality and morbidity due to cardiovascular complications [4]. It accounts for 80% of deaths in diabetic individuals due to CVD [5]. The hyperglycemia, along with lipid abnormalities, is a modifiable risk factor for CVD, and remains uncontrolled in T2DM individuals [4,6]. In spite of advancements in therapeutic strategies, there has been no significant decrease in the mortality related to CVD [7].

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