Interactive Research School for Health Affairs, Bharati Vidyapeeth, Deemed to be University, Pune-Satara Road, Pune 411043, Maharashtra, India.
Department of Pharmacology, Bharati Vidyapeeth Medical College, Bharati Vidyapeeth, Deemed to be University, Pune-Satara Road, Pune 411043, Maharashtra, India.
Nutrients. 2020 Nov 27;12(12):3652. doi: 10.3390/nu12123652.
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 ( ≤ 0.001) serum triglycerides and very low density lipoprotein and elevated ( ≤ 0.001) high density lipoprotein levels in diabetic rats. Total cholesterol and low-density lipoprotein level was decreased ( ≤ 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 ( ≤ 0.001) in the fish oil treatment group. Whereas, carnitine palmitoyltransferase 1 and fatty acid binding protein gene expression were upregulated ( ≤ 0.001) in both flax and fish oil intervention group.
2 型糖尿病是一种由于胰岛素作用和分泌受损而引起的疾病,同时伴有脂质异常。本研究旨在评估 ω-3 脂肪酸(亚麻籽油和鱼油)与格列本脲联合应用对高脂肪饮食伴低链脲佐菌素(STZ)诱导的糖尿病大鼠异常血脂谱、血糖升高、肝肾功能损害的影响,并探讨其可能的作用机制。将雄性 Wistar 大鼠(n = 48)分为 8 组。除健康组外,所有动物组均给予高脂肪饮食(HFD)90 天。此外,通过低剂量 STZ(35mg/kg)诱导糖尿病。糖尿病动物给予 ω-3 脂肪酸(500mg/kg),同时给予格列本脲(0.25mg/kg)。亚麻籽油和鱼油干预均降低(≤0.001)糖尿病大鼠血清三酰甘油和极低密度脂蛋白水平,升高(≤0.001)高密度脂蛋白水平。鱼油治疗组降低(≤0.001)总胆固醇和低密度脂蛋白水平,而亚麻籽油治疗组无影响。亚麻籽油和鱼油干预均下调脂肪酸代谢基因、转录因子(固醇调节元件结合蛋白-1c 和核因子-κβ)及其调节基因,即乙酰辅酶 A 羧化酶 α、脂肪酸合酶和肿瘤坏死因子-α的表达。鱼油治疗组过氧化物酶体增殖物激活受体γ基因表达上调(≤0.001)。而肉毒碱棕榈酰转移酶 1 和脂肪酸结合蛋白基因表达在亚麻籽油和鱼油干预组均上调(≤0.001)。