Role of Vernonia Amygdalina on Plasma Lipid Profile, Liver and Kidney Enzymes in Rats with Streptozotocin-Induced Diabetes

Gabriel Olukayode Ajayi, Elvis Uchechukwu Obi, Elizabeth Namesegua Elegbeleye, Precious Titilayo Obayemi, Oyindamola Mary Edamisan
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Abstract

Diabetes mellitus is a non-communicable disease which has been associated with liver and kidney injuries, and at the same time affects lipid profiles. The aim of this study was to investigate the role of Vernonia amygdalina (VAM) on plasma lipid profile, liver and kidney enzymes in rats with streptozotocin -induced diabetes. Twenty-five male albino wistar rats weighing between 137 and 223 g were randomly grouped into five of five rats per group as follows: control, diabetic, diabetic + metformin (MET), diabetic + VAM at 150, 300 mg/kg. Diabetes was induced by administration of 45 mg/kg body weight streptozotocin (STZ) dissolved in citrate buffer (0.01 M, pH 4.5) by single intraperitoneal injection. Three days after, when diabetes was confirmed, MET and VAM were administered daily by oral gavage for 7 days. Animals were fasted overnight after the last administration of MET and VAM, sacrificed, blood was collected and plasma prepared for lipid profile estimation. Liver and kidney were collected, weighed, homogenized and supernatants obtained for enzymes and biochemical assays. There were no significant (p>0.05) change in the weights of animal, liver and kidney, liver/rat and kidney/rat ratios, plasma cholesterol (CHOL) concentration, activities of liver and kidney aspartate aminotransferase (AST), alanine aminotransferase (ALT), liver gamma-glutamyl transferase (GGT), lactate dehydrogenase (LDH), and liver and kidney total protein (TPRO) concentrations; significant (p<0.05) decrease in triglyceride (TRIG), high density lipoprotein-cholesterol (HDL), low density lipoprotein-cholesterol (LDL), very low density lipoprotein-cholesterol (VLDL); and significant (p<0.05) increase in fasting blood glucose (FBG) level, kidney GGT, LDH activities, liver and kidney creatinine (CREA) and total bilirubin (TBIL) concentrations of diabetic (STZ) rats compared with normal control. The treatment of the diabetic rats with MET and VAM significantly modulated positively these parameters compared with the diabetic rats. This study further explains the protective role played by VAM in dyslipidaemia, liver and kidney injuries resulting from diabetes.
苦杏仁对链脲佐菌素诱导的糖尿病大鼠血脂及肝肾酶的影响
糖尿病是一种非传染性疾病,与肝脏和肾脏损伤有关,同时影响脂质谱。本研究旨在探讨苦杏仁素(VAM)对链脲佐菌素诱导的糖尿病大鼠血脂及肝肾酶的影响。选取体重为137 ~ 223 g的雄性白化wistar大鼠25只,随机分为5只(每组5只),分别为对照组、糖尿病、糖尿病+二甲双胍(MET)、糖尿病+ VAM(150、300 mg/kg)。用溶解于柠檬酸缓冲液(0.01 M, pH 4.5)中的链脲佐菌素(STZ) 45 mg/kg体重腹腔单次注射诱导糖尿病。确诊糖尿病后3 d,每日灌胃给予MET和VAM,连续7 d。末次给药MET和VAM后禁食过夜,处死,采集血液,制备血浆进行血脂测定。收集肝脏和肾脏,称重,均质,上清液用于酶和生化分析。动物体重、肝脏和肾脏、肝脏/大鼠和肾脏/大鼠比值、血浆胆固醇(CHOL)浓度、肝脏和肾脏天冬氨酸转氨酶(AST)、丙氨酸转氨酶(ALT)、肝脏γ -谷氨酰转移酶(GGT)、乳酸脱氢酶(LDH)活性以及肝脏和肾脏总蛋白(TPRO)浓度均无显著(p>0.05)变化;甘油三酯(TRIG)、高密度脂蛋白-胆固醇(HDL)、低密度脂蛋白-胆固醇(LDL)、极低密度脂蛋白-胆固醇(VLDL)显著(p<0.05)降低;糖尿病(STZ)大鼠空腹血糖(FBG)水平、肾脏GGT、LDH活性、肝肾肌酐(CREA)和总胆红素(TBIL)浓度较正常对照组显著(p<0.05)升高。与糖尿病大鼠相比,MET和VAM对糖尿病大鼠的这些参数有显著的正向调节。本研究进一步解释了VAM对糖尿病引起的血脂异常、肝肾损伤的保护作用。
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