Department of Zoology, Guru Ghasidas Vishwavidayalaya (A Central University), Bilaspur, India.
Division Zoology, Department of Biosciences, Career Point University, Hamirpur, India.
Neuroendocrinology. 2022;112(8):807-822. doi: 10.1159/000520280. Epub 2021 Oct 21.
The present study was designed to evaluate the therapeutic efficacy of melatonin and insulin coadministration in diabetes-induced renal injury in rats.
Diabetes was achieved by giving streptozotocin (15 mg/kg) for 6 consecutive days. The diabetic condition was confirmed by assessing the blood glucose level; animals having blood glucose levels above 250 mg were considered as diabetic. Following the confirmation, animals were randomly divided into different experimental groups, viz group I served as the control (CON), group II diabetic (D), group III D+melatonin (MEL), group IV D+insulin (INS), group V D+MEL+INS, group VI D+glibenclamide (GB), group VII CON+MEL, group VIII CON+INS, and group IX CON+GB. Following the completion of the experimental period, animals were sacrificed, blood was collected via a retro-orbital puncture, and kidneys were harvested. Diabetic rats exhibited a significant increment in blood glucose and biochemical indexes of renal injury (tubular disruption, swollen glomeruli with loss of glomerular spaces, and distortion of the endothelial lining) including augmented levels of serum creatinine, urea, uric acid, Na+, and K+, and inhibition/suppression of the activity of glutathione (GSH) peroxidase, GSH reductase, glucose-6-phosphate dehydrogenase, and GSH-S-transferase in the renal cortex.
By examining thiobarbiturate reactive substances, reduced GSH, superoxide dismutase activity, and catalase activity in the renal cortex of control and diabetic rats, it was documented that treatment with melatonin or insulin alone or in combination showed a significant ad integrum recovery of GSH-dependent antioxidative enzymatic activities. Melatonin and insulin coadministration caused greater reductions in circulating tumor necrosis factor-α, tumor growth factor-β1, interleukin (IL)-1β, and IL-6 levels in diabetic rats, whereas IL-10 levels increased, as compared to each treatment alone. Diabetic rats showed a significant increase in the expression of both MT1 and MT2 melatonin receptor genes. Melatonin or insulin treatment alone or in combination resulted in significant restoration of the relative expression of both melatonin receptors in the renal cortex.
The coadministration of exogenous melatonin and insulin abolished many of the deleterious effects of type 1 diabetes on rat renal function.
本研究旨在评估褪黑素和胰岛素联合给药对糖尿病诱导的大鼠肾损伤的治疗效果。
连续 6 天给予链脲佐菌素(15mg/kg)以诱导糖尿病。通过评估血糖水平来确认糖尿病状态;血糖水平高于 250mg 的动物被认为患有糖尿病。确认后,动物被随机分为不同的实验组,即第 I 组作为对照组(CON),第 II 组为糖尿病组(D),第 III 组为 D+褪黑素(MEL)组,第 IV 组为 D+胰岛素(INS)组,第 V 组为 D+MEL+INS 组,第 VI 组为 D+格列本脲(GB)组,第 VII 组为 CON+MEL 组,第 VIII 组为 CON+INS 组,第 IX 组为 CON+GB 组。实验期结束后,处死动物,通过眼眶后穿刺采集血液,并收获肾脏。糖尿病大鼠的血糖和肾功能损伤的生化指标(肾小管破坏、肾小球肿胀伴肾小球间隙丧失和内皮衬里扭曲)显著升高,包括血清肌酐、尿素、尿酸、Na+和 K+水平升高,以及肾脏皮质中谷胱甘肽(GSH)过氧化物酶、GSH 还原酶、葡萄糖-6-磷酸脱氢酶和 GSH-S-转移酶的活性抑制/降低。
通过检测硫代巴比妥酸反应性物质、还原型 GSH、超氧化物歧化酶活性和过氧化氢酶活性,发现在对照组和糖尿病大鼠的肾脏皮质中,褪黑素或胰岛素单独或联合治疗均显著恢复了 GSH 依赖性抗氧化酶活性。褪黑素和胰岛素联合治疗可使糖尿病大鼠循环肿瘤坏死因子-α、转化生长因子-β1、白细胞介素(IL)-1β和 IL-6 水平显著降低,而 IL-10 水平升高,与每种药物单独治疗相比。糖尿病大鼠的 MT1 和 MT2 褪黑素受体基因表达均显著增加。褪黑素或胰岛素单独或联合治疗均可显著恢复肾脏皮质中两种褪黑素受体的相对表达。
外源性褪黑素和胰岛素的联合给药消除了 1 型糖尿病对大鼠肾功能的许多有害影响。