格列美脲与格列吡嗪对妊娠链脲佐菌素诱导的糖尿病Wistar大鼠肾脏微结构及氧化应激标志物安全性的比较研究

Esubi Ju, Olojede So, Lawal Sk, Medubi Lj, Adekoya Aj, Dauda Ff, Olus Ap, A. Osinubi
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引用次数: 2

摘要

妊娠期糖尿病(GDM)和2型糖尿病的共同特征是胰岛素分泌相对减少和机体对胰岛素的反应受损。口服降糖药侵入性小,提高患者依从性,可有效维持妊娠期血糖水平。目的:研究格列美脲和格列吡嗪对链脲佐菌素(STZ)诱导的妊娠糖尿病大鼠肾脏及母体某些指标的影响。方法:35只体重120 ~ 160 g的雌性Sprague-Dawley大鼠分为5组。2 ~ 5组腹腔注射链脲佐菌素(STZ)诱导糖尿病。1组(对照组给予蒸馏水),2组(糖尿病患者给予格列美脲),3组(糖尿病患者给予胰岛素),4组(糖尿病患者给予格列吡嗪),5组(糖尿病患者给予柠檬酸缓冲液)。结果:格列美脲和格列吡嗪治疗组与糖尿病组和胰岛素组相比,氧化应激指标、血糖水平、体重、血液学指标和血脂均有显著改善(p=0.05)。与格列吡嗪组和糖尿病组相比,格列美脲组氧化应激指标、体重及肾组织恢复效果均有统计学意义(p=0.05)。结论:这两种口服降糖药可有效控制妊娠期葡萄糖耐受不良、肾脏氧化应激以及与胰岛素相当的肾脏细胞结构特性。因此,由于其对肾脏氧化应激和肾脏微结构特性的改善和恢复作用,格列美脲可能是妊娠期间充分控制葡萄糖耐受不良的诱人替代药物选择。
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Comparative Studies on Safety of Glimepiride and Glipizide on Renal Microarchitecture and Oxidative Stress Markers of Pregnant Streptozotocin-Induced Diabetic Wistar Rats
Introduction: A relatively decreased insulin secretion and impaired response of the body to insulin are the common attributes of gestational diabetes mellitus (GDM) and Type 2 diabetes mellitus. The oral hypoglycemic agents are less invasive, improve patients’ compliance, which can be effective in maintaining the blood sugar level during pregnancy. Aim: The overall aim of this research was to ascertain the comparative evaluation of the glimepiride and glipizide on the kidney and some maternal parameters of pregnant streptozotocin (STZ)-induced diabetic rats. Methodology: Thirty-five (35) female Sprague-Dawley rats weighing between 120-160 g were divided into 5 groups. Groups 2-5 were induced with diabetes mellitus by intraperitoneal injection of streptozotocin (STZ). Group 1: (Control given distilled water), Group 2: (Diabetic treated with Glimepiride), Group 3: (Diabetic treated with Insulin), Group 4: (Diabetic treated with Glipizide), Group 5: (Diabetic given citrate buffer). Results: Glimepiride and Glipizide treated groups showed statistically significant (p=0.05) improvement in oxidative stress markers, blood glucose level, body weight, hematological parameters and lipid profile when compared with diabetic and insulin groups. There was statistically significant (p=0.05) improvement on the oxidative stress marker, body weight and the restorative effect on renal histology in the group treated glimepiride when compared with glipizide and diabetic groups. Conclusion: This work has demonstrated that the two oral hypoglycaemic agents were effective in controlling glucose intolerance during pregnancy, renal oxidative stress as well as cytoarchitectonic properties of the kidney comparable with insulin. Therefore, because of its ameliorative and restorative effects on renal oxidative stress and micro-architectonic properties of the kidney, glimepiride could be tempting alternative drug of choice for adequate control of glucose intolerance during pregnancy.
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