Combined administration of gallic acid and glibenclamide mitigate systemic complication and histological changes in the cornea of diabetic rats induced with streptozotocin.

Acta cirurgica brasileira Pub Date : 2024-02-05 eCollection Date: 2024-01-01 DOI:10.1590/acb390124
Jing Zhao, Shaik Althaf Hussain, Narendra Maddu
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Abstract

Purpose: To determine the effect of gallic acid or its combination with glibenclamide on some biochemical markers and histology of the cornea of streptozotocin (STZ) induced diabetic rats.

Methods: Following induction of diabetes, 24 male albino rats were divided into four groups of six rats each. Groups 1 and 2 (control and diabetic) received rat pellets and distilled water; group 3 (gallic acid) received rat pellets and gallic acid (10 mg/kg, orally) dissolved in the distilled water; and group 4 (gallic acid + glibenclamide) received rat pellets, gallic acid (10 mg/kg, orally), and glibenclamide (5 mg/kg, orally) dissolved in the distilled water. The treatments were administered for three months after which the rats were sacrificed after an overnight fast. Blood and sera were collected for the determination of biochemical parameters, while their eyes were excised for histology.

Results: STZ administration to the rats induced insulin resistance, hyperglycemia, microprotenuria, loss of weight, oxidative stress, inflammation, and alteration of their cornea histology, which was abolished following supplementation with gallic acid or its combination with glibenclamide.

Conclusions: The study showed the potentials of gallic acid and glibenclamide in mitigating systemic complication and histological changes in the cornea of diabetic rats induced with STZ.

联合服用没食子酸和格列本脲可减轻全身并发症和链脲佐菌素诱导的糖尿病大鼠角膜的组织学变化。
目的:确定没食子酸或其与格列本脲联合使用对链脲佐菌素(STZ)诱导的糖尿病大鼠角膜的一些生化指标和组织学的影响:诱导糖尿病大鼠后,将 24 只雄性白化大鼠分为 4 组,每组 6 只。第 1 组和第 2 组(对照组和糖尿病组)接受大鼠颗粒和蒸馏水;第 3 组(没食子酸组)接受大鼠颗粒和溶于蒸馏水的没食子酸(10 毫克/千克,口服);第 4 组(没食子酸 + 格列本脲组)接受大鼠颗粒、没食子酸(10 毫克/千克,口服)和溶于蒸馏水的格列本脲(5 毫克/千克,口服)。治疗持续三个月后,大鼠在禁食一夜后被处死。收集血液和血清以测定生化指标,同时切除大鼠眼睛以进行组织学检查:结果:给大鼠服用 STZ 会诱发胰岛素抵抗、高血糖、微量蛋白尿、体重减轻、氧化应激、炎症和角膜组织学改变:研究表明,没食子酸和格列本脲具有减轻STZ诱导的糖尿病大鼠全身并发症和角膜组织学变化的潜力。
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