首页> 外文期刊>Human and Experimental Toxicology >Evaluation of 4-methyl-2-[(2-methylbenzyl) amino]-1,3-thiazole-5-carboxylic acid against hyperglycemia, insulin sensitivity, and oxidative stress-induced inflammatory responses and -cell damage in the pancreas of streptozotocin-induced diabetic rats
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Evaluation of 4-methyl-2-[(2-methylbenzyl) amino]-1,3-thiazole-5-carboxylic acid against hyperglycemia, insulin sensitivity, and oxidative stress-induced inflammatory responses and -cell damage in the pancreas of streptozotocin-induced diabetic rats

机译:评价4-甲基-2 - [(2-甲基苄基)氨基] -1,3-噻唑-5-羧酸对高血糖,胰岛素敏感性和氧化应激诱导的炎症反应和 - 链脲佐菌素胰腺胰腺损伤 - 诱发糖尿病大鼠

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摘要

4-Methyl-2-[(2-methylbenzyl) amino]-1,3-thiazole-5-carboxylic acid (bioactive compound (BAC)), a novel thiazole derivative, is a xanthine oxidase inhibitor and free radical scavenging agent. Effects of BAC on hyperglycemia, insulin sensitivity, oxidative stress, and inflammatory mediators were evaluated in streptozotocin (STZ)-induced neonatal models of non-insulin-dependent diabetes mellitus (NIDDM) rats where NIDDM was induced in neonatal pups with single intraperitoneal injection of STZ (100 mg/kg). The effect of BAC (10 and 20 mg/kg, p.o.) for 3 weeks was evaluated by the determination of blood glucose, oral glucose tolerance test (OGTT), HbA1c level, insulin level, insulin sensitivity, and insulin resistance (IR). Furthermore, inflammatory mediators (tumor necrosis factor-alpha and interleukin-6) and oxidative stress were estimated in serum and pancreatic tissue, respectively. Significant alteration in the level of blood glucose, OGTT, HbA1c, insulin level, insulin sensitivity, in addition variation in the antioxidant status and inflammatory mediators, and alteration in histoarchitecture of pancreatic tissue confirmed the potential of BAC in STZ-induced neonatal models of NIDDM rats. Pretreatment with BAC restored the level of glucose by decreasing the IR and increasing the insulin sensitivity. Furthermore, BAC balanced the antioxidant status and preserved the inflammatory mediators. Histological studies of pancreatic tissues showed normal architecture after BAC administration to diabetic rats. Altogether, our results suggest that BAC successfully reduces the blood glucose level and possesses antioxidant as well as anti-inflammatory activities. This leads to decreased histological damage in diabetic pancreatic tissues, suggesting the possibility of future diabetes treatments.
机译:4-甲基-2 - [(2-甲基苄基)氨基] -1,3-噻唑-5-羧酸(生物活性化合物(BAC)),一种新型噻唑衍生物,是黄嘌呤氧化酶抑制剂和自由基清除剂。在链脲佐菌素(STZ) - 诱导的非胰岛素依赖性糖尿病(Niddm)大鼠的新生儿模型中评估了BAC对高血糖,胰岛素敏感性,氧化应激和炎症介质的影响,其中单人腹腔注射NIDDM在新生儿幼豆中诱导NIDDM STZ(100 mg / kg)。通过测定血糖,口服葡萄糖耐量试验(OGTT),HBA1C水平,胰岛素水平,胰岛素敏感性和胰岛素抗性(IR)评估BAC(10和20mg / kg,p.o.)对3周的影响。此外,炎症介质(肿瘤坏死因子-α和白细胞介素-6)分别估计在血清和胰腺组织中。血糖水平的显着变化,ogtt,HBA1c,胰岛素水平,胰岛素敏感性,抗氧化状态和炎症介质的变化以及胰组织组织建筑的改变证实了Bac在STZ诱导的Niddm新生儿模型中的潜力老鼠。通过降低IR并增加胰岛素敏感性,BAC的预处理恢复了葡萄糖水平。此外,BAC平衡了抗氧化状态并保存了炎症介质。胰腺组织的组织学研究表明,BAC施用糖尿病大鼠后的正常结构。完全,我们的结果表明BAC成功减少了血糖水平,并具有抗氧化剂以及抗炎活动。这导致糖尿病胰腺组织中的组织学损伤降低,表明未来糖尿病治疗的可能性。

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