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Herba Artemisiae Capillaris Extract Prevents the Development of Streptozotocin-Induced Diabetic Nephropathy of Rat

机译:茵陈提取物可预防链脲佐菌素诱导的大鼠糖尿病性肾病的发展

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摘要

Diabetic nephropathy (DN) is a major cause of end-stage renal disease throughout the world; until now there is no specific drug available. In this work, we use herba artemisiae capillaris extract (HACE) to alleviate renal fibrosis characterized by the excessive accumulation of extracellular matrix (ECM) in rats, aiming to investigate the protective effect of the HACE on DN. We found that the intragastric treatment of high-dose HACE could reverse the effect of streptozotocin not only to decrease the level of blood glucose and blood lipid in different degree but also further to improve renal functions. It is worth mentioning that the effect of HACE treatment was comparable to the positive drug benazepril. Moreover, we found that HACE treatment could on one hand inhibit oxidative stress in DN rats through regulating enzymatic activity for scavenging reactive oxygen species and on the other hand increase the ECM degradation through regulating the activity of metalloproteinase-2 (MMP-2) and the expression of tissue transglutaminase (tTG), which explained why HACE treatment inhibited ECM accumulation. On the basis of above experimental results, we conclude that HACE prevents DN development in a streptozotocin-induced DN rat model, and HACE is a promising candidate to cure DN in clinic.
机译:糖尿病肾病(DN)是全世界终末期肾脏疾病的主要原因。到目前为止,尚无特定药物。在这项工作中,我们使用草蒿提取物(HACE)缓解以大鼠细胞外基质(ECM)过量积累为特征的肾纤维化,旨在研究HACE对DN的保护作用。我们发现,大剂量HACE的胃内治疗可以逆转链脲佐菌素的作用,不仅可以不同程度地降低血糖和血脂水平,而且可以进一步改善肾脏功能。值得一提的是,HACE治疗的效果与贝那普利阳性药物相当。此外,我们发现HACE处理一方面可以通过调节酶活性来清除活性氧,从而抑制DN大鼠的氧化应激,另一方面可以通过调节金属蛋白酶2(MMP-2)和金属蛋白酶的活性来增加ECM降解。转谷氨酰胺酶(tTG)的表达,这解释了为什么HACE治疗抑制ECM积累。根据以上实验结果,我们得出结论,HACE可以预防链脲佐菌素诱导的DN大鼠模型中DN的发展,并且HACE是临床上有望治愈DN的候选药物。

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