首页> 外文期刊>Toxicology Letters: An International Journal Providing a Forum for Original and Pertinent Contributions in Toxicology Research >Effect of 2-dodecyl-6-methoxycyclohexa-2,5-diene-1,4-dione, isolated from Averrhoa carambola L. (Oxalidaceae) roots, on advanced glycation end-product-mediated renal injury in type 2 diabetic KKAy mice
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Effect of 2-dodecyl-6-methoxycyclohexa-2,5-diene-1,4-dione, isolated from Averrhoa carambola L. (Oxalidaceae) roots, on advanced glycation end-product-mediated renal injury in type 2 diabetic KKAy mice

机译:从杨桃根中分离的2-十二烷基-6-甲氧基环己-2,5-二烯-1,4-二酮对晚期糖基化终产物介导的2型糖尿病KKAy小鼠肾损伤的影响

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摘要

The roots of Averrhoa carambola L. (Oxalidaceae) have a long history of medical use in traditional Chinese medicine for treating diabetes and diabetic nephropathy. 2-Dodecyl-6-methoxycyclohexa-2,5-diene-1,4-dione (DMDD) was isolated from the tuberous roots of A. carambola L. The purpose of this study was to investigate the beneficial effect of DMDD on the advanced glycation end-product-mediated renal injury in type 2 diabetic KKAy mice with regard to prove its efficacy by local traditional practitioners in the treatment of kidney frailties in diabetics. KKAy mice were orally administrated DMDD (12.5, 25, 50mg/kg body weight/d) or aminoguanidine (200mg/kg body weight/d) for 8 weeks. Hyperglycemia, renal AGE formation, and the expression of related proteins, such as the AGE receptor, nuclear factor-?B, transforming growth factor-?1, and Ne-(carboxymethyl)lysine, were markedly decreased by DMDD. Diabetes-dependent alterations in proteinuria, serum creatinine, creatinine clearance, and serum urea-N and glomerular mesangial matrix expansion were attenuated after treatment with DMDD for 8 weeks. The activities of superoxide dismutase and glutathione peroxidase, which are reduced in the kidneys of KKAy mice, were enhanced by DMDD. These findings suggest that DMDD may inhibit the progression of diabetic nephropathy and may be a therapeutic agent for regulating several pharmacological targets to treat or prevent of diabetic nephropathy.
机译:杨桃的根源在治疗糖尿病和糖尿病性肾病的中药中具有悠久的医学应用历史。从杨桃A的块根中分离出2-十二烷基-6-甲氧基环己-2,5-二烯-1,4-二酮(DMDD)。关于糖基化终产物介导的2型糖尿病KKAy小鼠肾损伤的研究,以证明其由当地传统医生从实践中治疗糖尿病性肾衰的功效。给予KKAy小鼠DMDD(12.5、25、50mg / kg体重/ d)或氨基胍(200mg / kg体重/ d)8周。 DMDD显着降低了高血糖症,肾脏AGE的形成以及AGE受体,核因子-βB,转化生长因子-α1和Ne-(羧甲基)赖氨酸等相关蛋白的表达。 DMDD治疗8周后,蛋白尿,血清肌酐,肌酐清除率,血清尿素-N和肾小球系膜基质扩张的糖尿病依赖性改变减弱。 DMDD增强了KKAy小鼠肾脏中超氧化物歧化酶和谷胱甘肽过氧化物酶的活性。这些发现表明DMDD可以抑制糖尿病性肾病的进展,并且可以是调节几种药理学靶标以治疗或预防糖尿病性肾病的治疗剂。

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