首页> 外文期刊>Molecular and Cellular Biochemistry: An International Journal for Chemical Biology >Reversal of endothelial dysfunction in aorta of streptozotocin-nicotinamide-induced type-2 diabetic rats by S-Allylcysteine
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Reversal of endothelial dysfunction in aorta of streptozotocin-nicotinamide-induced type-2 diabetic rats by S-Allylcysteine

机译:S-烯丙基 - 烯丙基胺诱导的22型糖尿病大鼠主动脉内皮功能障碍的逆转

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摘要

Dietary measures and plant-based therapies as prescribed by native systems of medicine have gained attraction among diabetics with claims of efficacy. The present study investigated the effects of S-Allylcysteine (SAC) on body weight gain, glucose, insulin, insulin resistance, and nitric oxide synthase in plasma and argininosuccinate synthase (AS) and argininosuccinate lyase (ASL), lipid peroxides and antioxidant enzymes in aorta of control and streptozotocin-nicotinamide (STZ-NA)-induced diabetic rats. Changes in body weight, glucose, insulin, insulin resistance, and antioxidant profiles of aorta and mRNA expressions of nitric oxide synthase, AS, and ASL were observed in experimental rats. SAC (150 mg/kg b.w) showed its therapeutic effects similar to gliclazide in decreasing glucose, insulin resistance, lipid peroxidation, and increasing body weight; insulin, antioxidant enzymes, and mRNA levels of nitric oxide synthase, argininosuccinate synthase, and argininosuccinate lyase genes in STZ-NA rats. Histopathologic studies also revealed the protective nature of SAC on aorta. In conclusion, garlic and its constituents mediate the anti-diabetic potential through mitigating hyperglycemic status, changing insulin resistance by alleviating endothelial dysregulation in both plasma and tissues.
机译:原生药物制定的饮食措施和基于植物的疗法在糖尿病患者中获得了疗效的吸引力。本研究研究了S-烯丙基胞嘧啶(SAC)对体重增加,葡萄糖,胰岛素,胰岛素抗性和一氧化氮合酶(AS),脂质过氧化物和抗氧化酶中控制和链脲酰基胺酰胺(STZ-NA)诱导糖尿病大鼠主动脉。在实验大鼠中观察到体重,葡萄糖,胰岛素,胰岛素抗性的体重,葡萄糖,胰岛素,胰岛素抵抗和抗氧化剂曲线,如实验大鼠。 SAC(150mg / kg B.w)显示其治疗效果类似于葡萄糖,胰岛素抵抗,脂质过氧化和增加体重的神经脂醛。胰岛素,抗氧化酶和MRNA水平在STZ-NA大鼠中的一氧化氮合酶,氨基膦酸盐合酶和精氨酸琥珀酸裂解酶基因。组织病理学研究还揭示了主动脉囊的保护性质。总之,大蒜及其成分通过减轻高血糖地位介导抗糖尿病势,通过减轻血浆和组织中的内皮剂量抑制来改变胰岛素抵抗力。

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