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Hypoglycemic, Hypolipidemic and Antioxidant Effects of Peptides from Red Deer Antlers in Streptozotocin-Induced Diabetic Mice

机译:马鹿鹿角肽对链脲佐菌素诱导的糖尿病小鼠的降血糖,降血脂和抗氧化作用

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Diabetes mellitus is a serious chronic metabolic disorder. To develop novel anti-diabetic drugs from nature sources has always been the focus of research. Red deer (Cervus elaphu Linnaeus) antler is one of the most famous Chinese traditional medicines. We found that the peptides of 5-10 kDa from red deer antlers (PRDA) promoted the growth of cultured rat islet cells. The purpose of this study was to investigate the anti-diabetic actions of PRDA in vivo and purify a pure active peptide. We therefore investigated the hypoglycemic, hypolipidemic and antioxidant effects of PRDA in streptozotocin-induced diabetic mice and isolated a pure anti-diabetic peptide. PRDA, given intraperitoneally (75, 150, or 300 mu g/kg), significantly decreased the blood glucose levels, significantly increased the insulin concentrations, and remarkably improved the lipid metabolism in the diabetic mice. PRDA significantly increased the superoxide dismutase activity, catalase activity and the total antioxidant capacity in the serum and liver, and simultaneously decreased the malondialdehyde levels. The activities of hexokinase and pyruvate kinase, two important enzymes involved in glucose utilization, were also significantly increased in the liver of the PRDA-treated diabetic mice. Moreover, a novel anti-diabetic peptide isolated from PRDA significantly promoted the viability of cultured rat insulinoma cells. The molecular mass of the purified peptide was 7064.8 Da under mass spectrometry, and its N-terminal amino acid sequence was identified as LSPFTTKTYFPHFDLSHGSA. Thus, PRDA may be useful in managing the hyperglycemia, hyperlipidemia, and oxidative stress in diabetes, and the anti-diabetic peptide is a promising drug for the treatment of diabetes. (C) 2015 Tohoku University Medical Press
机译:糖尿病是一种严重的慢性代谢性疾病。从自然资源开发新型抗糖尿病药物一直是研究的重点。马鹿鹿角(鹿)是最著名的中药之一。我们发现,来自马鹿鹿角(PRDA)的5-10 kDa的肽促进了培养的大鼠胰岛细胞的生长。这项研究的目的是研究PRDA在体内的抗糖尿病作用并纯化纯活性肽。因此,我们研究了链脲佐菌素诱导的糖尿病小鼠中PRDA的降血糖,降血脂和抗氧化作用,并分离了纯的抗糖尿病肽。腹膜内给予PRDA(75、150或300μg/ kg),可显着降低血糖水平,显着增加胰岛素浓度,并显着改善糖尿病小鼠的脂质代谢。 PRDA显着增加了血清和肝脏中的超氧化物歧化酶活性,过氧化氢酶活性和总抗氧化能力,同时降低了丙二醛水平。在参与PRDA治疗的糖尿病小鼠的肝脏中,己糖激酶和丙酮酸激酶(参与葡萄糖利用的两个重要酶)的活性也显着增加。而且,从PRDA分离的新型抗糖尿病肽显着促进了培养的大鼠胰岛素瘤细胞的活力。质谱分析纯化的肽的分子量为7064.8Da,其N端氨基酸序列鉴定为LSPFTTKTYFPHFDLSHGSA。因此,PRDA可用于控制糖尿病中的高血糖,高血脂和氧化应激,并且抗糖尿病肽是用于治疗糖尿病的有前途的药物。 (C)2015年东北大学医学出版社

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