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Peptides from frog skin with potential for development into agents for Type 2 diabetes therapy

机译:青蛙皮肤的肽具有潜力的糖尿病患者的发育潜力

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摘要

Several frog skin peptides, first identified as result of their antimicrobial or immunomodulatory activities, have subsequently been shown to stimulate insulin release both in vitro and in vivo and so show potential for development into incretin-based drugs for treatment of patients with Type 2 diabetes mellitus. However, their therapeutic potential as anti-diabetic agents is not confined to this activity as certain frog skin-derived peptides, such as magainin-AM2 and CPF-SE1 and analogs of hymenochirin-1B, tigerinin-1R, and esculentin-2CHa, have been shown to increase insulin sensitivity, promote beta-cell proliferation, suppress pancreatic and circulating glucagon concentrations, improve the lipid profile, and selectively alter expression of genes involved in insulin secretion and action in mice with diet-induced obesity, insulin resistance and impaired glucose tolerance. This review assesses the therapeutic possibilities of peptides from frogs belonging to the Pipidae, Dicroglossidae, and Ranidae families, focusing upon work that has been carried out since 2014.
机译:随后证明了几只嘴唇皮肤肽,首先被鉴定为抗微调或免疫调节活动的结果,以刺激体外和体内的胰岛素释放,因此显示出促进胰岛素的药物的发育潜力,用于治疗2型糖尿病患者。然而,它们作为抗糖尿病药剂的治疗潜力不仅限于该活性,作为某些蛙皮肤衍生的肽,例如Magainin-AM2和CPF-SE1和Hymenochirin-1B,Tigerinin-1R和Escuburinin-2Cha的类似物已被证明提高胰岛素敏感性,促进β-细胞增殖,抑制胰腺和循环胰高血糖素浓度,改善脂质谱,并选择性地改变饮食肥胖,胰岛素抵抗,胰岛素抵抗和血糖胰岛素分泌物中参与胰岛素分泌和作用的基因的表达宽容。该审查评估了属于Pipidae,Dicroglossidae和Ranidae家族的青蛙肽的治疗可能性,重点是自2014年以来已经进行的工作。

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