Masuno H, Ohara T, Ide A, Okuda H
J Biochem. 1984 Apr;95(4):1083-90. doi: 10.1093/oxfordjournals.jbchem.a134696.
The effects of various synthetic peptides on basal and ACTH-stimulated lipolysis in fat cells were examined. Glu-Arg-Gly-Phe-Phe-Phe possessed lipolytic activity and increased ACTH-stimulated lipolysis at concentrations higher than 0.5 mumol/ml. Glu-Arg-Gly-Phe-Phe-Tyr did not cause any release of FFA from fat cells. Glu-Arg-Gly-Leu-Leu-Leu had no lipolytic activity but inhibited ACTH-stimulated lipolysis at concentrations higher than 0.25 mumol/ml. Glu-Arg-Gly-Leu-Leu-Leu also inhibited epinephrine-stimulated lipolysis. The effects of the peptides on basal and insulin-stimulated lipogenesis in fat cells were examined. Glu-Arg-Gly-Phe-Phe-Tyr increased both basal and insulin-stimulated lipogenesis. A tripeptide, Glu-Arg-Gly, inhibited both basal and insulin-stimulated lipogenesis. Glu-Arg-Gly-Leu-Leu-Leu had no effect on either basal or insulin-stimulated lipogenesis. Glu-Arg-Gly-Phe-Phe-Phe and ACTH, which elicit FFA release from fat cells, also stimulated formation of [14C]triglyceride from [14C]glucose.
研究了各种合成肽对脂肪细胞基础脂解和促肾上腺皮质激素(ACTH)刺激脂解的影响。Glu-Arg-Gly-Phe-Phe-Phe具有脂解活性,在浓度高于0.5 μmol/ml时可增加ACTH刺激的脂解作用。Glu-Arg-Gly-Phe-Phe-Tyr不会引起脂肪细胞释放游离脂肪酸(FFA)。Glu-Arg-Gly-Leu-Leu-Leu没有脂解活性,但在浓度高于0.25 μmol/ml时可抑制ACTH刺激的脂解作用。Glu-Arg-Gly-Leu-Leu-Leu也抑制肾上腺素刺激的脂解作用。研究了这些肽对脂肪细胞基础和胰岛素刺激的脂肪生成的影响。Glu-Arg-Gly-Phe-Phe-Tyr增加基础和胰岛素刺激的脂肪生成。一种三肽Glu-Arg-Gly抑制基础和胰岛素刺激的脂肪生成。Glu-Arg-Gly-Leu-Leu-Leu对基础或胰岛素刺激的脂肪生成均无影响。能引起脂肪细胞释放FFA的Glu-Arg-Gly-Phe-Phe-Phe和ACTH也刺激了由[14C]葡萄糖生成[14C]甘油三酯。