Iudaev N A, Pankov Iu A, Keda Iu M, Shvachkin Iu P, Riabtsev M N
Biokhimiia. 1976 Aug;41(8):1484-7.
Fat mobilyzing activity of synthetic tetradecapeptide, which corresponds in 31--44 amino acid sequence of human growth hormone, is studied in vitro in human fat tissue. The peptide at concentrations of 3--33 microng/ml considerably stimulated lipolysis in subdermal fat tissue, omentum and shoulder ateroma. Minimal efficient peptide concentration was 3 microng/ml in most experiments, sometimes it was 0.3 microng/ml. Direct dependency between dose logarithm and lipolysis rate was observed at dose interval of 0.3--18 microng/ml. Native growth hormone produced no activity in human fat tissue even in concentrations of 50--100 microng/ml.
在人体脂肪组织中对体外研究了与人生长激素31 - 44氨基酸序列相对应的合成十四肽的脂肪动员活性。该肽浓度为3 - 33微克/毫升时,能显著刺激皮下脂肪组织、网膜和肩部动脉粥样硬化斑块中的脂肪分解。在大多数实验中,肽的最小有效浓度为3微克/毫升,有时为0.3微克/毫升。在0.3 - 18微克/毫升的剂量间隔内,观察到剂量对数与脂肪分解速率之间存在直接相关性。天然生长激素即使在浓度为50 - 100微克/毫升时,在人体脂肪组织中也没有活性。