Campbell R M, Scanes C G
Proc Soc Exp Biol Med. 1987 Apr;184(4):456-60. doi: 10.3181/00379727-184-42500.
The ability of growth hormone (GH) to inhibit the early (first hour) lipolytic response to glucagon and cAMP was investigated using chicken adipose tissue explants in vitro. In the first hour of incubation, GH inhibited glucagon, 8-bromo-3',5'-cyclic adenosine monophosphate (8-bromo-cAMP), and 1-isobutyl-3-methyl-xanthine (IBMX) induced glycerol release. The antilipolytic effect of GH was dose dependent, with inhibition of glucagon and 8-bromo-cAMP observed in the presence of as little as 100 ng/ml GH. In the fourth hour of incubation (late lipolytic response), GH (10, 100, or 1000 ng/ml) enhanced the lipolytic action of glucagon.
利用鸡脂肪组织外植体在体外研究了生长激素(GH)抑制对胰高血糖素和环磷酸腺苷(cAMP)早期(第一小时)脂解反应的能力。在孵育的第一小时,GH抑制了胰高血糖素、8-溴-3',5'-环磷酸腺苷(8-溴-cAMP)和1-异丁基-3-甲基黄嘌呤(IBMX)诱导的甘油释放。GH的抗脂解作用呈剂量依赖性,在低至100 ng/ml的GH存在下即可观察到对胰高血糖素和8-溴-cAMP的抑制作用。在孵育的第四小时(晚期脂解反应),GH(10、100或1000 ng/ml)增强了胰高血糖素的脂解作用。