Schimmel R J, McMahon K K
Biochim Biophys Acta. 1980 Dec 1;633(2):237-44. doi: 10.1016/0304-4165(80)90409-2.
The effects of adenosine, N6-phenylisopropyl adenosine and 2',5'-dideoxyadenosine on lipolysis and cyclic AMP accumulation, in hamster adipocytes treated with cholera toxin, were studied. Cholera toxin caused an increase in lipolysis and cyclic AMP accumulation that was dependent upon the concentration of toxin and the length of time cells were exposed to the toxin. When N6-phenylisopropyl adenosine or 2',5'-dideoxyadenosine were present, the lipolytic and cyclic AMP responses to cholera toxin were inhibited. The adenosine analogues were equally effective inhibitors of lipolysis and cyclic AMP accumulation, when they were added 1 or 2 h after exposure to the toxin. Enzymatic removal of endogenously produced adenosine with adenosine deaminase potentiated both the lipolytic and cyclic AMP responses to cholera toxin. In addition, the inhibitory effects of N6-phenylisopropyl adenosine, 2'5'-dideoxyadenosine and clonidine on lipolysis and cyclic AMP were enhanced consequent to enzymatic removal of adenosine. These data show responses of intact fat cells to N6-phenylisopropyl adenosine, 2',5'-dideoxyadenosine or removal of endogenous adenosine and provide evidence for an adenosine sensitivity of fat cells exposed to cholera toxin.
研究了腺苷、N6-苯基异丙基腺苷和2',5'-二脱氧腺苷对经霍乱毒素处理的仓鼠脂肪细胞中脂解作用和环磷酸腺苷(cAMP)积累的影响。霍乱毒素导致脂解作用增强和cAMP积累增加,这取决于毒素的浓度以及细胞暴露于毒素的时间长度。当存在N6-苯基异丙基腺苷或2',5'-二脱氧腺苷时,对霍乱毒素的脂解和cAMP反应受到抑制。当在暴露于毒素1或2小时后添加腺苷类似物时,它们对脂解和cAMP积累的抑制效果相同。用腺苷脱氨酶酶促去除内源性产生的腺苷可增强对霍乱毒素的脂解和cAMP反应。此外,在酶促去除腺苷后,N6-苯基异丙基腺苷、2',5'-二脱氧腺苷和可乐定对脂解和cAMP的抑制作用增强。这些数据显示了完整脂肪细胞对N6-苯基异丙基腺苷、2',5'-二脱氧腺苷或去除内源性腺苷的反应,并为暴露于霍乱毒素的脂肪细胞的腺苷敏感性提供了证据。