Mills I, García-Sainz J A, Fain J N
Biochim Biophys Acta. 1986 May 21;876(3):619-30. doi: 10.1016/0005-2760(86)90051-2.
Adipocytes from hypothyroid rats have a decreased responsiveness to agents that activate adenylate cyclase, whereas cells from hyperthyroid rats have an increased responsiveness as compared to the controls. This is reflected in cyclic AMP accumulation as well as lipolysis. Administration of pertussis toxin to rats or its in vitro addition to adipocytes increased basal lipolysis and cyclic AMP accumulation as well as the response to norepinephrine or forskolin. The effects of thyroid status was not abolished by toxin treatment. Pertussis toxin-catalyzed ADP ribosylation of Ni was increased in adipocyte membranes from hypothyroid rats as compared to those from euthyroid rats. However, no change in sensitivity to N6-(phenylisopropyl)adenosine was observed. The data suggest that the amount of Ni might not be rate-limiting for the inhibitory action of adenosine. A consistent decrease in maximal lipolysis was observed in freshly isolated adipocytes from hypothyroid animals as compared to those from the controls. Such defective maximal lipolysis was not corrected by adenosine deaminase or in vivo administration of pertussis toxin. The relationship between cyclic AMP levels and lipolysis suggests that in fat cells from hypothyroid rats either the cyclic AMP-dependent protein kinase or the lipase activity itself may limit maximal lipolysis. There appears to be multiple effects of thyroid status on lipolysis involving factors other than those affecting adenylate cyclase activation.
甲状腺功能减退大鼠的脂肪细胞对激活腺苷酸环化酶的物质反应性降低,而甲状腺功能亢进大鼠的细胞与对照组相比反应性增加。这在环磷酸腺苷积累以及脂肪分解中都有体现。给大鼠注射百日咳毒素或在体外将其添加到脂肪细胞中,会增加基础脂肪分解和环磷酸腺苷积累以及对去甲肾上腺素或福斯高林的反应。毒素处理并未消除甲状腺状态的影响。与甲状腺功能正常大鼠的脂肪细胞膜相比,甲状腺功能减退大鼠的脂肪细胞膜中百日咳毒素催化的Ni的ADP核糖基化增加。然而,对N6 -(苯异丙基)腺苷的敏感性未观察到变化。数据表明,Ni的量可能不是腺苷抑制作用的限速因素。与对照组相比,甲状腺功能减退动物新鲜分离的脂肪细胞中观察到最大脂肪分解持续下降。腺苷脱氨酶或体内注射百日咳毒素并未纠正这种有缺陷的最大脂肪分解。环磷酸腺苷水平与脂肪分解之间的关系表明,在甲状腺功能减退大鼠的脂肪细胞中,要么环磷酸腺苷依赖性蛋白激酶要么脂肪酶活性本身可能限制最大脂肪分解。甲状腺状态对脂肪分解似乎有多种影响,涉及除影响腺苷酸环化酶激活之外的其他因素。