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百日咳毒素对甲状腺功能减退、甲状腺功能正常和甲状腺功能亢进大鼠脂肪细胞中腺苷酸环化酶活性、环磷酸腺苷积累及脂肪分解的影响。

Pertussis toxin effects on adenylate cyclase activity, cyclic AMP accumulation and lipolysis in adipocytes from hypothyroid, euthyroid and hyperthyroid rats.

作者信息

Mills I, García-Sainz J A, Fain J N

出版信息

Biochim Biophys Acta. 1986 May 21;876(3):619-30. doi: 10.1016/0005-2760(86)90051-2.

DOI:10.1016/0005-2760(86)90051-2
PMID:3011106
Abstract

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.

摘要

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。

相似文献

1
Pertussis toxin effects on adenylate cyclase activity, cyclic AMP accumulation and lipolysis in adipocytes from hypothyroid, euthyroid and hyperthyroid rats.百日咳毒素对甲状腺功能减退、甲状腺功能正常和甲状腺功能亢进大鼠脂肪细胞中腺苷酸环化酶活性、环磷酸腺苷积累及脂肪分解的影响。
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2
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Human fat cell lipolysis is primarily regulated by inhibitory modulators acting through distinct mechanisms.人类脂肪细胞的脂解作用主要受通过不同机制起作用的抑制性调节剂调控。
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Activation of lipolysis and cyclic AMP accumulation in rabbit adipocytes by isoproterenol in the presence of forskolin or pertussis toxin.在存在福斯高林或百日咳毒素的情况下,异丙肾上腺素对兔脂肪细胞脂解作用的激活及环磷酸腺苷的积累。
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Promotion of lipolysis in rat adipocytes by pertussis toxin: reversal of endogenous inhibition.百日咳毒素对大鼠脂肪细胞脂解作用的促进:内源性抑制的逆转
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Short-term hyperthyroidism modulates adenosine receptors and catalytic activity of adenylate cyclase in adipocytes.短期甲状腺功能亢进会调节脂肪细胞中腺苷受体和腺苷酸环化酶的催化活性。
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Res Commun Chem Pathol Pharmacol. 1989 Dec;66(3):397-410.

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Regulation of beta 1- and beta 3-adrenergic agonist-stimulated lipolytic response in hyperthyroid and hypothyroid rat white adipocytes.甲状腺功能亢进和减退大鼠白色脂肪细胞中β1-和β3-肾上腺素能激动剂刺激的脂解反应的调节
Br J Pharmacol. 2000 Feb;129(3):448-56. doi: 10.1038/sj.bjp.0703008.
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Effect of tri-iodothyronine on leptin release and leptin mRNA accumulation in rat adipose tissue.
三碘甲状腺原氨酸对大鼠脂肪组织中瘦素释放及瘦素mRNA积累的影响。
Biochem J. 1998 Jun 1;332 ( Pt 2)(Pt 2):361-6. doi: 10.1042/bj3320361.
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Expression of leptin and beta 3-adrenergic receptors in rat adipose tissue in altered thyroid states.甲状腺状态改变时大鼠脂肪组织中瘦素和β3-肾上腺素能受体的表达
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Biochem J. 1987 Oct 1;247(1):223-7. doi: 10.1042/bj2470223.
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Short-term hyperthyroidism modulates adenosine receptors and catalytic activity of adenylate cyclase in adipocytes.短期甲状腺功能亢进会调节脂肪细胞中腺苷受体和腺苷酸环化酶的催化活性。
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Adipocyte plasma-membrane Gi and Gs in insulinopenic diabetic patients.胰岛素缺乏型糖尿病患者脂肪细胞质膜中的Gi和Gs
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Guanine-nucleotide-binding proteins Gi and Gs in fat-cells from normal, hypothyroid and obese human subjects.正常、甲状腺功能减退和肥胖人类受试者脂肪细胞中的鸟嘌呤核苷酸结合蛋白Gi和Gs
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