Hyperleptinaemia in mice induced by administration of the tyrosine hydroxylase inhibitor α‐methyl‐p‐tyrosine

FEBS Letters

Rayner, D.Vernon¹  Simón, Edurne²  Duncan, Jacqueline S.¹  Trayhurn, Paul¹ 

[1] Molecular Physiology Group, Rowett Research Institute, Bucksburn, Aberdeen AB21 9SB, Scotland, UK;Department of Nutrition and Food Science, Universidad Pais Vasco, Paseo de la Universidad 7, 01006 Vitoria, Spain

关键词: α-Methyl-p-tyrosine;    β3-Adrenoceptor;    Leptin;    ob gene;    Sympathetic nervous system;    White adipose tissue;    αMPT;    α-methyl-p-tyrosine;   

DOI  :  10.1016/S0014-5793(98)00642-5

学科分类：生物化学/生物物理

来源: John Wiley & Sons Ltd.

【 摘 要 】

α-methyl-p-tyrosine (αMPT), an inhibitor of tyrosine hydroxylase, was administered to mice to block noradrenaline synthesis. Ten hours after injection of αMPT there was a 6-fold increase in plasma leptin. The level of ob mRNA in epididymal white adipose tissue was also increased, but UCP1 mRNA in brown fat fell. In contrast to lean mice, ob mRNA in white fat of ob/ob mice was not increased by αMPT. αMPT raised plasma leptin in fasted as well as fed mice. Hyperleptinaemia was attenuated by treatment with a β3-adrenoceptor agonist. Inhibition of noradrenaline synthesis leads to the rapid induction of hyperleptinaemia; it is suggested that sympathetic tone plays a pivotal role in regulating leptin production.

【 授权许可】

Unknown