Münzberg Heike, Jobst Erin E, Bates Sarah H, Jones Justin, Villanueva Eneida, Leshan Rebecca, Björnholm Marie, Elmquist Joel, Sleeman Mark, Cowley Michael A, Myers Martin G
Internal Medicine, University of Michigan, Ann Arbor, Michigan 48109, USA.
J Neurosci. 2007 Jan 3;27(1):69-74. doi: 10.1523/JNEUROSCI.3168-06.2007.
Leptin directly suppresses the activity of orexigenic neurons in the hypothalamic arcuate nucleus (ARC). We examined c-Fos-like immunoreactivity (CFLIR) as a marker of ARC neuronal activity in db/db mice devoid of the signaling form of the leptin receptor (LRb) and s/s mice that express LRb(S1138) [which is defective for STAT3 (signal transducer and activator of transcription) signaling]. Both db/db and s/s animals are hyperphagic and obese. This analysis revealed that CFLIR in agouti related peptide-expressing orexigenic ARC neurons is basally elevated in db/db but not s/s mice. Consistent with these observations, electrophysiologic evaluation of a small number of neurons in s/s animals suggested that leptin appropriately suppresses the frequency of IPSCs on ARC proopiomelanocortin (POMC) neurons that are mediated by the release of GABA from orexigenic ARC neurons. CFLIR in POMC neurons of s/s mice was also increased compared with db/db animals. Thus, these data suggest that, although LRb-->STAT3 signaling is crucial for the regulation of feeding, it is not required for the acute or chronic regulation of orexigenic ARC neurons, and the activation of STAT3-mediated transcription by leptin is not required for the appropriate development of leptin responsiveness in these neurons.
瘦素直接抑制下丘脑弓状核(ARC)中促食欲神经元的活性。我们检测了c-Fos样免疫反应性(CFLIR),以此作为缺乏瘦素受体信号传导形式(LRb)的db/db小鼠和表达LRb(S1138)[其STAT3(信号转导和转录激活因子)信号传导存在缺陷]的s/s小鼠中ARC神经元活性的标志物。db/db和s/s动物均食欲亢进且肥胖。该分析显示,表达刺鼠相关肽的促食欲ARC神经元中的CFLIR在db/db小鼠中基础水平升高,但在s/s小鼠中未升高。与这些观察结果一致,对s/s动物中少数神经元的电生理评估表明,瘦素可适当抑制ARC促阿黑皮素原(POMC)神经元上由促食欲ARC神经元释放γ-氨基丁酸介导的抑制性突触后电流(IPSC)频率。与db/db动物相比,s/s小鼠POMC神经元中的CFLIR也增加。因此,这些数据表明,尽管LRb→STAT3信号传导对进食调节至关重要,但它对于促食欲ARC神经元的急性或慢性调节并非必需,并且瘦素对这些神经元中瘦素反应性的适当发育也不需要STAT3介导的转录激活。