Wittmann Gábor, Liposits Zsolt, Lechan Ronald M, Fekete Csaba
Department of Endocrine Neurobiology, Institute of Experimental Medicine, Hungarian Academy of Sciences, Budapest 1083, Hungary.
Endocrinology. 2005 Jul;146(7):2985-91. doi: 10.1210/en.2005-0178. Epub 2005 Apr 14.
Cocaine- and amphetamine-regulated transcript (CART) has stimulatory effects on the hypothalamic-pituitary-adrenal axis through direct effects on hypophysiotropic CRH neurons. Recently CART-containing axons have been demonstrated to densely innervate the hypophysiotropic CRH neurons. Based on the sources of the CART-immunoreactive (IR) innervation of the paraventricular nucleus, the putative origins of these CART-containing fibers include neurons of the hypothalamic arcuate nucleus that coexpress alphaMSH and medullary adrenaline-producing neurons. To determine whether these cell groups contribute to the CART innervation of the hypophysiotropic CRH neurons, we performed a quadruple-labeling immunofluorescent study using antisera against CRH, CART, alphaMSH, and phenylethanolamine-N-methyl-transferase (PNMT), the latter as a marker for adrenaline. Consistent with previous observations, PNMT- and CART-IR axons densely innervated all CRH neurons, whereas the alphaMSH-IR innervation was sparse. Although approximately 60% of CART-IR varicosities in juxtaposition to CRH neurons cocontained PNMT, only approximately 18% of them were immunopositive for alphaMSH. All alphaMSH-IR boutons and approximately 90% of PNMT-containing varicosities on the surface of CRH neurons were also labeled for CART. The remaining 22% of CART axon varicosities in contact with CRH neurons contained neither alphaMSH nor PNMT. These results indicate that medullary adrenergic/CART neurons are the major source for the CART innervation of CRH neurons in the paraventricular nucleus; however, to a lesser extent the arcuate nucleus also contributes to the CART-IR innervation of these neurons. The observation that nearly 20% of the CART-IR afferents contain neither alphaMSH nor PNMT, however, suggests that additional sources also contribute to the CART-IR input of hypophysiotropic CRH neurons.
可卡因和苯丙胺调节转录肽(CART)通过对促垂体促肾上腺皮质激素释放激素(CRH)神经元的直接作用,对下丘脑-垂体-肾上腺轴具有刺激作用。最近已证实,含CART的轴突密集支配促垂体CRH神经元。根据室旁核CART免疫反应性(IR)神经支配的来源,这些含CART纤维的假定起源包括共表达α-黑素细胞刺激素(αMSH)的下丘脑弓状核神经元和髓质肾上腺素生成神经元。为了确定这些细胞群是否对促垂体CRH神经元的CART神经支配有贡献,我们使用抗CRH、CART、αMSH和苯乙醇胺-N-甲基转移酶(PNMT,后者作为肾上腺素的标志物)的抗血清进行了四重标记免疫荧光研究。与先前的观察结果一致,PNMT和CART-IR轴突密集支配所有CRH神经元,而αMSH-IR神经支配稀疏。尽管与CRH神经元并列的CART-IR曲张体中约60%同时含有PNMT,但其中只有约18%对αMSH呈免疫阳性。CRH神经元表面所有的αMSH-IR终扣和约90%含PNMT的曲张体也被标记为CART。与CRH神经元接触的其余22%的CART轴突曲张体既不含有αMSH也不含有PNMT。这些结果表明,髓质肾上腺素能/CART神经元是室旁核中CRH神经元CART神经支配的主要来源;然而,弓状核在较小程度上也对这些神经元的CART-IR神经支配有贡献。然而,近20%的CART-IR传入纤维既不含有αMSH也不含有PNMT这一观察结果表明,其他来源也对促垂体CRH神经元的CART-IR输入有贡献。