Muschamp John W, Hull Elaine M
Department of Psychology and Program in Neuroscience, Florida State University, Tallahassee, FL 32306-1270, USA.
Neurosci Lett. 2007 Nov 12;427(3):123-6. doi: 10.1016/j.neulet.2007.09.031. Epub 2007 Sep 22.
In male rats, estradiol (E(2)) exerts marked anorectic effects. One mechanism proposed for this effect is an E(2)-mediated down-regulation of the orexigenic neuropeptide melanin concentrating hormone (MCH). Previous anatomical work has shown that both MCH and estrogen receptor alpha (ERalpha) are found in quantity in the lateral hypothalamic area (LHA), a structure long associated with appetite and ingestive behavior. It has been hypothesized that the most direct manner by which E(2) could affect MCH expression and feeding would be via classical nuclear ERalpha located in MCH neurons. To evaluate this notion, we performed double-label immunohistochemistry for MCH and ERalpha in male rat hypothalamus. We report here that MCH neurons do not contain ERalpha, suggesting that the primary locus for estrogenic control of feeding is not the MCH neurons themselves. Rather, we show substantial overlap in the anatomical distribution of both cell types, raising the possibility that E(2) influences MCH signaling indirectly via adjacent ERalpha-containing cells.
在雄性大鼠中,雌二醇(E₂)具有显著的厌食作用。针对这种作用提出的一种机制是E₂介导的促食欲神经肽黑色素浓集激素(MCH)的下调。先前的解剖学研究表明,MCH和雌激素受体α(ERα)在下丘脑外侧区(LHA)大量存在,LHA是一个长期以来与食欲和摄食行为相关的结构。据推测,E₂影响MCH表达和进食的最直接方式是通过位于MCH神经元中的经典核ERα。为了评估这一观点,我们对雄性大鼠下丘脑进行了MCH和ERα的双重标记免疫组织化学研究。我们在此报告,MCH神经元不含ERα,这表明雌激素对进食控制的主要位点不是MCH神经元本身。相反,我们发现这两种细胞类型在解剖分布上有大量重叠,这增加了E₂通过相邻含ERα的细胞间接影响MCH信号传导的可能性。