Yang Xuejuan, Yan Jianqun, Lu Bo, Zhao Xiaolin, Lei Qi, Yang Dejun, Chen Ke, Zhao Shiru, Zhu Guangjing
Department of Physiology and Pathophysiology, Key Laboratory of Environment and Genes Related to Diseases, Ministry of Education, Xi'an Jiaotong University School of Medicine, Xi'an, Shaanxi 710061, China.
Brain Res. 2009 Jun 1;1273:83-91. doi: 10.1016/j.brainres.2009.03.058. Epub 2009 Apr 5.
Previous studies have shown that lesions of the posterodorsal amygdala (PDA) produce hyperphagia and obesity in female rats. To better understand the role of the PDA in the regulation of feeding behavior, the current study examined the effects of electrical stimulation of the PDA of female rats on food intake and identified neurons activated by PDA stimulation using Fos immunohistochemistry. Hormonal levels following stimulation of the PDA were also investigated. Electrical stimulation (100 muA, 0.2 ms, 20 Hz, 10 min) of the PDA remarkably decreased 1 h food intake of rats. Following PDA stimulation, the number of Fos-like immunoreactive neurons increased in the caudal and intermediate parts of the nucleus of the solitary tract (NST), the area postrema (AP), the external lateral subnucleus of the parabrachial nucleus (PBN), the arcuate nucleus of the hypothalamus (Arc), and the central amygdaloid nucleus (CeA). The level of circulating leptin was elevated significantly by PDA stimulation as well. Together with previous studies, the results suggest that the PDA may play an important role in the regulation of feeding behavior, at least partly by modulating the circulating leptin, and that the caudal and intermediate parts of the NST, AP, external lateral PBN, Arc, and CeA probably participate in this regulation.
先前的研究表明,后背部杏仁核(PDA)损伤会导致雌性大鼠出现摄食过量和肥胖。为了更好地理解PDA在进食行为调节中的作用,本研究检测了对雌性大鼠PDA进行电刺激对食物摄入量的影响,并使用Fos免疫组织化学方法鉴定了由PDA刺激激活的神经元。还研究了PDA刺激后的激素水平。对PDA进行电刺激(100微安、0.2毫秒、20赫兹、10分钟)显著降低了大鼠1小时的食物摄入量。PDA刺激后,孤束核(NST)尾侧和中间部分、最后区(AP)、臂旁核外侧亚核(PBN)、下丘脑弓状核(Arc)和中央杏仁核(CeA)中Fos样免疫反应性神经元的数量增加。PDA刺激还使循环瘦素水平显著升高。与先前的研究一起,结果表明PDA可能在进食行为调节中起重要作用,至少部分是通过调节循环瘦素,并且NST、AP、PBN外侧、Arc和CeA的尾侧和中间部分可能参与了这种调节。