Han Y, Shaikh M B, Siegel A
Department of Neurosciences, University of Medicine and Dentistry of New Jersey, Newark 07103, USA.
Brain Res. 1996 Apr 15;716(1-2):59-71. doi: 10.1016/0006-8993(95)01586-8.
The medial amygdala is known to powerfully suppress predatory attack behavior in the cat, but the mechanisms underlying such modulation remain unknown. The present study tested the hypothesis that medial amygdaloid suppression of predatory attack is mediated, in part, by a pathway from the medial amygdala to the medial hypothalamus which utilizes substance P as a neurotransmitter. Stimulating electrodes were implanted into the medial amygdala and cannula electrodes were implanted into both the medial and lateral hypothalamus. Predatory attack behavior was elicited by electrical stimulation of the lateral hypothalamus. In the first phase of the study, paired trials compared attack latencies of single stimulation of the lateral hypothalamus with those following dual stimulation of the lateral hypothalamus and medial amygdala. Attack latencies were significantly elevated following dual stimulation of the medial amygdala and lateral hypothalamus. In the second phase of the study, dose and time dependent decreases in response suppression were noted following the infusion of the substance P (NK1) receptor antagonist, CP96.345 (in doses of 0.05, 0.5 and 2.5 nmol) into the medial hypothalamus. In third phase of the study, the effects of microinjections of the substance P receptor agonist, [Sar9.Met(O2)11]-substance P (in doses of 0.5, 1.0 and 2.0 nmol), directly into the medial hypothalamus upon lateral hypothalamically elicited predatory attack behavior were determined. Microinfusion of this drug elevated attack response latencies in a dose- and time-dependent manner. In addition, pretreatment with CP96,345 into the medial hypothalamus blocked the suppressive effects of subsequent delivery of [Sar9,Met(O2)11]-substance P into the same medial hypothalamic site. Other parts of the study demonstrated the presence of: (1) high densities of substance P receptors in the ventromedial hypothalamus, and (2) neurons that are positively labeled for substance P that project from the medial amygdala to the ventromedial hypothalamus as demonstrated by retrograde labeling with Fluoro-Gold. These findings provide support for the hypothesis that medial amygdaloid suppression of lateral hypothalamically elicited predatory attack behavior includes a substance P pathway from the medial amygdala to the medial hypothalamus. The findings further suggest that stimulation of the medial amygdala activates substance P receptors in the medial hypothalamus, thus triggering an inhibitory mechanism from the medial to the lateral hypothalamus, resulting in suppression of predatory attack behavior.
内侧杏仁核能够有力地抑制猫的捕食攻击行为,但其调控机制尚不清楚。本研究验证了如下假设:内侧杏仁核对捕食攻击行为的抑制作用,部分是通过一条从内侧杏仁核到内侧下丘脑的通路介导的,该通路以P物质作为神经递质。将刺激电极植入内侧杏仁核,将套管电极植入内侧和外侧下丘脑。通过电刺激外侧下丘脑诱发捕食攻击行为。在研究的第一阶段,配对试验比较了单独刺激外侧下丘脑与同时刺激外侧下丘脑和内侧杏仁核后的攻击潜伏期。内侧杏仁核和外侧下丘脑同时受到刺激后,攻击潜伏期显著延长。在研究的第二阶段,向内侧下丘脑注射P物质(NK1)受体拮抗剂CP96.345(剂量分别为0.05、0.5和2.5 nmol)后,观察到反应抑制呈剂量和时间依赖性降低。在研究的第三阶段,确定了向内侧下丘脑直接微量注射P物质受体激动剂[Sar9.Met(O2)11]-P物质(剂量分别为于0.5、1.0和2.0 nmol)对外侧下丘脑诱发的捕食攻击行为的影响。微量注射这种药物后,攻击反应潜伏期呈剂量和时间依赖性延长。此外,预先向内侧下丘脑注射CP96,345可阻断随后向同一内侧下丘脑部位注射[Sar9,Met(O2)11]-P物质的抑制作用。研究的其他部分表明:(1)腹内侧下丘脑存在高密度的P物质受体;(2)通过荧光金逆行标记显示,从内侧杏仁核投射到腹内侧下丘脑的神经元被P物质阳性标记。这些发现支持了如下假设:内侧杏仁核对外侧下丘脑诱发的捕食攻击行为的抑制作用包括一条从内侧杏仁核到内侧下丘脑的P物质通路。这些发现还进一步表明,刺激内侧杏仁核可激活内侧下丘脑中的P物质受体,从而触发从内侧下丘脑到外侧下丘脑的抑制机制,导致捕食攻击行为受到抑制。