Koob G F, Heinrichs S C
Department of Neuropharmacology, CVN-7, The Scripps Research Institute, La Jolla, CA 92037, USA.
Brain Res. 1999 Nov 27;848(1-2):141-52. doi: 10.1016/s0006-8993(99)01991-5.
Corticotropin-releasing factor (CRF) and CRF-related neuropeptides have an important role in the central nervous system to mediate behavioral responses to stressors. CRF receptor antagonists are very effective in reversing stress-induced suppression and activation in behavior. An additional CRF-like neuropeptide, urocortin, has been identified in the brain and has a high affinity for the CRF-2 receptor in addition to the CRF-1 receptor. Urocortin has many of the effects of CRF but also is significantly more potent than CRF in decreasing feeding in both meal-deprived and free-feeding rats. In mouse genetic models, mice over-expressing CRF show anxiogenic-like responses compared to wild-type mice, and mice lacking the CRF-1 receptor showed an anxiolytic-like behavioral profile compared to wild-type mice. Results to date have led to the hypothesis that CRF-1 receptors may mediate CRF-like neuropeptide effects on behavioral responses to stressors, but CRF-2 receptors may mediate the suppression of feeding produced by CRF-like neuropeptides. Brain sites for the behavioral effects of CRF include the locus coeruleus (LC), paraventricular nucleus (PVN) of the hypothalamus, the bed nucleus of the stria terminalis (BNST), and the central nucleus of the amygdala. CRF may also be activated during acute withdrawal from all major drugs of abuse, and recent data suggest that CRF may contribute to the dependence and vulnerability to relapse associated with chronic administration of drugs of abuse. These data suggest that CRF systems in the brain have a unique role in mediating behavioral responses to diverse stressors. These systems may be particularly important in situations were an organism must mobilize not only the pituitary adrenal system, but also the central nervous system in response to environmental challenge. Clearly, dysfunction in such a fundamental brain-activating system may be the key to a variety of pathophysiological conditions involving abnormal responses to stressors such as anxiety disorders, affective disorders, and anorexia nervosa.
促肾上腺皮质激素释放因子(CRF)及相关神经肽在中枢神经系统中发挥着重要作用,可介导对应激源的行为反应。CRF受体拮抗剂在逆转应激诱导的行为抑制和激活方面非常有效。另外一种类CRF神经肽——尿皮质素已在大脑中被鉴定出来,它除了对CRF-1受体有高亲和力外,对CRF-2受体也有高亲和力。尿皮质素具有许多CRF的作用,但在减少禁食和自由进食大鼠的进食量方面,其效力也显著高于CRF。在小鼠遗传模型中,与野生型小鼠相比,过度表达CRF的小鼠表现出类似焦虑的反应,而缺乏CRF-1受体的小鼠与野生型小鼠相比则表现出抗焦虑样行为特征。迄今为止的研究结果提出了这样一个假说,即CRF-1受体可能介导类CRF神经肽对应激源行为反应的影响,但CRF-2受体可能介导类CRF神经肽对进食的抑制作用。CRF产生行为效应的脑区包括蓝斑(LC)、下丘脑室旁核(PVN)、终纹床核(BNST)和杏仁核中央核。在从所有主要滥用药物中急性戒断期间,CRF也可能被激活,最近的数据表明,CRF可能与长期滥用药物导致的依赖和复发易感性有关。这些数据表明,大脑中的CRF系统在介导对各种应激源的行为反应中具有独特作用。在机体不仅必须动员垂体-肾上腺系统,而且还必须动员中枢神经系统以应对环境挑战的情况下,这些系统可能尤为重要。显然,这样一个基本的大脑激活系统功能失调可能是涉及对应激源异常反应的各种病理生理状况(如焦虑症、情感障碍和神经性厌食症)的关键所在。