Koob G F
Department of Neuropharmacology, Scripps Research Institute, La Jolla, CA 92037, USA.
Biol Psychiatry. 1999 Nov 1;46(9):1167-80. doi: 10.1016/s0006-3223(99)00164-x.
Corticotropin-releasing factor (CRF) and related peptides in the central nervous system appears to have activating properties on behavior and to enhance behavioral responses to stressors. CRF and urocortin injected into the brain produces increases in arousal as measured by locomotor activation and increased responsiveness to stressful stimuli. These effects of CRF appear to be independent of the pituitary adrenal axis and can be reversed by specific and selective CRF antagonists alpha-helical CRF9-41 and D-Phe CRF12-41. Perhaps more importantly, CRF antagonists can reverse behavioral responses to many stressors. These results suggest that endogenous CRF systems in the brain may have a role in mediating behavioral responses to stressors. Norepinephrine systems emanating from the nucleus locus coeruleus also long have been hypothesized to be involved in mediating behavioral constructs associated with alertness, arousal, and stress. Pharmacologic, physiologic, and neuroanatomic evidence supports an important role for a CRF-norepinephrine interaction in the region of the locus coeruleus in response to stressors that may be modality-specific where CRF neurons activate the locus coeruleus. One may hypothesize that another norepinephrine-CRF interaction may occur in the terminal projections of the forebrain norepinephrine systems in the paraventricular nucleus of the hypothalamus, the bed nucleus of the stria terminalis, and the central nucleus of the amygdala where norepinephrine stimulates CRF release. Such a feed-forward system may be particularly important in situations where an organism must mobilize not only the pituitary adrenal system but also the central nervous system, in response to environmental challenge. However, such a feed-forward mechanism in a fundamental brain-activating system may be particularly vulnerable to dysfunction and thus, may be the key to a variety of pathophysiologic conditions involving abnormal responses to stressors such as anorexia nervosa, anxiety, and affective disorders.
中枢神经系统中的促肾上腺皮质激素释放因子(CRF)及相关肽似乎对行为具有激活特性,并能增强对应激源的行为反应。向脑内注射CRF和尿皮质素会使觉醒增加,这可通过运动激活以及对应激刺激反应性增强来衡量。CRF的这些作用似乎独立于垂体 - 肾上腺轴,并且可被特异性和选择性的CRF拮抗剂α - 螺旋CRF9 - 41和D - Phe CRF12 - 41逆转。或许更重要的是,CRF拮抗剂可逆转对多种应激源的行为反应。这些结果表明,脑内的内源性CRF系统可能在介导对应激源的行为反应中发挥作用。长期以来,人们一直推测源自蓝斑核的去甲肾上腺素系统参与介导与警觉、觉醒和应激相关的行为结构。药理学、生理学和神经解剖学证据支持在蓝斑核区域CRF - 去甲肾上腺素相互作用在对应激源的反应中起重要作用,这种反应可能是模式特异性的,即CRF神经元激活蓝斑核。有人可能推测,另一种去甲肾上腺素 - CRF相互作用可能发生在下丘脑室旁核、终纹床核和杏仁核中央核的前脑去甲肾上腺素系统的终末投射中,其中去甲肾上腺素刺激CRF释放。在生物体必须不仅动员垂体 - 肾上腺系统而且动员中枢神经系统以应对环境挑战的情况下,这样的前馈系统可能特别重要。然而,这样一个基本的脑激活系统中的前馈机制可能特别容易出现功能障碍,因此,可能是涉及对诸如神经性厌食症、焦虑症和情感障碍等应激源异常反应的各种病理生理状况的关键。