Rodgers R J, Ishii Y, Halford J C G, Blundell J E
School of Psychology, University of Leeds, Leeds, UK.
Neuropeptides. 2002 Oct;36(5):303-25. doi: 10.1016/s0143-4179(02)00085-9.
Initial research on the functional significance of two novel hypothalamic neuropeptides, orexin-A and orexin-B, suggested an important role in appetite regulation. Since then, however, these peptides have also been shown to influence a wide range of other physiological and behavioural processes. In this paper, we review the now quite extensive literature on orexins and appetite control, and consider their additional effects within this context. Although the evidence for orexin (particularly orexin-A and the orexin-1 receptor) involvement in many aspects of ingestive physiology and behaviour is incontrovertible, central administration of orexins is also associated with increased EEG arousal and wakefulness, locomotor activity and grooming, sympathetic and HPA activity, and pain thresholds. Since the orexin system is selectively activated by signals indicating severe nutritional depletion, it would be highly adaptive for a hungry animal not only to seek sustenance but also to remain fully alert to dangers in the environment. Crucial evidence indicates that orexin-A increases food intake by delaying the onset of a behaviourally normal satiety sequence. In contrast, a selective orexin-1 receptor antagonist (SB-334867) suppresses food intake and advances the onset of a normal satiety sequence. These data suggest that orexin-1 receptors mediate the episodic signalling of satiety and appear to bridge the transition from eating to resting in the rats' feeding-sleep cycle. The argument is developed that the diverse physiological and behavioural effects of orexins can best be understood in terms of an integrated set of reactions which function to rectify nutritional status without compromising personal survival. Indeed, many of the non-ingestive effects of orexin administration are identical to the cluster of active defences mediated via the lateral and dorsolateral columns of the midbrain periaqueductal gray matter, i.e., somatomotor activation, vigilance, tachycardia, hypertension and non-opioid analgesia. In our view, therefore, the LH orexin system is very well placed to orchestrate the diverse subsystems involved in foraging under potentially dangerous circumstances, i.e., finding and ingesting food without oneself becoming a meal for someone else.
对两种新型下丘脑神经肽——食欲素A和食欲素B的功能意义的初步研究表明,它们在食欲调节中起重要作用。然而,从那时起,这些肽也被证明会影响广泛的其他生理和行为过程。在本文中,我们回顾了目前关于食欲素与食欲控制的相当广泛的文献,并在此背景下考虑它们的其他作用。尽管食欲素(特别是食欲素A和食欲素1受体)参与摄食生理和行为许多方面的证据是无可争议的,但向中枢给予食欲素也与脑电图觉醒和清醒程度增加、运动活动和梳理行为、交感神经和下丘脑-垂体-肾上腺(HPA)活动以及痛阈提高有关。由于食欲素系统会被表明严重营养消耗的信号选择性激活,对于饥饿的动物来说,不仅寻求食物而且对环境中的危险保持完全警觉将具有高度适应性。关键证据表明,食欲素A通过延迟行为上正常的饱腹感序列的开始来增加食物摄入量。相反,一种选择性食欲素1受体拮抗剂(SB - 334867)会抑制食物摄入并提前正常饱腹感序列的开始。这些数据表明,食欲素1受体介导饱腹感的间歇性信号传递,并且似乎在大鼠的进食 - 睡眠周期中架起了从进食到休息的过渡桥梁。有人提出这样的观点,即食欲素的多种生理和行为作用最好从一组综合反应的角度来理解,这些反应的作用是在不危及个体生存的情况下纠正营养状态。事实上,给予食欲素的许多非摄食作用与通过中脑导水管周围灰质的外侧和背外侧柱介导的一系列主动防御相同,即躯体运动激活、警觉、心动过速、高血压和非阿片类镇痛。因此,我们认为,下丘脑外侧区食欲素系统非常适合协调在潜在危险情况下觅食所涉及的各种子系统,即在不使自己成为他人食物的情况下寻找和摄取食物。