Morrison Shaun F, Nakamura Kazuhiro, Madden Christopher J
Neurological Sciences Institute, Oregon Health & Science University, 505 NW 185th Avenue, Beaverton, OR 97006, USA.
Exp Physiol. 2008 Jul;93(7):773-97. doi: 10.1113/expphysiol.2007.041848. Epub 2008 May 9.
Thermogenesis, the production of heat energy, is an essential component of the homeostatic repertoire to maintain body temperature in mammals and birds during the challenge of low environmental temperature and plays a key role in elevating body temperature during the febrile response to infection. The primary sources of neurally regulated metabolic heat production are mitochondrial oxidation in brown adipose tissue, increases in heart rate and shivering in skeletal muscle. Thermogenesis is regulated in each of these tissues by parallel networks in the central nervous system, which respond to feedforward afferent signals from cutaneous and core body thermoreceptors and to feedback signals from brain thermosensitive neurons to activate the appropriate sympathetic and somatic efferents. This review summarizes the research leading to a model of the feedforward reflex pathway through which environmental cold stimulates thermogenesis and discusses the influence on this thermoregulatory network of the pyrogenic mediator, prostaglandin E(2), to increase body temperature. The cold thermal afferent circuit from cutaneous thermal receptors ascends via second-order thermosensory neurons in the dorsal horn of the spinal cord to activate neurons in the lateral parabrachial nucleus, which drive GABAergic interneurons in the preoptic area to inhibit warm-sensitive, inhibitory output neurons of the preoptic area. The resulting disinhibition of thermogenesis-promoting neurons in the dorsomedial hypothalamus and possibly of sympathetic and somatic premotor neurons in the rostral ventromedial medulla, including the raphe pallidus, activates excitatory inputs to spinal sympathetic and somatic motor circuits to drive thermogenesis.
产热,即热能的产生,是哺乳动物和鸟类在环境低温挑战期间维持体温的稳态机制的重要组成部分,并且在感染引起的发热反应中体温升高过程中起关键作用。神经调节的代谢产热的主要来源是棕色脂肪组织中的线粒体氧化、心率增加以及骨骼肌颤抖。中枢神经系统中的平行网络对这些组织中的产热进行调节,这些网络对来自皮肤和核心体温感受器的前馈传入信号以及来自脑热敏神经元的反馈信号作出反应,以激活适当的交感神经和躯体传出神经。本综述总结了导致建立环境寒冷刺激产热的前馈反射通路模型的研究,并讨论了致热介质前列腺素E(2)对该体温调节网络的影响,以升高体温。来自皮肤热感受器的冷觉传入回路通过脊髓背角的二级热感觉神经元上行,以激活外侧臂旁核中的神经元,这些神经元驱动视前区中的GABA能中间神经元,以抑制视前区中对温暖敏感的抑制性输出神经元。由此对视前区背内侧下丘脑促进产热的神经元以及可能对延髓头端腹内侧包括中缝苍白核的交感神经和躯体运动前神经元的去抑制,激活对脊髓交感神经和躯体运动回路的兴奋性输入,以驱动产热。