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视前区-中缝核连接控制体温调节血管舒缩。

Preoptic-raphé connections for thermoregulatory vasomotor control.

机构信息

Howard Florey Institute, Florey Neuroscience Institutes, University of Melbourne, Parkville, Victoria 3010, Australia.

出版信息

J Neurosci. 2011 Mar 30;31(13):5078-88. doi: 10.1523/JNEUROSCI.6433-10.2011.

Abstract

Blood flow to glabrous skin such as the rat's tail determines heat dissipation from the body and is regulated by sympathetic vasoconstrictor nerves. Tail vasoconstrictor activity is tonically inhibited by neurons in two distinct preoptic regions, rostromedial (RMPO) and caudolateral (CLPO) regions, whose actions may be via direct projections to medullary raphé premotor neurons. In urethane-anesthetized rats, we sought single preoptic neurons that were antidromically activated from the medullary raphé and could subserve this function. Nine of 45 raphé-projecting preoptic neurons, predominantly in the CLPO, showed spontaneous activity under warm conditions and were inhibited by cooling the trunk skin (warm-responsive). Unexpectedly, 14 raphé-projecting preoptic neurons (mostly in the RMPO) were activated by skin cooling (cold-responsive), suggesting that an excitatory pathway from this region could contribute to tail vasoconstriction. Supporting this, neuronal disinhibition in the RMPO by microinjecting the GABA(A) receptor antagonist bicuculline (0.5 mm, 15 nl) caused a rapid increase in tail sympathetic nerve activity (SNA). Similar injections into the CLPO were without effect. Electrical stimulation of the RMPO also activated tail SNA, with a latency ∼25 ms longer than to stimulation of the medullary raphé. Injection of the glutamate receptor antagonist kynurenate (50 mm, 120 nl) into the medullary raphé suppressed tail SNA responses to both RMPO bicuculline and skin cooling. These findings suggest that both inhibitory and excitatory descending drives regulate tail vasoconstriction in the cold and that warm- and cold-responsive raphé-projecting preoptic neurons may mediate these actions.

摘要

血流到无毛皮肤,如老鼠的尾巴,决定身体散热,由交感缩血管神经调节。尾巴缩血管活性由两个不同的视前区神经元,即前内侧(RMPO)和尾外侧(CLPO),神经元紧张性抑制,其作用可能是通过直接投射到延髓中缝前运动神经元。在乌拉坦麻醉的大鼠中,我们寻找从延髓中缝背侧投射并能发挥此作用的单个视前区神经元。45 个投射到中缝的视前区神经元中,有 9 个(主要在 CLPO)在温暖条件下表现出自发活动,并在躯干皮肤冷却时被抑制(温暖反应)。出乎意料的是,14 个投射到中缝的视前区神经元(主要在 RMPO)被皮肤冷却激活(冷反应),这表明该区域的兴奋性通路可能有助于尾巴血管收缩。支持这一点,在 RMPO 中微注射 GABA(A)受体拮抗剂荷包牡丹碱(0.5 mM,15 nl)抑制神经元,导致尾巴交感神经活动(SNA)迅速增加。在 CLPO 中进行类似的注射则没有效果。RMPO 的电刺激也激活了尾巴 SNA,潜伏期比刺激延髓中缝长约 25 毫秒。将谷氨酸受体拮抗剂 kynurenate(50 mM,120 nl)注入延髓中缝抑制了尾巴 SNA 对 RMPO 荷包牡丹碱和皮肤冷却的反应。这些发现表明,抑制性和兴奋性下行驱动都调节了寒冷时尾巴的血管收缩,而温暖和寒冷反应性投射到中缝的视前区神经元可能介导这些作用。

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