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中脑视前区谷氨酸能神经元促进小鼠体温调节性散热和水的摄入。

Median preoptic glutamatergic neurons promote thermoregulatory heat loss and water consumption in mice.

机构信息

Department of Neurology, Beth Israel-Deaconess Medical Center - Harvard Medical School, Boston, MA, USA.

The Heart Research Institute, Sydney, Australia.

出版信息

J Physiol. 2017 Oct 15;595(20):6569-6583. doi: 10.1113/JP274667. Epub 2017 Sep 13.

Abstract

KEY POINTS

Glutamatergic neurons in the median preoptic area were stimulated using genetically targeted Channelrhodopsin 2 in transgenic mice. Stimulation of glutamatergic median preoptic area neurons produced a profound hypothermia due to cutaneous vasodilatation. Stimulation also produced drinking behaviour that was inhibited as water was ingested, suggesting pre-systemic feedback gating of drinking. Anatomical mapping of the stimulation sites showed that sites associated with hypothermia were more anteroventral than those associated with drinking, although there was substantial overlap.

ABSTRACT

The median preoptic nucleus (MnPO) serves an important role in the integration of water/electrolyte homeostasis and thermoregulation, but we have a limited understanding these functions at a cellular level. Using Cre-Lox genetic targeting of Channelrhodospin 2 in VGluT2 transgenic mice, we examined the effect of glutamatergic MnPO neuron stimulation in freely behaving mice while monitoring drinking behaviour and core temperature. Stimulation produced a strong hypothermic response in 62% (13/21) of mice (core temperature: -4.6 ± 0.5°C, P = 0.001 vs. controls) caused by cutaneous vasodilatation. Stimulating glutamatergic MnPO neurons also produced robust drinking behaviour in 82% (18/22) of mice. Mice that drank during stimulation consumed 912 ± 163 μl (n = 8) during a 20 min trial in the dark phase, but markedly less during the light phase (421 ± 83 μl, P = 0.0025). Also, drinking during stimulation was inhibited as water was ingested, suggesting pre-systemic feedback gating of drinking. Both hypothermia and drinking during stimulation occurred in 50% of mice tested. Anatomical mapping of the stimulation sites showed that sites associated with hypothermia were more anteroventral than those associated with drinking, although there was substantial overlap. Thus, activation of separate but overlapping populations of glutamatergic MnPO neurons produces effects on drinking and autonomic thermoregulatory mechanisms, providing a structural basis for their frequently being coordinated (e.g. during hyperthermia).

摘要

要点

使用转基因小鼠中基因靶向的 Channelrhodopsin 2 刺激中脑prefrontal 区的谷氨酸能神经元。刺激谷氨酸能中脑prefrontal 区神经元会导致皮肤血管扩张,从而产生明显的体温过低。刺激还产生了饮水行为,但随着水的摄入而被抑制,这表明饮水的前系统反馈门控。刺激部位的解剖学映射显示,与低温相关的部位比与饮水相关的部位更靠前腹侧,尽管存在大量重叠。

摘要

中脑prefrontal 核(MnPO)在水/电解质稳态和体温调节的整合中起着重要作用,但我们对这些功能在细胞水平上的理解有限。使用 Cre-Lox 基因靶向 VGluT2 转基因小鼠中的 Channelrhodospin 2,我们在自由活动的小鼠中检查了刺激谷氨酸能 MnPO 神经元的效果,同时监测了饮水行为和核心体温。刺激在 62%(13/21)的小鼠中产生了强烈的低温反应(核心温度:-4.6±0.5°C,P=0.001 与对照组相比),这是由皮肤血管扩张引起的。刺激谷氨酸能 MnPO 神经元也在 82%(18/22)的小鼠中产生了强烈的饮水行为。在黑暗期 20 分钟的试验中,刺激期间饮水的小鼠消耗了 912±163μl(n=8),但在光照期明显减少(421±83μl,P=0.0025)。此外,由于水的摄入,刺激期间的饮水被抑制,这表明饮水的前系统反馈门控。在测试的 50%的小鼠中,既出现了低温又出现了刺激期间的饮水。刺激部位的解剖学映射显示,与低温相关的部位比与饮水相关的部位更靠前腹侧,尽管存在大量重叠。因此,激活分离但重叠的谷氨酸能 MnPO 神经元群体会对饮水和自主体温调节机制产生影响,为它们经常协调(例如在发热时)提供了结构基础。

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