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证据表明,BDNF 通过一种涉及增加脑干副交感神经元兴奋性的机制来调节心率。

Evidence that BDNF regulates heart rate by a mechanism involving increased brainstem parasympathetic neuron excitability.

机构信息

Laboratory of Neurosciences, National Institute on Aging Intramural Research Program, Baltimore, Maryland, USA.

出版信息

J Neurochem. 2014 May;129(4):573-80. doi: 10.1111/jnc.12656. Epub 2014 Feb 10.

Abstract

Autonomic control of heart rate is mediated by cardioinhibitory parasympathetic cholinergic neurons located in the brainstem and stimulatory sympathetic noradrenergic neurons. During embryonic development the survival and cholinergic phenotype of brainstem autonomic neurons is promoted by brain-derived neurotrophic factor (BDNF). We now provide evidence that BDNF regulates heart rate by a mechanism involving increased brainstem cardioinhibitory parasympathetic activity. Mice with a BDNF haploinsufficiency exhibit elevated resting heart rate, and infusion of BDNF intracerebroventricularly reduces heart rate in both wild-type and BDNF+/- mice. The atropine-induced elevation of heart rate is diminished in BDNF+/- mice and is restored by BDNF infusion, whereas the atenolol-induced decrease in heart rate is unaffected by BDNF levels, suggesting that BDNF signaling enhances parasympathetic tone which is diminished with BDNF haploinsufficiency. Whole-cell recordings from pre-motor cholinergic cardioinhibitory vagal neurons in the nucleus ambiguus indicate that BDNF haploinsufficiency reduces cardioinhibitory vagal neuron activity by increased inhibitory GABAergic and diminished excitatory glutamatergic neurotransmission to these neurons. Our findings reveal a previously unknown role for BDNF in the control of heart rate by a mechanism involving increased activation of brainstem cholinergic parasympathetic neurons.

摘要

心率的自主控制是由位于脑干的抑制性副交感胆碱能神经元和兴奋性交感去甲肾上腺素能神经元介导的。在胚胎发育过程中,脑源性神经营养因子(BDNF)促进脑干自主神经元的存活和胆碱能表型。我们现在提供的证据表明,BDNF 通过涉及增加脑干抑制性副交感神经活动的机制来调节心率。BDNF 半不足的小鼠表现出静息心率升高,并且脑室内输注 BDNF 可降低野生型和 BDNF+/- 小鼠的心率。BDNF+/- 小鼠中阿托品诱导的心率升高降低,并且 BDNF 输注可恢复该作用,而 BDNF 水平对阿替洛尔诱导的心率降低没有影响,这表明 BDNF 信号增强了副交感神经张力,而 BDNF 半不足则降低了这种张力。在疑核中的前运动性抑制性副交感迷走神经元中进行的全细胞膜片钳记录表明,BDNF 半不足通过增加抑制性 GABA 能和减少兴奋性谷氨酸能神经传递来降低抑制性副交感迷走神经元活性。我们的研究结果揭示了 BDNF 在通过增加脑干胆碱能副交感神经元的激活来控制心率方面的一个以前未知的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7322/4137462/9e57cad2bd03/nihms561276f1.jpg

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