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谷氨酸能调节高血压下丘脑前交感神经元。

Glutamatergic Regulation of Hypothalamic Presympathetic Neurons in Hypertension.

机构信息

Center for Neuroscience and Pain Research, Division of Anesthesiology and Critical Care, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, TX, 77030, USA.

出版信息

Curr Hypertens Rep. 2017 Sep 19;19(10):78. doi: 10.1007/s11906-017-0776-4.

Abstract

Elevated sympathetic vasomotor tone emanating from the brain is a major mechanism involved in the development of hypertension. Increased glutamatergic excitatory input to presympathetic neurons in the paraventricular nucleus (PVN) of the hypothalamus leads to increased sympathetic outflow in various animal models of hypertension. Recent studies have revealed molecular and cellular mechanisms underlying enhanced glutamatergic synaptic input to PVN presympathetic neurons in hypertension. In this review article, we summarize recent findings on changes in inotropic and metabotropic glutamate receptors, at both presynaptic and postsynaptic sites, responsible for increased glutamatergic input to PVN presympathetic neurons in hypertension. Particular emphasis is placed on the role of protein kinases and phosphatases in the potentiated activity of synaptic NMDA receptors in the PVN in hypertension. New findings about glutamatergic synaptic plasticity in the PVN not only improve the understanding of molecular mechanisms involved in heightened activity of the sympathetic nervous system but also suggest new therapeutic targets for treating drug-resistant, neurogenic hypertension.

摘要

大脑发出的交感血管运动张力升高是高血压发展的主要机制。在下丘脑室旁核 (PVN) 的交感节前神经元中,谷氨酸能兴奋性传入增加,导致各种高血压动物模型中的交感传出增加。最近的研究揭示了高血压中增强的谷氨酸能突触传入到 PVN 交感节前神经元的分子和细胞机制。在这篇综述文章中,我们总结了最近关于在高血压中负责增加谷氨酸能传入到 PVN 交感节前神经元的变构和代谢型谷氨酸受体在突触前和突触后位点的变化的发现。特别强调了蛋白激酶和磷酸酶在高血压中 PVN 中 NMDA 受体突触活性增强中的作用。关于 PVN 中谷氨酸能突触可塑性的新发现不仅提高了对交感神经系统活动增强所涉及的分子机制的理解,还为治疗耐药性、神经性高血压提供了新的治疗靶点。

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