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向孤束核微量注射L-谷氨酸所引起的心血管反应可被还原型谷胱甘肽消除。

Cardiovascular responses to l-glutamate microinjection into the NTS are abrogated by reduced glutathione.

作者信息

Granato Álisson Silva, Gomes Paula Magalhães, Martins Sá Renato William, Borges Gabriel Silva Marques, Alzamora Andréia Carvalho, de Oliveira Lisandra Brandino, Toney Glenn M, Cardoso Leonardo M

机构信息

Federal University of Ouro Preto, Department of Biological Sciences/NUPEB, Campus Universitário Morro do Cruzeiro, Ouro Preto, MG, 35,400-000 Brazil.

Department of Physiology, University of Texas Health Science Center at San Antonio, San Antonio, TX 78229, USA.

出版信息

Neurosci Lett. 2017 Mar 6;642:142-147. doi: 10.1016/j.neulet.2017.02.019. Epub 2017 Feb 9.

Abstract

Redox imbalance in regions of the CNS controlling blood pressure is increasingly recognized as a leading factor for hypertension. Nucleus tractus solitarius (NTS) of the dorsomedial medulla is the main region receiving excitatory visceral sensory inputs that modulate autonomic efferent drive to the cardiovascular system. This study sought to determine the capacity of reduced glutathione, a major bioactive antioxidant, to modulate NTS-mediated control of cardiovascular function in unanaesthetized rats. Male Fischer 344 rats were used for microinjection experiments. Cardiovascular responses to l-glutamate were first used to verify accurate placement of injections into the dorsomedial region comprising the NTS. Next, responses to GSH or vehicle were recorded followed by responses to l-glutamate again at the same site. GSH microinjection increased mean arterial pressure (MAP) compared to vehicle and abrogated responses to subsequent injection of l-glutamate. These data indicate that GSH microinjection into the NTS affects blood pressure regulation by dorsomedial neuronal circuits and blunts l-glutamate driven excitation in this region. These findings raise the possibility that increased antioxidant actions of GSH in NTS could contribute to autonomic control dysfunctions of the cardiovascular system.

摘要

中枢神经系统中控制血压区域的氧化还原失衡日益被认为是高血压的主要因素。延髓背内侧的孤束核(NTS)是接受兴奋性内脏感觉输入的主要区域,这些输入调节对心血管系统的自主传出驱动。本研究旨在确定主要生物活性抗氧化剂还原型谷胱甘肽调节未麻醉大鼠中NTS介导的心血管功能控制的能力。雄性Fischer 344大鼠用于显微注射实验。首先利用对L-谷氨酸的心血管反应来验证注射到包含NTS的背内侧区域的准确性。接下来,记录对谷胱甘肽或赋形剂的反应,然后在同一部位再次记录对L-谷氨酸的反应。与赋形剂相比,显微注射谷胱甘肽可提高平均动脉压(MAP),并消除对随后注射L-谷氨酸的反应。这些数据表明,向NTS显微注射谷胱甘肽会影响背内侧神经元回路对血压的调节,并减弱该区域中L-谷氨酸驱动 的兴奋。这些发现增加了一种可能性,即NTS中谷胱甘肽抗氧化作用的增强可能导致心血管系统的自主控制功能障碍。

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