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Regulation of Hypothalamic Presympathetic Neurons and Sympathetic Outflow by Group II Metabotropic Glutamate Receptors in Spontaneously Hypertensive Rats

机译:II型代谢型谷氨酸受体在自发性高血压大鼠下丘脑前交感神经元和交感神经流出的调节。

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摘要

Increased glutamatergic input in the hypothalamic paraventricular nucleus (PVN) plays an important role in the development of hypertension. Group II metabotropic glutamate receptors (mGluRs) are expressed in the PVN, but their involvement in regulating synaptic transmission and sympathetic outflow in hypertension is unclear. Here we show that the group II mGluRs agonist (2S,2'R,3'R)-2-(2',3'-dicarboxycyclopropyl)glycine (DCG-IV) produced a significantly greater reduction in the frequency of spontaneous and miniature excitatory postsynaptic currents and the amplitude of electrically evoked excitatory postsynaptic currents in retrogradely labeled spinally projecting PVN neurons in spontaneously hypertensive rats (SHRs) than in normotensive control rats. DCG-IV similarly decreased the frequency of GABAergic inhibitory postsynaptic currents of labeled PVN neurons in the two groups of rats. Strikingly, DCG-IV suppressed the firing of labeled PVN neurons only in SHRs. DCG-IV failed to inhibit the firing of PVN neurons of SHRs in the presence of ionotropic glutamate receptor antagonists. Lowering blood pressure with celiac ganglionectomy in SHRs normalized the DCG-IV effect on excitatory postsynaptic currents to the same level seen in control rats. Furthermore, microinjection of DCG-IV into the PVN significantly reduced blood pressure and sympathetic nerve activity in SHRs. Our findings provide new information that presynaptic group II mGluR activity at the glutamatergic terminals increases in the PVN in SHRs. Activation of group II mGluRs in the PVN inhibits sympathetic vasomotor tone through attenuation of increased glutamatergic input and neuronal hyperactivity in SHRs.
机译:下丘脑室旁核(PVN)中谷氨酸能输入的增加在高血压的发展中起重要作用。 II组代谢型谷氨酸受体(mGluRs)在PVN中表达,但尚不清楚它们是否参与调节高血压的突触传递和交感性流出。在这里,我们显示了II组mGluRs激动剂(2S,2'R,3'R)-2-(2',3'-二羧基环丙基)甘氨酸(DCG-IV)产生的自发频率和微型频率明显降低与正常血压对照组相比,自发性高血压大鼠(SHRs)中逆行标记的脊柱投射PVN神经元的兴奋性突触后突触电流和电诱发的兴奋性突触后突触电流的幅度。 DCG-IV类似地降低了两组大鼠中标记的PVN神经元的GABA能抑制突触后电流的频率。令人惊讶的是,DCG-IV仅在SHR中抑制了标记的PVN神经元的放电。在存在离子型谷氨酸受体拮抗剂的情况下,DCG-IV无法抑制SHRs的PVN神经元的放电。通过在SHR中进行腹腔神经节切除术来降低血压,可使DCG-IV对兴奋性突触后突触电流的作用正常化,达到与对照组大鼠相同的水平。此外,将DCG-IV微量注射到PVN中可显着降低SHR的血压和交感神经活动。我们的发现提供了新的信息,即SHRs中的谷氨酸能末端的突触前II组mGluR活性增加。 PVN中II组mGluRs的激活通过减少SHRs中增加的谷氨酸能输入和神经元过度活跃来抑制交感性血管舒缩。

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