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向大鼠延髓腹外侧微量注射L-脯氨酸所引起的降压反应是由离子型兴奋性氨基酸受体介导的。

Depressor responses to L-proline microinjected into the rat ventrolateral medulla are mediated by ionotropic excitatory amino acid receptors.

作者信息

Takemoto Yumi

机构信息

Department of Neurophysiology, Division of Integrated Medical Science, Programs for Biomedical Research, Graduate School of Biomedical Sciences, Hiroshima University, Japan.

出版信息

Auton Neurosci. 2005 Jun 15;120(1-2):108-12. doi: 10.1016/j.autneu.2005.05.004.

Abstract

The essential amino acid L-proline produces a depressor response when microinjected into the caudal ventrolateral medulla (CVLM) of anesthetized rats. L-proline may activate some excitatory amino acid (EAA) receptors. The present study tested this hypothesis by investigating the effects of two ionotropic excitatory amino acid receptor antagonists on the depressor response to L-proline in the CVLM: the alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid (AMPA)/kainate receptor-selective antagonist 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX) and the N-methyl-D-aspartate (NMDA) receptor-selective antagonist MK801. Urethane-anesthetized rats received arterial catheters and their ventrolateral medulla surface was exposed. Injections of the antagonists CNQX and MK801 (2 mM, 68 nl in each case) into the CVLM completely blocked depressor responses to subsequent administration of AMPA (2 pmol/34 nl) and NMDA (2 pmol/34 nl), respectively. The depressor response to L-proline (3.4 nmol/34 nl) was strongly inhibited by prior injection of CNQX (2 mM, 68 nl) and significantly attenuated by prior injection of a high dose (20 mM, 68 nl), but not a low dose (2 mM, 68 nl), of MK801. The results indicate that the depressor response to L-proline in the CVLM includes mechanisms of ionotropic excitatory amino acid receptors.

摘要

必需氨基酸L-脯氨酸微量注射到麻醉大鼠的延髓尾端腹外侧区(CVLM)时会产生降压反应。L-脯氨酸可能激活某些兴奋性氨基酸(EAA)受体。本研究通过研究两种离子型兴奋性氨基酸受体拮抗剂对CVLM中L-脯氨酸降压反应的影响来验证这一假设:α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)/海人藻酸受体选择性拮抗剂6-氰基-7-硝基喹喔啉-2,3-二酮(CNQX)和N-甲基-D-天冬氨酸(NMDA)受体选择性拮抗剂MK801。用乌拉坦麻醉的大鼠插入动脉导管并暴露其延髓腹外侧表面。分别向CVLM注射拮抗剂CNQX和MK801(均为2 mM,68 nl),完全阻断了随后给予AMPA(2 pmol/34 nl)和NMDA(2 pmol/34 nl)时的降压反应。预先注射CNQX(2 mM,68 nl)可强烈抑制对L-脯氨酸(3.4 nmol/34 nl)的降压反应,预先注射高剂量(20 mM,68 nl)而非低剂量(2 mM,68 nl)的MK801可使该反应显著减弱。结果表明,CVLM中对L-脯氨酸的降压反应包括离子型兴奋性氨基酸受体机制。

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