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多胺亚精胺对自由活动大鼠NMDA诱导的动脉高血压的影响。

Effects of the polyamine spermidine on NMDA-induced arterial hypertension in freely moving rats.

作者信息

Maione S, Berrino L, Pizzirusso A, Leyva J, Filippelli A, Vitagliano S, Rossi F

机构信息

Institute of Pharmacology and Toxicology, Faculty of Medicine and Surgery, II University of Naples, Italy.

出版信息

Neuropharmacology. 1994 Jun;33(6):789-93. doi: 10.1016/0028-3908(94)90118-x.

Abstract

We investigated the effect of the polyamine spermidine (SPD) (0.01-1 microgram/rat) on hypertension induced by N-methyl-D-aspartate (NMDA) (0.1 microgram/rat) microinjected into the latero-caudal periaqueductal gray (PAG) area of freely moving rats. Pretreatment with a low dose of SPD (0.01 microgram/rat) significantly increased NMDA-induced hypertension. On the contrary, higher doses of SPD (0.1 and 1 microgram/rat) significantly decreased NMDA-induced cardiovascular changes. SPD alone did not modify arterial blood pressure. Arcaine (1 microgram/rat), a putative antagonist at the polyamine recognition site on NMDA receptors, when microinjected into the PAG area, prevented the negative but not the positive modulatory effects of SPD on the NMDA-induced cardiovascular changes. Pretreatment with SPD did not affect cardiovascular effects induced by quisqualic acid (QUIS), a non-NMDA receptor agonist. These data, in agreement with the in vitro results, suggest that at the level of the PAG area, the polyamines also show multiple actions at NMDA receptors in vivo.

摘要

我们研究了多胺亚精胺(SPD)(0.01 - 1微克/大鼠)对自由活动大鼠尾侧导水管周围灰质(PAG)区域微量注射N - 甲基 - D - 天冬氨酸(NMDA)(0.1微克/大鼠)所诱发高血压的影响。低剂量SPD(0.01微克/大鼠)预处理显著增加了NMDA诱发的高血压。相反,较高剂量的SPD(0.1和1微克/大鼠)显著降低了NMDA诱发的心血管变化。单独使用SPD不会改变动脉血压。精肌肽(1微克/大鼠),一种假定的NMDA受体多胺识别位点拮抗剂,微量注射到PAG区域时,可阻止SPD对NMDA诱发心血管变化的负性调节作用,但不能阻止正性调节作用。SPD预处理不影响非NMDA受体激动剂quisqualic acid(QUIS)诱发的心血管效应。这些数据与体外实验结果一致,表明在PAG区域水平,多胺在体内对NMDA受体也表现出多种作用。

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