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慢性摄入NG-硝基-L-精氨酸甲酯期间Brattleboro大鼠的局部血流动力学

Regional haemodynamics in Brattleboro rats during chronic ingestion of NG-nitro-L-arginine methyl ester.

作者信息

Gardiner S M, Kemp P A, Bennett T

机构信息

Department of Physiology and Pharmacology, Medical School, Queen's Medical Centre, Nottingham, UK.

出版信息

Blood Press. 1993 Sep;2(3):228-32. doi: 10.3109/08037059309077556.

DOI:10.3109/08037059309077556
PMID:8205318
Abstract

The aim of this study was to assess regional haemodynamic changes in conscious Brattleboro rats during chronic ingestion of the nitric oxide (NO) synthase inhibitor, NG-nitro-L-arginine methyl ester (L-NAME). Animals were instrumented with renal, mesenteric and hindquarters pulsed Doppler flow probes and an intra-arterial catheter, and haemodynamic measurements were made before, during and after 14 days' exposure to L-NAME (0.01 mg ml-1 in the drinking water). Within 6 h after addition of L-NAME to the drinking water, mean arterial blood pressure was increased (maximum, 33 +/- 6 mm Hg), and remained so until L-NAME was withdrawn, whereupon blood pressure returned to normal levels within 24 h. The hypertension was accompanied by a transient reduction in mesenteric blood flow, and a more persistent reduction in hindquarters blood flow. Mesenteric and, particularly, hindquarters vascular conductance showed a sustained reduction. However, during ingestion of L-NAME, renal blood flow was not diminished and, over the final 4 days of exposure to L-NAME there was no significant renal vasoconstriction. All regional haemodynamic effects of L-NAME were lost within 24 h of its withdrawal. Hence, as with shorter periods of exposure to the less potent NO synthase inhibitor, NG-monomethyl-L-arginine, the hypertension caused by L-NAME is dependent on its continued administration, and is associated with a particularly marked hindquarters vasoconstriction.

摘要

本研究的目的是评估清醒的布拉特洛维大鼠在长期摄入一氧化氮(NO)合酶抑制剂NG-硝基-L-精氨酸甲酯(L-NAME)期间的局部血流动力学变化。给动物安装肾、肠系膜和后肢脉冲多普勒血流探头以及动脉内导管,并在暴露于L-NAME(饮用水中浓度为0.01 mg/ml)前、期间和14天后进行血流动力学测量。在饮用水中添加L-NAME后6小时内,平均动脉血压升高(最高升高33±6 mmHg),并一直保持升高,直到停止给予L-NAME,此时血压在24小时内恢复到正常水平。高血压伴有肠系膜血流短暂减少以及后肢血流更持续的减少。肠系膜尤其是后肢的血管传导性持续降低。然而,在摄入L-NAME期间,肾血流量并未减少,并且在暴露于L-NAME的最后4天内没有明显的肾血管收缩。L-NAME停药后24小时内,其所有局部血流动力学效应均消失。因此,与短期暴露于效力较弱的NO合酶抑制剂NG-单甲基-L-精氨酸的情况一样,L-NAME引起的高血压依赖于其持续给药,并且与特别明显的后肢血管收缩有关。

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