Preliminary research on possible relationship of NO with agmatine at the vascular level.

I Haulică, W Bild, R Iliescu, R Georgescu, F Frunză
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Abstract

The comparative study of the vascular effects of agmatine and L-arginine as physiological precursors of NO indicated the following: When administered intravenously, both vasoactive substances produced a decrease of the systemic blood pressure in rats and rabbits, diminished in the case of agmatine and suppressed in that of arginine by the previous administration of L-NAME. Myorelaxing vascular effects were obtained in isolated thoracic aorta rings, precontracted with phenylephrine and noradrenaline. Endothelium removal suppressed the myorelaxing properties of L-arginine, without affecting the effects of agmatine, both before and after administration of L-NAME or yohimbine. The persistence of the relaxing effects of agmatine after NOS and guanylate-cyclase inhibition with methylene blue excludes the participation of NO and cGMP in their occurrence. The enhancement of agmatine myorelaxation by moxonidine pleads for the stimulation of imidazoline receptors.

血管水平一氧化氮与胍丁氨酸可能关系的初步研究。
对作为NO生理前体的胍丁氨酸和l -精氨酸的血管作用的比较研究表明:当静脉给药时,这两种血管活性物质都能降低大鼠和家兔的全身血压,胍丁氨酸的血压降低,精氨酸的血压被先前给药的L-NAME所抑制。用苯肾上腺素和去甲肾上腺素预收缩胸主动脉环,获得肌舒张血管效应。在给予L-NAME或育亨宾前后,内皮去除抑制了l -精氨酸的肌肉松弛特性,而不影响胍丁氨酸的作用。在NOS和亚甲基蓝抑制鸟苷酸环化酶后,胍丁氨酸的松弛作用持续存在,排除了NO和cGMP参与其发生。莫替尼定对胍丁氨酸肌松弛的增强是通过刺激咪唑啉受体实现的。
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