Sahach V F, Kotsiuruba A V, Baziliuk O V, Mehed' O F, Stepanenko L H
Fiziol Zh (1994). 2004;50(6):9-18.
It has been studied an action of chronic urea introduction (40 mg/kg, 14 and 28 days) as arginase inhibitor on nonoxidative (arginase activity, urea, polyamines content) and oxidative (NOS activity, nitrite- and nitrate-anion content) metabolism of L-arginine in aorta, heart, plasma and erythrocytes of SHR. It has been shown that urea is an inhibitor of not arginase only, but also ornitinedecarboxilase (ODK) reactions, limiting L-arginine consumption for urea and polyamines synthesis and thus facilitating its utilization for nitric oxide synthesis by NOS. These exogenous effects of urea are not accompanied by amelioration of tissue ischaemization within cardiovascular system. It has been shown that exogenous urea down regulate blood pressure without any normalization of endothelim-dependent reactions of smooth muscle cells on acetylcholine in SHR.
研究了慢性注射尿素(40毫克/千克,14天和28天)作为精氨酸酶抑制剂对自发性高血压大鼠(SHR)主动脉、心脏、血浆和红细胞中L-精氨酸的非氧化代谢(精氨酸酶活性、尿素、多胺含量)和氧化代谢(一氧化氮合酶活性、亚硝酸盐和硝酸盐阴离子含量)的作用。结果表明,尿素不仅是精氨酸酶的抑制剂,也是鸟氨酸脱羧酶(ODC)反应的抑制剂,限制了L-精氨酸用于尿素和多胺合成的消耗,从而促进其被一氧化氮合酶用于一氧化氮合成。尿素的这些外源性作用并未伴随着心血管系统内组织缺血情况的改善。结果表明,外源性尿素可降低血压,但自发性高血压大鼠平滑肌细胞对乙酰胆碱的内皮依赖性反应并未恢复正常。