Sahach V F, Kotsiuruba A V, Baziliuk O V, Mehed' O F, Bykhanevich O M, Hula N M, Stepanenko L H
A.A. Bogomolets Institute of Physiology, National Academy of Science of Ukraine, Kiev.
Fiziol Zh (1994). 2001;47(5):3-11.
Have studied action of chronic urea--an arginase inhibitor--introduction (40 mg/kg, 28 days) on blood pressure, endothelium-dependent reactions of aorta smooth muscle cells (SMC) and nonenzymatic (contents of diene conjugates and H2O2) and enzymatic (contents of free arachidonic acid and vasoconstrictic eicosanoids LTC4 and TXA2) oxidizing lipid metabolism of heart, aorta, plasma and erythrocytes of spontaneously hypertensive rats. Have shown, that urea down regulate blood pressure without any normalization of endothelium-dependent reactions of SMC of aorta and down regulate both enzymatic and nonenzymatic oxidizing lipid metabolism. Down regulation of two alternative (by cyclooxygenase and by lipoxygenase) enzymatic pathways of free arachidonic acid oxidizing metabolism by urea can be one of mechanisms of its antihypertensive action. The possibility of urea use at hypertension and various pathophysiological conditions are discussed.
研究了慢性给予精氨酸酶抑制剂尿素(40毫克/千克,28天)对自发性高血压大鼠的血压、主动脉平滑肌细胞(SMC)的内皮依赖性反应以及心脏、主动脉、血浆和红细胞的非酶促(二烯共轭物和H2O2含量)和酶促(游离花生四烯酸和血管收缩性类二十烷酸LTC4和TXA2含量)氧化脂质代谢的作用。结果表明,尿素可降低血压,但主动脉SMC的内皮依赖性反应未恢复正常,且可下调酶促和非酶促氧化脂质代谢。尿素对游离花生四烯酸氧化代谢的两条替代(通过环氧化酶和脂氧化酶)酶促途径的下调可能是其降压作用的机制之一。文中还讨论了在高血压和各种病理生理条件下使用尿素的可能性。