Xin Yan-Fei, Zhou Xiang-Jun, Cheng Xi, Wang Yong-Xiang
Laboratory of Pharmacology, School of Pharmacy, Shanghai Jiao Tong University, Shanghai 200030, China.
J Pharmacol Exp Ther. 2005 Mar;312(3):1090-6. doi: 10.1124/jpet.104.077123. Epub 2004 Oct 20.
N(G)-nitro-d-arginine (d-NNA), i.v. injected into rats, produced a pressor response, and was presumed to act via chiral inversion into N(G)-nitro-l-arginine (l-NNA), an inhibitor of nitric oxide synthase. We examined the possible role of renal d-amino acid oxidase (DAAO) in the chiral inversion of d-NNA to l-NNA. In pentobarbital-anesthetized rats, l-NNA was detected via capillary electrochromatography in the blood immediately after i.v. injection of d-NNA. The time course of appearance of l-NNA paralleled the increase in blood pressure elicited by d-NNA. Unilateral renal ligation partially, and bilateral ligation completely, blocked the pressor response as well as the conversion of d-NNA to l-NNA. Furthermore, injection into conscious rats of sodium benzoate, a selective DAAO inhibitor, completely blocked the pressor response to naive d-NNA, but not pressor response to d-NNA preincubated with homogenates of the kidney. Homogenates of the kidneys, liver (lesser degree), and brain (much lesser degree) converted d-NNA to l-NNA, and the chiral inversion was blocked by the addition of benzoate. Moreover, d-NNA chiral inversion correlates with the activity of DAAO. Our results reveal a novel pathway of chiral inversion of d-amino acids where the renal DAAO plays an essential role that accounts for the biological activity of d-NNA.
静脉注射给大鼠的N(G)-硝基-d-精氨酸(d-NNA)会产生升压反应,据推测其作用是通过手性转化为一氧化氮合酶抑制剂N(G)-硝基-l-精氨酸(l-NNA)来实现的。我们研究了肾d-氨基酸氧化酶(DAAO)在d-NNA向l-NNA手性转化中的可能作用。在戊巴比妥麻醉的大鼠中,静脉注射d-NNA后立即通过毛细管电色谱法在血液中检测到l-NNA。l-NNA出现的时间进程与d-NNA引起的血压升高平行。单侧肾结扎部分阻断,双侧肾结扎完全阻断升压反应以及d-NNA向l-NNA的转化。此外,向清醒大鼠注射选择性DAAO抑制剂苯甲酸钠可完全阻断对未处理的d-NNA的升压反应,但不能阻断对与肾匀浆预孵育的d-NNA的升压反应。肾、肝(程度较轻)和脑(程度更轻)的匀浆可将d-NNA转化为l-NNA,并且加入苯甲酸钠可阻断手性转化。此外,d-NNA的手性转化与DAAO的活性相关。我们的结果揭示了一种新的d-氨基酸手性转化途径,其中肾DAAO起着关键作用,这解释了d-NNA的生物学活性。