Renal D-amino acid oxidase mediates chiral inversion of N(G)-nitro-D-arginine.
نویسندگان
چکیده
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.
منابع مشابه
Inhibitory effects of benzoate on chiral inversion and clearance of N(G)-nitro-arginine in conscious rats.
N(G)-nitro-arginine (NNA) is known to exhibit stereoselective pharmacokinetics in which N(G)-nitro-d-arginine (d-NNA) has a faster clearance rate than N(G)-nitro-l-arginine (l-NNA) in anesthetized rats, and d-NNA undergoes unidirectional chiral inversion. It was postulated that chiral inversion of d-NNA was performed in a two-step pathway by d-amino acid oxidase (DAAO) followed by an unidentifi...
متن کاملInhibitory effects of benzoate on chiral inversion and clearance of N-nitro-arginine in conscious rats
N-nitro-arginine (NNA) is known to exhibit stereoselective pharmacokinetics in which D-NNA has a faster clearance rate than L-NNA in anesthetized rats, and D-NNA undergoes unidirectional chiral inversion. It was postulated that chiral inversion of D-NNA was performed in a two-step pathway by D-amino acid oxidase (DAAO) followed by an unidentified transaminase. Such chiral inversion contributes ...
متن کاملShort Communication Inhibitory Effects of Benzoate on Chiral Inversion and Clearance of N-Nitro-Arginine in Conscious Rats
N-nitro-arginine (NNA) is known to exhibit stereoselective pharmacokinetics in which N-nitro-D-arginine (D-NNA) has a faster clearance rate than N-nitro-L-arginine (L-NNA) in anesthetized rats, and D-NNA undergoes unidirectional chiral inversion. It was postulated that chiral inversion of D-NNA was performed in a twostep pathway by D-amino acid oxidase (DAAO) followed by an unidentified transam...
متن کاملShort Communication Inhibitory Effects of Benzoate on Chiral Inversion and Clearance of N-Nitro-Arginine in Conscious Rats
N-nitro-arginine (NNA) is known to exhibit stereoselective pharmacokinetics in which N-nitro-D-arginine (D-NNA) has a faster clearance rate than N-nitro-L-arginine (L-NNA) in anesthetized rats, and D-NNA undergoes unidirectional chiral inversion. It was postulated that chiral inversion of D-NNA was performed in a twostep pathway by D-amino acid oxidase (DAAO) followed by an unidentified transam...
متن کاملShort Communication Inhibitory Effects of Benzoate on Chiral Inversion and Clearance of N-Nitro-Arginine in Conscious Rats
N-nitro-arginine (NNA) is known to exhibit stereoselective pharmacokinetics in which N-nitro-D-arginine (D-NNA) has a faster clearance rate than N-nitro-L-arginine (L-NNA) in anesthetized rats, and D-NNA undergoes unidirectional chiral inversion. It was postulated that chiral inversion of D-NNA was performed in a twostep pathway by D-amino acid oxidase (DAAO) followed by an unidentified transam...
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عنوان ژورنال:
- The Journal of pharmacology and experimental therapeutics
دوره 312 3 شماره
صفحات -
تاریخ انتشار 2005