Evaluation of D-amino acid oxidase activity in rat kidney using a D-kynurenine derivative, 6-methylthio-D-kynurenine: An in vivo microdialysis study.

IF 1.9 Q3 PHARMACOLOGY & PHARMACY
Drug Discoveries and Therapeutics Pub Date : 2024-01-12 Epub Date: 2023-12-03 DOI:10.5582/ddt.2023.01083
Takeshi Fukushima, Ayano Kansaku, Maho Umino, Tatsuya Sakamoto, Mayu Onozato
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引用次数: 0

Abstract

D-Amino acid oxidase (DAO), a D-amino acid metabolizing enzyme, is reportedly associated with the psychiatric disease schizophrenia, suggesting a role for DAO inhibitors in its treatment. We have previously reported that DAO catalyzes the conversion of nonfluorescent 6-methylthio-D-kynurenine (MeS-D-KYN) to fluorescent 5-methylthiokynurenic acid (MeS-KYNA) in vitro. The present study aimed to determine the potential of MeS-D-KYN in evaluating DAO activity in vivo using renal microdialysis technique in rats. Male Sprague-Dawley rats were subjected to linear microdialysis probe implantation in the left kidney. Continuous perfusion of MeS-D-KYN was maintained, and DAO activity in the kidney cortex was evaluated by measuring the MeS-KYNA content in the microdialysate. The microdialysate was collected every 30 min and analyzed by high-performance liquid chromatography with fluorescence detection, monitored at 450 nm with an excitation wavelength of 364 nm. A significant production of MeS-KYNA was observed during, but not before, infusion of MeS-D-KYN, indicating that this compound is not endogenous. MeS-KYNA production was suppressed by the co-infusion of DAO inhibitor, 5-chlorobenzo[d]isoxazol-3-ol (CBIO), suggesting that MeS-D-KYN was converted to MeS-KYNA by renal DAO. Moreover, oral administration of CBIO effectively suppressed DAO activity in a dose-dependent manner. DAO converted MeS-D-KYN to MeS-KYNA in vivo, suggesting the potential of this compound in evaluating DAO activity. The use of the renal microdialysis technique developed in this study facilitates the monitoring of DAO activity in live experimental animals.

用d -犬尿氨酸衍生物6-甲基硫代d -犬尿氨酸评价大鼠肾脏d -氨基酸氧化酶活性:体内微透析研究。
d -氨基酸氧化酶(DAO)是一种d -氨基酸代谢酶,据报道与精神疾病精神分裂症有关,表明DAO抑制剂在其治疗中起作用。我们之前报道过DAO在体外催化非荧光6-甲基硫代- d -犬尿氨酸(MeS-D-KYN)转化为荧光5-甲基硫代-犬尿氨酸(MeS-KYNA)。本研究旨在确定MeS-D-KYN在大鼠肾脏微透析技术中评估DAO活性的潜力。在雄性sd大鼠左肾内植入线性微透析探针。维持MeS-D-KYN持续灌注,通过测定微透析液中MeS-KYNA含量来评价肾皮质DAO活性。微透析液每隔30 min收集一次,采用高效液相色谱法进行荧光检测,在450 nm处监测,激发波长为364 nm。在输注MeS-D-KYN期间观察到大量MeS-KYNA的产生,而在输注MeS-D-KYN之前则没有,这表明该化合物不是内源性的。联合输注DAO抑制剂5-氯苯并[d]异恶唑-3-醇(CBIO)可抑制MeS-KYNA的生成,提示MeS-D-KYN可通过肾脏DAO转化为MeS-KYNA。此外,口服CBIO可有效抑制DAO活性,且呈剂量依赖性。DAO在体内将MeS-D-KYN转化为MeS-KYNA,表明该化合物在评估DAO活性方面具有潜力。利用本研究开发的肾脏微透析技术,便于在活体实验动物中监测DAO活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Drug Discoveries and Therapeutics
Drug Discoveries and Therapeutics PHARMACOLOGY & PHARMACY-
CiteScore
3.20
自引率
3.20%
发文量
51
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