Korotkina R N, Papin A A, Voronina T A, Karelin A A
Biull Eksp Biol Med. 1988 Nov;106(11):565-8.
Experiments in vivo and in vitro on 90 rats were made to study the influence of 1,4-benzodiazepine tranquilizers (phenazepam, nitrazepam and diazepam) on cerebral xanthine oxidase activity. Phenazepam, nitrazepam and diazepam in the dose of 5 mg per 200 g bw were shown to reduce xanthine oxidase activity by 80.4%, 64.3% and 55.8%, respectively 2 h after intraperitoneal injection. 6 h after the injection of benzodiazepines the enzyme activity grows, but control values are achieved only after nitrazepam injection. In vitro experiments revealed direct influence of the tranquilizers on xanthine oxidase. Phenazepam inhibits xanthine oxidase activity in concentration as long as 10(-10) M (to 36.6%), and practically completely in 10(-6) M concentration. Nitrazepam and diazepam inhibit xanthine oxidase activity within concentration range between 10(-8) M (to 51.5% and 33.2%, respectively), and 10(-4) M (practically completely). The inhibition of xanthine oxidase activity is shown to be caused by the competition between hypoxanthine, the reaction substrate, and tranquilizer, to bind with the active site of the enzyme.
在90只大鼠身上进行了体内和体外实验,以研究1,4 - 苯二氮䓬类镇静剂(非那西泮、硝西泮和地西泮)对脑黄嘌呤氧化酶活性的影响。腹腔注射后2小时,每200克体重给予5毫克的非那西泮、硝西泮和地西泮,分别使黄嘌呤氧化酶活性降低80.4%、64.3%和55.8%。注射苯二氮䓬类药物6小时后,酶活性升高,但仅在注射硝西泮后达到对照值。体外实验揭示了镇静剂对黄嘌呤氧化酶的直接影响。非那西泮在浓度低至10(-10) M时就抑制黄嘌呤氧化酶活性(至36.6%),在10(-6) M浓度时几乎完全抑制。硝西泮和地西泮在10(-8) M(分别至51.5%和33.2%)至10(-4) M(几乎完全抑制)的浓度范围内抑制黄嘌呤氧化酶活性。黄嘌呤氧化酶活性的抑制表明是由反应底物次黄嘌呤与镇静剂竞争结合酶的活性位点所致。