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小鼠血吸虫病慢性期肝脏微粒体酶的活性

Activity of liver microsomal enzymes during the chronic phase of murine schistosomiasis.

作者信息

Conte F P, Fidalgo-Neto A A, Manhães-Rocha D A, Paumgartten F J R, De-Oliveira A C A X

机构信息

Laboratório de Toxicologia Ambiental, Departamento de Ciências Biológicas, Escola Nacional de Saúde Pública, Fundação Oswaldo Cruz, Rio de Janeiro, RJ, Brasil.

出版信息

Braz J Med Biol Res. 2007 May;40(5):657-62.

Abstract

The effects of schistosomiasis on microsomal enzymes were studied on post-infection day 90 when accumulated damage and fibrosis are most intense but granulomatous reaction around the eggs harbored in the liver is smaller than during the earlier phases. Swiss Webster (SW) and DBA/2 mice of either sex (N = 12 per sex per group) were infected with 100 Schistosoma mansoni cercariae on postnatal day 10 and killed on post-infection day 90. Cytochrome P-450 (CYP) concentration and alkoxyresorufin-O-dealkylases (EROD, MROD, BROD, and PROD), p-nitrophenol-hydroxylase (PNPH), coumarin-7-hydroxylase (COH), and UDP-glucuronosyltransferase (UGT) activities were measured in hepatic microsomes. Age-matched mice of the same sex and strain were used as controls. In S. mansoni-infected mice, CYP1A- and 2B-mediated activities (control = 100%) were reduced in SW (EROD: male (M) 36%, female (F) 38%; MROD: M 38%, F 39%; BROD: M 46%, F 19%; PROD: M 50%, F 28%) and DBA/2 mice (EROD: M 64%, F 58%; MROD: M 60%; BROD: F 49%; PROD: M 73%) while PNPH (CYP2E1) was decreased in SW (M 31%, F 38%) but not in DBA/2 mice. COH did not differ between infected and control DBA/2 and UGT, a phase-2 enzyme, was not altered by infection. In conclusion, chronic S. mansoni infection reduced total CYP content and all CYP-mediated activities evaluated in SW mice, including those catalyzed by CYP2E1 (PNPH), CYP1A (EROD, MROD) and 2B (BROD, PROD). In DBA/2 mice, however, CYP2A5- and 2E1-mediated activities remained unchanged while total CYP content and activities mediated by other CYP isoforms were depressed during chronic schistosomiasis.

摘要

在感染后第90天研究了血吸虫病对微粒体酶的影响,此时累积损伤和纤维化最为严重,但肝脏中虫卵周围的肉芽肿反应比早期阶段小。在出生后第10天,将100只曼氏血吸虫尾蚴感染瑞士韦伯斯特(SW)小鼠和DBA/2小鼠(每组每种性别12只),并在感染后第90天处死。测定肝微粒体中细胞色素P-450(CYP)浓度以及烷氧基试卤灵-O-脱烷基酶(EROD、MROD、BROD和PROD)、对硝基苯酚羟化酶(PNPH)、香豆素-7-羟化酶(COH)和尿苷二磷酸葡萄糖醛酸基转移酶(UGT)的活性。使用相同性别和品系、年龄匹配的小鼠作为对照。在感染曼氏血吸虫的小鼠中,SW小鼠(EROD:雄性(M)36%,雌性(F)38%;MROD:M 38%,F 39%;BROD:M 46%,F 19%;PROD:M 50%,F 28%)和DBA/2小鼠(EROD:M 64%,F 58%;MROD:M 60%;BROD:F 49%;PROD:M 73%)中CYP1A和2B介导的活性(对照=100%)降低,而SW小鼠中PNPH(CYP2E1)降低(M 31%,F 38%),但DBA/2小鼠中未降低。感染组和对照组DBA/2小鼠的COH没有差异,UGT作为一种二期酶,不受感染影响。总之,慢性曼氏血吸虫感染降低了SW小鼠中的总CYP含量以及所有评估的CYP介导的活性,包括由CYP2E1(PNPH)、CYP1A(EROD、MROD)和2B(BROD、PROD)催化的活性。然而,在DBA/2小鼠中,CYP2A5和2E1介导的活性保持不变,而在慢性血吸虫病期间,总CYP含量和其他CYP同工型介导的活性降低。

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