Protective effects of 5-methoxypsoralen against acetaminophen-induced hepatotoxicity in mice

被引:31
|
作者
Liu, Wei-Xia [1 ]
Jia, Feng-Lan [1 ]
He, Yue-Ying [1 ]
Zhang, Bao-Xu [1 ]
机构
[1] Peking Univ, Sch Publ Hlth, Dept Toxicol, Beijing 100191, Peoples R China
关键词
5-Methoxypsoralen; Protection; Acetaminophen; Hepatotoxicity; Antioxidation; ACUTE LIVER-FAILURE; INDUCTION; INCREASES; PSORALENS; APOPTOSIS; INJURY; 5-MOP; CELLS;
D O I
10.3748/wjg.v18.i18.2197
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AIM: To investigate the hepatic protective effects of 5-methoxypsoralen (5-MOP) and to learn if 5-MOP causes hepatotoxicity at protective doses. METHODS: C57BL/6J mice were administrated orally with 5-MOP at doses of 12.5, 25 and 50 mg/kg body weight respectively every morning for 4 d before given acetaminophen (APAP) subcutaneously at a dose of 500 mg/kg. The 5-MOP alone group was treated with 5-MOP orally at a dose of 50 mg/kg body weight for 4 d without APAP. Twenty-four hours after APAP administration, blood samples of mice were analyzed for serum enzyme alanine transaminase (ALT), aspartate transaminase (AST), lactate dehydrogenase (LDH) levels, and malondialdehyde (MDA), reduced glutathione (GSH) and oxidized glutathione (GSSG) of liver tissues were measured and histopathologic changes of the liver were observed. RESULTS: Compared with the vehicle control group, the serum levels (IU/L) of ALT, AST and LDH were all increased significantly in APAP group (8355 +/- 3940 vs 30 +/- 21, P < 0.05; 6482 +/- 4018 vs 146 +/- 58, P < 0.05; 24627 +/- 10975 vs 1504 +/- 410, P < 0.05). Compared with APAP group, the serum ALT levels (IU/L) (1674 +/- 1810 vs 8355 +/- 3940, P < 0.05; 54 +/- 39 vs 8355 +/- 3940, P < 0.05; 19 +/- 9 vs 8355 +/- 3940, P < 0.05), AST levels (IU/L) (729 +/- 685 vs 6482 +/- 4108, P < 0.05; 187 +/- 149 vs 6482 +/- 4108, P < 0.05; 141 +/- 12 vs 6482 +/- 4108, P < 0.05) and LDH levels (IU/L) (7220 +/- 6317 vs 24 627 +/- 10 975, P < 0.05; 1618 +/- 719 vs 24 627 +/- 10 975, P < 0.05; 1394 +/- 469 vs 24 627 +/- 10 975, P < 0.05) were all decreased drastically in the three-dosage 5-MOP pretreatment groups. Pretreatment of 5-MOP could attenuate histopathologic changes induced by APAP, including hepatocellular necrosis and infiltration of inflammatory cells, and the effect was dose-dependent. MDA levels (nmol/mg) were decreased by 5-MOP in a dose-dependent manner (0.98 +/- 0.45 vs 2.15 +/- 1.07, P > 0.05; 0.59 +/- 0.07 vs 2.15 +/- 1.07, P < 0.05; 0.47 +/- 0.06 vs 2.15 +/- 1.07, P < 0.05). The pretreatment of 5-MOP could also increase the GSH/GSSG ratio (3.834 +/- 0.340 vs 3.306 +/- 0.282, P > 0.05; 5.330 +/- 0.421 vs 3.306 +/- 0.282, P < 0.05; 6.180 +/- 0.212 vs 3.306 +/- 0.282, P < 0.05). In the group treated with 5-MOP but without APAP, the serum enzyme levels, the liver histopathologic manifestation, and the values of MDA and GSH/GSSG ratio were all normal. CONCLUSION: 5-MOP can effectively protect C57BL/63 mice from APAP-induced hepatotoxicity and possesses an antioxidative activity, and does not cause liver injury at the protective doses. (C) 2012 Baishideng. All rights reserved.
引用
收藏
页码:2197 / 2202
页数:6
相关论文
共 50 条
  • [21] Effects of Photoperiod on Acetaminophen-Induced Hepatotoxicity in Mice
    Jihong Lu
    Hu Wang
    Rumeng Zhang
    Zhikang Wan
    Hang Gao
    Jie Cai
    Yujia Cheng
    Dong Pu
    Tengfei Lin
    Chenyu Fan
    Ying Sun
    Digestive Diseases and Sciences, 2020, 65 : 178 - 188
  • [22] Protective effects of resveratrol against acetaminophen-induced toxicity in mice
    Sener, Goksel
    Toklu, Hale Z.
    Sehirli, A. Ozer
    Velioglu-Ogunc, Ayliz
    Cetinel, Sule
    Gedik, Nursal
    HEPATOLOGY RESEARCH, 2006, 35 (01) : 62 - 68
  • [23] Chitohexaose protects against acetaminophen-induced hepatotoxicity in mice
    Barman, P. K.
    Mukherjee, R.
    Prusty, B. K.
    Suklabaidya, S.
    Senapati, S.
    Ravindran, B.
    CELL DEATH & DISEASE, 2016, 7 : e2224 - e2224
  • [24] Calcitriol Protects against Acetaminophen-Induced Hepatotoxicity in Mice
    Sriphoosanaphan, Supachaya
    Rattanachaisit, Pakkapon
    Somanawat, Kanjana
    Wanpiyarat, Natcha
    Komolmit, Piyawat
    Werawatganon, Duangporn
    BIOMEDICINES, 2023, 11 (06)
  • [25] Role of β-carotene against acetaminophen-induced hepatotoxicity in mice
    Manda, K
    Bhatia, AL
    NUTRITION RESEARCH, 2003, 23 (08) : 1097 - 1103
  • [26] Chitohexaose protects against acetaminophen-induced hepatotoxicity in mice
    P K Barman
    R Mukherjee
    B K Prusty
    S Suklabaidya
    S Senapati
    B Ravindran
    Cell Death & Disease, 2016, 7 : e2224 - e2224
  • [27] Protective effects of salidroside against acetaminophen-induced toxicity in mice
    Wu, Yan-Ling
    Piao, Dong-Ming
    Han, Xue-Hua
    Nan, Ji-Xing
    BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2008, 31 (08) : 1523 - 1529
  • [28] PROTECTIVE EFFECTS OF SELENIUM ON ACETAMINOPHEN-INDUCED HEPATOTOXICITY IN THE RAT
    SCHNELL, RC
    PARK, KS
    DAVIES, MH
    MERRICK, BA
    WEIR, SW
    TOXICOLOGY AND APPLIED PHARMACOLOGY, 1988, 95 (01) : 1 - 11
  • [29] Protective effects of garlic and related organosulfur compounds on acetaminophen-induced hepatotoxicity in mice
    Wang, EJ
    Li, Y
    Lin, M
    Chen, LS
    Stein, AP
    Reuhl, KR
    Yang, CS
    TOXICOLOGY AND APPLIED PHARMACOLOGY, 1996, 136 (01) : 146 - 154
  • [30] ACETAMINOPHEN-INDUCED HEPATOTOXICITY IN MICE
    WALKER, RM
    RACZ, WJ
    MCELLIGOTT, TF
    LABORATORY INVESTIGATION, 1980, 42 (02) : 181 - 189