Hepatoprotective efficacy of certain flavonoids against microcystin induced toxicity in mice

被引:66
作者
Jayaraj, R.
Deb, Utsab
Bhaskar, A. S. B.
Prasad, G. B. K. S.
Rao, P. V. Lakshmana
机构
[1] Def Res & Dev Estab, Div Pharmacol & Toxicol, Gwalior 474002, India
[2] Jiwaji Univ, Sch Studies Biochem, Gwalior 474002, India
关键词
microcystin-LR; flavonoids; quercetin; morin; silybin; microcystin adduct; OXIDATIVE STRESS; ADDUCT FORMATION; IN-VIVO; LR; CYANOBACTERIAL; LIVER; PROFILE; CHEMOPROTECTANTS; IDENTIFICATION; INHIBITION;
D O I
10.1002/tox.20283
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Toxic cyanobacteria (blue-green algae) water blooms have become a serious problem in several industrialized areas of the world. Microcystin-LR (MC-LR) is a cyanobacterial heptapeptide that represents acute and chronic hazards to animal and human health. Identification of suitable chemprotectants against microcystin is essential considering human health hazards. In the present study, we have evaluated the protective efficacy of three flavanoids namely quercetin (200 mg/kg), silybin (400 mg/kg), and morin (400 mg/kg) pretreatment against microcystin toxicity (0.75 LD50, 57.5 mu g/kg) in mice. Various biochemical variables were measured to study the recovery profile of protected animals at 1- and 3-days post-toxin treatment. The serum alanine amino transferase (ALT) shows 17-fold increase in MC-LR treated animals compared with control group at 1 day. The silybin and quercetin group showed a decrease in level of ALT compared with MC-LR group but still higher than control group. No significant protection was observed with aspartate aminotransaminase (AST) and lactate dehydrogenase (LDH) levels in flavanoid-treated groups at 1-day post-treatment. But at 3 days, the serum levels of AST and ALT were normalized to control values, but the serum LDH levels were still significantly higher than the control group. No significant changes were observed in glutathione peroxidase and reduced glutathione levels at both 1- and 3-day postexposure. The catalase activity shows a significant decrease in quercetin-treated animals at 3day postexposure. The protein phosphatase was significantly inhibited in MC-LR group compared to control. The silybin pretreated group showed recovery after 1 day. At 3 days, the PPAse activity was reversed to control values in all the flavanoid-treated groups. Immunoblotting analysis showed microcystin-PPAse adduct in liver tissues of toxin-treated as well as flavanoid-treated mice even after 3 days. The results of this study show that flavanoids, quercetin, silybin, and morin could reverse the hepatotoxic effects of MC-LR in vivo. (c) 2007 Wiley Periodicals, Inc.
引用
收藏
页码:472 / 479
页数:8
相关论文
共 35 条
[11]   HEPATOCYTE DEFORMATION INDUCED BY CYANOBACTERIAL TOXINS REFLECTS INHIBITION OF PROTEIN PHOSPHATASES [J].
ERIKSSON, JE ;
TOIVOLA, D ;
MERILUOTO, JAO ;
KARAKI, H ;
HAN, YG ;
HARTSHORNE, D .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 173 (03) :1347-1353
[12]  
FLOHE L, 1984, METHOD ENZYMOL, V105, P114
[13]   Comparative toxicity evaluation of cyanobacterial cyclic peptide toxin microcystin variants (LR, RR, YR) in mice [J].
Gupta, N ;
Pant, SC ;
Vijayaraghavan, R ;
Rao, PVL .
TOXICOLOGY, 2003, 188 (2-3) :285-296
[14]   EVALUATION OF POTENTIAL CHEMOPROTECTANTS AGAINST MICROCYSTIN-LR HEPATOTOXICITY IN MICE [J].
HERMANSKY, SJ ;
STOHS, SJ ;
ELDEEN, ZM ;
ROCHE, VF ;
MEREISH, KA .
JOURNAL OF APPLIED TOXICOLOGY, 1991, 11 (01) :65-74
[15]   CYCLOSPORINE-A - A CHEMOPROTECTANT AGAINST MICROCYSTIN-LR TOXICITY [J].
HERMANSKY, SJ ;
CASEY, PJ ;
STOHS, SJ .
TOXICOLOGY LETTERS, 1990, 54 (2-3) :279-285
[16]   FLUOROMETRIC METHOD FOR DETERMINATION OF OXIDIZED AND REDUCED GLUTATHIONE IN TISSUES [J].
HISSIN, PJ ;
HILF, R .
ANALYTICAL BIOCHEMISTRY, 1976, 74 (01) :214-226
[17]   Cyanobacterial toxins:: Removal during drinking water treatment, and human risk assessment [J].
Hitzfeld, BC ;
Höger, SJ ;
Dietrich, DR .
ENVIRONMENTAL HEALTH PERSPECTIVES, 2000, 108 :113-122
[18]   Fulminant hepatocyte apoptosis in vivo following microcystin-LR administration to rats [J].
Hooser, SB .
TOXICOLOGIC PATHOLOGY, 2000, 28 (05) :726-733
[19]   Protein phosphorylation profile and adduct formation in liver and kidney of microcystin-LR-treated mice [J].
Jayaraj, R. ;
Rao, P. V. Lakshmana .
TOXICON, 2006, 48 (03) :272-277
[20]   Activity and gene expression profile of certain antioxidant enzymes to microcystin-LR induced oxidative stress in mice [J].
Jayaraj, R ;
Anand, T ;
Rao, PVL .
TOXICOLOGY, 2006, 220 (2-3) :136-146