Protective Effect of Flos Puerariae Extract Following Acute Alcohol Intoxication in Mice

被引:44
作者
Chen, Xiao [1 ]
Cai, Fei [1 ]
Guo, Shuang [1 ]
Ding, Fang [2 ]
He, Yi [2 ]
Wu, Jiliang [1 ]
Liu, Chao [1 ]
机构
[1] Hubei Univ Sci & Technol, Hubei Prov Key Lab Cardiovasc Cerebrovasc & Metab, Xianning 437100, Peoples R China
[2] Xianning Cent Hosp, Xianning, Peoples R China
基金
中国国家自然科学基金;
关键词
Flos Puerariae; Alcoholism; Alcohol Dehydrogenase; Aldehyde Dehydrogenase; Antioxidant; LIVER-DISEASE; OXIDATIVE STRESS; HANGOVER; ETHANOL; MEMORY; PATHOGENESIS; DISORDERS; MECHANISM; BEHAVIOR; SYSTEM;
D O I
10.1111/acer.12437
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
Background: The effect of Flos Puerariae extract (FPE) on alcohol metabolism, hepatic injury, and memory impairment was assessed following acute ethanol (EtOH) intoxication in mice. Methods: The model of acute EtOH intoxication was established by intragastric administration with 8 g/kg EtOH in mice. FPE was orally administrated (gavage) once a day for 7 consecutive days. Mice were randomly divided into 4 groups: control group, model group, and FPE groups (100, 200 mg/kg). Alcohol tolerance and intoxication time, blood alcohol concentration, the activities of alcohol dehydrogenase (ADH) and aldehyde dehydrogenase (ALDH) in liver, aspartate amino transferase (AST) and alanine amino transferase (ALT) in serum, superoxide dismutase (SOD), glutathione peroxidase (GSH-px), catalase and the formation of malondialdehyde (MDA) in both liver and brain, as well as memory ability were determined after acute alcohol exposure. Results: Compared with model group, pretreatment with FPE significantly prolonged alcohol tolerance time and shortened intoxication time, which is accompanied by decreased blood alcohol concentration and elevated activities of ADH and ALDH in liver. Moreover, the index of hepatic injury, ALT, and AST activities in serum was markedly decreased by pretreatment with FPE. Additionally, decreased MDA level, enhanced GSH-px and catalase activities in liver, as well as enhanced SOD and catalase activities in brain were found in FPE pretreated mice after acute exposure to EtOH. Furthermore, FPE pretreated mice showed markedly relieved memory disruption following acute EtOH intoxication. Conclusions: This study suggests that FPE pretreatment could enhance alcohol metabolism, prevent hepatic injury, and relieve memory impairment after acute alcohol intoxication and that this effect is likely related to its modulation on the alcohol metabolizing and antioxidant enzymes.
引用
收藏
页码:1839 / 1846
页数:8
相关论文
共 37 条
[1]  
Augustyniak Agnieszka, 2005, Postepy Hig Med Dosw (Online), V59, P464
[2]  
Cai Fei Cai Fei, 2014, African Journal of Pharmacy and Pharmacology, V8, P1
[3]   Mechanisms of Neurodegeneration and Regeneration in Alcoholism [J].
Crews, Fulton T. ;
Nixon, Kim .
ALCOHOL AND ALCOHOLISM, 2009, 44 (02) :115-127
[4]   Laboratory Models Available to Study Alcohol-Induced Organ Damage and Immune Variations: Choosing the Appropriate Model [J].
El-Guindy, Nympha B. D'Souza ;
Kovacs, Elizabeth J. ;
De Witte, Philippe ;
Spies, Claudia ;
Littleton, John M. ;
de Villiers, Willem J. S. ;
Lott, Amanda J. ;
Plackett, Timothy P. ;
Lanzke, Nadine ;
Meadows, Gary G. .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 2010, 34 (09) :1489-1511
[5]   Acetaldehyde-induced mitochondrial dysfunction sensitizes hepatocytes to oxidative damage [J].
Farfan Labonne, Blanca Eugenia ;
Gutierrez, Mario ;
Enrique Gomez-Quiroz, Luis ;
Konigsberg Fainstein, Mina ;
Bucio, Leticia ;
Souza, Veronica ;
Flores, Oscar ;
Ortiz, Victor ;
Hernandez, Elizabeth ;
Kershenobich, David ;
Concepcion Gutierrez-Ruiz, Maria .
CELL BIOLOGY AND TOXICOLOGY, 2009, 25 (06) :599-609
[6]  
Field Matt, 2008, Curr Drug Abuse Rev, V1, P263
[7]   The transcriptional and DNA binding activity of peroxisome proliferator-activated receptor α is inhibited by ethanol metabolism -: A novel mechanism for the development of ethanol-induced fatty liver [J].
Galli, A ;
Pinaire, J ;
Fischer, M ;
Dorris, R ;
Crabb, DW .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (01) :68-75
[8]   Alcoholic Liver Disease: Pathogenesis and New Therapeutic Targets [J].
Gao, Bin ;
Bataller, Ramon .
GASTROENTEROLOGY, 2011, 141 (05) :1572-1585
[9]   REACTIVE OXYGEN SPECIES AND THE CENTRAL-NERVOUS-SYSTEM [J].
HALLIWELL, B .
JOURNAL OF NEUROCHEMISTRY, 1992, 59 (05) :1609-1623
[10]   In vitro evaluation of tectoridin, tectorigenin and tectorigenin sodium sulfonate on antioxidant properties [J].
Han, Ting ;
Cheng, Gang ;
Liu, Ying ;
Yang, Hong ;
Hu, Yu-tao ;
Huang, Wen .
FOOD AND CHEMICAL TOXICOLOGY, 2012, 50 (02) :409-414