Effect of Oyster mushroom in Paracetamol Induced Toxicity of Liver in Wistar albino Rats

Afroza Khanam Sumy, N. Jahan, N. Sultana, A. M. Sikder
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引用次数: 3

Abstract

Backgroud : Liver is an important metabolic organ. It has wide range of functions including detoxification, storage of glycogen, vitamins A, D and B12, production of several coagulation factors, growth factors such as insulin-like growth factor-1 (IGF-1), angiotensinogen, and biochemicals necessary for digestion (bile). Its damage occurs due to its multidimensional functions, various xenobiotics and oxidative stress leading to distortion of all of its functions. Oyster mushroom which is excellently edible and nutritious has got free radical scavenging activity, and so may be considered as a hepatoprotective agent. Objective : To observe the hepatoprotective effect of Oyster mushroom (Pleurotus florida) against paracetamol induced liver damage in Wistar albino rats. Materials and Methods : This experimental study was carried out in the Department of Physiology, Sir Salimullah Medical College (SSMC), Dhaka from 1st July 2009 to 30th June 2010. Thirty four Wistar albino rats, aged 90 to 120 days, weighing between 150 to 210 grams were used for the study. After acclimatization for 14 days, they were divided into two groups –– control group (Group A) and experimental group (Group B, mushroom-pretreated and paracetamol-treated group). Control group was again subdivided into Group A1 (baseline control group) and Group A2 (paracetamol-treated control group). Animals of all groups received basal diet for 30 consecutive days. In addition, Group A1 rats received propylene glycol (2 mL/kg body weight orally) only on 30th day, Group A2 rats received single dose of paracetamol suspension (750 mg/kg body weight orally) only on 30th day and Group B rats received mushroom extract (200 mg/kg body weight orally) for 30 consecutive days and paracetamol suspension (750 mg/kg body weight orally) only on 30th day. All the animals were sacrificed on 31st day. Then liver specimens were collected. Histology of liver was done by using standard laboratory procedure. Statistical analysis was done by one way ANOVA test by using SPSS version 15.0. Result : In this study, histological examination of liver reveals abnormal histological findings in 100% of rats in paracetamol-treated group (Group A2), almost normal structure in 80% of rats and mild histological changes in 20% rats in mushroom-pretreated and paracetamol-treated group (Group B). Conclusion : The present study reveals the hepatoprotective effect of Oyster mushroom (Pleurotus florida) against paracetamol induced liver damage in Wistar albino rats. DOI: http://dx.doi.org/10.3329/jemc.v4i3.20945 J Enam Med Col 2014; 4(3): 161-167
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平菇对扑热息痛致Wistar白化大鼠肝脏毒性的影响
背景:肝脏是人体重要的代谢器官。它具有广泛的功能,包括解毒、储存糖原、维生素A、D和B12、产生几种凝血因子、生长因子如胰岛素样生长因子-1 (IGF-1)、血管紧张素原和消化所需的生化物质(胆汁)。其损伤是由于其多方面的功能,各种外源物质和氧化应激导致其所有功能的扭曲。平菇具有良好的食用性和营养价值,具有清除自由基的活性,可作为肝保护剂。目的:观察平菇(Pleurotus florida)对扑热息痛致Wistar白化大鼠肝损伤的保护作用。材料和方法:本实验研究于2009年7月1日至2010年6月30日在达卡萨里穆拉爵士医学院(SSMC)生理学系进行。34只年龄在90至120天、体重在150至210克之间的Wistar白化大鼠被用于这项研究。驯化14 d后,分为对照组(A组)和试验组(B组,蘑菇预处理组和扑热息痛组)。对照组再次分为A1组(基线对照组)和A2组(扑热息痛对照组)。各组动物连续饲喂基础饲粮30 d。此外,A1组大鼠仅在第30天口服丙二醇(2 mL/kg体重),A2组大鼠仅在第30天口服单剂量扑热息痛混悬液(750 mg/kg体重),B组大鼠连续30天口服蘑菇提取物(200 mg/kg体重),第30天口服扑热息痛混悬液(750 mg/kg体重)。第31天处死所有动物。然后采集肝脏标本。采用标准实验室程序进行肝脏组织学检查。统计学分析采用SPSS 15.0版本单因素方差分析。结果:在本研究中,对乙酰氨基酚处理组(A2组)肝脏组织学检查显示100%的大鼠肝脏组织异常,蘑菇预处理组和对乙酰氨基酚处理组(B组)80%的大鼠肝脏组织基本正常,20%的大鼠肝脏组织有轻微改变。结论:本研究揭示了平菇(Pleurotus florida)对扑热息痛引起的Wistar白化大鼠肝脏损伤的保护作用。DOI: http://dx.doi.org/10.3329/jemc.v4i3.20945 J Enam Med Col 2014;4 (3): 161 - 167
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