Pharmacognosy Division, Bengal School of Technology (A College of Pharmacy), Delhi Road, Sugandha, Hooghly 712102, West Bengal, India.
Biol Trace Elem Res. 2012 Aug;148(2):232-41. doi: 10.1007/s12011-012-9363-3. Epub 2012 Mar 1.
The present work was focused to evaluate the ameliorative property of aqueous extract of Trichosanthes dioica fruit (AQ T. dioica fruit) against arsenic-induced toxicity in male Wistar albino rats. AQ T. dioica fruit was administered orally to rats at 50 and 100 mg/kg body weight for 20 consecutive days prior to oral administration of sodium arsenite (10 mg/kg) for 10 days. Then the rats were sacrificed for the evaluation of body weights, organ weights, hematological profile, serum biochemical profile, and hepatic and renal antioxidative parameters viz. lipid peroxidation, reduced and oxidized glutathione, glutathione-S-transferase, glutathione peroxidase, glutathione reductase, superoxide dismutase, catalase, and DNA fragmentation. Pretreatment with AQ T. dioica fruit at both doses markedly and significantly normalized body weights, organ weights, hematological profiles, and serum biochemical profile in arsenic-treated animals. Further, AQ T. dioica fruit pretreatment significantly modulated all the aforesaid hepatic and renal biochemical perturbations and reduced DNA fragmentation in arsenic-intoxicated rats. Therefore, from the present findings, it can be concluded that T. dioica fruit possessed remarkable value in amelioration of arsenic-induced hepatic and renal toxicity, mediated by alleviation of arsenic-induced oxidative stress by multiple mechanisms in male albino rats.
本研究旨在评估三叶木通(AQ T. dioica fruit)水提物对雄性 Wistar 白化大鼠砷中毒的改善作用。AQ T. dioica fruit 在给予亚砷酸钠(10mg/kg)之前,以 50 和 100mg/kg 体重连续口服给药 20 天。然后处死大鼠,评估体重、器官重量、血液学特征、血清生化特征以及肝肾功能抗氧化参数,如脂质过氧化、还原型和氧化型谷胱甘肽、谷胱甘肽-S-转移酶、谷胱甘肽过氧化物酶、谷胱甘肽还原酶、超氧化物歧化酶、过氧化氢酶和 DNA 片段化。AQ T. dioica fruit 在两个剂量下预处理可显著且明显地使砷处理动物的体重、器官重量、血液学特征和血清生化特征正常化。此外,AQ T. dioica fruit 预处理可显著调节上述所有肝肾功能生化紊乱,并减少砷中毒大鼠的 DNA 片段化。因此,从目前的研究结果可以得出结论,三叶木通果实具有显著的价值,可以通过多种机制减轻砷诱导的氧化应激,从而改善雄性白化大鼠的砷诱导的肝肾功能毒性。