EFFECTS OF VIRGIN COCONUT OIL AND LAURIC ACID “WITH OR WITHOUT 5-FLUOROURACIL” ON DIMETHYLHYDRAZINE-INDUCED HEPATOTOXICITY IN MALE RATS

Adel A. El Bagoury, Hala El-Tantawi, S. El-Naggar, Amel M. Kwilla, Amal M. Khalaf
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Abstract

Dimethylhydrazine (DMH) is highly toxic for the different body organs, including the liver. The current study aimed to investigate the potential protective role of virgin coconut oil (VCO) and lauric acid (LA) in presence/absence of a chemotherapy drug “5-fluorouracil (5-FU)” against the hepatoxicity induced by DMH in male rats (Rattus norvegicus). Ninety rats were randomly divided into nine groups (n = 10). (G1) control group; (G2) rats received 4 mL VCO/kg body weight (b.wt) , orally/day after day for six weeks starting from week 13; (G3) rats received LA (200 mg/kg b.wt), orally/day after day for six weeks as in G2; (G4) rats were injected subcutaneously (s.c.) with DMH (20 mg/kg b.wt), once/week for the first six weeks; (G5) rats received DMH as in G4 and intraperitoneally (i.p.) injected with 5-FU (75 mg/kg b.wt), once/week starting from week 13 for three successive weeks; (G6) rats received DMH and VCO as in G4 and G2, respectively; (G7) rats received DMH and LA as in G4 and G3, respectively; (G8) rats received DMH, 5-FU, and VCO as in G4, G5, and G2, respectively; (G9) rats received DMH, 5-FU, and LA as in G4, G5, and G3, respectively. The results showed that DMH injection caused oxidative stress and histopathological alterations in the liver tissue, as well as dyslipidaemia. However, treatment of male rats with VCO or LA in presence/absence of 5-FU reduced significantly the DMH-induced hepatotoxicity.
初榨椰子油和月桂酸“加或不加5-氟尿嘧啶”对二甲肼诱导的雄性大鼠肝毒性的影响
二甲肼(DMH)对包括肝脏在内的不同身体器官都有剧毒。本研究旨在探讨在化疗药物“5-氟尿嘧啶(5-FU)”存在/不存在的情况下,初生椰子油(VCO)和月桂酸(LA)对DMH诱导的雄性大鼠(Rattus norvegicus)肝毒性的潜在保护作用。90只大鼠随机分为9组(n = 10)。(G1)对照组;(G2)大鼠从第13周开始,每天口服4 mL VCO/kg体重(b.wt),连续6周;(G3)大鼠给予LA (200 mg/kg b.wt),每日口服,连续6周,与G2组相同;(G4)大鼠皮下注射DMH (20 mg/kg b.wt),前6周每周1次;(G5)大鼠于G4给予DMH,并从第13周开始腹腔注射5-FU (75 mg/kg b.wt),每周1次,连续3周;(G6) DMH和VCO分别与G4和G2组相同;(G7)大鼠分别在G4和G3时给予DMH和LA;(G8)大鼠分别在G4、G5、G2组给予DMH、5-FU、VCO;(G9)大鼠分别在G4、G5、G3组给予DMH、5-FU、LA。结果表明,注射DMH引起肝组织氧化应激和组织病理学改变,并引起血脂异常。然而,在5-FU存在或不存在的情况下,用VCO或LA治疗雄性大鼠可显著降低dmh诱导的肝毒性。
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