Salahshoor Mohammad Reza, Vahabi Arman, Roshankhah Shiva, Darehdori Ahmad Shabanizadeh, Jalili Cyrus
Department of Anatomical Sciences, Medical School, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Department of Anatomical Sciences, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Int J Prev Med. 2018 Jan 29;9:8. doi: 10.4103/ijpvm.IJPVM_144_16. eCollection 2018.
Morphine is a pain medication. It is mostly processed in liver and reasons disturbing effects. It can increase the production of free radicals. Thymoquinone is a phytochemical compound found in the plant . It has diverse pharmacological properties such as antioxidant and anticancer. This study was intended to assess the effects of thymoquinone against morphine damages on the liver of mice.
In this study, various doses of thymoquinone (4.5, 9, and 18 mg/kg) and thymoquinone plus morphine was administered (once a day) intraperitoneally to 48 male mice for 20 consequent days. These mice were randomly assigned to eight groups ( = 6). Aspartate aminotransferase, alanine aminotransferase, alkaline phosphatase, serum nitric oxide (NO) levels, liver weight, and histology have been studied.
The results indicated that morphine administration significantly increased the mean diameter of central hepatic vein and hepatocyte, blood serum NO level, liver enzymes level, and decreased liver weight compared to saline group ( < 0.05). However, thymoquinone and thymoquinone plus morphine administration significantly enhanced liver weight and reduced the mean diameter of hepatocyte, central hepatic vein, liver enzymes, and NO levels in all groups compared to morphine group ( < 0.05).
It seems that antioxidant effect of thymoquinone could protect damage of liver parameters against morphine toxicity.
吗啡是一种止痛药物。它主要在肝脏中进行代谢,会产生不良影响。它会增加自由基的产生。百里醌是一种存在于植物中的植物化学化合物。它具有多种药理特性,如抗氧化和抗癌作用。本研究旨在评估百里醌对吗啡所致小鼠肝脏损伤的影响。
在本研究中,将不同剂量的百里醌(4.5、9和18毫克/千克)以及百里醌加吗啡(每天一次)腹腔注射给48只雄性小鼠,连续注射20天。这些小鼠被随机分为八组(每组 = 6只)。研究了天冬氨酸转氨酶、丙氨酸转氨酶、碱性磷酸酶、血清一氧化氮(NO)水平、肝脏重量和组织学。
结果表明,与生理盐水组相比,给予吗啡显著增加了肝中央静脉和肝细胞的平均直径、血清NO水平、肝酶水平,并降低了肝脏重量(P < 0.05)。然而,与吗啡组相比,给予百里醌和百里醌加吗啡显著增加了所有组的肝脏重量,并降低了肝细胞、肝中央静脉、肝酶和NO水平的平均直径(P < 0.05)。
百里醌的抗氧化作用似乎可以保护肝脏参数免受吗啡毒性的损害。