Osuntokun Opeyemi Samson, Babatunde Ademola Adeniyi, Olayiwola Gbola, Atere Tope Gafar, Oladokun Olayemi Olutobi, Adedokun Kabiru Isola
Department of Physiology, Faculty of Basic Medical Sciences, College of Health Sciences, Osun State University Osogbo, Nigeria.
Department of Clinical Pharmacy and Pharmacy Administration, Faculty of Pharmacy, Obafemi Awolowo University, Ile-Ife, Nigeria.
Toxicol Rep. 2021 Mar 10;8:592-598. doi: 10.1016/j.toxrep.2021.03.008. eCollection 2021.
This study examined some of the biomarkers of hepatotoxicity following chronic treatment with carbamazepine (CBZ), levetiracetam (LEV), and CBZ + LEV adjunctive treatment in male rats.
Twenty-four male Wistar rats (140-150 g) were randomized into four groups (n = 6) to receive oral dose of normal saline (0.1 mL), CBZ (25 mg/kg), LEV (50 mg/kg) or sub-therapeutic dose of CBZ (12.5 mg/kg) together with LEV (25 mg/kg) for 28 days. Activities of the liver enzymes and oxidative stress markers were determined while liver histomorphology was also carried out. Data were analyzed using descriptive and inferential statistics. The results were presented as mean ± SEM in graphs or tables, while the level of significance was taken at p < 0.05.
The activities of alkaline-phosphatase and malondialdehyde concentrations increased significantly in all the drug treatment groups, while the activities of superoxide dismutase decreased significantly following CBZ, and CBZ + LEV treatment. Alanine-aminotransferase activities increased significantly in the CBZ and CBZ + LEV treated rats compared with control. The liver section of CBZ treated rats showed mild vascular congestion.
None of these AEDs treatment is devoid of hepatotoxicity. However, the adverse effects in CBZ were greater than LEV, or CBZ + LEV adjunctive treatment.
本研究检测了雄性大鼠长期服用卡马西平(CBZ)、左乙拉西坦(LEV)以及CBZ + LEV联合治疗后的一些肝毒性生物标志物。
将24只雄性Wistar大鼠(140 - 150克)随机分为四组(每组n = 6),分别口服生理盐水(0.1毫升)、CBZ(25毫克/千克)、LEV(50毫克/千克)或低于治疗剂量的CBZ(12.5毫克/千克)与LEV(25毫克/千克),持续28天。测定肝酶活性和氧化应激标志物,同时进行肝脏组织形态学检查。使用描述性和推断性统计方法分析数据。结果以平均值±标准误的形式呈现在图表中,显著性水平设定为p < 0.05。
所有药物治疗组的碱性磷酸酶活性和丙二醛浓度均显著增加,而CBZ和CBZ + LEV治疗后超氧化物歧化酶活性显著降低。与对照组相比,CBZ和CBZ + LEV治疗的大鼠丙氨酸转氨酶活性显著增加。CBZ治疗大鼠的肝脏切片显示轻度血管充血。
这些抗癫痫药物治疗均存在肝毒性。然而,CBZ的不良反应大于LEV或CBZ + LEV联合治疗。