Department of Pharmacology, NGSM Institute of Pharmaceutical Sciences, Deralakatte, Mangalore, Karnataka, India.
Indian J Pharmacol. 2013 Mar-Apr;45(2):121-5. doi: 10.4103/0253-7613.108280.
Aripiprazole, a new atypical antipsychotic drug extensively metabolized by enzyme CYP3A4, is found to produce asymptomatic elevation of serum transaminase levels on long-term treatment. The present study aims to evaluate the hepatotoxic effect of aripiprazole when coprescribed with carbamazepine and fluvoxamine.
The rats were subjected to chronic treatment with two different doses, therapeutic dose (TD) and maximum therapeutic dose (MTD), of aripiprazole in combination with carbamazepine and fluvoxamine. The changes in hepatic function was assessed by various biochemical liver enzyme markers like serum glutamate oxaloacetate transaminase (SGOT), serum glutamate pyruvate transaminase (SGPT), alkaline phosphatase (ALP), total bilirubin, histological studies, and physical parameters (liver weight, liver volume, and body weight).
The combination of aripiprazole with fluvoxamine at both TD and MTD showed the hepatic damage and significant elevation in serum transaminase level which is supported by histological reports. The coadministration of aripiprazole with carbamazepine leads to significant decrease in blood concentration of aripiprazole possibly due to induction of enzyme CYP3A4 resulting in loss or reduction of clinical efficacy.
There would be an accumulation of aripiprazole when coadministered with fluvoxamine, a known inhibitor of CYP3A4, leading to hepatic damage and reduction in aripiprazole when administered along with carbamazepine. Therefore, aripiprazole with fluvoxamine and carbamazepine should be coprescribed with caution. The patients should be monitored for signs of adverse effects like hepatic damage or decreased efficacy of these drugs.
阿立哌唑是一种新型非典型抗精神病药物,广泛被 CYP3A4 酶代谢,在长期治疗中发现会导致血清转氨酶水平无症状升高。本研究旨在评估阿立哌唑与卡马西平和氟伏沙明合用时的肝毒性作用。
大鼠分别接受两种不同剂量(治疗剂量[TD]和最大治疗剂量[MTD])的阿立哌唑与卡马西平和氟伏沙明联合治疗。通过各种生化肝酶标志物如血清谷氨酸草酰乙酸转氨酶(SGOT)、血清谷氨酸丙酮酸转氨酶(SGPT)、碱性磷酸酶(ALP)、总胆红素来评估肝功能变化,进行组织学研究以及检测生理参数(肝重、肝体积和体重)。
TD 和 MTD 时阿立哌唑与氟伏沙明联合使用均显示出肝损伤和血清转氨酶水平显著升高,组织学报告也证实了这一点。阿立哌唑与卡马西平联合使用会导致阿立哌唑血药浓度显著降低,可能是由于 CYP3A4 酶的诱导,导致临床疗效丧失或降低。
当与氟伏沙明(已知的 CYP3A4 抑制剂)合用时,阿立哌唑会蓄积,导致肝损伤,并与卡马西平合用时降低阿立哌唑的疗效。因此,阿立哌唑与氟伏沙明和卡马西平合用时应谨慎。应监测患者是否有肝损伤或这些药物疗效降低的不良反应迹象。