Hosseinzadeh Hossein, Parvardeh Siavash, Masoudi Alireza, Moghimi Mahsa, Mahboobifard Fatemeh
Pharmaceutical Research Center, Department of Pharmacodynamy and Toxicology, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran.
Department of Pharmacology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Avicenna J Phytomed. 2016 Jan-Feb;6(1):55-66.
Dependence and tolerance are major restricting factors in the clinical use of opioid analgesics. In the present study, the effects of thymoquinone, the major constituent of Nigella sativa seeds, on morphine dependence and tolerance were investigated in mice.
Male adult NMRI mice were made tolerant and dependent by repeated injections of morphine (50, 50, and 75 mg/kg, i.p. on 9 a.m., 1 p.m., and 5 p.m., respectively) during a 3-day administration schedule. The hot-plate test was used to assess tolerance to the analgesic effects of morphine. Naloxone (2 mg/kg, i.p.) was injected to precipitate withdrawal syndrome in order to assess the morphine dependence. To evaluate the effects of thymoquinone on tolerance and dependence to morphine, different single or repeated doses of thymoquinone were administered in mice. Rotarod was used to assess the motor coordination.
Administration of single or repeated doses of thymoquinone (20 and 40 mg/kg, i.p.) significantly decreased the number of jumps in morphine dependent animals. Repeated administration of thymoquinone (20 and 40 mg/kg, for 3 days) and also single injection of thymoquinone (40 mg/kg, on the fourth day) attenuated tolerance to the analgesic effect of morphine. None of the thymoquinone doses (10, 20, and 40 mg/kg) produced any antinociceptive effects on their own. Motor coordination of animals was impaired by the high dose of thymoquinone (40 mg/kg).
Based on these results, it can be concluded that thymoquinone prevents the development of tolerance and dependence to morphine.
依赖性和耐受性是阿片类镇痛药临床应用中的主要限制因素。在本研究中,对黑种草籽的主要成分百里醌对小鼠吗啡依赖性和耐受性的影响进行了研究。
雄性成年NMRI小鼠在为期3天的给药方案中,分别于上午9点、下午1点和下午5点腹腔注射吗啡(50、50和75mg/kg),使其产生耐受性和依赖性。采用热板试验评估对吗啡镇痛作用的耐受性。注射纳洛酮(2mg/kg,腹腔注射)以诱发戒断综合征,从而评估吗啡依赖性。为评估百里醌对吗啡耐受性和依赖性的影响,对小鼠给予不同的单次或重复剂量的百里醌。采用转棒试验评估运动协调性。
给予单次或重复剂量的百里醌(20和40mg/kg,腹腔注射)可显著减少吗啡依赖动物的跳跃次数。重复给予百里醌(20和40mg/kg,共3天)以及单次注射百里醌(40mg/kg,在第4天)可减弱对吗啡镇痛作用的耐受性。百里醌各剂量(10、20和40mg/kg)自身均未产生任何镇痛作用。高剂量的百里醌(40mg/kg)会损害动物的运动协调性。
基于这些结果,可以得出结论,百里醌可预防对吗啡耐受性和依赖性的形成。