Hakimizadeh Elham, Fatemi Iman, Hassanshahi Jalal, Kaeidi Ayat
Physiology-Pharmacology Research Center, Research Institute of Basic Medical Sciences, Rafsanjan University of Medical Sciences, Rafsanjan, Iran.
Research Center of Tropical and Infectious Diseases, Kerman University of Medical Sciences, Kerman, Iran.
Res Pharm Sci. 2024 Aug 19;19(4):366-375. doi: 10.4103/RPS.RPS_85_22. eCollection 2024 Aug.
Chronic consumption of morphine (Mor) induces tolerance and dependence. This study aimed to survey the effects of pistachio extract (PX) on the induction and expression of Mor analgesic tolerance and physical dependency in mice.
Animals were randomly separated into six groups (n = 7): control, DMSO, Mor (10 mg/kg), Mor + saline, Mor + PX (10 mg/kg), and Mor + PX (100 mg/kg). Mor was injected (10 mg/kg, twice a day, s.c.) for 7 days to induce tolerance. PX was administered (10 and 100 mg/kg, orally) during the examination period. On each day and 20 min after Mor administration, a tail-flick test was done to measure the analgesic response and induction of tolerance. On day 7, naloxone (5 mg/kg, s.c.) was injected into the Mor-dependent animals to evaluate dependence, and animals were monitored for 30 min for jumping. Also, malondialdehyde (MDA), superoxide dismutase (SOD), and glutathione peroxidase (GPx) were assessed in the brain tissue.
FINDINGS/RESULTS: Our results indicated that co-administration of PX with Mor for 7 days diminished the induction of Mor tolerance. PX administration for 7 days alongside Mor reduced the frequency of withdrawal signs in naloxone-injected animals during dependence induction. Also, Mor increased the level of MDA and decreased the activities of SOD and GPx. Treatment with PX (100 mg/kg) restored all of the mentioned abnormalities.
According to the results presented in this study, chronic administration of PX forbade the induction of Mor analgesic tolerance and dependency in mice.
长期服用吗啡(Mor)会导致耐受性和依赖性。本研究旨在探讨开心果提取物(PX)对小鼠吗啡镇痛耐受性诱导及表达以及身体依赖性的影响。
将动物随机分为六组(n = 7):对照组、二甲基亚砜组、吗啡组(10 mg/kg)、吗啡+生理盐水组、吗啡+PX组(10 mg/kg)和吗啡+PX组(100 mg/kg)。注射吗啡(10 mg/kg,每天两次,皮下注射),持续7天以诱导耐受性。在检测期间口服给予PX(10和100 mg/kg)。每天在给予吗啡后20分钟进行甩尾试验,以测量镇痛反应和耐受性诱导情况。在第7天,对吗啡依赖的动物注射纳洛酮(5 mg/kg,皮下注射)以评估依赖性,并对动物进行30分钟的跳跃监测。此外,还对脑组织中的丙二醛(MDA)、超氧化物歧化酶(SOD)和谷胱甘肽过氧化物酶(GPx)进行了评估。
我们的结果表明,PX与吗啡共同给药7天可减少吗啡耐受性的诱导。在诱导依赖性期间,与吗啡一起给予PX 7天可降低注射纳洛酮动物的戒断症状频率。此外,吗啡增加了MDA水平,降低了SOD和GPx的活性。用PX(100 mg/kg)治疗可恢复所有上述异常情况。
根据本研究结果,长期给予PX可抑制小鼠吗啡镇痛耐受性和依赖性的诱导。