Protective effects of pistachio hydroalcoholic extract on morphine-induced analgesic tolerance and dependence: investigating the impact of oxidative stress.

IF 2.1 Q3 CHEMISTRY, MEDICINAL Research in Pharmaceutical Sciences Pub Date : 2024-08-19 eCollection Date: 2024-08-01 DOI:10.4103/RPS.RPS_85_22
Elham Hakimizadeh, Iman Fatemi, Jalal Hassanshahi, Ayat Kaeidi
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Abstract

Background and purpose: 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.

Experimental approach: 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.

Conclusion and implications: According to the results presented in this study, chronic administration of PX forbade the induction of Mor analgesic tolerance and dependency in mice.

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开心果水醇提取物对吗啡引起的镇痛耐受性和依赖性的保护作用:研究氧化应激的影响。
背景和目的:长期服用吗啡(Morine)会产生耐受性和依赖性。本研究旨在调查开心果提取物(PX)对小鼠吗啡镇痛耐受性和身体依赖性的诱导和表达的影响:实验方法:将小鼠随机分为六组(n = 7):对照组、二甲基亚砜组、Mor(10 毫克/千克)组、Mor + 生理盐水组、Mor + PX(10 毫克/千克)组和 Mor + PX(100 毫克/千克)组。连续 7 天注射 Mor(10 毫克/千克,每天两次,静脉注射)以诱导耐受。检查期间口服 PX(10 毫克/千克和 100 毫克/千克)。每天给药20分钟后,进行尾弹试验,以测量镇痛反应和诱导耐受性。第 7 天,向对 Mor 有依赖性的动物注射纳洛酮(5 毫克/千克,静脉注射)以评估其依赖性,并在 30 分钟内监测动物的跳跃情况。此外,还评估了脑组织中的丙二醛(MDA)、超氧化物歧化酶(SOD)和谷胱甘肽过氧化物酶(GPx):我们的研究结果表明,PX 与 Mor 联合给药 7 天会降低 Mor 耐受性的诱导。PX与Mor同时给药7天可减少纳洛酮注射动物在依赖性诱导过程中出现戒断症状的频率。此外,Mor 还增加了 MDA 的水平,降低了 SOD 和 GPx 的活性。使用 PX(100 毫克/千克)治疗可恢复上述所有异常现象:根据本研究的结果,长期服用 PX 可阻止小鼠对莫氏镇痛剂产生耐受性和依赖性。
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来源期刊
Research in Pharmaceutical Sciences
Research in Pharmaceutical Sciences CHEMISTRY, MEDICINAL-
CiteScore
3.60
自引率
19.00%
发文量
50
审稿时长
34 weeks
期刊介绍: Research in Pharmaceutical Sciences (RPS) is included in Thomson Reuters ESCI Web of Science (searchable at WoS master journal list), indexed with PubMed and PubMed Central and abstracted in the Elsevier Bibliographic Databases. Databases include Scopus, EMBASE, EMCare, EMBiology and Elsevier BIOBASE. It is also indexed in several specialized databases including Scientific Information Database (SID), Google Scholar, Iran Medex, Magiran, Index Copernicus (IC) and Islamic World Science Citation Center (ISC).
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