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Single and combined effects of cannabinoids on neuropathic pain and cognition.

机译:大麻素对神经性疼痛和认知的单一或联合作用。

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摘要

Rationale. For centuries, medications derived from the marijuana plant have been used for therapeutic purposes across numerous cultures. In 1964, the primary psychoactive ingredient in cannabis, delta-9-tetrahydrocannabinol (Delta-9-THC) was defined. This, followed by the discovery of the endocannabinoid system, marked the beginning of comprehensive research into the beneficial exploitation of this system.;The cannabis plant contains various other cannabinoids besides Delta-9-THC. Most of the effects of cannabinoid-based therapies are based on the agonistic action of Delta-9-THC through cannabinoid receptors. Alternatively, some of these effects are caused by the actions of other cannabinoids, like cannabidiol, which does not have high affinity for cannabinoid receptors. Like Delta-9-THC, cannabidiol (CBD), the non-psychoactive phytocannabinoid in Cannabis sativa, has been hypothesized to ameliorate adverse effects of Delta-9-THC. Cannabidiol possesses neuroprotective, antiemetic, and anti-inflammatory properties. Sativex, a 1:1 ratio of CBD and Delta-9-THC, is currently an approved medication in Europe for the treatment of conditions such as neuropathic pain, and has been fast tracked by the USFDA for late stage clinical trials for a host of disorders, ranging from epilepsy to irritable bowel disease. Additionally, increasing preclinical evidence demonstrates that treatment with Cannabidiol alone produces efficacy on a variety of nervous system injuries, including neuropathic pain, schizophrenia and anxiety disorders.;Furthermore, there is mounting evidence of an "entourage effect" in cannabinoid-based pharmacotherapies. This effect occurs when treatment with a combination of cannabinoids derived from the plant produce more efficacy than treatment with a single cannabinoid (1). As cannabinoid-based treatments continue to develop and clinical data increases, further investigation of the entourage effect is necessary to facilitate the appropriate future treatment regimens for nervous system disorders.;Hypotheses. We hypothesized that treatment with the non-psychoactive cannabis compound cannabidiol would be as effective as the psychoactive cannabis compound Delta-9-THC, or a combination of the two, in mitigating neuropathic pain in a mouse model of chemotherapy-induced peripheral neuropathy. We additionally hypothesized that cannabidiol would not affect classic cannabinoid-agonist induced cognitive impairment in rodent models of learning and memory.;Methodology. Neuropathic pain was induced by repeated injections of the chemotherapeutic agent Paclitaxel. Mechanical hypersensitivity to Paclitaxel was assessed using the Von Frey assay. Cognition was assessed using three rodent models of learning and memory: 1) Conditional Discrimination, 2) Conditional Discrimination with a reversal component, and 3) Barnes Maze.;Results. Cannabidiol was found to be more potent and more effective than Delta-9-THC in attenuating neuropathic pain in a dose dependent manner. Combinations of CBD+Delta-9-THC revealed that lower, ineffective doses of CBD and Delta-9-THC display supra-additive effects when given in combination while higher, individually effective doses exhibit sub-additive effects in combination.;Cognitively, no deficits were observed over a range of doses of any cannabinoid tested in the conditional discrimination tasks, although a slight trend was observed in animals administered the synthetic mixed CB1/CB2 agonist WIN55,212-2. In the Barnes Maze task, treatment with Delta-9-THC alone dose-dependently decreased number of entries and total time spent in the target zone. Cannabidiol did not produce any effects in the Barnes Maze alone, nor did it attenuate the effects seen in animals treated with Delta-9-THC alone. Lastly, Delta-9-THC did not affect total distance traveled or average speed, whereas combination treatment increased both locomotor measurements at all but the highest combination dose.;Conclusions.The results of these studies indicate that cannabidiol is more potent than Delta-9-THC in attenuating neuropathic pain. Results of cognitive testing indicate subtle impairment in animals treated with Delta-9-THC and WIN55,212-2 that were not reversed by CBD.
机译:基本原理。几个世纪以来,源自大麻植物的药物已用于多种文化的治疗目的。 1964年,大麻中的主要精神活性成分被定义为delta-9-四氢大麻酚(delta-9-THC)。随后,发现内源性大麻素系统,标志着对该系统的有益开发进行了全面研究的开始。大麻植物除Delta-9-THC外还含有其他多种大麻素。基于大麻素的疗法的大多数效果都基于Delta-9-THC通过大麻素受体的激动作用。或者,其中一些影响是由其他大麻素(例如大麻二酚)的作用引起的,这些大麻素对大麻素受体的亲和力不高。像Delta-9-THC一样,大麻中的非精神活性植物大麻素大麻二酚(CBD)已被认为可减轻Delta-9-THC的不良影响。卡那比二醇具有神经保护,止吐和消炎的特性。 Sativex是CBD和Delta-9-THC的1:1比例,目前在欧洲已被批准用于治疗神经性疼痛等疾病,并且已被USFDA迅速跟踪用于许多宿主的后期临床试验。疾病,从癫痫病到肠易激病。此外,越来越多的临床前证据表明,单用大麻二酚治疗可对多种神经系统损伤(包括神经性疼痛,精神分裂症和焦虑症)产生疗效。此外,越来越多的证据表明,基于大麻素的药物治疗具有“刺激作用”。当使用衍生自植物的大麻素组合进行治疗比单用大麻素治疗具有更高的功效时,就会出现这种效果(1)。随着基于大麻素的治疗方法的不断发展和临床数据的增加,有必要对随行人员的影响进行进一步研究,以促进神经系统疾病的适当的未来治疗方案。我们假设使用非精神活性大麻化合物大麻二酚治疗与化学活性大麻化合物Delta-9-THC或两者的组合在缓解化疗诱导的周围神经病的小鼠模型中的神经性疼痛方面一样有效。我们还假设大麻脂不会在学习和记忆的啮齿动物模型中影响经典的大麻素激动剂引起的认知障碍。反复注射化疗药物紫杉醇可诱发神经性疼痛。使用Von Frey分析评估对紫杉醇的机械性超敏反应。使用三种啮齿动物的学习和记忆模型评估认知能力:1)有条件的歧视,2)带有逆向成分的有条件的歧视和3)Barnes Maze。发现卡纳比多二醇以剂量依赖性方式在减轻神经性疼痛方面比Delta-9-THC更有效且更有效。 CBD + Delta-9-THC的组合显示,当组合使用时,较低的无效剂量的CBD和Delta-9-THC表现出超加性效应,而较高的单独有效剂量组合显示出亚加性效应。在条件歧视任务中测试的任何大麻素剂量范围内都观察到了维生素A缺乏,尽管在使用合成的混合CB1 / CB2激动剂WIN55,212-2的动物中观察到了轻微的趋势。在Barnes Maze任务中,单独使用Delta-9-THC进行治疗可剂量依赖性地减少进入靶区的次数和总时间。仅在巴恩斯迷宫中,卡纳比多二醇不会产生任何作用,也不会减弱仅用Delta-9-THC处理的动物所见的作用。最后,Delta-9-THC不会影响总的行进距离或平均速度,而联合治疗除了增加了最高的联合剂量外,全部都提高了运动能力;结论。这些研究结果表明,大麻酚比Delta-9更有效。 -THC可减轻神经性疼痛。认知测试的结果表明,用Delta-9-THC和WIN55,212-2治疗的动物受到了CBD不能逆转的轻微损伤。

著录项

  • 作者

    Myers, Alyssa M.;

  • 作者单位

    Temple University.;

  • 授予单位 Temple University.;
  • 学科 Neurosciences.
  • 学位 M.S.
  • 年度 2016
  • 页码 51 p.
  • 总页数 51
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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