Select Minor Cannabinoids from Cannabis sativa Are Cannabimimetic and Antinociceptive in a Mouse Model of Chronic Neuropathic Pain.

IF 3.1 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Abigail M Schwarz, Dea Kobeci, Joseph A Mancuso, Valeria Moreno-Rodríguez, Caleb Seekins, Thai Bui, Alyssa Welborn, Jerry Carr, John M Streicher
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引用次数: 0

Abstract

Chronic pain conditions affect nearly 20% of the population in the United States. Current medical interventions, such as opioid drugs, are effective at relieving pain but are accompanied by many undesirable side effects. This is one reason increased numbers of chronic pain patients have been turning to Cannabis for pain management. Cannabis contains many bioactive chemical compounds; however, current research looking into lesser-studied minor cannabinoids in Cannabis lacks uniformity between experimental groups and/or excludes female mice from investigation. This makes it challenging to draw conclusions between experiments done with different minor cannabinoid compounds between laboratories or parse out potential sex differences that could be present. We chose five minor cannabinoids found in lower quantities within Cannabis: cannabinol (CBN), cannabidivarin (CBDV), cannabigerol (CBG), Δ8-tetrahydrocannabinol (Δ8-THC), and Δ9-tetrahydrocannabivarin (THCV). These compounds were then tested for their cannabimimetic and pain-relieving behaviors in a cannabinoid tetrad assay and a chemotherapy-induced peripheral neuropathy (CIPN) pain model in male and female CD-1 mice. We found that the minor cannabinoids we tested differed in the cannabimimetic behaviors evoked, as well as the extent. We found that CBN, CBG, and high-dose Δ8-THC evoked some tetrad behaviors in both sexes, while THCV and low-dose Δ8-THC exhibited cannabimimetic tetrad behaviors only in females. Only CBN efficaciously relieved CIPN pain, which contrasts with reports from other researchers. Together these findings provide further clarity to the pharmacology of minor cannabinoids and suggest further investigation into their mechanism and therapeutic potential. SIGNIFICANCE STATEMENT: Minor cannabinoids are poorly studied ligands present in lower levels in Cannabis than cannabinoids like THC. In this study, we evaluated five minor cannabinoids (CBN, CBDV, CBG, THCV, and Δ8-THC) for their cannabimimetic and analgesic effects in mice. We found that four of the five minor cannabinoids showed cannabimimetic activity, while one was efficacious in relieving chronic neuropathic pain. This work is important in further evaluating the activity of these drugs, which are seeing wider public use with marijuana legalization.

在慢性神经性疼痛小鼠模型中,大麻中精选的少量大麻素具有大麻拟效和抗痛觉作用。
慢性疼痛影响着美国近 20% 的人口。目前的医疗干预措施,如阿片类药物,虽然能有效缓解疼痛,但却伴随着许多不良副作用。这也是越来越多的慢性疼痛患者转而使用大麻治疗疼痛的原因之一。大麻中含有许多生物活性化学物质;然而,目前对大麻中研究较少的次要大麻素的研究缺乏实验组之间的一致性和/或将雌性小鼠排除在调查之外。这使得在不同实验室之间用不同的次要大麻素化合物进行实验得出结论或分析可能存在的潜在性别差异具有挑战性。我们选择了在大麻中含量较低的五种次要大麻素:大麻酚(CBN)、大麻二萜(CBDV)、大麻萜醇(CBG)、Δ8-四氢大麻酚(Δ8-THC)和Δ9-四氢大麻萜(THCV)。然后,我们在大麻素四分体试验和化疗诱导的CD-1雌雄小鼠周围神经病变(CIPN)疼痛模型中测试了这些化合物的大麻拟效和镇痛行为。我们发现,我们测试的次要大麻素在诱发的大麻拟效行为和程度上存在差异。我们发现,CBN、CBG 和高剂量 Δ8-THC 在雌雄小鼠中都能诱发一些四联行为,而 THCV 和低剂量 Δ8-THC 仅在雌性小鼠中表现出大麻拟态四联行为。只有 CBN 能有效缓解 CIPN 疼痛,这与其他研究人员的报告形成鲜明对比。这些发现进一步阐明了小大麻素的药理学,并建议进一步研究其机制和治疗潜力。意义声明 次要大麻素是一种研究较少的配体,在大麻中的含量低于四氢大麻酚等大麻素。在这项研究中,我们评估了 5 种次要大麻素(CBN、CBDV、CBG、THCV 和 Δ8-THC)对小鼠的大麻拟效作用和镇痛作用。我们发现,5 种次要大麻素中有 4 种具有大麻拟效活性,其中一种对缓解慢性神经性疼痛有效。这项工作对于进一步评估这些药物的活性非常重要,随着大麻合法化,这些药物正被更多的公众使用。
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来源期刊
CiteScore
6.90
自引率
0.00%
发文量
115
审稿时长
1 months
期刊介绍: A leading research journal in the field of pharmacology published since 1909, JPET provides broad coverage of all aspects of the interactions of chemicals with biological systems, including autonomic, behavioral, cardiovascular, cellular, clinical, developmental, gastrointestinal, immuno-, neuro-, pulmonary, and renal pharmacology, as well as analgesics, drug abuse, metabolism and disposition, chemotherapy, and toxicology.
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