The Minor Phytocannabinoid Delta-8-Tetrahydrocannabinol Attenuates Collagen-Induced Arthritic Inflammation and Pain-Depressed Behaviors.

IF 3.1 3区 医学 Q2 PHARMACOLOGY & PHARMACY
S Olivia Vanegas, Arsalan Zaki, Caroline N Dealy, Steven G Kinsey
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引用次数: 0

Abstract

Patients with arthritis report using cannabis for pain management, and the major cannabinoid delta-9-tetrahydrocannabinol (Δ9-THC) has anti-inflammatory properties, yet the effects of minor cannabinoids on arthritis are largely unknown. The goal of the present study was to determine the antiarthritic potential of the minor cannabinoid delta-8-tetrahydrocannabinol (Δ8-THC) using the collagen-induced arthritis (CIA) mouse model. Adult male DBA/1J mice were immunized and boosted 21 days later with an emulsion of collagen and complete Freund's adjuvant. Beginning on the day of the booster, mice were administered twice-daily injections of Δ8-THC (3 or 30 mg/kg), the steroid dexamethasone (2 mg/kg), or vehicle for two weeks. Dorsal-ventral paw thickness and qualitative measures of arthritis were recorded daily, and latency to fall from an inverted grid was measured on alternating days, to determine arthritis severity and functional impairment. On the final day of testing, spontaneous wire-climbing behavior and temperature preference in a thermal gradient ring were measured to assess CIA-depressed behavior. The Δ8-THC treatment (30 mg/kg) reduced paw swelling and qualitative signs of arthritis. Δ8-THC also blocked CIA-depressed climbing and CIA-induced preference for a heated floor without producing locomotor effects but did not affect latency to fall from a wire grid. In alignment with the morphologic and behavioral assessments in vivo, histology revealed that Δ8-THC reduced synovial inflammation, proteoglycan loss and cartilage and bone erosion in the foot joints in a dose-dependent manner. Together, these findings suggest that Δ8-THC not only blocked morphologic changes but also prevented functional loss caused by collagen-induced arthritis. SIGNIFICANCE STATEMENT: Despite increasing use of cannabis products, the potential effects of minor cannabinoids are largely unknown. Here, the minor cannabinoid delta-8-tetrahydrocannabinol blocked the development of experimentally induced arthritis by preventing both pathophysiological as well as functional effects of the disease model. These data support the development of novel cannabinoid treatments for inflammatory arthritis.

次要植物大麻素 delta-8-tetrahydrocannabinol 可减轻胶原蛋白诱发的关节炎和疼痛抑郁行为。
据报道,关节炎患者使用大麻来止痛,主要大麻素Δ9-THC 具有抗炎特性,但次要大麻素对关节炎的影响在很大程度上还不为人所知。本研究的目的是利用胶原诱发关节炎(CIA)小鼠模型确定次要大麻素Δ8-THC 的抗关节炎潜力。对成年雄性 DBA/1J 小鼠进行免疫接种,21 天后用胶原蛋白乳液和完全弗氏佐剂进行强化。从加强免疫当天开始,小鼠每天两次注射Δ8-THC(3或30毫克/千克)、类固醇地塞米松(2毫克/千克)或载体,持续两周。每天记录爪子的背腹侧厚度和关节炎的定性指标,并隔天测量从倒置网格上跌落的潜伏期,以确定关节炎的严重程度和功能障碍。在测试的最后一天,测量自发的爬网行为和在热梯度环中的温度偏好,以分别评估CIA抑制行为和条件行为。Δ8-THC治疗(30毫克/千克)减轻了爪肿和关节炎的定性症状。Δ8-THC还能阻止CIA抑制的攀爬行为和CIA诱发的对加热地板的偏好,但不会产生运动效应,也不会影响从铁丝网上跌落的潜伏期。与体内形态学和行为学评估结果一致,组织学显示Δ8-THC以剂量依赖的方式减少了足关节的滑膜炎症、蛋白多糖损失以及软骨和骨侵蚀。这些研究结果表明,Δ8-THC 不仅能阻止形态学变化,还能防止胶原蛋白诱导的关节炎造成的功能损失。意义声明 尽管大麻产品的使用越来越多,但次要大麻素的潜在作用在很大程度上仍不为人所知。在这里,小大麻素Δ8-THC 通过防止疾病模型的病理生理和功能影响,阻止了实验诱导的关节炎的发展。这些数据支持开发治疗炎症性关节炎的新型大麻素疗法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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