Δ9-Tetrahydrocannabinol Alleviates Hyperalgesia in a Humanized Mouse Model of Sickle Cell Disease.

IF 3.1 3区 医学 Q2 PHARMACOLOGY & PHARMACY Journal of Pharmacology and Experimental Therapeutics Pub Date : 2024-10-18 DOI:10.1124/jpet.124.002285
Alex Mabou Tagne, Yannick Fotio, Kalpna Gupta, Daniele Piomelli
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Abstract

People with sickle cell disease (SCD) often experience chronic pain as well as unpredictable episodes of acute pain, which significantly affects their quality of life and life expectancy. Current treatment strategies for SCD-associated pain primarily rely on opioid analgesics, which have limited efficacy and cause serious adverse effects. Cannabis has emerged as a potential alternative, yet its efficacy remains uncertain. In this study, we investigated the antinociceptive effects of Δ9-tetrahydrocannabinol (THC), cannabis' intoxicating constituent, in male HbSS mice, which express >99% human sickle hemoglobin, and male HbAA mice, which express normal human hemoglobin A, as a control. Acute THC administration (0.1-3 mg/kg-1, i.p.) dose-dependently reduced mechanical and cold hypersensitivity in human sickle hemoglobin (HbSS) but not human normal hemoglobin A (HbAA) mice. In the tail-flick assay, THC (1 and 3 mg/kg-1, i.p.) produced substantial antinociceptive effects in HbSS mice. By contrast, THC (1 mg/kg-1, i.p.) did not alter anxiety-like behavior (elevated plus maze) or long-term memory (24-hour novel object recognition). Subchronic THC treatment (1 and 3 mg/kg-1, i.p.) provided sustained relief of mechanical hypersensitivity but led to tolerance in cold hypersensitivity in HbSS mice. Together, the findings identify THC as a possible therapeutic option for the management of chronic pain in SCD. Further research is warranted to elucidate its mechanism of action and possible interaction with other cannabis constituents. SIGNIFICANCE STATEMENT: The study explores Δ9-tetrahydrocannabinol (THC)'s efficacy in alleviating pain in sickle cell disease (SCD) using a humanized mouse model. Findings indicate that acute THC administration reduces mechanical and cold hypersensitivity in SCD mice without impacting emotional and cognitive dysfunction. Subchronic THC treatment offers sustained relief of mechanical hypersensitivity but leads to cold hypersensitivity tolerance. These results offer insights into THC's potential as an alternative pain management option in SCD, highlighting both its benefits and limitations.

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Δ 9 -四氢大麻酚可减轻镰状细胞病人性化小鼠模型的痛觉过度。
镰状细胞病(SCD)患者经常会经历慢性疼痛以及不可预测的急性疼痛发作,这严重影响了他们的生活质量和预期寿命。目前针对 SCD 相关疼痛的治疗策略主要依赖于阿片类镇痛药,但这些药物的疗效有限,而且会产生严重的不良反应。大麻已成为一种潜在的替代药物,但其疗效仍不确定。在本研究中,我们研究了大麻的麻醉成分Δ9-四氢大麻酚(THC)对雄性 HbSS 小鼠(表达超过 99% 的人类镰状血红蛋白)和雄性 HbAA 小鼠(表达正常人类血红蛋白 A)的抗痛觉作用。急性 THC 给药(0.1-3 mg-kg-1,腹腔注射)剂量依赖性地降低了 HbSS 小鼠的机械过敏性和冷过敏性,但没有降低 HbAA 小鼠的机械过敏性和冷过敏性。在弹尾试验中,THC(1 和 3 mg-kg-1,腹腔注射)对 HbSS 小鼠产生了显著的抗痛觉作用。相比之下,THC(1 毫克-千克-1,静注)不会改变焦虑样行为(高架加迷宫)或长期记忆(24 小时新物体识别)。亚慢性 THC 治疗(1 毫克-公斤-1 和 3 毫克-公斤-1,静注)可持续缓解 HbSS 小鼠的机械过敏性,但会导致其耐受冷过敏性。综上所述,这些研究结果表明 THC 是治疗 SCD 慢性疼痛的一种可能选择。还需要进一步研究以阐明其作用机制以及与其他大麻成分之间可能存在的相互作用。意义声明 该研究利用人源化小鼠模型探讨了 THC 在缓解镰状细胞病(SCD)疼痛方面的功效。研究结果表明,急性服用 THC 可降低 SCD 小鼠的机械和冷过敏性,但不会影响情绪和认知功能障碍。亚慢性 THC 治疗可持续缓解机械过敏,但会导致冷过敏耐受。这些结果让我们深入了解了 THC 作为 SCD 患者替代性疼痛治疗方案的潜力,同时强调了它的益处和局限性。
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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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