Walker J M, Hohmann A G
Department of Psychology, Indiana University Bloomington, IN 47405-7007, USA.
Handb Exp Pharmacol. 2005(168):509-54. doi: 10.1007/3-540-26573-2_17.
A large body of literature indicates that cannabinoids suppress behavioral responses to acute and persistent noxious stimulation in animals. This review examines neuroanatomical, behavioral, and neurophysiological evidence supporting a role for cannabinoids in suppressing pain at spinal, supraspinal, and peripheral levels. Localization studies employing receptor binding and quantitative autoradiography, immunocytochemistry, and in situ hybridization are reviewed to examine the distribution of cannabinoid receptors at these levels and provide a neuroanatomical framework with which to understand the roles of endogenous cannabinoids in sensory processing. Pharmacological and transgenic approaches that have been used to study cannabinoid antinociceptive mechanisms are described. These studies provide insight into the functional roles of cannabinoid CB1 (CB1R) and CB2 (CB2R) receptor subtypes in cannabinoid antinociceptive mechanisms, as revealed in animal models of acute and persistent pain. The role of endocannabinoids and related fatty acid amides that are implicated in endogenous mechanisms for pain suppression are discussed. Human studies evaluating therapeutic potential of cannabinoid pharmacotherapies in experimental and clinical pain syndromes are evaluated. The potential of exploiting cannabinoid antinociceptive mechanisms in novel pharmacotherapies for pain is discussed.
大量文献表明,大麻素可抑制动物对急性和持续性有害刺激的行为反应。本综述考察了神经解剖学、行为学和神经生理学方面的证据,这些证据支持大麻素在脊髓、脊髓上和外周水平抑制疼痛中所起的作用。对采用受体结合、定量放射自显影、免疫细胞化学和原位杂交的定位研究进行了综述,以考察这些水平上大麻素受体的分布,并提供一个神经解剖学框架,用以理解内源性大麻素在感觉处理中的作用。描述了用于研究大麻素抗伤害感受机制的药理学和转基因方法。这些研究深入探讨了大麻素CB1(CB1R)和CB2(CB2R)受体亚型在大麻素抗伤害感受机制中的功能作用,这在急性和持续性疼痛的动物模型中得到了揭示。讨论了内源性大麻素和相关脂肪酸酰胺在疼痛抑制内源性机制中的作用。对评估大麻素药物疗法在实验性和临床疼痛综合征中的治疗潜力的人体研究进行了评估。探讨了在新型疼痛药物疗法中利用大麻素抗伤害感受机制的潜力。