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阿片受体对激动剂-拮抗剂镇痛药的亲和力。

Opioid receptor affinity for agonist-antagonist analgesics.

作者信息

Jacobs A M, Youngblood F

机构信息

Reconstructive Surgery of the Foot and Ankle, Deaconess Hospital, St. Louis, MO.

出版信息

J Am Podiatr Med Assoc. 1992 Oct;82(10):520-4. doi: 10.7547/87507315-82-10-520.

Abstract

Analgesic medications are distributed to a variety of receptors within the central nervous system. Activity at these receptors (mu 1, mu, sigma, delta, kappa) results in both the beneficial pain-relieving effects of analgesics as well as undesirable side effects. The mixed agonist-antagonist class of analgesics offers the potential benefit of greater receptor site selectivity while diminishing the incidence of adverse sequelae, such as respiratory depression. Traditionally, it has been suggested that mixed agonist-antagonist medications may be associated with decreased analgesic effectiveness. However, newer agents of this mixed class may result in effective analgesia while diminishing the incidence of side effects.

摘要

镇痛药作用于中枢神经系统内的多种受体。这些受体(μ1、μ、σ、δ、κ)的活性既产生了镇痛药有益的止痛效果,也带来了不良副作用。混合激动 - 拮抗剂类镇痛药具有更大的受体部位选择性这一潜在优势,同时能降低诸如呼吸抑制等不良后果的发生率。传统观点认为,混合激动 - 拮抗剂类药物可能会降低镇痛效果。然而,这类新型混合药物可能在减少副作用发生率的同时产生有效的镇痛作用。

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