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阿片类药物的非镇痛作用:外周阿片受体作为未来止痒治疗的有前途的靶点。

Non-analgesic effects of opioids: peripheral opioid receptors as promising targets for future anti-pruritic therapies.

机构信息

Department of Dermatology, Venereology and Allergology, Wroclaw Medical University, Poland.

出版信息

Curr Pharm Des. 2012;18(37):6021-4. doi: 10.2174/138161212803582405.

Abstract

Administration of opioids for analgesia may produce pruritus. It was believed, that this effect is mediated centrally by activation of μ-opioid receptors (MOR). However, recent data suggested that opioids may also mediate pruritus directly in the skin. A number of skin cell types, including keratinocytes, dermal mast cells, fibroblasts or macrophages, were shown to express both MOR as well as other opioid receptors. It was demonstrated, that the activation of MOR in the skin elicited pruritus, while activation of cutaneous κ-opioid receptors had anti-pruritic effect. Moreover, activation of opioid receptors in the skin modulated not only pruritus, but also inflammatory response. Taking these observations into consideration it could be suggested, that substances acting solely on peripheral opioid receptors could be potent anti-pruritic or even anti-inflammatory drugs, but devoided of typical side effects related to the activation of central opioid system.

摘要

阿片类药物用于镇痛可能会引起瘙痒。人们认为,这种作用是通过激活μ-阿片受体(MOR)而在中枢介导的。然而,最近的数据表明,阿片类药物也可能直接在皮肤中介导瘙痒。许多皮肤细胞类型,包括角质形成细胞、真皮肥大细胞、成纤维细胞或巨噬细胞,均被证明表达 MOR 以及其他阿片受体。研究表明,皮肤中 MOR 的激活会引起瘙痒,而皮肤 κ-阿片受体的激活则具有止痒作用。此外,皮肤中阿片受体的激活不仅调节瘙痒,还调节炎症反应。考虑到这些观察结果,我们可以推测,仅作用于外周阿片受体的物质可能是有效的止痒甚至抗炎药物,而没有与激活中枢阿片系统相关的典型副作用。

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