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Chronic Opioid Therapy and Opioid Tolerance: A New Hypothesis

机译:慢性阿片类药物治疗和阿片类药物耐受性:新假说

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摘要

Opioids are efficacious and cost-effective analgesics, but tolerance limits their effectiveness. This paper does not present any new clinical or experimental data but demonstrates that there exist ascending sensory pathways that contain few opioid receptors. These pathways are located by brain PET scans and spinal cord autoradiography. These nonopioid ascending pathways include portions of the ventral spinal thalamic tract originating in Rexed layers VI–VIII, thalamocortical fibers that project to the primary somatosensory cortex (S1), and possibly a midline dorsal column visceral pathway. One hypothesis is that opioid tolerance and opioid-induced hyperalgesia may be caused by homeostatic upregulation during opioid exposure of nonopioid-dependent ascending pain pathways. Upregulation of sensory pathways is not a new concept and has been demonstrated in individuals impaired with deafness or blindness. A second hypothesis is that adjuvant nonopioid therapies may inhibit ascending nonopioid-dependent pathways and support the clinical observations that monotherapy with opioids usually fails. The uniqueness of opioid tolerance compared to tolerance associated with other central nervous system medications and lack of tolerance from excess hormone production is discussed. Experimental work that could prove or disprove the concepts as well as flaws in the concepts is discussed.
机译:阿片类药物是有效且具有成本效益的止痛药,但耐受性限制了其有效性。本文没有提供任何新的临床或实验数据,但是证明存在上升的感觉途径,该途径包含少量的阿片受体。这些通路通过大脑PET扫描和脊髓放射自显影定位。这些非阿片类药物的上升途径包括源自第六至第八层雷克斯层的腹侧丘脑束道,伸向初级体感皮质(S1)的丘脑皮质纤维,以及可能是中线背柱内脏途径。一种假设是阿片类药物耐受性和阿片类药物诱导的痛觉过敏可能是由非阿片类药物依赖性上升疼痛途径的阿片类药物暴露期间体内稳态上调引起的。感觉途径的上调不是一个新概念,并且已在耳聋或失明受损的个体中得到证实。第二个假设是,非阿片类药物辅助治疗可能会抑制非阿片类药物依赖的上升途径,并支持单用阿片类药物治疗通常失败的临床观察。讨论了与其他中枢神经系统药物相关的耐受性相比,阿片类药物耐受性的独特性以及由于过量激素产生引起的耐受性不足。讨论了可以证明或否定概念以及概念缺陷的实验性工作。

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