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康诺利定:一种用于慢性疼痛的新型植物提取物。

Conolidine: A Novel Plant Extract for Chronic Pain.

作者信息

Edinoff Amber N, Patel Akash S, Baker Mitchell W, Lawson Jesse, Wolcott Christopher, Cornett Elyse M, Sadegi Kambiz, Kaye Adam M, Kaye Alan D

机构信息

Department of Psychiatry and Behavioral Medicine, Louisiana State University Health Science Center Shreveport, Shreveport, LA, USA.

Department of Anesthesiology, Perioperative and Pain Medicine, Brigham and Women's Hospital, 75 Francis Street, Boston, MA, USA.

出版信息

Anesth Pain Med. 2021 Dec 8;11(6):e121438. doi: 10.5812/aapm.121438. eCollection 2021 Dec.

Abstract

Pain, the most common symptom reported among patients in the primary care setting, is complex to manage. Opioids are among the most potent analgesics agents for managing pain. Since the mid-1990s, the number of opioid prescriptions for the management of chronic non-cancer pain (CNCP) has increased by more than 400%, and this increased availability has significantly contributed to opioid diversion, overdose, tolerance, dependence, and addiction. Despite the questionable effectiveness of opioids in managing CNCP and their high rates of side effects, the absence of available alternative medications and their clinical limitations and slower onset of action has led to an overreliance on opioids. Conolidine is an indole alkaloid derived from the bark of the tropical flowering shrub used in traditional Chinese, Ayurvedic, and Thai medicine. Conolidine could represent the beginning of a new era of chronic pain management. It is now being investigated for its effects on the atypical chemokine receptor (ACK3). In a rat model, it was found that a competitor molecule binding to ACKR3 resulted in inhibition of ACKR3's inhibitory activity, causing an overall increase in opiate receptor activity. Although the identification of conolidine as a potential novel analgesic agent provides an additional avenue to address the opioid crisis and manage CNCP, further studies are necessary to understand its mechanism of action and utility and efficacy in managing CNCP.

摘要

疼痛是初级保健机构中患者报告的最常见症状,其管理很复杂。阿片类药物是治疗疼痛最有效的镇痛药之一。自20世纪90年代中期以来,用于治疗慢性非癌性疼痛(CNCP)的阿片类药物处方数量增加了400%以上,这种可得性的增加显著导致了阿片类药物的转移、过量使用、耐受性、依赖性和成瘾。尽管阿片类药物在治疗CNCP方面的有效性存疑且副作用发生率高,但由于缺乏可用的替代药物及其临床局限性以及起效较慢,导致人们过度依赖阿片类药物。康力定是一种吲哚生物碱,源自热带开花灌木的树皮,用于传统中医、阿育吠陀医学和泰国医学。康力定可能代表着慢性疼痛管理新时代的开端。目前正在研究其对非典型趋化因子受体(ACK3)的作用。在大鼠模型中发现,一种与ACKR3结合的竞争分子会抑制ACKR3的抑制活性,导致阿片受体活性总体增加。尽管将康力定鉴定为一种潜在的新型镇痛药为解决阿片类药物危机和治疗CNCP提供了一条额外途径,但仍需要进一步研究以了解其作用机制以及在治疗CNCP中的效用和疗效。

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