Kaczocha Martin, Azim Syed, Nicholson James, Rebecchi Mario J, Lu Yong, Feng Tian, Romeiser Jamie L, Reinsel Ruth, Rizwan Sabeen, Shodhan Shivam, Volkow Nora D, Benveniste Helene
Department of Anesthesiology, Stony Brook University, Stony Brook, New York, USA.
Department of Orthopaedics, Stony Brook University, Stony Brook, New York, USA.
BMC Anesthesiol. 2018 Feb 27;18(1):27. doi: 10.1186/s12871-018-0489-5.
The primary goal of this study was to determine whether administration of intrathecal morphine reduces postoperative pain. The secondary goal was to determine the effect of intrathecal morphine upon circulating levels of the weakly analgesic endocannabinoids, anandamide (AEA) and 2-arachidonoylglycerol (2-AG), and the related lipids palmitoylethanolamide (PEA) and oleoylethanolamide (OEA).
Forty two total knee arthroplasty (TKA) patients were enrolled in a prospective, double-blinded, randomized study. The intervention consisted of intrathecal morphine (200 μg) or placebo administered at the time of the spinal anesthesia. Postoperative pain was measured during the first 4 h after surgery while serum levels of AEA, 2-AG, PEA, OEA, and cortisol were measured at baseline and 4 h after surgery.
Administration of intrathecal morphine reduced postoperative pain 4 h after TKA surgery compared to placebo (p = 0.005) and reduced postoperative systemic opioid consumption (p = 0.001). At baseline, intrathecal morphine led to a significant reduction in AEA, 2-AG, and OEA levels but did not affect PEA or cortisol levels. In patients administered intrathecal placebo, 2-AG levels were elevated 4 h after surgery; whereas patients receiving intrathecal morphine showed reductions in AEA, PEA, and OEA when compared to placebo. At 4 h after TKA surgery cortisol levels were significantly elevated in the placebo group and reduced in those receiving morphine.
These results indicate that intrathecal morphine reduces postoperative pain in TKA patients. Furthermore, activation of central opioid receptors negatively modulates the endocannabinoid tone, suggesting that potent analgesics may reduce the stimulus for production of peripheral endocannabinoids. This study is the first to document the existence of rapid communication between the central opioid and peripheral endocannabinoid systems in humans.
This trial was registered retrospectively.
NCT02620631 . Study to Examine Pain Relief With Supplemental Intrathecal Morphine in TKA Patients, NCT02620631 , 12/03/2015.
本研究的主要目的是确定鞘内注射吗啡是否能减轻术后疼痛。次要目的是确定鞘内注射吗啡对弱镇痛性内源性大麻素、花生四烯酸乙醇胺(AEA)和2-花生四烯酸甘油酯(2-AG)以及相关脂质棕榈酰乙醇胺(PEA)和油酰乙醇胺(OEA)循环水平的影响。
42例全膝关节置换术(TKA)患者被纳入一项前瞻性、双盲、随机研究。干预措施包括在脊髓麻醉时给予鞘内吗啡(200μg)或安慰剂。术后4小时内测量术后疼痛,同时在基线和术后4小时测量血清中AEA、2-AG、PEA、OEA和皮质醇的水平。
与安慰剂相比,鞘内注射吗啡可减轻TKA术后4小时的疼痛(p = 0.005),并减少术后全身阿片类药物的消耗量(p = 0.001)。在基线时,鞘内注射吗啡导致AEA、2-AG和OEA水平显著降低,但不影响PEA或皮质醇水平。鞘内注射安慰剂的患者术后4小时2-AG水平升高;而与安慰剂相比,接受鞘内注射吗啡的患者AEA、PEA和OEA水平降低。TKA术后4小时,安慰剂组皮质醇水平显著升高,而接受吗啡治疗的患者皮质醇水平降低。
这些结果表明,鞘内注射吗啡可减轻TKA患者的术后疼痛。此外,中枢阿片受体的激活对内源性大麻素张力产生负性调节,提示强效镇痛药可能减少外周内源性大麻素产生的刺激。本研究首次证明了人类中枢阿片系统与外周内源性大麻素系统之间存在快速通讯。
本试验为回顾性注册。
NCT02620631。在TKA患者中使用鞘内补充吗啡检查疼痛缓解的研究,NCT02620631,2015年3月12日。