Cheppudira Bopaiah P, Trevino Alex V, Petz Lawrence N, Christy Robert J, Clifford John L
Burn Injuries Task Area, United States Army Institute of Surgical Research, 3698 Chambers Pass, San Antonio Military Medical Center, Fort Sam Houston, San Antonio, Texas, 78234, USA.
Department of Clinical Investigation, United States Army Institute of Surgical Research, 3698 Chambers Pass, San Antonio Military Medical Center, Fort Sam Houston, San Antonio, Texas, 78234, USA.
BMC Anesthesiol. 2016 Sep 5;16(1):73. doi: 10.1186/s12871-016-0242-x.
Nerve growth factor (NGF) is known to induce inflammation and pain; however its role in opioid-induced tolerance has not been studied. This study investigated the effects of an anti-NGF neutralizing antibody on the development of tolerance following chronic morphine treatment in naïve rats.
Four groups of rats were used in this study; one treated with saline alone, one with 10 mg/kg of morphine, one with 10 μg of anti-NGF and the other with 10 mg/kg of morphine + 10 μg of anti-NGF, twice per day for 5 days. The route of treatment was subcutaneous (S.C.) for morphine and saline, and intraperitoneal (i.p.) for anti-NGF. Response to a noxious thermal stimulus during the course of drug treatment was assessed (Hargreaves' test). Further, the change in the NGF levels in the lumbar spinal cord was measured by ELISA.
Our results showed that repeated administration of morphine produced an apparent tolerance which was significantly attenuated by co-administration of anti-NGF (P < 0.001). Additionally, the area under the curve (AUC) of the analgesic effect produced by the combination of morphine and anti-NGF was significantly (P < 0.001) greater than for saline controls and chronic morphine treated rats. Moreover, the level of NGF in the spinal cord of chronic morphine treated rats was significantly higher (P < 0.05) than in both the saline control group and the group receiving simultaneous administration of anti-NGF with morphine. These results indicate that anti-NGF has the potential to attenuate morphine-induced tolerance behavior by attenuating the effects of NGF at the spinal level.
Taken together, our study strongly suggests that the NGF signaling system is a potential novel target for treating opioid-induced tolerance.
已知神经生长因子(NGF)可诱发炎症和疼痛;然而,其在阿片类药物诱导的耐受性中的作用尚未得到研究。本研究调查了抗NGF中和抗体对未用药大鼠慢性吗啡治疗后耐受性发展的影响。
本研究使用了四组大鼠;一组仅用生理盐水治疗,一组用10mg/kg吗啡治疗,一组用10μg抗NGF治疗,另一组用10mg/kg吗啡 + 10μg抗NGF治疗,每天两次,共5天。吗啡和生理盐水的给药途径为皮下注射(S.C.),抗NGF为腹腔注射(i.p.)。评估药物治疗过程中对有害热刺激的反应(哈格里夫斯试验)。此外,通过酶联免疫吸附测定法测量腰脊髓中NGF水平的变化。
我们的结果表明,重复给予吗啡产生了明显的耐受性,而联合给予抗NGF可显著减弱这种耐受性(P < 0.001)。此外,吗啡和抗NGF联合产生的镇痛作用的曲线下面积(AUC)显著大于生理盐水对照组和慢性吗啡治疗组(P < 0.001)。而且,慢性吗啡治疗组大鼠脊髓中的NGF水平显著高于生理盐水对照组和同时接受抗NGF与吗啡治疗的组(P < 0.05)。这些结果表明,抗NGF有可能通过减弱脊髓水平的NGF作用来减轻吗啡诱导的耐受行为。
综上所述,我们的研究强烈表明,NGF信号系统是治疗阿片类药物诱导的耐受性的潜在新靶点。