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与吗啡或芬太尼治疗相比,丁丙诺啡可改善手术对大鼠下丘脑-垂体-肾上腺轴、自然杀伤细胞活性和转移定植的影响。

Buprenorphine ameliorates the effect of surgery on hypothalamus-pituitary-adrenal axis, natural killer cell activity and metastatic colonization in rats in comparison with morphine or fentanyl treatment.

作者信息

Franchi Silvia, Panerai Alberto E, Sacerdote Paola

机构信息

Department of Pharmacology, University of Milano, via Vanvitelli 32, Milano, Italy.

出版信息

Brain Behav Immun. 2007 Aug;21(6):767-74. doi: 10.1016/j.bbi.2007.01.001. Epub 2007 Feb 8.

Abstract

Not all opioids employed in clinical practice share the same immunosuppressive properties. The potent partial micro-agonist buprenorphine appears to exhibit a neutral effect on the immune responses. Surgery stress is associated with decreased natural killer cell activity (NK) and enhancement of tumor metastasis in rats. We analyzed the ability of buprenorphine to prevent the effects of experimental surgery on HPA activation (plasma corticosterone levels), NK activity and lung diffusion of the NK sensitive tumor MADB106. Buprenorphine (0.1mg/kg) was compared with equianalgesic doses of fentanyl (0.1mg/kg) and morphine (10mg/kg) in this animal model. In normal animals morphine and fentanyl stimulate the HPA axis, decrease NK activity and augment tumor metastasis, while buprenorphine is devoid of these effects. Surgery significantly raised corticosterone levels, suppressed NK activity and increased MADB106 metastasis. Only buprenorphine was able to prevent the neuroendocrine and immune system alterations and ameliorate the increase of tumor metastasis induced by surgical stress. These preclinical findings suggest that an adequate treatment of surgically induced stress immunosuppression with an opioid drug devoid of immunosuppressive effects may also play a protective role against the metastatic diffusion following cancer surgery.

摘要

并非所有临床实践中使用的阿片类药物都具有相同的免疫抑制特性。强效部分μ-激动剂丁丙诺啡似乎对免疫反应表现出中性作用。手术应激与大鼠自然杀伤细胞活性(NK)降低及肿瘤转移增强有关。我们分析了丁丙诺啡预防实验性手术对HPA激活(血浆皮质酮水平)、NK活性及NK敏感肿瘤MADB106肺转移影响的能力。在该动物模型中,将丁丙诺啡(0.1mg/kg)与等效镇痛剂量的芬太尼(0.1mg/kg)和吗啡(10mg/kg)进行比较。在正常动物中,吗啡和芬太尼刺激HPA轴,降低NK活性并增加肿瘤转移,而丁丙诺啡没有这些作用。手术显著提高了皮质酮水平,抑制了NK活性并增加了MADB106转移。只有丁丙诺啡能够预防神经内分泌和免疫系统改变,并改善手术应激诱导的肿瘤转移增加。这些临床前研究结果表明,用无免疫抑制作用的阿片类药物充分治疗手术诱导的应激性免疫抑制,可能对癌症手术后的转移扩散也起到保护作用。

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