Anton Benito, Leff Phillipe, Calva Juan C, Acevedo Rodolfo, Salazar Alberto, Matus Maura, Pavón Lenin, Martinez Martin, Meissler Joseph J, Adler Martin W, Gaughan John P, Eisenstein Toby K
Molecular Neurobiology and Addictive Neurochemistry Laboratory, National Institute of Psychiatry, Mexico City, Mexico.
Brain Behav Immun. 2008 Aug;22(6):824-32. doi: 10.1016/j.bbi.2008.02.004. Epub 2008 Apr 18.
Endomorphin 1 (EM-1) and endomorphin 2 (EM-2) were tested for their capacity to alter immune function. Addition of either of these peptides to murine spleen cells in vitro inhibited antibody formation to sheep red blood cells in a bi-phasic dose dependent manner. Maximal inhibition was achieved at doses in the range of 10(-13) to 10(-15)M. Neither naloxone (general opioid receptor antagonist) nor CTAP (selective mu opioid receptor antagonist) blocked the immunosuppressive effect. To show that there was specificity to the immunosuppressive activity of the peptides, affinity-purified rabbit antibodies were raised against each of the synthetic EM peptides haptenized to KLH and tested for capacity to inhibit immunosuppression. Antibody responses were monitored by a standard solid phase antibody capture ELISA, and antibodies were purified by immunochromatography using the synthetic peptides coupled to a Sepharose 6B resin. Verification of the specificity of affinity-purified antisera was performed by immunodot-blot and solid-phase RIA assays. The antisera specific for both EM-1 and EM-2 neutralized the immunosuppressive effects of their respective peptides in a dose-related manner. Control normal rabbit IgG had no blocking activity on either EM-1 or EM-2. These studies show that the endomorphins are immunomodulatory at ultra-low concentrations, but the data do not support a mechanism involving the mu-opioid receptor.
对内吗啡肽1(EM-1)和内吗啡肽2(EM-2)改变免疫功能的能力进行了测试。在体外将这些肽中的任何一种添加到小鼠脾细胞中,均以双相剂量依赖性方式抑制针对绵羊红细胞的抗体形成。在10^(-13)至10^(-15)M的剂量范围内可实现最大抑制。纳洛酮(通用阿片受体拮抗剂)和CTAP(选择性μ阿片受体拮抗剂)均未阻断免疫抑制作用。为了表明这些肽的免疫抑制活性具有特异性,制备了针对与钥孔血蓝蛋白(KLH)偶联的每种合成EM肽的亲和纯化兔抗体,并测试其抑制免疫抑制的能力。通过标准的固相抗体捕获ELISA监测抗体反应,并使用偶联到琼脂糖凝胶6B树脂上的合成肽通过免疫色谱法纯化抗体。通过免疫斑点印迹和固相放射免疫分析(RIA)测定法验证亲和纯化抗血清的特异性。对EM-1和EM-2均具有特异性的抗血清以剂量相关的方式中和了其各自肽的免疫抑制作用。对照正常兔IgG对EM-1或EM-2均无阻断活性。这些研究表明,内吗啡肽在超低浓度下具有免疫调节作用,但数据不支持涉及μ阿片受体的机制。