Garssadi S I, Mándi Y, Régely K, Taródi B, Béládi I
Institute of Microbiology, Albert Szent-Györgyi Medical University, Szeged, Hungary.
Brain Behav Immun. 1993 Jun;7(2):164-75. doi: 10.1006/brbi.1993.1018.
Serotonin (5-HT) at a concentration of 10(-4) to 10(-10) M impaired the cytotoxicity of human natural killer cells in whole blood. 5-HT added at the onset of the short-term cytotoxic assay had a pronounced inhibitory effect. It is very likely that the 5-HT2 receptor is involved in the inhibition of cytotoxicity because ketanserin, an inhibitor of the 5-HT2 receptor, partially prevented the effect of 5-HT. Treatment with 10(2)-10(4) IU/ml of interferon-alpha before or after the application of 5-HT decreased its inhibitory effect on the cytotoxicity. Radioligand binding studies revealed that the antagonistic effect of interferon was not due to the competition for the 5-HT2 receptors. Cycloheximide, an inhibitor of protein synthesis, did not block the suppression of natural killer activity by 5-HT, but it exerted a blocking effect on the acquisition of resistance to 5-HT induced by interferon.
浓度为10⁻⁴至10⁻¹⁰ M的血清素(5-羟色胺,5-HT)损害了全血中人类自然杀伤细胞的细胞毒性。在短期细胞毒性试验开始时添加5-HT具有显著的抑制作用。5-HT2受体很可能参与了细胞毒性的抑制,因为5-HT2受体抑制剂酮色林可部分阻止5-HT的作用。在应用5-HT之前或之后用10²-10⁴ IU/ml的α干扰素进行处理,可降低其对细胞毒性的抑制作用。放射性配体结合研究表明,干扰素的拮抗作用并非由于对5-HT2受体的竞争。蛋白质合成抑制剂环己酰亚胺并未阻断5-HT对自然杀伤活性的抑制,但它对干扰素诱导的对5-HT抗性的获得具有阻断作用。