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作 者:李俊[1] 汤晓林[1] 吴成义[1] 徐叔云[1]
机构地区:[1]安徽医科大学临床药理研究所
出 处:《中国药理学通报》1997年第3期220-222,共3页Chinese Pharmacological Bulletin
基 金:安徽省教委自然科学基金
摘 要:目的:进一步研究海马内微量注射(ih)褪黑素(MT)的免疫调节机制。方法:采用放射免疫法检测β-End和[3H]-TdR参入法检测脾淋巴细胞增殖实验。结果:ip纳络酮(2.5mg·kg-1)能部分抑制ihMT的免疫调节作用,ihMT可明显提高下丘脑β-End水平,降低垂体的β-End。体外Nal(0.25nmol·L-1~0.25μmol·L-1)对ihMT脾淋巴细胞增殖反应也呈剂量依赖性抑制作用,抗β-End抗体对ihMT增高的脾淋巴细胞增殖反应呈明显抑制作用。结论:ihMT的免疫调节作用可能主要与外周内源性阿片肽有关,而脾细胞产生的β-End可能在ihMT的免疫调节中发挥重要作用。AIM:To study the immunoregulatory mechanisms of melatonin(MT) microinjected into hippocampus (ih). METHODS: The levels of β endophin (β End) were measured by radioimmunoassay in different centeral nervous areas in ih MT rats, the proliferative responses of splenocytes were simultaneously conducted with TdR incorporation. RESULTS: The enhanced proliferations of splenocytes in ih MT rats were partly inhibited by naloxone (ip, 2 5 mg·kg -1 ) and the levels of β End were increased in the hypothalamus, however decreased in the pituitary. In vitro , the enhanced proliferation of splenocytes was also inhibited by Nal (0 25 nmol·L -1  ̄0 25 μmol·L -1 ) with dose dependent manner. The same actions as Nals were observed in splenocyte culture added anti β End serum. CONCLUSIONS:The immunoregulatory effects of MT(ih) could be related to the peripheral endogenous opioids, and β End produced by the splenocytes could have an important role in the immunoregulatory actions in ih MT rats.
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