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作 者:邱一华[1] 彭聿平[1] 戴丽[1] 黄慧伟[1]
机构地区:[1]南通医学院生理学教研室
出 处:《中国应用生理学杂志》1999年第2期119-122,共4页Chinese Journal of Applied Physiology
摘 要:目的:观察不同浓度乙酰胆碱(ACh,10-10~10-5mol/L)对大鼠体外抗体生成的影响,并初步探讨其作用机制,从细胞水平了解乙酰胆碱与免疫功能之间的关系。方法:用体外抗体生成的检测方法,用绵羊红细胞(SRBC)刺激大鼠肠系膜淋巴结B细胞转化成抗体形成细胞(AFC),然后检测其抗体生成量。结果:①10-10~10-7mol/LACh能显著抑制体外抗体生成,其中10-8和10-7mol/LACh的作用较强,而10-6和10-5mol/LACh无明显的抑制作用;②M型胆碱能受体激动剂毛果芸香碱(10-8和10-7mol/L)能明显减弱体外抗体生成,而N型受体激动剂烟碱(10-8和10-7mol/L)没有显著的减弱作用,M型受体拮抗剂阿托品(10-7和10-6mol/L)可完全阻断ACh抑制体外抗体生成的作用;③ACh分别在B细胞用SRBC刺激后3~48h中的6个不同时间与淋巴细胞作用,其抗体生成仍然是减少的。结论:ACh可非浓度依赖性地抑制大鼠的体外抗体生成;此作用可能由B细胞上的M型胆碱能受体介导;且ACh可能主要影响B细胞转化的后期过程。Aim and Methods: In the present study, the effect of acetylcholine (ACh) on the antibody synthesis and the primary mechanism of the action were investigated by means of the assay for antibody synthesis in vitro . The B lymphocytes in the mesenteric lymphaden of rats were stimulated with sheep red blood cells (SRBC) and incubated five days. Various concentrations of ACh (10 -10 to 10 -5 mol/L), muscarinic and nicotinic cholinergic receptor agonist and muscarinic receptor antagonist were respectively added to the lymphocyte suspension with SRBC. Results: ACh at 10 -10 to 10 -7 mol/L range significantly suppressed the antibody synthesis in vitro, having a stronger action at 10 -8 to 10 -7 mol/L, but having not remarked effect at 10 -6 to 10 -5 mol/L. Pilocarpine, a muscarinic cholinergic receptor agonist, significantly inhibited the antibody synthesis in vitro, but nicotine, a nicotinic cholinergic receptor agonist did not remarkably reduce the antibody synthesis in vitro. Atropine, a muscarinic receptor antagonist, abolished completely the inhibitory effect of ACh on the antibody synthesis in vitro. The antibody synthesis was still low when ACh was added at six different times to lymphocyte suspension that had been incubated with SRBC for 3 to 48 hours. Conclusion:ACh can cause concentration independent suppression of the antibody synthesis of rats in vitro, and the action of ACh may be mediated by the muscarinic receptor and occur in the later stage of B lymphocyte transformation.
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