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机构地区:[1]上海第二医科大学细胞调控研究室
出 处:《中国中医基础医学杂志》1997年第6期15-17,共3页JOURNAL OF BASIC CHINESE MEDICINE
基 金:国家自然科学基金
摘 要:本文目的是用原代培养的神经细胞探讨知母皂甙元(ZMS)对神经细胞M受体的调节作用。主要方法是:用原代培养的神经细胞,用M受体非选择性拮抗剂3H-QNB结合分析法测定M受体密度,并以M受体不可逆阻断剂苯甲基偶酰基胆碱氮芥(BCM)为工具,测定M受体代谢动力学参数。主要结果:向不同培养天数(9~15天)的神经细胞加入ZMS(0.1mmolL-1),作用48小时后对M受体密度均有显著的上调作用(P<0.01)。各种浓度的ZMS(0.1~100umolL-1)对3H-QNB的结合均无明显抑制作用。用(0.1mmolL-1)的ZMS显著升高M受体的合成速率(P<0.01),而对降解速率常数无影响(P>0.05)。结论:ZMS能使培养9~15天的原代配养的大鼠神经细胞的M受体密度上调,这种作用和激动剂或拮抗剂不同,并非ZMS直接作用于M受体结合位点所引起,而是由于ZMS能促进M受体的生成。离体培养的环境相对衡定,可以排除神经体液的间接作用。Aim: To study the regulatory effects of ZMS, a Sapogenin from Zhimu (Rhizoma Anemarrhenae) on the neuronal muscarinic cholinergic receptors of primary culture of neonatal rat brain. Method:\ muscarinic antagonist 3H QNB was used to determine the receptor and the metabolic kinetic parameters were obtained by using the irreversible muscarinic blockade Benzilyl choline mustrad (BCM). Results:\ After being added to the culture medium for 48 hours, ZMS (0.1 mmol·L-1) significantly upregulated muscarinic receptor densities in different culture period ( P <0.01). No marked inhibition of 3H QNB binding was found when the range of ZMS was from 0.1 ̄100 umol·L-1. ZMS significantly elevated the production rate of neuronal muscarinic receptors ( P<0.01 ), with no influence on dissociation rate constant ( P>0.05 ). Conclusion:\ ZMS can significantly evelate the density of M cholinergic recptors in primary cultured rat brain cells. Such an action is not due to the direct binding of ZMS to the cells like agonists or antagonists. Instead, it is due to an stimulatory action of ZMS on the synthesis of M receptors
分 类 号:R282.710.5[医药卫生—中药学]
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