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作 者:李和[1] 王小丽[1] 张亦农[1] 杨世明[1] 李肇春[1]
机构地区:[1]同济医科大学组织学胚胎学教研室
出 处:《解剖学报》1999年第3期193-196,I001,共4页Acta Anatomica Sinica
基 金:国家自然科学基金;国家教委留学回国人员科研基金
摘 要:目的在光镜及电镜下观察大鼠脊髓后角内μ阿片受体(MOR)与C纤维的关系,为进一步揭示阿片镇痛的突触机制提供形态学证据。方法根据辣椒素对初级传入神经中C纤维的特异性神经毒性,在大鼠蛛网膜下腔注射辣椒素以毁损C纤维,用免疫组织化学ABC法比较脊髓后角内MOR免疫反应性的变化;根据西非单叶豆同工凝集素I-B4(grifoniasimplicifoliaisolectinI-B4,I-B4)与初级传入C纤维选择性结合的特性,应用双标(免疫)组织化学电镜技术(ABC-纳金法)分别标记脊髓后角内I-B4结合位点和MOR。结果大鼠蛛网膜下腔注射辣椒素3~7d后,其脊髓后角Ⅰ~Ⅱ层内的MOR免疫反应性较对照动物明显减弱;电镜下在大鼠脊髓后角浅层内观察到,MOR不仅定位于树突内,也分布在含I-B4结合位点的C纤维终末内。无论在树突内还是在轴突终末内,MOR主要分布在非突触部位,仅少量MOR与突触前膜和/或突触后膜有关。结论脊髓后角中部分MOR来源于辣椒素敏感的C纤维,外源性吗啡或内源性吗啡样物质如内吗啡肽等MOR激动剂在脊髓后角内既可通过突触后(树突内)的MOR发挥作用,也可通过突触前(轴突终末内)的MOR对C纤维产生突触前?Objective\ To provide morphological evidences for further revealing synaptic mechanism of opioid analgesia,the relation of μ opioid receptor(MOR) to primary afferent C fiber in the spinal dorsal horn of the rat was light and electron microscopically observed.Methods\ According to the specific neurotoxicity of capsaicin to C fiber,capsaicin was injected subarachnoidally in the rat and the change of MOR immunoreactivity was detected in the rat spinal dorsal horn by using immunohistochemistry(ABC method);Based upon the selectivity of isolectin I B4 from griffonia simpliciflia binding to C fiber,the I B4 binding sites and MOR in the spinal dorsal horn were double labeled(immunohistochemical)histochemical electron microscopy(ABC Nanogold method).Results\ During 3~7 days after subarachnoidal injetion of capsaicin,the MOR immunorecativity in the laminae Ⅰ~Ⅱ of the spinal dorsal horn of the rat treated with capsaicin was markedly decreased as compared with that of the control rat.Under electron microscope,it was observed that in the superficial layers of the spinal cord,MOR was distributed in some axonal terminals including the terminals of C fibers containing I B4 binding sites as well as in the dendrites.In both the dendrites and the axonal terminals,MORs were mainly localized in the non synaptic membranes except for the minority associated with pre and/or post synaptic membranes.Conclusion\ A considerable amount of MOR in the spinal dorsal horn originates from the primary afferent C fibers and morphine or endogenous morphine like substances such as endomorphin may act not only on postsynaptic MOR in the dendrites but also on presynaptic MOR in the axonal terminal of C fiber to inhibit the input of C fiber,and in these processes,the nonsynaptic action of MOR agonists is likely essential.
分 类 号:R338[医药卫生—人体生理学] R971.1[医药卫生—基础医学]
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