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大鼠脊髓中[125I-酪氨酸8]缓激肽受体结合位点的定量放射自显影定位:新生期辣椒素、去甲肾上腺素能传入神经切断、背根切断和外周轴突切断的影响

Quantitative autoradiographic localization of [125I-Tyr8]bradykinin receptor binding sites in the rat spinal cord: effects of neonatal capsaicin, noradrenergic deafferentation, dorsal rhizotomy and peripheral axotomy.

作者信息

Lopes P, Kar S, Chrétien L, Regoli D, Quirion R, Couture R

机构信息

Department of Physiology, Faculty of Medicine, Université de Montréal, Québec, Canada.

出版信息

Neuroscience. 1995 Oct;68(3):867-81. doi: 10.1016/0306-4522(95)00161-b.

Abstract

In vitro receptor autoradiography was used to localize, quantify and characterize [125I-Tyr8]bradykinin binding sites in all major spinal cord segments of normal rats and animals subjected to various chemical treatments and surgical lesions. [125I-Tyr8]bradykinin specific binding sites were predominantly located to superficial laminae of the rat dorsal horn, with the substantia gelatinosa showing the highest density of labelling (values ranging from 3.1 fmol/mg tissue in cervical to 4.5 fmol/mg tissue in lumbar segments). A moderate density (1.8-3.0 fmol/mg tissue) of specific binding was observed in lamina III, whereas in other areas, i.e. laminae I and IV-X, lower amounts of labelling were detected. Within the superficial laminae of the dorsal horn, [125I-Tyr8]bradykinin binding was largely distributed over the neurophil with some perikarya showing concentrations of labelling. In contrast, the ventral horn showed a rather homogeneous distribution of [125I-Tyr8]bradykinin binding over the neuropil, with silver grain alignments surrounding motoneuron perikaryas and proximal processes. Bradykinin, [Tyr8]bradykinin and B2 receptor antagonists (D-Arg[Hyp3,Thi5,D-Tic7,Oic8]bradykinin (Hoe 140), D-Arg[Tyr3,D-Phe7,Leu8]bradykinin, D-Arg[Hyp3, Leu8]bradykinin, D-Arg[Hyp2, Thi5,8,-Phe7]bradykinin D-Arg[Hyp3, D-Phe7, Leu8]bradykinin, Tyr0, D-Arg[Hyp3, D-Phe7, Leu8]bradykinin inhibited [125I-Tyr8]-bradykinin binding with very high subnanomolar affinities, while the B1 receptor agonist (Tyr0,des-Arg10-kallidin) and antagonist ([Leu8]-des-Arg9-bradykinin) did not significantly affect [125I-Tyr8]bradykinin binding at up to micromolar concentrations. Two weeks after unilateral lumbar dorsal rhizotomy (L1-L6) or peripheral lesions of the sciatic nerve, significant decreases ( +/- 50%) in [125I-Tyr8]bradykinin binding sites were found in ipsilateral laminae I-III of lumbar spinal cord.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

采用体外受体放射自显影技术,对正常大鼠以及接受各种化学处理和手术损伤的动物的所有主要脊髓节段中[125I - Tyr8]缓激肽结合位点进行定位、定量和特性分析。[125I - Tyr8]缓激肽特异性结合位点主要位于大鼠背角浅层,其中胶状质的标记密度最高(颈段为3.1 fmol/mg组织,腰段为4.5 fmol/mg组织)。在第III层观察到中等密度的特异性结合(1.8 - 3.0 fmol/mg组织),而在其他区域,即第I层和第IV - X层,检测到的标记量较低。在背角浅层内,[125I - Tyr8]缓激肽结合主要分布在神经纤维网,一些核周体有标记聚集。相比之下,腹角中[125I - Tyr8]缓激肽结合在神经纤维网上分布较为均匀,运动神经元核周体和近端突起周围有银粒排列。缓激肽、[Tyr8]缓激肽和B2受体拮抗剂(D - Arg[Hyp3,Thi5,D - Tic7,Oic8]缓激肽(Hoe 140)、D - Arg[Tyr3,D - Phe7,Leu8]缓激肽、D - Arg[Hyp3,Leu8]缓激肽、D - Arg[Hyp2,Thi5,8,-Phe7]缓激肽、D - Arg[Hyp3,D - Phe7,Leu8]缓激肽、Tyr0,D - Arg[Hyp3,D - Phe7,Leu8]缓激肽)以非常高的亚纳摩尔亲和力抑制[125I - Tyr8] - 缓激肽结合,而B1受体激动剂(Tyr0,des - Arg10 - 胰激肽)和拮抗剂([Leu8] - des - Arg9 - 缓激肽)在高达微摩尔浓度时对[125I - Tyr]缓激肽结合没有显著影响。单侧腰背部神经根切断术(L1 - L6)或坐骨神经外周损伤两周后,在腰脊髓同侧的第I - III层中,[125I - Tyr8]缓激肽结合位点显著减少(±50%)。(摘要截短于250字)

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