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大鼠黑质单侧6-羟基多巴胺损伤伴随的生化变化。

Biochemical changes accompanying unilateral 6-hydroxydopamine lesions in the rat substantia nigra.

作者信息

Saavedra J M, Setler P E, Kebabian J W

出版信息

Brain Res. 1978 Aug 4;151(2):339-52. doi: 10.1016/0006-8993(78)90889-2.

DOI:10.1016/0006-8993(78)90889-2
PMID:679013
Abstract

The biochemical consequences of a unilateral 6-hydroxydopamine injection into the substantia nigra of the rat brain were investigated. Projections of dopaminergic neurons from the A8-A9-A10 regions to a number of forebrain areas were confirmed. No innervation to the hypothalamus, including the median eminence, or to the brain stem, could be found with the present techniques. No destruction of serotonergic or GABAergic fibers could be demonstrated in the lesioned substantia nigra. Increases in glutamic acid decarboxylase activity were found restricted to the caudate and zona compacta of the substantia nigra ipsilateral to the lesion, indicating the possibility of a physiological interaction between GABAergic and dopaminergic systems. The neuroanatomical localization of the nigral dopamine-sensitive adenylate cyclase was also studied. No change in enzyme activity was found after destruction of a great proportion of the dopaminergic cells, suggesting that this enzyme has an extradopaminergic localization in the substantia nigra.

摘要

研究了向大鼠脑黑质单侧注射6-羟基多巴胺的生化后果。证实了多巴胺能神经元从A8-A9-A10区域向多个前脑区域的投射。用现有技术未发现向包括正中隆起在内的下丘脑或脑干的神经支配。在受损黑质中未发现5-羟色胺能或γ-氨基丁酸能纤维的破坏。发现谷氨酸脱羧酶活性的增加仅限于损伤同侧的尾状核和黑质致密部,表明γ-氨基丁酸能和多巴胺能系统之间存在生理相互作用的可能性。还研究了黑质多巴胺敏感腺苷酸环化酶的神经解剖定位。在大部分多巴胺能细胞被破坏后,未发现酶活性有变化,这表明该酶在黑质中有一个多巴胺能外的定位。

相似文献

1
Biochemical changes accompanying unilateral 6-hydroxydopamine lesions in the rat substantia nigra.大鼠黑质单侧6-羟基多巴胺损伤伴随的生化变化。
Brain Res. 1978 Aug 4;151(2):339-52. doi: 10.1016/0006-8993(78)90889-2.
2
Dopamine-sensitive adenylate cyclase: location in substantia nigra.多巴胺敏感腺苷酸环化酶:在黑质中的定位。
Science. 1977 Feb 4;195(4277):503-5. doi: 10.1126/science.13499.
3
Dissociation between the presynaptic dopamine-sensitive adenylate cyclase and [3H]spiperone binding sites in rat substantia nigra.大鼠黑质中突触前多巴胺敏感性腺苷酸环化酶与[3H]螺哌隆结合位点之间的解离。
Brain Res. 1979 May 11;167(2):355-65. doi: 10.1016/0006-8993(79)90829-1.
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Localization of nigral dopamine-sensitive adenylate cyclase on neurons originating from the corpus striatum.黑质多巴胺敏感腺苷酸环化酶在源自纹状体的神经元上的定位。
Science. 1977 Jun 17;196(4296):1343-5. doi: 10.1126/science.17159.
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Dopamine-sensitive adenylate cyclase occurs in a region of substantia nigra containing dopaminergic dendrites.多巴胺敏感腺苷酸环化酶存在于黑质中含有多巴胺能树突的区域。
Science. 1976 Aug 20;193(4254):683-5. doi: 10.1126/science.181842.
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Topographic projections of substance P and GABA pathways in the striato- and pallido-nigral system: a biochemical and immunohistochemical study.P物质和γ-氨基丁酸通路在纹状体-苍白球-黑质系统中的拓扑投射:一项生物化学与免疫组织化学研究
Brain Res. 1978 Sep 8;152(3):487-98. doi: 10.1016/0006-8993(78)91104-6.
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Regulation of neurotensin-containing neurons in the rat striatum and substantia nigra. Effects of unilateral nigral lesion with 6-hydroxydopamine on neurotensin content and its binding site density.大鼠纹状体和黑质中含神经降压素神经元的调节。6-羟基多巴胺单侧黑质损伤对神经降压素含量及其结合位点密度的影响。
Brain Res. 1990 Mar 5;510(2):203-10. doi: 10.1016/0006-8993(90)91368-q.
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Partial lesions of the dopaminergic nigrostriatal system in rat brain: biochemical characterization.大鼠脑多巴胺能黑质纹状体系统的部分损伤:生化特征
Brain Res. 1980 Aug 11;195(1):123-37. doi: 10.1016/0006-8993(80)90871-9.
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GABAergic nerve terminals decrease in the substantia nigra following hemitransections of the striatonigral and pallidonigral pathways.在纹状体黑质和苍白球黑质通路进行半横断后,黑质中的γ-氨基丁酸能神经末梢减少。
Brain Res. 1980 Jun 23;192(2):413-20. doi: 10.1016/0006-8993(80)90893-8.
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Region specific regulation of glutamic acid decarboxylase mRNA expression by dopamine neurons in rat brain.大鼠脑中多巴胺神经元对谷氨酸脱羧酶mRNA表达的区域特异性调控。
Exp Brain Res. 1989;77(3):611-20. doi: 10.1007/BF00249614.

引用本文的文献

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Increases in [3H]FK-506 and [3H]L-N(G)-nitro-arginine binding in the rat brain after nigrostriatal dopaminergic denervation.黑质纹状体多巴胺能去神经支配后大鼠脑中[3H]FK-506和[3H]L-N(G)-硝基精氨酸结合增加。
Metab Brain Dis. 1999 Mar;14(1):21-31. doi: 10.1023/a:1020605429535.