Suppr超能文献

(±)-12-氯番荔枝碱对多巴胺D2自身受体反馈调节的阻断作用

[Blockade of (+/-) 12-chloroscoulerine on feed-back regulation of dopamine D2 autoreceptors].

作者信息

Chen L J, Zhang X X, Guo X

机构信息

Shanghai Institute of Materia Medica, Chinese Academy of Sciences, China.

出版信息

Zhongguo Yao Li Xue Bao. 1996 Sep;17(5):477-80.

PMID:9863180
Abstract

AIM

To verify whether (+/-) 12-chloroscoulerine (CSL) is antagonist or agonist effect to D2 autoreceptors.

METHODS

The levodopa content accumulated in the rat striatum was measured by HPLC-ECD, and the DA neuron firing activity in the substantia nigra zona compacta (SNC) was recorded.

RESULTS

The accumulated levodopa content induced by CSL 40 mg.kg-1 was much more than that of 1,4-butyro-lactone (BL) group (P < 0.01). After i.p. injection of apomorphine (Apo) 5 mg.kg-1, the levodopa content was decreased below that of BL group (P < 0.05). The Apo inhibition on levodopa content was completely reversed by CSL (40 mg.kg-1, i.p.) and then increased the levodopa content (2.5 +/- 1.1 micrograms.g-1) over that of Apo group (0.7 +/- 0.3 microgram.g-1, P < 0.01). In the electrophysiologic recording, Apo (15 micrograms.kg-1, i.v.) induced the decrease of SNC DA cell firing rate nearly to zero. At the accumulated dose of CSL up to 80 micrograms.kg-1 (i.v.), the inhibition of Apo was attenuated and the firing activity was restored to predrug level.

CONCLUSION

CSL showed an antagonistic action, an action to D2 autoreceptors.

摘要

目的

验证(±)12-氯番荔枝碱(CSL)对D2自身受体是拮抗作用还是激动作用。

方法

采用高效液相色谱-电化学检测法(HPLC-ECD)测定大鼠纹状体中积累的左旋多巴含量,并记录黑质致密部(SNC)中多巴胺能神经元的放电活动。

结果

40mg·kg-1的CSL诱导积累的左旋多巴含量远高于1,4-丁内酯(BL)组(P<0.01)。腹腔注射5mg·kg-1阿扑吗啡(Apo)后,左旋多巴含量降至低于BL组(P<0.05)。CSL(40mg·kg-1,腹腔注射)完全逆转了Apo对左旋多巴含量的抑制作用,然后使左旋多巴含量(2.5±1.1μg·g-1)高于Apo组(0.7±0.3μg·g-1,P<0.01)。在电生理记录中,Apo(15μg·kg-1,静脉注射)使SNC多巴胺能细胞放电率几乎降至零。当CSL静脉注射累计剂量达80μg·kg-1时,Apo的抑制作用减弱,放电活动恢复到给药前水平。

结论

CSL对D2自身受体表现出拮抗作用。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验