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苯丁胺对清醒大鼠纹状体多巴胺和5-羟色胺释放的影响:体内微透析研究

Effects of phentermine on striatal dopamine and serotonin release in conscious rats: in vivo microdialysis study.

作者信息

Balcioglu A, Wurtman R J

机构信息

Massachusetts Institute of Technology, Department of Brain and Cognitive Sciences, Cambridge 02139, USA.

出版信息

Int J Obes Relat Metab Disord. 1998 Apr;22(4):325-8. doi: 10.1038/sj.ijo.0800589.

Abstract

OBJECTIVE

To measure the effects of phentermine, an appetite supressant, on the release of brain dopamine (DA) and serotonin (5-HT) into striatal dialysates of freely moving rats.

DESIGN

Microdialysis and high performance liquid chromatography.

SUBJECTS

Unanesthetized rats.

MEASUREMENTS

Samples collected every 20 min were assayed for both neurotransmitters in a single run, using high performance liquid chromatography with electrochemical detection.

RESULTS

Baseline levels of DA and 5-HT in dialysates were 56+/-16 and 3+/-0.6 fmol/20 microl, respectively. Administration of phentermine (2 or 5 mg/kg) increased dialysate DA concentrations to 147+/-17% (P < 0.01) and 320+/-89% (P < 0.01) of baseline, respectively, without significantly affecting 5-HT concentrations. Pretreatment with tetrodotoxin (TTX, 60 min, 1 microM), which abolished the basal release of DA and 5-HT into striatal dialysates, diminished the increase in DA concentrations induced by phentermine, but did not completely block it. Phentermine (2 or 5 mg/kg, i.p.) still stimulated DA release to 27+/-13% and 85+/-15% of baseline, respectively, in the presence of TTX.

CONCLUSION

Phentermine increases brain DA but not 5-HT release in freely moving rats, and TTX reduces, but does not fully block this effect. This pattern is similar to that known to be produced by d-amphetamine.

摘要

目的

测定食欲抑制剂芬特明对自由活动大鼠纹状体透析液中脑多巴胺(DA)和5-羟色胺(5-HT)释放的影响。

设计

微透析和高效液相色谱法。

对象

未麻醉大鼠。

测量

每20分钟收集的样本在单次运行中使用带电化学检测的高效液相色谱法对两种神经递质进行检测。

结果

透析液中DA和5-HT的基线水平分别为56±16和3±0.6 fmol/20微升。给予芬特明(2或5毫克/千克)后,透析液中DA浓度分别增加至基线的147±17%(P<0.01)和320±89%(P<0.01),而对5-HT浓度无显著影响。用河豚毒素(TTX,60分钟,1微摩尔)预处理可消除DA和5-HT向纹状体透析液中的基础释放,减少芬特明诱导的DA浓度升高,但未完全阻断。在存在TTX的情况下,芬特明(2或5毫克/千克,腹腔注射)仍分别将DA释放刺激至基线的27±13%和85±15%。

结论

芬特明增加自由活动大鼠脑内DA的释放,但不增加5-HT的释放,TTX可降低但不能完全阻断这种作用。这种模式与已知的右旋苯丙胺产生的模式相似。

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