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钾离子刺激大鼠纹状体切片中亮氨酸脑啡肽和甲硫氨酸脑啡肽的释放:吗啡和纳洛酮无作用

K-stimulated release of leu- and met-enkephalin from rat striatal slices: lack of effect of morphine and naloxone.

作者信息

Richter J A, Wesche D L, Frederickson R C

出版信息

Eur J Pharmacol. 1979 Jun;56(1-2):105-13. doi: 10.1016/0014-2999(79)90439-4.

Abstract

The release of leu- and met-enkephalin from rat striatal slices was determined by superfusing the slices in vitro and running the superfusates directly over columns of Amberlite XAD-2 from which the peptides were eluted with methanol and measured by radioimmunoassay. Depolarization by high K concentrations increased the release of both pentapeptides many fold; the degree of increase, however, depended in part on the length of time chosen for the stimulation period, suggesting that the stimulation effect was very short lived. The stimulated release of both peptides (but not the resting release) was at least partially dependent on Ca in the medium and was totally inhibited by high Mg concentrations. Selected concentrations of naloxone and morphine in the superfusing medium had no effect on the resting or stimulated release of the peptides. The results support the hypothesis that these peptides serve as neurotransmitters in the striatum, but autoregulation of their release by morphine and naloxone could not be demonstrated.

摘要

通过体外灌注大鼠纹状体切片并将灌注液直接流经Amberlite XAD - 2柱来测定亮氨酸脑啡肽和甲硫氨酸脑啡肽的释放,肽段用甲醇从柱上洗脱后,通过放射免疫测定法进行测量。高钾浓度引起的去极化使两种五肽的释放增加了许多倍;然而,增加的程度部分取决于所选刺激期的时长,这表明刺激作用持续时间非常短。两种肽的刺激释放(而非静息释放)至少部分依赖于培养基中的钙,并且被高镁浓度完全抑制。灌注培养基中选定浓度的纳洛酮和吗啡对肽的静息或刺激释放没有影响。这些结果支持了这样的假设,即这些肽在纹状体中充当神经递质,但未证实吗啡和纳洛酮对其释放有自动调节作用。

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