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纳洛酮可阻断麻醉大鼠外侧而非内侧穿通通路中长时程增强的诱导。

Naloxone blocks the induction of long-term potentiation in the lateral but not in the medial perforant pathway in the anesthetized rat.

作者信息

Bramham C R, Errington M L, Bliss T V

机构信息

Department of Physiology, University of Bergen, Norway.

出版信息

Brain Res. 1988 May 24;449(1-2):352-6. doi: 10.1016/0006-8993(88)91052-9.

Abstract

The possible importance of opioid peptides in the induction of long-term potentiation (LTP) was investigated in the perforant path-granule cell system. A high-frequency train (400 Hz) was delivered to the lateral or medial perforant path, during push-pull perfusion of the dentate molecular layer with artificial cerebrospinal fluid (CSF) alone, or with CSF containing naloxone (10(-4) M). Naloxone effectively blocked the induction, but not the maintenance of LTP in the lateral perforant path, a putative proenkephalin system. Naloxone did not affect the production of LTP in the medial pathway. These findings suggest that activation of naloxone-sensitive receptors is necessary for the full expression of LTP in the lateral perforant pathway.

摘要

在穿通通路-颗粒细胞系统中研究了阿片肽在诱导长时程增强(LTP)中的潜在重要性。在单独用人工脑脊液(CSF)或含纳洛酮(10⁻⁴ M)的CSF对齿状分子层进行推挽灌注期间,向外侧或内侧穿通通路施加高频串刺激(400 Hz)。纳洛酮有效地阻断了外侧穿通通路(一种假定的前脑啡肽系统)中LTP的诱导,但不影响其维持。纳洛酮不影响内侧通路中LTP的产生。这些发现表明,纳洛酮敏感受体的激活对于外侧穿通通路中LTP的充分表达是必要的。

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