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肝氧素A3可阻断去甲肾上腺素从大鼠海马切片中的释放。

Hepoxilin A3 blocks the release of norepinephrine from rat hippocampal slices.

作者信息

Pace-Asciak C R, Wong L, Corey E J

机构信息

Research Institute, Hospital for Sick Children, Toronto, Canada.

出版信息

Biochem Biophys Res Commun. 1990 Dec 31;173(3):949-53. doi: 10.1016/s0006-291x(05)80877-0.

Abstract

Hepoxilin A3 was previously shown to display neuromodulatory actions on rat hippocampal CA1 neurons, with hyperpolarization of the membrane potential, an increase in the amplitude and duration of the post-spike train after hyperpolarization and an increase in the inhibitory post synaptic potential. The present report describes new biochemical evidence of a presynaptic action of hepoxilin A3 in rat hippocampal slices prelabeled with [3H]-norepinephrine. Hepoxilin A3 on its own had a marginal effect on the release of label, but blocked release which was induced by 4-aminopyridine (4-AP). Prostaglandin E2 also behaved in a similar way. These results demonstrate that hepoxilins modulate neurotransmission in the mammalian CNS through both pre- and postsynaptic actions.

摘要

先前的研究表明,肝氧素A3对大鼠海马CA1神经元具有神经调节作用,可使膜电位超极化,超极化后动作电位序列的幅度和持续时间增加,抑制性突触后电位增加。本报告描述了在预先用[3H] -去甲肾上腺素标记的大鼠海马切片中,肝氧素A3突触前作用的新生化证据。肝氧素A3自身对标记物释放的影响较小,但可阻断由4-氨基吡啶(4-AP)诱导的释放。前列腺素E2也表现出类似的作用。这些结果表明,肝氧素通过突触前和突触后作用调节哺乳动物中枢神经系统中的神经传递。

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