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蛋白激酶C激活参与米那普明对大鼠海马脑片乙酰胆碱释放的调节。

Involvement of protein kinase C activation in regulation of acetylcholine release from rat hippocampal slices by minaprine.

作者信息

Chaki S, Muramatsu M, Otomo S

机构信息

Department of Pharmacology, Taisho Pharmaceutical Co. Ltd., Saitama, Japan.

出版信息

Neurochem Int. 1994 Jan;24(1):37-41. doi: 10.1016/0197-0186(94)90127-9.

Abstract

Involvement of protein kinase C (PKC) activation in the regulation of acetylcholine (ACh) release from rat hippocampal slices by minaprine, [3(2-morpholinoethylamino)-4-methyl-6-phenylpyridazine] was investigated. Phorbol esters such as 4 beta-phorbol 12,13-dibutylate (PDBu) and 12-o-tetradecanoylphorbol 13-acetate (TPA) enhanced high K(+)-evoked [3H]ACh release from rat hippocampal slices. The enhancing effect of phorbol ester was attenuated by PKC inhibitors, staurosporine and 1-(5-isoquinolinesulfonyl)-2-methylpiperazine (H-7). However, the inactive phorbol analogue, 4 alpha-phorbol 12,13-didecanoate (PDD) had no effect on [3H]ACh release. Minaprine and 4-aminopyridine (4-AP) attenuated the inhibitory effect of 5-hydroxytryptamine (5-HT) on high K(+)-evoked [3H]ACh release from rat hippocampal slices. The attenuating effect of minaprine on the inhibition of [3H]ACh release by 5-HT was prevented by staurosporine, while that of 4-AP was not influenced. Furthermore, PDBu blocked voltage-dependent, rapidly inactivating 42K efflux from rat brain synaptosomes. These results suggest that minaprine attenuates the inhibitory effect of 5-HT on ACh release via PKC activation in rat hippocampus, and that the blockade of the K+ channel with PKC activation might be involved in the action of minaprine.

摘要

研究了蛋白激酶C(PKC)激活在米那普明[3-(2-吗啉代乙氨基)-4-甲基-6-苯基哒嗪]对大鼠海马脑片乙酰胆碱(ACh)释放的调节中的作用。佛波酯如4β-佛波醇12,13-二丁酸酯(PDBu)和12-O-十四烷酰佛波醇13-乙酸酯(TPA)增强了高钾(K⁺)诱发的大鼠海马脑片[³H]ACh释放。PKC抑制剂星形孢菌素和1-(5-异喹啉磺酰基)-2-甲基哌嗪(H-7)减弱了佛波酯的增强作用。然而,无活性的佛波类似物4α-佛波醇12,13-二癸酸酯(PDD)对[³H]ACh释放没有影响。米那普明和4-氨基吡啶(4-AP)减弱了5-羟色胺(5-HT)对高钾(K⁺)诱发的大鼠海马脑片[³H]ACh释放的抑制作用。星形孢菌素可阻止米那普明对5-HT抑制[³H]ACh释放的减弱作用,而4-AP的减弱作用则不受影响。此外,PDBu阻断了大鼠脑突触体电压依赖性、快速失活的42K外流。这些结果表明,米那普明通过激活大鼠海马中的PKC减弱了5-HT对ACh释放的抑制作用,并且PKC激活对钾通道的阻断可能参与了米那普明的作用。

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