Magnani M, Mantovani P, Pepeu G
Pharmacol Res Commun. 1985 Jul;17(7):653-8. doi: 10.1016/0031-6989(85)90072-4.
The noradrenergic influence on cortical acetylcholine (ACh) release was investigated by the cortical cup technique in urethane anaestetized rats treated with 4-aminopyridine (4-AP). The following results were obtained: 1) The increase in ACh release induced by 4-AP (3 mg/kg i.p.) was strongly potentiated by pretreatment with -methyl-p-tyrosine (alpha-MPT) which inhibits catecholamine biosynthesis or by N-(2-chloroethyl)-N-ethyl-bromobenzylamine (DSP4) bringing about a selective degeneration of noradrenergic fibres. Neither pretreatment enhanced the spontaneous ACh output. 2) Pretreatment with p-chlorophenylalanine (PCPA), an inhibitor of serotonin synthesis, did not modify 4-AP effect on ACh output. 3) The alpha blockers, yohimbine (1 mg/kg i.p.) and prazosin (4 mg/kg i.p.), did not enhance the 4-AP effect on ACh release but only delayed its onset. 4) Yohimbine (7 mg/kg i.p.) completely reversed 4-AP effect on ACh release which was significantly decreased. It is concluded therefore that pretreatments with alpha-MPT and DSP4 remove an inhibitory noradrenergic control on cortical ACh release. On the other hand, the alpha blockers might interfere with the ionic mechanisms underlaying the 4-AP effect thus, masking the removal of the noradrenergic control, due to an alpha blockade.
采用皮质杯技术,在经4-氨基吡啶(4-AP)处理的氨基甲酸乙酯麻醉大鼠中,研究了去甲肾上腺素能对皮质乙酰胆碱(ACh)释放的影响。获得了以下结果:1)用抑制儿茶酚胺生物合成的α-甲基对酪氨酸(α-MPT)或导致去甲肾上腺素能纤维选择性变性的N-(2-氯乙基)-N-乙基溴苄胺(DSP4)预处理,可强烈增强由4-AP(3mg/kg腹腔注射)诱导的ACh释放增加。两种预处理均未增强ACh的自发输出量。2)用血清素合成抑制剂对氯苯丙氨酸(PCPA)预处理,未改变4-AP对ACh输出量的影响。3)α受体阻滞剂育亨宾(1mg/kg腹腔注射)和哌唑嗪(4mg/kg腹腔注射)未增强4-AP对ACh释放的作用,但仅延迟了其起效时间。4)育亨宾(7mg/kg腹腔注射)完全逆转了4-AP对ACh释放的作用,使ACh释放显著减少。因此得出结论,用α-MPT和DSP4预处理可消除去甲肾上腺素能对皮质ACh释放的抑制性控制。另一方面,α受体阻滞剂可能会干扰4-AP作用的离子机制,从而由于α受体阻滞而掩盖了去甲肾上腺素能控制的消除。