The yohimbine-induced anticonflict effect in the rat, Part II. Neurochemical findings.

A Söderpalm, F Ehrenström, B Söderpalm
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引用次数: 5

Abstract

In a companion paper the alpha 2-adrenoceptor antagonist yohimbine was found to produce a dose-dependent anticonflict effect in a modified Vogel's conflict test. The behavioral data further indicated that noradrenergic and serotonergic neurons as well as the benzodiazepine (BDZ) receptor may be involved in the anticonflict effect of yohimbine. In the present study the effects on rat brain monoamine neurochemistry and GABAA/BDZ receptor function (36Cl-uptake in corticohippocampal synaptoneurosomes) of a maximally anticonflict producing dose of yohimbine (4.0 mg/kg, i.p.) were studied. The levels of rat brain catecholamines and indoleamines were measured ex vivo using high performance liquid chromatography with electrochemical detection (HPLC-ED). Yohimbine decreased noradrenaline levels both in the hippocampus and the hemispheres but instead increased DOPAC levels in these brain regions as well as in the limbic forebrain. Yohimbine also markedly enhanced DOPA accumulation in the hippocampus and the hemispheres after inhibition of 1-aromatic amino acid decarboxylase by means of NSD 1015, whereas in the limbic system only a modest increase was obtained. The yohimbine-induced effects on the catecholamine synthesis rate were largely abolished in animals severely depleted of NA by means of 6-hydroxy-dopamine (6-OH-DA) pretreatment. Yohimbine decreased both the 5-HIAA/5-HT quotient (an indicator of 5-HT turnover) and 5-HTP accumulation after NSD 1015 in the hemispheres, whereas in the hippocampus and the limbic system only 5-HTP accumulation was decreased. The yohimbine-induced effect on the indoleamine synthesis rate was not influenced by 6-OH-DA pretreatment, whereas this effect and that on the catecholamine synthesis rate were both abolished by reserpine pretreatment. Neither in vivo nor in vitro administration of yohimbine significantly altered baseline or GABA-induced accumulation of 36Cl- in corticohippocampal synaptoneurosomes. In conclusion, the present study provides neurochemical support for the suggestion that yohimbine may exert its anticonflict effect in a modified Vogel's conflict test by increasing and decreasing NA and 5-HT neurotransmission, respectively, whereas no evidence was obtained for a direct interaction of yohimbine with GABAA/BDZ receptor function.

育亨宾诱导大鼠的抗冲突作用,第二部分。影响神经系统的结果。
在一篇配套的论文中,在改进的Vogel冲突试验中,发现α 2-肾上腺素受体拮抗剂育亨宾产生剂量依赖性的抗冲突效应。行为学数据进一步表明,去甲肾上腺素能和血清素能神经元以及苯二氮卓(BDZ)受体可能参与育亨宾的抗冲突作用。本研究研究了最大抗冲突产生剂量育喜宾(4.0 mg/kg, i.p)对大鼠脑单胺神经化学和GABAA/BDZ受体功能(皮质海马突触体36cl摄取)的影响。采用高效液相色谱-电化学检测(HPLC-ED)法测定大鼠脑内儿茶酚胺和吲哚胺的含量。育亨宾降低了海马体和大脑半球的去甲肾上腺素水平,但却增加了这些大脑区域以及前脑边缘的多巴胺水平。育亨宾通过NSD 1015抑制1-芳香氨基酸脱羧酶后,也显著增加了海马和大脑半球的多巴积累,而在边缘系统中只得到适度的增加。在NA严重衰竭的动物中,育亨宾对儿茶酚胺合成速率的影响通过6-羟基多巴胺(6-OH-DA)预处理基本消除。育亨宾降低了NSD 1015后大脑半球的5-HIAA/5-羟色胺商(5-羟色胺转换的指标)和5-羟色胺积累,而海马和边缘系统仅降低了5-羟色胺积累。育亨宾对吲哚胺合成速率的影响不受6-OH-DA预处理的影响,而利血平预处理可消除育亨宾对儿茶酚胺合成速率的影响。育亨宾在体内和体外均未显著改变基线或gaba诱导的皮质海马突触体中36Cl-的积累。综上所述,本研究为育亨宾可能通过增加和减少NA和5-HT神经传递来发挥其在改良Vogel冲突试验中的抗冲突作用提供了神经化学支持,而育亨宾与GABAA/BDZ受体功能的直接相互作用尚未得到证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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