Talalaenko A N, Panfilov V Iu, Vozdigan S A, Pokramovich A I, Markova O P, Okhrimenko S V
Eksp Klin Farmakol. 1997 Jul-Aug;60(4):7-9.
In experiments on rats with tests for avoidance of an "illuminated area" and a "threatening situation", microinjection into the septal nucleus accumbens of monoamines and GABA, adreno- and dopaminomimetics, and their antagonists demonstrated a different neurochemical profile of this brain structure in anxiety states of different genesis. Local injections of chlordiazepoxide, pnenibut, indoter, campiron, and campironin into the nucleus weakened the alarm in the test for avoidance of an "illuminated area" and/or a "threatening situation", showing a similarity to the effects of GABA and serotonin but not to those of mesaton (phenylephrine hydrochloride) and dopamine. It is concluded that the antialarm effect of benzodiazepine and nonbenzodiazepine anxiolytics may be mediated by switching into action of neuron matrices of the accumbens nucleus with a different neurochemical profile responsible for the operative control of behavior in changed modality of the aversive stimulus.
在对大鼠进行的避免“光照区域”和“威胁情境”测试的实验中,向伏隔核内微量注射单胺类物质、γ-氨基丁酸(GABA)、肾上腺素能和多巴胺能拟似物及其拮抗剂,结果表明在不同成因的焦虑状态下,该脑结构具有不同的神经化学特征。向伏隔核内局部注射氯氮卓、苯乙肼、吲哚洛尔、坎皮隆和坎皮隆宁,在避免“光照区域”和/或“威胁情境”的测试中减弱了警觉性,显示出与GABA和5-羟色胺的作用相似,但与美速克新命(盐酸去氧肾上腺素)和多巴胺的作用不同。得出的结论是,苯二氮卓类和非苯二氮卓类抗焦虑药的抗警觉作用可能是通过激活伏隔核具有不同神经化学特征的神经元基质来介导的,这些神经元基质负责在厌恶刺激的变化模式下对行为进行有效控制。