Kryzhanovsky G N, Aliev M N
Pharmacol Biochem Behav. 1981 Mar;14(3):273-81. doi: 10.1016/0091-3057(81)90390-7.
The stereotyped behavior syndrome was induced in rats through local impairment of inhibitory GABA-ergic mechanisms in both caudate nuclei by bilateral microinjection of tetanus toxin, penicillin, or picrotoxin into the rostral part of the caudate nucleus. Intraperitoneally injected haloperidol suppressed the syndrome; this effect was dose-dependent. The same effect on the tetanus toxin-induced stereotyped behavior was produced by GABA microinjected bilaterally into the rostral part of the caudate nucleus of unrestrained rats. It was found in this model of tetanus toxin-induced stereotyped behavior that lithium chloride and diazepam can suppress the syndrome. Combined application of lithium chloride, diazepam, and haloperidol in minimal effective doses resulted in a much more complete and longer-lasting suppression of the syndrome than the separate use of these drugs. This effect is attributed to the joint specific actions of the drugs on pathogenetically interrelated components of a hyperactive determinant structure that arises in the caudate nuclei after impairment of the GABA control and this is responsible for the stereotyped behavior syndrome.
通过向尾状核头部双侧微量注射破伤风毒素、青霉素或印防己毒素,损伤双侧尾状核中抑制性γ-氨基丁酸(GABA)能机制,在大鼠中诱发刻板行为综合征。腹腔注射氟哌啶醇可抑制该综合征,且这种作用具有剂量依赖性。对未束缚大鼠双侧尾状核头部微量注射GABA,对破伤风毒素诱导的刻板行为产生同样的作用。在这种破伤风毒素诱导的刻板行为模型中发现,氯化锂和地西泮可抑制该综合征。以最小有效剂量联合应用氯化锂、地西泮和氟哌啶醇,与单独使用这些药物相比,能更完全、更持久地抑制该综合征。这种作用归因于这些药物对在GABA控制受损后尾状核中出现的过度活跃决定结构的致病相关成分的联合特定作用,而该结构是刻板行为综合征的起因。