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对大鼠使用对氯苯丙氨酸(pCPA)刺激特定驱力(捕食行为)

Stimulation of a specific drive (predatory behaviour) by p-chlorophenylalanine (pCPA) in the rat.

作者信息

Kreiskott H, Hofmann H P

出版信息

Pharmakopsychiatr Neuropsychopharmakol. 1975 May;8(3):136-40. doi: 10.1055/s-0028-1094452.

DOI:10.1055/s-0028-1094452
PMID:135265
Abstract

In contrast to wild rats the percentage of animals showing predatory behaviour is very low among laboratory rats. Stimulation of this specific drive by systemic drug application has been mentioned only for pCPA and delta9-tetrahydrocannabinole. As detailed investigations concerning this stimulating property of pCPA are not published, the effect was studied in selected non-biting rats (without starvation and isolation) regarding dose- and time-dependence after single and repeated drug administration; further, D- and L-isomers of pCPA were included in the investigation. After single oral application of 200 to 3200 mg/kg DL-pCPA a dose-dependent stimulation of predatory behaviour was found. Smaller doses (200 or 400 mg/kg p.o.) given repeatedly on 3 consecutive days showed effects comparable with those after single administration of much higher doses (1600 or 3200 mg/kg p.o.). With repeated oral application of 50, 100 or 200 mg/kg on 10 consecutive days no difference was found between D- and L-pCPA concerning efficacy and time course of drug effect. Both after single and repeated administration in all series of tests the effect reached its maximum not before several days and faded almost completely in the drug-free after-period. D-methamphetamine HCl, investigated comparatively as a CNS stimulant, provoked no predatory behaviour in a wide dose-range (0.125 to 8.0 mg/kg p.o.) with repeated administration on 10 consecutive days. Within the control groups (total number of rats = 100) no animal showed predatory attach during an observation-period of at least 3 weeks.

摘要

与野生大鼠相比,在实验室大鼠中表现出捕食行为的动物比例非常低。仅提及通过全身给药应用pCPA和δ9-四氢大麻酚来刺激这种特定驱力。由于关于pCPA这种刺激特性的详细研究尚未发表,因此在选定的非咬杀大鼠(无饥饿和隔离)中研究了单次和重复给药后该效应的剂量和时间依赖性;此外,还研究了pCPA的D-和L-异构体。单次口服200至3200mg/kg DL-pCPA后,发现捕食行为有剂量依赖性刺激。连续3天重复给予较小剂量(200或400mg/kg口服),其效果与单次给予高得多的剂量(1600或3200mg/kg口服)后的效果相当。连续10天重复口服50、100或200mg/kg,D-和L-pCPA在疗效和药物作用时间过程方面没有差异。在所有系列试验中,单次和重复给药后,效应在数天前均未达到最大值,并且在停药后的时期几乎完全消退。作为中枢神经系统兴奋剂进行比较研究的D-甲基苯丙胺盐酸盐,在连续10天重复给药的宽剂量范围(0.125至8.0mg/kg口服)内未引发捕食行为。在对照组(大鼠总数 = 100)中,在至少3周的观察期内没有动物表现出捕食性攻击。

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Stimulation of a specific drive (predatory behaviour) by p-chlorophenylalanine (pCPA) in the rat.对大鼠使用对氯苯丙氨酸(pCPA)刺激特定驱力(捕食行为)
Pharmakopsychiatr Neuropsychopharmakol. 1975 May;8(3):136-40. doi: 10.1055/s-0028-1094452.
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