Kilic Fatma S, Kulluk Dilek, Musmul Ahmet
Department of Pharmacology, Medical Faculty, Eskisehir Osmangazi University, Meselik 26480, Eskisehir, Turkey. Tel. +90 (222) 2392979 Ext. 4564. Fax. +90 (222) 2393772. E-mail:
Neurosciences (Riyadh). 2014 Apr;19(2):100-5.
To examine the effects of dehydroepiandrosterone (DHEA) on animal models of schizophrenia.
Seventy Swiss albino female mice (25-35 g) were divided into 4 groups: amphetamine-free (control), amphetamine, 50, and 100 mg/kg DHEA. The DHEA was administered intraperitoneally (ip) for 5 days. Amphetamine (3 mg/kg ip) induced hyper locomotion, apomorphine (1.5 mg/kg subcutaneously [sc]) induced climbing, and haloperidol (1.5 mg/kg sc) induced catalepsy tests were used as animal models of schizophrenia. The study was conducted at the Animal Experiment Laboratories, Department of Pharmacology, Medical School, Eskisehir Osmangazi University, Eskisehir, Turkey between March and May 2012. Statistical analysis was carried out using Kruskal-Wallis test for hyper locomotion, and one-way ANOVA for climbing and catalepsy tests.
In the amphetamine-induced locomotion test, there were significant increases in all movements compared with the amphetamine-free group. Both DHEA 50 mg/kg (p<0.05), and 100 mg/kg (p<0.01) significantly decreased all movements compared with the amphetamine-induced locomotion group. There was a significant difference between groups in the haloperidol-induced catalepsy test (p<0.05). There was no significant difference between groups in terms of total climbing time in the apomorphine-induced climbing test (p>0.05).
We observed that DHEA reduced locomotor activity and increased catalepsy at both doses, while it had no effect on climbing behavior. We suggest that DHEA displays typical neuroleptic-like effects, and may be used in the treatment of schizophrenia.
研究脱氢表雄酮(DHEA)对精神分裂症动物模型的影响。
将70只瑞士白化雌性小鼠(25 - 35克)分为4组:无苯丙胺组(对照组)、苯丙胺组、50毫克/千克DHEA组和100毫克/千克DHEA组。DHEA腹腔注射(ip)5天。以苯丙胺(3毫克/千克ip)诱导的活动亢进、阿扑吗啡(1.5毫克/千克皮下注射[sc])诱导的攀爬以及氟哌啶醇(1.5毫克/千克sc)诱导的僵住症试验作为精神分裂症动物模型。该研究于2012年3月至5月在土耳其埃斯基谢希尔奥斯曼加齐大学医学院药理学系动物实验实验室进行。对活动亢进采用Kruskal - Wallis检验进行统计分析,对攀爬和僵住症试验采用单因素方差分析。
在苯丙胺诱导的活动试验中,与无苯丙胺组相比,所有运动均显著增加。与苯丙胺诱导的活动组相比,50毫克/千克(p<0.05)和100毫克/千克(p<0.01)的DHEA均显著降低了所有运动。在氟哌啶醇诱导的僵住症试验中,各组之间存在显著差异(p<0.05)。在阿扑吗啡诱导的攀爬试验中,各组在总攀爬时间方面无显著差异(p>0.05)。
我们观察到两种剂量的DHEA均降低了运动活性并增加了僵住症,而对攀爬行为无影响。我们认为DHEA表现出典型的抗精神病样作用,可能可用于精神分裂症的治疗。