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伊沙匹隆和8-羟基二苯丙胺对仓鼠(金黄地鼠)探究行为的作用:拮抗剂和对氯苯丙氨酸的影响

Action of ipsapirone and 8-OH-DPAT on exploratory behavior in hamsters (Mesocricetus auratus): effects of antagonists and p-CPA.

作者信息

Fernández-Guasti A, López-Rubalcava C

机构信息

Departamento de Farmacologíay Toxicología, CINVESTAV, D.F. México.

出版信息

Pharmacol Biochem Behav. 1995 Mar;50(3):375-82. doi: 10.1016/0091-3057(94)00278-q.

Abstract

The effect of the serotonergic drugs 8-OH-DPAT (0.0625, 0.125, and 0.25 mg/kg) and ipsapirone (5.0 and 10.0 mg/kg) on the exploratory behavior shown by hamsters under light:dark conditions was studied. These drugs produced an increase in the number of transitions similar to that induced by diazepam (0.25, 0.5, and 1.0 mg/kg), suggesting an anxiolytic action. The antagonists, methiotepin (0.31 mg/kg), pindolol (2.0 mg/kg), and alprenolol (5.0 mg/kg), did not modify the number of transitions per se and were partially effective in reverting ipsapirone's action. Similarly, methiotepin and pindolol partially blocked 8-OH-DPAT actions, whereas alprenolol lacked an effect. Drug-induced increases in this behavior occurred despite the administration of p-CPA (400 mg/kg x 3 days). The neurochemical analysis revealed that this treatment decreased 5-HT levels (from 40% to 60%). Motor activity was assessed to control unspecific drug actions; 8-OH-DPAT produced an increase that was effectively blocked by methiotepin, but was unaffected by pindolol, alprenolol, or p-CPA. These results suggest that the increase in the number of transitions produced by 8-OH-DPAT cannot be interpreted on the basis of a reduced anxiety state. Data are discussed in terms of the similarities and differences between the actions of 5-HT1A drugs in hamsters when compared with rats and mice.

摘要

研究了血清素能药物8-OH-DPAT(0.0625、0.125和0.25mg/kg)和ipsapirone(5.0和10.0mg/kg)对仓鼠在明/暗条件下探索行为的影响。这些药物使转换次数增加,类似于地西泮(0.25、0.5和1.0mg/kg)诱导的增加,提示有抗焦虑作用。拮抗剂美噻吨(0.31mg/kg)、吲哚洛尔(2.0mg/kg)和阿普洛尔(5.0mg/kg)本身并未改变转换次数,且在逆转ipsapirone的作用方面部分有效。同样,美噻吨和吲哚洛尔部分阻断了8-OH-DPAT的作用,而阿普洛尔则无此作用。尽管给予了对氯苯丙氨酸(400mg/kg×3天),药物仍诱导了这种行为的增加。神经化学分析显示,这种处理降低了5-羟色胺水平(从40%降至60%)。评估运动活性以控制非特异性药物作用;8-OH-DPAT使运动活性增加,这被美噻吨有效阻断,但不受吲哚洛尔、阿普洛尔或对氯苯丙氨酸的影响。这些结果表明,8-OH-DPAT引起的转换次数增加不能基于焦虑状态的降低来解释。根据与大鼠和小鼠相比,5-HT1A药物在仓鼠中的作用异同对数据进行了讨论。

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