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恶喹酸和地西泮:它们在啮齿动物中的相互拮抗作用。

Oxolinic acid and diazepam: their reciprocal antagonism in rodents.

作者信息

Thiébot M H, Kloczko J, Chermat R, Simon P, Soubrié P

出版信息

Psychopharmacology (Berl). 1980 Jan;67(1):91-5. doi: 10.1007/BF00427601.

Abstract

The stimulant effects of oxolinic acid were investigated in rats and mice. This drug, given orally, consistantly induced, in doses ranging from 16 to 256 mg.kg-1, locomotor stimulation and stereotyped behavior. These effects were antagonized by pimozide (1 mg.kg-1), alpha-methyltyrosine (64 mg.kg-1) or reserpine (4 mg.kg-1, 24 h before testing) pretreatment, suggesting a facilitatory role of oxolinic acid on catecholaminergic processes. Diazepam (4-16 mg.kg-1) reduced the stimulant effects induced by oxolinic acid but not those induced by amphetamine; oxolinic acid (8 mg.kg-1) markedly reduced the antipunishment effect elicited in rats by diazepam (2 mg.kg-1). Since benzodiazepines have been reported to enhance GABA functioning, these data suggest that oxolinic acid may impair GABA transmission. However, neither muscimol (0.5-1 mg.kg-1) or gamma-acetylenic-GABA (16-64 mg.kg-1) selectively reduced the stimulant effects elicited by oxolinic acid. Therefore, the possible facilitation exerted by this drug on catecholaminergic systems may not derive from the release of an inhibitory GABAergic control.

摘要

在大鼠和小鼠中研究了恶喹酸的兴奋作用。口服这种药物,剂量在16至256毫克·千克⁻¹范围内,持续诱导运动兴奋和刻板行为。这些作用可被匹莫齐特(1毫克·千克⁻¹)、α-甲基酪氨酸(64毫克·千克⁻¹)或利血平(测试前24小时给予4毫克·千克⁻¹)预处理所拮抗,提示恶喹酸对儿茶酚胺能过程有促进作用。地西泮(4至16毫克·千克⁻¹)可降低恶喹酸诱导的兴奋作用,但不降低苯丙胺诱导的兴奋作用;恶喹酸(8毫克·千克⁻¹)可显著降低地西泮(2毫克·千克⁻¹)在大鼠中引起的抗惩罚作用。由于已有报道苯二氮䓬类药物可增强γ-氨基丁酸(GABA)功能,这些数据提示恶喹酸可能损害GABA传递。然而,蝇蕈醇(0.5至1毫克·千克⁻¹)或γ-乙炔基-GABA(16至64毫克·千克⁻¹)均未选择性降低恶喹酸引起的兴奋作用。因此,该药物对儿茶酚胺能系统可能的促进作用可能并非源于抑制性GABA能控制的释放。

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