Criborn C O, Henriksson C, Ahlenius S, Hillegaart V
J Neural Transm. 1987;69(3-4):277-85. doi: 10.1007/BF01244348.
In the present report we have investigated the effects of apomorphine, (-)3-PPP, L-DOPA and haloperidol on the elicitation of convulsions induced in mice by exposure to oxygen at high pressure (HBO) (5 ata O2). It was found that the administration of apomorphine (0.025-0.1 mg X kg-1 s.c.), (-)3-PPP (4 mg X kg-1 i.p.) L-DOPA (200-400 mg X kg-1 i.p.) as well as haloperidol (0.25-2.0 mg X kg-1 i.p.) produced a significant protection against HBO-induced convulsions. Haloperidol was the only drug to produce a dose-dependent decrease in respiration, and this effect does probably explain the anticonvulsant effects observed. The low doses at which apomorphine was effective, and the effects produced by (-)3-PPP, indicate an effect mediated via DA autoreceptors. Alternatively, and more likely taking the effects of L-DOPA into account, the DA receptors involved are sensitive enough to disclose postsynaptic agonist properties of apomorphine and (-)3-PPP at the doses employed.
在本报告中,我们研究了阿扑吗啡、(-)3 - PPP、左旋多巴和氟哌啶醇对小鼠在高压氧(HBO)(5个绝对大气压O₂)暴露下诱发惊厥的影响。发现皮下注射阿扑吗啡(0.025 - 0.1 mg·kg⁻¹)、腹腔注射(-)3 - PPP(4 mg·kg⁻¹)、腹腔注射左旋多巴(200 - 400 mg·kg⁻¹)以及腹腔注射氟哌啶醇(0.25 - 2.0 mg·kg⁻¹)均能对HBO诱导的惊厥产生显著保护作用。氟哌啶醇是唯一一种能使呼吸呈剂量依赖性降低的药物,这种效应可能解释了所观察到的抗惊厥作用。阿扑吗啡发挥作用的低剂量以及(-)3 - PPP产生的效应表明其作用是通过多巴胺自身受体介导的。另外,考虑到左旋多巴的作用,更有可能的是,所涉及的多巴胺受体足够敏感,能够在所用剂量下揭示阿扑吗啡和(-)3 - PPP的突触后激动剂特性。