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氟西汀的多巴胺能和5-羟色胺能特性。

Dopaminergic and serotonergic properties of fluoxetine.

作者信息

Simon B, Appel J B

机构信息

Department of Psychology, University of South Carolina, Columbia, USA.

出版信息

Prog Neuropsychopharmacol Biol Psychiatry. 1997 Jan;21(1):169-81. doi: 10.1016/s0278-5846(96)00167-4.

Abstract
  1. Rats were trained to discriminate i.p. injections of a 5-HT agonist, LSD (0.08 mg/kg, n = 12) or a DA agonist, cocaine (10 mg/kg; n = 16) in a two lever, drug discrimination situation. 2. Animals were tested with fluoxetine (0.625-10 mg/kg) alone and in combination with low doses of the training drugs. 3. Fluoxetine did not substitute for either LSD or cocaine at any dose tested. A relatively low dose of fluoxetine (2.5 mg/kg) potentiated the discriminability of cocaine (2.5 mg/kg) from saline. A higher dose of fluoxetine (5.0 mg/kg) significantly enhanced the effects of a low dose of LSD (0.02 mg/kg), but only to 41.7% responses on the LSD-appropriate lever. 4. The data suggest that fluoxetine alters the discriminative stimulus properties of cocaine to a greater extent than those of LSD. 5. The ability of fluoxetine to potentiate the cocaine cue (but not to substitute for cocaine) suggests that both of those drugs affect DA systems, but do so through different mechanisms. For example, fluoxetine may not inhibit DA reuptake (to the same extent as cocaine), but may have other dopaminergic actions such as increasing DA receptor density.
摘要
  1. 在双杠杆药物辨别实验中,训练大鼠通过腹腔注射辨别5-羟色胺(5-HT)激动剂麦角酸二乙胺(LSD,0.08毫克/千克,n = 12)或多巴胺(DA)激动剂可卡因(10毫克/千克;n = 16)。2. 单独用氟西汀(0.625 - 10毫克/千克)以及与低剂量的训练药物联合对动物进行测试。3. 在任何测试剂量下,氟西汀都不能替代LSD或可卡因。相对低剂量的氟西汀(2.5毫克/千克)增强了可卡因(2.5毫克/千克)与生理盐水之间的辨别能力。较高剂量的氟西汀(5.0毫克/千克)显著增强了低剂量LSD(0.02毫克/千克)的效果,但仅使在LSD相应杠杆上的反应达到41.7%。4. 数据表明,氟西汀对可卡因辨别刺激特性的改变程度大于对LSD的改变。5. 氟西汀增强可卡因线索(但不替代可卡因)的能力表明,这两种药物都影响多巴胺系统,但作用机制不同。例如,氟西汀可能不会(像可卡因那样程度地)抑制多巴胺再摄取,但可能具有其他多巴胺能作用,如增加多巴胺受体密度。

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