Campbell A D, McBride W J
Department of Psychiatry, Indiana University School of Medicine, Indianapolis 46202-4887, USA.
Pharmacol Biochem Behav. 1995 Aug;51(4):835-42. doi: 10.1016/0091-3057(95)00050-7.
The present study was undertaken to examine the involvement of activation of 5-HT3 receptors in the rat nucleus accumbens (Acb) on the effects of ethanol-induced increases of dopamine (DA) using the selective agonist 1-(m-chlorophenyl)-biguanide (CPBG). Perfusion of CPBG through the microdialysis probe concentration-dependently (3.3-100 microM) enhanced the extracellular levels of DA in the Acb. Extracellular DA concentrations increased as high as 1000% of baseline. The CPBG-induced increases in DA levels were Ca++ dependent and inhibited by local perfusion with the 5-HT3 antagonist ICS 205-930 (100 microM). In addition, CPBG at high concentrations caused significant decreases in the extracellular levels of DA metabolites. Intraperitoneal (IP) injection of 1 g/kg ethanol produced no changes in extracellular DA levels in the Acb; coadministration of 1 g/kg ethanol (IP) and 5 microM CPBG (local) produced increases equal to 5 microM CPBG alone. Administration of 2 g/kg ethanol (IP) alone enhanced extracellular DA levels by approximately 60% above baseline, whereas local perfusion of 5 microM CPBG alone produced an increase of approximately 100% above baseline. The coadministration of 2 g/kg ethanol (IP) and 5 microM CPBG (local) enhanced DA levels by approximately 170% above baseline; this apparent additive enhancement was almost completely prevented when 100 microM ICS 205-930 was locally coperfused. Local administration of 3.3-100 microM CPBG did not alter the extracellular levels of serotonin or 5-hydroxyindoleacetic acid. The results support an involvement of 5-HT3 receptors in regulating DA release in the Acb, and also in mediating ethanol-induced DA release.(ABSTRACT TRUNCATED AT 250 WORDS)
本研究旨在使用选择性激动剂1-(间氯苯基) - 双胍(CPBG),研究大鼠伏隔核(Acb)中5 - HT3受体的激活对乙醇诱导多巴胺(DA)增加效应的影响。通过微透析探针灌注CPBG呈浓度依赖性(3.3 - 100 microM)地提高了Acb中DA的细胞外水平。细胞外DA浓度增加高达基线的1000%。CPBG诱导的DA水平升高依赖于Ca++,并被5 - HT3拮抗剂ICS 205 - 930(100 microM)局部灌注所抑制。此外,高浓度的CPBG导致DA代谢物的细胞外水平显著降低。腹腔注射1 g/kg乙醇对Acb中细胞外DA水平无影响;同时给予1 g/kg乙醇(腹腔注射)和5 microM CPBG(局部)产生的增加与单独给予5 microM CPBG相同。单独给予2 g/kg乙醇(腹腔注射)使细胞外DA水平比基线提高约60%,而单独局部灌注5 microM CPBG使水平比基线提高约100%。同时给予2 g/kg乙醇(腹腔注射)和5 microM CPBG(局部)使DA水平比基线提高约170%;当局部同时灌注100 microM ICS 205 - 930时,这种明显的相加增强几乎完全被阻止。局部给予3.3 - 100 microM CPBG未改变血清素或5 - 羟基吲哚乙酸的细胞外水平。结果支持5 - HT3受体参与调节Acb中DA的释放,以及介导乙醇诱导的DA释放。(摘要截断于250字)