Department of Biomedical Engineering, Purdue University, West Lafayette, Indiana, USA.
Synapse. 2011 Sep;65(9):929-37. doi: 10.1002/syn.20921. Epub 2011 Mar 28.
Microdialysis studies report that systemic alcohol increases extracellular dopamine (DA) in the rat striatum. The present study examined whether changes in striatal DA could be detected in rats using small animal positron emission tomography (PET). PET images were acquired in 44 alcohol-naïve male Wistar and alcohol-preferring (P) rats. Subjects received up to three [(11) C]raclopride scans (rest, alcohol, and saline). Animals were anesthetized with isoflurane and secured on a stereotactic-like holder during all scans. Blood samples were collected from the tail or lateral saphenous vein of 12 animals 10 min after tracer injection for determination of blood alcohol concentration (BAC). Time activity curves were extracted from the striatum and the cerebellum and binding potential (BP(ND) ) was calculated as a measure of D(2) receptor availability. Wistars given 1.0 g kg(-1) alcohol (20%v/v) i.v. or 3.0 g kg(-1) alcohol (20%v/v) i.p. showed significant alcohol-induced decreases in BP(ND) . In P rats (given 1.5, 2.25, or 3.0 g kg(-1) alcohol), no individual group showed a statistical effect of alcohol on BP(ND) , but taken together, all P rats receiving i.p. alcohol had significantly lower BP(ND) than rest or saline scans. Large decreases in BP(ND) were primarily observed in rats with BAC above 200 mg%. Also, a significant difference was found between baseline BP(ND) of Wistars who had undergone jugular catheterization surgery for i.v. alcohol administration and those who had not. Preliminary results suggest that alcohol-induced DA release in the rat striatum is detectable using small animal PET given sufficiently large cohorts and adequate blood alcohol levels.
微透析研究报告,全身给予酒精可使大鼠纹状体细胞外多巴胺(DA)增加。本研究使用小动物正电子发射断层扫描(PET)检查大鼠是否能检测到纹状体 DA 的变化。PET 图像采集于 44 只酒精-naive 雄性 Wistar 和酒精偏好(P)大鼠。受试动物接受了多达 3 次 [(11)C]raclopride 扫描(休息、酒精、盐水)。所有扫描过程中,动物都在异氟烷麻醉下,用立体定向样固定器固定。12 只动物在示踪剂注射后 10 分钟,从尾或外侧隐静脉采集血样,用于测定血酒精浓度(BAC)。从纹状体和小脑提取时间活性曲线,并计算结合潜力(BP(ND))作为 D2 受体可用性的指标。Wistar 大鼠静脉内给予 1.0 g kg(-1)酒精(20%v/v)或腹腔内给予 3.0 g kg(-1)酒精(20%v/v),BP(ND) 明显下降。在 P 大鼠(给予 1.5、2.25 或 3.0 g kg(-1)酒精)中,没有一个组的 BP(ND) 有统计学上的酒精作用,但综合来看,所有接受腹腔内酒精的 P 大鼠的 BP(ND) 均显著低于休息或盐水扫描。在 BAC 高于 200 mg%的大鼠中,主要观察到 BP(ND) 的大幅度下降。此外,还发现接受颈内导管术静脉内给予酒精的 Wistar 大鼠与未接受手术的大鼠之间,基线 BP(ND) 存在显著差异。初步结果表明,在足够大的队列和足够高的血酒精水平下,使用小动物 PET 可以检测到大鼠纹状体中酒精诱导的 DA 释放。