{"title":"The Effect of Acute and Chronic Ethanol on Dopamine Turnover in the Caudate Nucleus of the Rat","authors":"R. El-Mallakh","doi":"10.29046/JJP.006.1.005","DOIUrl":null,"url":null,"abstract":"It is ge nerally bel ieved that acute and chro nic e thanol (EtO H) ad ministra tion alters th e ac t ivity of ca techolam ines in the brain , however, th e specific effects of EtO H on th e dopam inergic system are disputed ( I) . Acute EtOH ad m inis tration has been vari ously reported to decrease (2 ,3), increase (4,5) , and ca use no change (6 ,7) in dopamine (DA) synthesis and turnover. Lik ewise , chronic EtO H treatmen ts have been reported to decrease (2 ,8) and increase (9, I0) DA synthesis and turnover. Many of these apparently co nflicting results are ex plained by the use of d ifferent anima l models (rat (2, 3 ,6,7, I0) , rabbi t (6), and mouse (4,5,9», different meth ods of EtO H ad min ist ration (intraperitoneal (3 ,4,6,7), oral (2,5) , and inh ala tio n (9», and no assurance of a lcoho lic dependence with ch ron ic ex posure (2, I0). Furth er , the majority of th ese stu d ies were ca rr ied out prior to th e development of a very se nsitive h igh per for mance liquid ch romatography (H PLC) tech nique which ca n detect minute amounts of DA, d ih yrox yphenylalan ine (DO PA) , and di hydroxyp henylacetic acid (DO PAC) (11 ,12). Sin ce DA receptor superse ns itivity has been fou nd in the mesoli mbic syste m of EtOH-dependent rats (1, 13) and because EtOH increases DA release in vivo (14) (indica ting th at EtO H does affect the dopaminergic syste m), we elect ed to exa mine th e effec ts o f ac ute and chron ic EtO H ad mi nistration o n th e dopaminergic syste m in th e rat ca udate nucleus .","PeriodicalId":142486,"journal":{"name":"Jefferson Journal of Psychiatry","volume":"15 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Jefferson Journal of Psychiatry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.29046/JJP.006.1.005","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
It is ge nerally bel ieved that acute and chro nic e thanol (EtO H) ad ministra tion alters th e ac t ivity of ca techolam ines in the brain , however, th e specific effects of EtO H on th e dopam inergic system are disputed ( I) . Acute EtOH ad m inis tration has been vari ously reported to decrease (2 ,3), increase (4,5) , and ca use no change (6 ,7) in dopamine (DA) synthesis and turnover. Lik ewise , chronic EtO H treatmen ts have been reported to decrease (2 ,8) and increase (9, I0) DA synthesis and turnover. Many of these apparently co nflicting results are ex plained by the use of d ifferent anima l models (rat (2, 3 ,6,7, I0) , rabbi t (6), and mouse (4,5,9», different meth ods of EtO H ad min ist ration (intraperitoneal (3 ,4,6,7), oral (2,5) , and inh ala tio n (9», and no assurance of a lcoho lic dependence with ch ron ic ex posure (2, I0). Furth er , the majority of th ese stu d ies were ca rr ied out prior to th e development of a very se nsitive h igh per for mance liquid ch romatography (H PLC) tech nique which ca n detect minute amounts of DA, d ih yrox yphenylalan ine (DO PA) , and di hydroxyp henylacetic acid (DO PAC) (11 ,12). Sin ce DA receptor superse ns itivity has been fou nd in the mesoli mbic syste m of EtOH-dependent rats (1, 13) and because EtOH increases DA release in vivo (14) (indica ting th at EtO H does affect the dopaminergic syste m), we elect ed to exa mine th e effec ts o f ac ute and chron ic EtO H ad mi nistration o n th e dopaminergic syste m in th e rat ca udate nucleus .
人们普遍认为,急性和慢性乙醇(etoh)和给药会改变大脑中多巴胺的活性,然而,etoh对多巴胺能系统的具体影响是有争议的(1)。有不同的报道称,急性EtOH和m的注入会减少(2,3),增加(4,5),并且可能不会改变多巴胺(DA)的合成和转换(6,7)。同样,据报道,慢性etoh治疗会减少(2,8)和增加(9,10)DA合成和周转。许多这些明显相互矛盾的结果可以通过使用不同的动物模型(大鼠(2,3,6,7,0),拉比(6)和小鼠(4,5,9),不同的EtO - H方法和最小剂量(腹腔注射(3,4,6,7),口服(2,5)和腹腔注射(9)来解释,并且不能保证酒精依赖于慢性暴露(2,0)。此外,这些研究中的大多数都是在非常灵敏的高纯度液相色谱(hplc)技术发展之前完成的,该技术可以检测微量的DA, d与yrox -苯基alan ine (DO PA)和dihydroxyhenylacetic acid (DO PAC)(11,12)。罪ce DA受体superse ns敏感度已经喝醉的nd mesoli mbic体制EtOH-dependent老鼠(13)和因为EtOH增加DA释放体内(14)(H籼稻ting,埃托奥影响多巴胺能系统),我们选ed穰我th e代用ts o f ac ute和时间H ic埃托奥广告mi nistration o n th e多巴胺体制th e鼠ca udate细胞核。