The role of catecholamines in the prolactin release induced by salsolinol

被引:15
|
作者
Szekacs, D.
Bodnar, I.
Vizi, E. S.
Nagy, G. M.
Fekete, M. I. K.
机构
[1] Semmelweis Univ, H-1094 Budapest, Hungary
[2] Hungarian Acad Sci, Dept Human Morphol & Dev Biol, Neuromorphol & Neuroendocrine Lab, H-1094 Budapest, Hungary
[3] Hungarian Acad Sci, Inst Expt Med, Budapest, Hungary
基金
匈牙利科学研究基金会;
关键词
salsolinol; prolactin; dopamine; norepinephrine;
D O I
10.1016/j.neuint.2007.07.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Salsolinol (1,2,3,4-tetrahydro-6,7-dihydroxy-l-methylisoquinoline) is an endogenous prolactin releasing agent. Its action can be inhibited by another isoquinoline, 1-methyl-3,4-dihydroisoquinoline (1MeDIQ), which has a strong norepinephrine releasing activity. Salsolinol does not alter the dopamine release in median eminence in vitro, providing evidence for the lack of interaction with presynaptic D2 dopamine receptors. At the same time, lack of norepinephrine transporter abolishes salsolinol.'s action. Salsolinol decreases tissue level of dopamine and increases norepinephrine to dopamine ratio in organs innervated by the sympathetic nervous system indicating a possible decrease of norepinephrine release. Enzymes of catecholamine synthesis and metabolism are probably also, not the site of action of salsolinol. In summary, based upon all of these observations a physiologically relevant interplay might exist between the sympatho-neuronal system and the regulation of prolactin release. (C) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:319 / 322
页数:4
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