DOPAMINE SYNTHESIS AND RELEASE IN LLC-PK1 CELLS

被引:22
作者
DAWSON, R
PHILLIPS, MI
机构
[1] UNIV FLORIDA,DEPT PHARMACODYNAM,GAINESVILLE,FL 32611
[2] UNIV FLORIDA,DEPT PHYSIOL,GAINESVILLE,FL 32611
来源
EUROPEAN JOURNAL OF PHARMACOLOGY-MOLECULAR PHARMACOLOGY SECTION | 1990年 / 189卷 / 06期
关键词
DOPAMINE; LLC-PK1; CELLS; L-DOPA; KIDNEY; AROMATIC AMINO ACID DECARBOXYLASE; RENAL CATECHOLAMINES;
D O I
10.1016/0922-4106(90)90041-U
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A porcine-derived renal epithelial cell line, LLC-PK1, was used to examine dopamine (DA) synthesis from L-dopa and DA release into the media. DA synthesis and release were elevated by increasing either L-dopa concentration or incubation time. DA synthesis was shown to be entirely due to conversion of L-dopa to DA by aromatic amino acid decarboxylase. DA release from LLC-PK1 cells was stimulated by NaCl and other Na+ or Cl- salts. DA release by LLC-PK1 cells was not dependent on extracellular Ca2+ or significantly stimulated by the depolarizing actions of KCl. LLC-PK1 cells which are devoid of any neural contribution to renal DA production can synthesize DA from L-dopa and release DA in response to stimulation by either Na+ or Cl-.
引用
收藏
页码:423 / 426
页数:4
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