Chronic lithium treatment decreases brain phospholipase A2 activity

被引:68
作者
Chang, MCJ [1 ]
Jones, CR [1 ]
机构
[1] NIA, Bethesda, MD 20892 USA
关键词
lithium; phospholipase A(2); arachidonate; brain; phospholipids; phosphatidylcholine;
D O I
10.1023/A:1022415113421
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
Chronic lithium administration decreases the turnover of arachidonic acid (AA) in several brain phospholipids. This suggests that lithium may attenuate phospholipase A(2) (PLA(2)) activity in brain. We now report effects of chronic lithium treatment on PLA(2) activity in postnuclear supernatant from rat brain: Enzyme activity was determined by two assay methods, radiometric and fluorometric, and measured the release of the fatty acid on the second acyl position (sn2) from choline and ethanolamine phospholipids. PLA(2) activity in brain postnuclear supernatant from rats chronically treated with lithium in the diet was significantly decreased (20-50%) when compared with controls. In vehicle or lithium-treated rats, PLA(2) activity was not significantly augmented or attenuated by the addition of calcium chelators, divalent cations or LiCl supplementation (1.0 mM) to postnuclear supernatant. These results suggest that a major therapeutic effect of lithium is to attenuate brain PLA(2) activity involved in signal transduction.
引用
收藏
页码:887 / 892
页数:6
相关论文
共 44 条
[1]   SOME ASPECTS OF RAT PLATELET AND SERUM PHOSPHOLIPASE-A2 ACTIVITIES [J].
AARSMAN, AJ ;
ROOSENBOOM, CFP ;
VANGEFFEN, GEW ;
VANDENBOSCH, H .
BIOCHIMICA ET BIOPHYSICA ACTA, 1985, 837 (03) :288-295
[2]   PROTEIN-KINASE-C, CALCIUM AND PHOSPHOLIPID DEGRADATION [J].
ASAOKA, Y ;
NAKAMURA, S ;
YOSHIDA, K ;
NISHIZUKA, Y .
TRENDS IN BIOCHEMICAL SCIENCES, 1992, 17 (10) :414-417
[3]   LITHIUM INHIBITS ADRENERGIC AND CHOLINERGIC INCREASES IN GTP BINDING IN RAT CORTEX [J].
AVISSAR, S ;
SCHREIBER, G ;
DANON, A ;
BELMAKER, RH .
NATURE, 1988, 331 (6155) :440-442
[4]   RECEPTOR-MEDIATED ACTIVATION OF PHOSPHOLIPASE-A2 VIA GTP-BINDING PROTEINS - ARACHIDONIC-ACID AND ITS METABOLITES AS 2ND MESSENGERS [J].
AXELROD, J ;
BURCH, RM ;
JELSEMA, CL .
TRENDS IN NEUROSCIENCES, 1988, 11 (03) :117-123
[5]   CONTINUOUS, VESICLE-BASED FLUOROMETRIC ASSAYS OF 14- AND 85-KDA PHOSPHOLIPASES A(2) [J].
BAYBURT, T ;
YU, BZ ;
STREET, I ;
GHOMASHCHI, F ;
LALIBERTE, F ;
PERRIER, H ;
WANG, ZY ;
HOMAN, R ;
JAIN, MK ;
GELB, MH .
ANALYTICAL BIOCHEMISTRY, 1995, 232 (01) :7-23
[6]   INFLUENCE OF MAO-INHIBITORS, NEUROLEPTICS, MORPHINE, MESCALINE, DIVASCAN, ACONITINE, AND PYROGENES ON PROSTAGLANDIN-BIOSYNTHESIS [J].
BEKEMEIER, H ;
GIESSLER, AJ ;
VOGEL, E .
PHARMACOLOGICAL RESEARCH COMMUNICATIONS, 1977, 9 (06) :587-598
[7]   NEURAL AND DEVELOPMENTAL ACTIONS OF LITHIUM - A UNIFYING HYPOTHESIS [J].
BERRIDGE, MJ ;
DOWNES, CP ;
HANLEY, MR .
CELL, 1989, 59 (03) :411-419
[8]   LITHIUM AMPLIFIES AGONIST-DEPENDENT PHOSPHATIDYLINOSITOL RESPONSES IN BRAIN AND SALIVARY-GLANDS [J].
BERRIDGE, MJ ;
DOWNES, CP ;
HANLEY, MR .
BIOCHEMICAL JOURNAL, 1982, 206 (03) :587-595
[9]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[10]   INFLUENCE OF LITHIUM ON 2ND MESSENGER ACCUMULATION IN NG108-15 CELLS [J].
BRAMI, BA ;
LELI, U ;
HAUSER, G .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1991, 174 (02) :606-612