Glycerophospholipids in brain: their metabolism, incorporation into membranes, functions, and involvement in neurological disorders

被引:375
作者
Farooqui, AA [1 ]
Horrocks, LA [1 ]
Farooqui, T [1 ]
机构
[1] Ohio State Univ, Dept Mol & Cellular Biochem, Columbus, OH 43210 USA
关键词
glycerophospholipids; phospholipases A(1); A(2); C; and D; arachidonic acid; docosahexaenoic acid; platelet activating factor; diacylglycerol; cannabinoid receptors; membrane fluidity; membrane permeability; apoptosis; neurological disorders;
D O I
10.1016/S0009-3084(00)00128-6
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
Neural membranes contain several classes of glycerophospholipids which turnover at different rates with respect to their structure and localization in different cells and membranes. The glycerophospholipid composition of neural membranes greatly alters their functional efficacy. The length of glycerophospholipid acyl chain and the degree of saturation are important determinants of many membrane characteristics including the formation of lateral domains that are rich in polyunsaturated fatty acids. Receptor-mediated degradation of glycerophospholipids by phospholipases A(1), A(2), C, and D results in generation of second messengers such as arachidonic acid, eicosanoids, platelet activating factor and diacylglycerol. Thus, neural membrane phospholipids are a reservoir for second messengers. They are also involved in apoptosis, modulation of activities of transporters, and membrane-bound enzymes. Marked alterations in neural membrane glycerophospholipid composition have been reported to occur in neurological disorders. These alterations result in changes in membrane fluidity and permeability. These processes along with the accumulation of lipid peroxides and compromised energy metabolism may be responsible for the neurodegeneration observed in neurological disorders. (C) 2000 Elsevier Science Ireland Ltd. All rights reserved.
引用
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页码:1 / 29
页数:29
相关论文
共 223 条
[1]  
Adayev T, 1998, J NEUROCHEM, V71, P1854
[2]   Phospholipid metabolism and membrane dynamics [J].
Alb, JG ;
Kearns, MA ;
Bankaitis, VA .
CURRENT OPINION IN CELL BIOLOGY, 1996, 8 (04) :534-541
[3]   Phosphatidylinositol synthase from mammalian tissues [J].
Antonsson, B .
BIOCHIMICA ET BIOPHYSICA ACTA-LIPIDS AND LIPID METABOLISM, 1997, 1348 (1-2) :179-186
[4]   Control of membrane phosphatidylcholine biosynthesis by diacylglycerol levels in neuronal cells undergoing neurite outgrowth [J].
Araki, W ;
Wurtman, RJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (22) :11946-11950
[5]   INOSITOL MONOPHOSPHATASE - A PUTATIVE TARGET FOR LI+ IN THE TREATMENT OF BIPOLAR DISORDER [J].
ATACK, JR ;
BROUGHTON, HB ;
POLLACK, SJ .
TRENDS IN NEUROSCIENCES, 1995, 18 (08) :343-349
[6]  
BARABAN JM, 1989, AM J PSYCHIAT, V146, P1251
[7]   Apoptosis and spinal cord injury [J].
Beattie, MS ;
Shuman, SL ;
Bresnahan, JC .
NEUROSCIENTIST, 1998, 4 (03) :163-171
[8]   SYNTHESIS OF CHOLINE AND ETHANOLAMINE PHOSPHOGLYCERIDES IN NEURONAL AND GLIAL CELLS OF RABBIT IN-VITRO [J].
BINAGLIA, L ;
GORACCI, G ;
PORCELLATI, G ;
ROBERTI, R ;
WOELK, H .
JOURNAL OF NEUROCHEMISTRY, 1973, 21 (05) :1067-1082
[9]   Phosphatidic acid as the biosynthetic precursor of the endocannabinoid 2-arachidonoylglycerol in intact mouse neuroblastoma cells stimulated with ionomycin [J].
Bisogno, T ;
Melck, D ;
De Petrocellis, L ;
Di Marzo, V .
JOURNAL OF NEUROCHEMISTRY, 1999, 72 (05) :2113-2119
[10]  
BLEASDALE JE, 1985, INOSITOL PHOSPHOINOS, P1