Peroxide detoxification by brain cells

Journal of Neuroscience Research - Tập 79 Số 1-2 - Trang 157-165 - 2005
Ralf Dringen1, Petra G. Pawlowski, Johannes Hirrlinger
1Interfakultäres Institut für Biochemie der Universität Tübingen, Hoppe-Seyler-Strasse 4, D-72076 Tübingen, Germany. [email protected]

Tóm tắt

Abstract

Peroxides are generated continuously in cells that consume oxygen. Among the different peroxides, hydrogen peroxide is the molecule that is formed in highest quantities. In addition, organic hydroperoxides are synthesized as products of cellular metabolism. Generation and disposal of peroxides is a very important process in the human brain, because cells of this organ consume 20% of the oxygen used by the body. To prevent cellular accumulation of peroxides and damage generated by peroxide‐derived radicals, brain cells contain efficient antioxidative defense mechanisms that dispose of peroxides and protect against oxidative damage. Cultured brain cells have been used frequently to investigate peroxide metabolism of neural cells. Efficient disposal of exogenous hydrogen peroxide was found for cultured astrocytes, oligodendrocytes, microglial cells, and neurons. Comparison of specific peroxide clearance rates revealed that cultured oligodendrocytes dispose of the peroxide quicker than the other neural cell cultures. Both catalase and the glutathione system contribute to the clearance of hydrogen peroxide by brain cells. For efficient glutathione‐dependent reduction of peroxides, neural cells contain glutathione in high concentration and have substantial activity of glutathione peroxidase, glutathione reductase, and enzymes that supply the NADPH required for the glutathione reductase reaction. This article gives an overview on the mechanisms involved in peroxide detoxification in brain cells and on the capacity of the different types of neural cells to dispose of peroxides. © 2004 Wiley‐Liss, Inc.

Từ khóa


Tài liệu tham khảo

10.1007/BF03160100

10.1016/S0076-6879(84)05016-3

10.1016/S0197-0186(03)00133-5

10.1016/S1096-4959(02)00107-0

10.1016/B978-0-12-152829-4.50008-2

10.1038/nrd1330

10.1523/JNEUROSCI.3989-03.2004

10.1159/000112127

10.1046/j.1471-4159.1996.66062329.x

10.1016/1357-2725(95)00080-9

10.1111/j.1471-4159.1982.tb08637.x

Clarke DD, 1999, Basic neurochemistry: molecular, cellular, and medical aspects, 637

Cooper AJL, 1997, The molecular and genetic basis of neurological disease, 1195

10.1046/j.1471-4159.2001.00535.x

10.1074/jbc.273.35.22528

10.1016/S0301-0082(99)00060-X

10.1016/S0076-6879(02)48646-6

10.1016/S0006-8993(97)00233-3

10.1515/BC.2003.059

10.1016/S1385-299X(97)00047-0

10.1002/(SICI)1098-1136(199806)23:2<139::AID-GLIA5>3.0.CO;2-1

10.1046/j.1471-4159.1999.0722523.x

10.1023/A:1020261600498

10.1006/exnr.2002.7927

10.1006/nbdi.1997.0127

10.1146/annurev.bi.64.070195.000525

10.1074/jbc.M206835200

10.1046/j.1471-4159.1999.0731422.x

Halliwell B, 1999, Free radicals in biology and medicine

10.1159/000017464

10.1016/S1385-299X(99)00023-9

10.1046/j.1471-4159.2001.00101.x

10.1046/j.1471-4159.2002.00999.x

10.1074/jbc.272.26.16644

10.1016/S0891-5849(00)00214-8

10.1016/0006-8993(95)00209-9

10.1016/0006-8993(94)01291-O

10.2174/0929867033456477

10.1002/ana.10483

10.1074/jbc.M010120200

10.1002/(SICI)1096-9861(19960916)373:2<157::AID-CNE1>3.0.CO;2-2

10.1016/S0891-5849(02)00855-9

10.1111/j.1471-4159.1993.tb03309.x

10.1046/j.1471-4159.1999.0731246.x

10.1016/S0891-5849(02)00815-8

10.1016/j.neulet.2004.04.042

10.1016/j.bbrc.2004.03.075

10.2165/00002512-200421020-00002

10.1046/j.1471-4159.2003.01871.x

10.1136/jcp.57.1.6

10.1016/S0161-813X(03)00095-0

10.1002/(SICI)1098-1136(199910)28:1<13::AID-GLIA2>3.0.CO;2-L

10.1016/S0002-9440(10)64249-6

10.1016/S0304-3940(00)01369-0

10.1007/s002040000206

10.1007/BF00965842

10.1177/002215540305100606

10.1046/j.1432-1327.2000.01595.x

10.1016/S0304-3940(00)01689-X

10.2307/1543355

10.1016/0076-6879(95)52007-4

10.1046/j.1471-4159.1998.71020844.x

10.1016/S0304-3940(99)00748-X

10.1046/j.1471-4159.1999.0732501.x

10.1046/j.1471-4159.1999.0731549.x

10.1093/jnen/59.1.53

10.1074/jbc.M308143200