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Increased transcription and activity of glutathione synthase in response to deficiencies in folate, vitamin E, and apolipoprotein E
Author(s) -
Tchantchou Flaubert,
Graves Michael,
Ashline David,
Morin Amy,
Pimenta Aurea,
Ortiz Daniela,
Rogers Eugene,
Shea Thomas B.
Publication year - 2004
Publication title -
journal of neuroscience research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.72
H-Index - 160
eISSN - 1097-4547
pISSN - 0360-4012
DOI - 10.1002/jnr.10867
Subject(s) - glutathione , chemistry , biochemistry , transcription (linguistics) , enzyme , philosophy , linguistics
Oxidative stress is a major contributing factor in neurodegeneration and can arise from dietary, environmental, and genetic sources. Here we examine the separate and combined impact of deprivation of folate and vitamin E, coupled with dietary iron as a prooxidant, on normal mice and transgenic mice lacking apolipoprotein E (ApoE–/– mice). Both mouse strains exhibited increased levels of glutathione when deprived of folate and vitamin E, but a substantial further increase was observed in ApoE–/– mice. To determine the mechanism(s) underlying this increase, we quantified transcription and activity of glutathione synthase (GS). Both normal and ApoE–/– mice demonstrated increased GS activity when deprived of folate and vitamin E. However, transcription was increased only in ApoE–/– mice deprived of folate and vitamin E. These findings demonstrate that deficiency in one gene can result in compensatory up‐regulation in a second relevant gene and, furthermore, indicate that compensation for oxidative stress can occur in brain tissue at epigenetic and genetic levels depending on the nature and/or extent of oxidative stress. © 2004 Wiley‐Liss, Inc.