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Acute hypoxia differentially affects the γ‐aminobutyric acid type A receptor α 1 , α 2 , β 2 , and γ 2 subunit mRNA levels in the developing chick optic tectum: Stage‐dependent sensitivity
Author(s) -
Plazas Sara Fiszer de,
Rapacioli Melina,
Gil Diego J. Rodríguez,
Vacotto Marina,
Flores Vladimir
Publication year - 2007
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.21418
Subject(s) - hypoxia (environmental) , protein subunit , messenger rna , biology , receptor , endocrinology , medicine , microbiology and biotechnology , chemistry , biochemistry , gene , organic chemistry , oxygen
This investigation analyzes the effect of an acute hypoxic treatment on the level of four (α 1 , α 2 , β 2 , and γ 2 ) subunit mRNAs of the GABA A receptor in layer “i” of the developing chick optic tectum. Our results show that 1 hr of normobaric acute hypoxia significantly changes the subunit mRNA levels. Different subunit mRNAs display different sensitivity to hypoxia: α 1 , β 2 , and γ 2 mRNAs are highly sensitive, whereas α 2 mRNA is almost not affected. The sensitivity of the mRNA levels to hypoxia is stage dependent. The mean percentages of variation produced by the hypoxia in the level of expression of the four subunits were 20% at ED12, 5% at ED16, and only 2% at ED18. These changes in the mean percentages of expression modify the probability of coexpression. In the case of double mRNA combinations, the hypoxia produced a mean variation in the probability of coexpression of 37% at ED12, 8% at ED16, and only 4% at ED18. With regard to the triple subunit mRNAs combinations, the variations were 206% at ED12, 11% at ED16, and only 7% at ED18. The quadruple combination values were 1,500% at ED12, 21% at ED16, and only 11% at ED18. This study demonstrates that the subunit mRNA levels are highly sensitive during the early stages, suggesting that GABA A receptor composition might undergo environment‐dependent plastic changes providing a high degree of plasticity to the GABA neurotransmitter system development. © 2007 Wiley‐Liss, Inc.