Sex- and age-related changes in GABA signaling components in the human cortex

Gamma-aminobutyric acid (GABA) is the primary inhibitory neurotransmitter in the nervous system. Previous studies have shown fluctuations in expression levels of GABA signaling components-glutamic acid decarboxylase (GAD), GABA receptor (GABAR) subunit, and GABA transporter (GAT)-with increasing age and between sexes; however, this limited knowledge is highly based on animal models that produce inconsistent findings. This study is the first analysis of the age- and sex-specific changes of the GAD, GABA(A B)R subunits, and GAT expression in the human primary sensory and motor cortices; superior (STG), middle (MTG), and inferior temporal gyrus (ITG); and cerebellum. Utilizing Western blotting, we found that the GABAergic system is relatively robust against sex and age-related differences in all brain regions examined. However, we observed several sex-dependent differences in GABA(A)R subunit expression in STG along with age-dependent GABA(A)R subunit and GAD level alteration. No significant age-related differences were found in alpha1, alpha2, alpha5, beta3, and gamma2 subunit expression in the STG. However, we found significantly higher GABA(A)R alpha3 subunit expression in the STG in young males compared to old males. We observed a significant sex-dependent difference in alpha1 subunit expression: males presenting significantly higher levels compared to women across all stages of life in STG. Older females showed significantly lower alpha2, alpha5, and beta3 subunit expression compared to old males in the STG. These changes found in the STG might significantly influence GABAergic neurotransmission and lead to sex- and age-specific disease susceptibility and progression.Gamma-aminobutyric acid (GABA) is the primary inhibitory neurotransmitter in the nervous system. Previous studies have shown fluctuations in expression levels of GABA signaling components-glutamic acid decarboxylase (GAD), GABA receptor (GABAR) subunit, and GABA transporter (GAT)-with increasing age and between sexes; however, this limited knowledge is highly based on animal models that produce inconsistent findings. This study is the first analysis of the age- and sex-specific changes of the GAD, GABA(A B)R subunits, and GAT expression in the human primary sensory and motor cortices; superior (STG), middle (MTG), and inferior temporal gyrus (ITG); and cerebellum. Utilizing Western blotting, we found that the GABAergic system is relatively robust against sex and age-related differences in all brain regions examined. However, we observed several sex-dependent differences in GABA(A)R subunit expression in STG along with age-dependent GABA(A)R subunit and GAD level alteration. No significant age-related differences were found in alpha1, alpha2, alpha5, beta3, and gamma2 subunit expression in the STG. However, we found significantly higher GABA(A)R alpha3 subunit expression in the STG in young males compared to old males. We observed a significant sex-dependent difference in alpha1 subunit expression: males presenting significantly higher levels compared to women across all stages of life in STG. Older females showed significantly lower alpha2, alpha5, and beta3 subunit expression compared to old males in the STG. These changes found in the STG might significantly influence GABAergic neurotransmission and lead to sex- and age-specific disease susceptibility and progression.