Age-related changes in tonic activation of presynaptic versus extrasynaptic γ-amniobutyric acid type B receptors in rat medial prefrontal cortex

• Published in: Neurobiology of aging 2016-09, Vol.45, p.88-97
• Main Authors: Carpenter, Haley E., Kelly, Kyle B., Bizon, Jennifer L., Frazier, Charles J.
• Format: Article
• Language: English
• Subjects: Age-related cognitive decline; Aging - metabolism; Aging - psychology; Animals; Beclomethasone; Cognition; Executive Function; GABAA; GABAB; gamma-Aminobutyric Acid - physiology; L2/3 pyramidal neurons; Male; Neural Inhibition; Patch-Clamp Techniques; Prefrontal cortex; Prefrontal Cortex - metabolism; Pyramidal Cells - physiology; Rats, Inbred F344; Receptors, GABA - metabolism; Receptors, GABA-B - metabolism; Receptors, GABA-B - physiology; Receptors, Presynaptic - metabolism; Signal Transduction - physiology; Working memory
• ISSN: 0197-4580; 1558-1497
• DOI: 10.1016/j.neurobiolaging.2016.05.015

The present study examined the effect of age on both glutamatergic and γ-aminobutyric acid mediated (GABAergic) signaling in the rodent medial prefrontal cortex (mPFC), with an emphasis on revealing novel changes contributing to increased inhibition in age. Whole-cell patch clamp recordings were obtained from layer 2/3 mPFC pyramidal neurons in acute cortical slices prepared from either young (4 months) or aged (20–24 months) male F344 rats. Results indicated that GABAB receptors on GABAergic, but not on glutamatergic, inputs to layer 2/3 pyramidal cells are tonically activated by ambient GABA in young animals and further demonstrated that this form of tonic inhibition is significantly attenuated in aged mPFC. Moreover, concurrent with loss of tonic presynaptic GABAB autoreceptor activation, layer 2/3 pyramidal cells in aged mPFC are subjected to increased tonic activation of extrasynaptic GABAA and GABAB receptors. These data demonstrate a shift in the site of GABAB receptor-mediated inhibitory tone in the aged mPFC that clearly promotes increased inhibition of pyramidal cells in aged animals, and that may plausibly contribute to impaired executive function.