Time-dependent Actions of Corticosterone on Infralimbic Cortex Pyramidal Neurons of Adult Male Rats.

Abstract

Responses to acute stress function to restore homeostasis. Hence, the study of neurophysiological responses to acute stress helps to understand mechanisms underlying adaptive coping in the face of environmental demands. The infralimbic medial prefrontal cortex (IL-mPFC) modulates the switch between behavioral coping styles, and acute stress enhances glutamatergic neurotransmission on mPFC projection neurons. However, the role of acute stress responses and stress hormones on the physiology of IL-mPFC projection neurons during adulthood remains underexplored. Here, we studied rapid and slow effects of acute corticosterone exposure on synaptic transmission and intrinsic membrane excitability in layer 5 pyramidal neurons of the IL (L5-IL PNs) in adult male rats using ex vivo whole-cell patch-clamp of mPFC slices. We report that corticosterone dynamically modulates the physiology of L5-IL PNs in a time-dependent manner. Specifically, corticosterone elicits a strong rapid shift of the excitatory-inhibitory balance towards enhanced excitation with mineralocorticoid (MR) and glucocorticoid receptors (GR) playing complementarily roles. Also, corticosterone rapidly and transently decreases the firing rate of L5-IL PNs via GR. Moreover, acute stress or corticosterone slowly enhance glutamatergic neurotransmission via MR and GR without modulating inhibitory neurotransmission or intrinsic excitability of adult L5-IL PNs. Our findings highlight the potential relevance of corticosterone effects on L5-IL PNs to promote a homeostatic response in adult male rats. First, corticosterone rapidly attenuates IL intrinsic excitability during the rapid initial phase of the acute stress response. Later on, corticosterone slowly restores IL output function over time to promote adaptive executive responses when context changes.Significance statement Corticosterone modulates physiological processes during stress to support adaptation. However, acute effects of corticosterone on stress control networks remains underexplored. Here, we explored mechanisms underlying corticosterone regulation of the activity of stress regulatory neurons of the infralimbic cortex (IL). Stress levels of corticosterone rapidly shift the excitatory-inhibitory balance of synaptic transmission towards enhanced excitation while diminishing firing of IL excitatory long-range neurons (IL PNs). Slow, lasting effects of corticosterone primarily target excitatory synaptic activity. Synaptic actions of glucocorticoids are cooperatively mediated by the mineralocorticoid (MRs) and glucocorticoid receptors (GRs), whereas the transient reduction in firing relies on GR in IL PNs. Thus, corticosterone provides an adaptive signal that controls IL output over time, promoting adaptive responses to environmental context.