Stress signalling pathways that impair prefrontal cortex structure and function

Abstract

The prefrontal cortex (PFC) - the most evolved brain region - subserves our highest-order cognitive abilities. However, it is also the brain region that is most sensitive to the detrimental effects of stress exposure. Even quite mild acute uncontrollable stress can cause a rapid and dramatic loss of prefrontal cognitive abilities, and more prolonged stress exposure causes architectural changes in prefrontal dendrites. Recent research has begun to reveal the intracellular signalling pathways that mediate the effects of stress on the PFC. This research has provided clues as to why genetic or environmental insults that disinhibit stress signalling pathways can lead to symptoms of profound prefrontal cortical dysfunction in mental illness.

Figures

Figure 1. Spatial working memory networks in the dorsolateral prefrontal cortex

a | The oculomotor delayed response (ODR) task is a spatial working memory task that is used to probe the physiological profiles of prefrontal cortex (PFC) neurons. The subject must remember the spatial position of the most recent cue over a delay period of several seconds and then indicate that position with a saccade to the memorized location. b | The region of the monkey dorsolateral PFC (Walker’s area 46) where neurons show persistent, spatially tuned firing during the delay period in the ODR task. c | An example of a PFC neuron that showed persistent firing during the delay period if the cue had occurred at 90° — the ‘preferred direction’ for this neuron (left middle plot) — but not if the cue appeared in a ‘non-preferred’ direction (other plots). The rasters show the firing of the neuron over seven trials at each spatial position. d | A schematic drawing of the PFC microcircuits that underlie spatial working memory as described by Goldman-Rakic. Layer III pyramidal cells receive highly processed spatial information (represented by the green lines) from parietal association cortices. Pyramidal cells with similar spatial characteristics engage in recurrent excitation to maintain persistent activity over the delay period (note that the subcellular localization of these excitatory connections is not currently known; they could be on the apical and/or basal dendrites). GABA (γ-aminobutyric acid)-ergic interneurons, such as basket cells (B) and chandelier cells (C) help to spatially tune neurons through lateral inhibition. Inputs from cross-directional microcircuits (neurons with different tuning characteristics) are shown in grey. AS, arcuate sulcus; PS, principal sulcus. Parts a–c are modified, with permission, from REF. ©(2007) Cell Press.

Figure 2. Catecholamine influences on prefrontal cortex physiology and function

Both noradrenaline (NA, part a) and dopamine (DA, part b) have ‘inverted U-shaped’ influences on prefrontal cortex (PFC) physiology and cognition, whereby either too little or too much of the neurotransmitter impairs PFC function. In an oculomotor delayed response task, with optimal levels of NA or DA release under alert, non-stressed conditions (top of the curves), PFC neurons fire (as shown in the green traces) during the delay period following cues for preferred but not non-preferred directions. NA enhances delay-related firing in response to cues in preferred directions by stimulating α2A-receptors (increasing the ‘signal’), whereas DA weakens delay-related firing in response to cues in non-preferred directions by stimulating D1 receptors (decreasing the ‘noise’). Administration of appropriate concentrations of the α2A-receptor agonist guanfacine or the D1 receptor agonist SKF81297 also has this effect. With high levels of NA release during stress (right side of the curve), NA engages the lower-affinity α1-receptors and so reduces neuronal firing. Similarly, excessive D1 receptor stimulation during stress suppresses cell firing. Administration of the α1-receptor agonist phenylephrine or a high concentration of SKF81297 can mimick the effects of high NA and DA levels, respectively. In each graph, the dotted lines indicate the transition between (from left to right) the fixation period, the cue period, the delay period and the oculomotor response period.

Figure 3. Intracellular signalling pathways that impair prefrontal cortex working memory functions during stress

Intracellular signalling pathways activated by stress exposure have feedforward interactions that rapidly impair prefrontal cortex (PFC) cognitive function. High levels of dopamine (DA) D1 receptor stimulation (and probably noradrenaline (NA) β1-receptor stimulation as well) activate adenylyl cyclases (ACs) to produce cyclic AMP. cAMP opens hyperpolarization-activated cyclic nucleotide-gated cation channels (HCN channels) on dendritic spines to produce the h current (Ih), which weakens network inputs and decreases delay-related firing. High levels of NA also stimulate α1-receptors, which activate phosphatidylinositol biphosphate (PIP2)–protein kinase C (PKC) signalling. Subsequent inositol-1,4,5-trisphosphate (InsP3)-mediated Ca2+ release has been shown to reduce PFC cell firing by opening SK channels, leading to a current (ISK), and has been shown to maintain firing through the depolarizing current ICAN. ICAN can be reduced by PKC and cAMP, such that the suppressive effects of ISK probably predominate under conditions of stress. The two signalling pathways interact to potentiate each other’s actions (dotted arrows); for example, cAMP can potentiate InsP3-medicated Ca2+ release through protein kinase A-mediated phosphorylation of InsP3 receptors. Conversely, Ca2+ can activate many isoforms of AC to generate more cAMP. Glucocorticoids might also activate these pathways (see main text). Enzymes that normally provide the molecular brakes on these stress signalling pathways (disrupted in schizophrenia 1 (DISC1), regulator of G-protein signalling 4 (RGS4) and DAG kinase (DGK)) are often genetically altered in families with serious mental illness, thus increasing susceptibility to stress exposure. Note that the cAMP and PKC signalling pathways have also been shown to be activated in the amygdala during stress, where they strengthen long-term memory consolidation and fear conditioning. DAG, diacyglycerol; PDE4B, phosphodiesterase 4B.

Figure 4. A working model showing how prefrontal cortex pyramidal cell activity might be regulated under optimal versus stress conditions

a | The efficacy of network inputs onto dendritic spines of the apical and/or basal dendrites is dynamically regulated by cyclic AMP–hyperpolarization-activated cyclic nucleotide-gated cation channel (HCN channel) signalling. Under optimal conditions, appropriate network connections are strengthened by α2A-receptor inhibition of cAMP–HCN channel signalling, whereas inappropriate network connections are weakened by dopamine D1 receptor activation of cAMP–HCN channel signalling. The small volume of the spine compartment probably allows very localized regulation of nearby HCN channels. The resulting specific pattern of network connectivity allows accurate representation of the cue’s spatial position in the oculomotor delayed response task, and the breadth of connectivity can be dynamically regulated based on current cognitive demands. b | HCN channels on the plasma membrane of dendritic shafts probably regulate excitability. They might not be open when the dendrite is depolarized by large numbers of excitatory network connections. c | Under optimal conditions, the cell body probably receives network signals and fires accordingly. d | Under optimal conditions the PFC shows highly patterned activity, whereby specific subsets of neurons are active to represent the precise spatial position of a stimulus. This is denoted in the figure, in which only the microcircuit representing 90° is active. Note that interneurons are not shown in this diagram for the sake of clarity. Network inputs are shown on the apical dendrites, but they might actually be on basal dendrites. Red circles represent α2A-receptor strengthening of network inputs; grey circles represent D1 receptor–cAMP weakening of a network connection. e | Under conditions of stress, high levels of cAMP open HCN channels throughout the dendrite, weakening all network connections. f | With loss of network excitatory inputs the dendrite might hyperpolarize, and HCN channels on dendritic shafts might open to help maintain dendritic excitability. HCN channel opening would also reduce the effectiveness of inputs onto the distal portions of the dendrite. g | High levels of phosphatidylinositol signalling during stress would increase inositol-1,4,5-trisphosphate (InsP3)-mediated waves of intracellular Ca2+ release. When the Ca2+ waves invade the soma, they open small-conductance, Ca2+-activated K+ channels (SK channels) and reduce cell firing. h | Under stressful conditions, network connections are weakened (grey circles) and, as a result, network firing is reduced and unpatterned. Thus, prefrontal cortex neurons are unable to accurately represent information in working memory. Unpatterned, generalized activity might serve another function — for example, stimulating stress pathways in the brainstem.

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