Cortical-brainstem circuitry attenuates stress reactivity

biorxiv(2023)

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摘要
Exposure to stressful stimuli promotes multi-system biological responses to restore homeostasis. Catecholaminergic neurons in the rostral ventrolateral medulla (RVLM) facilitate sympathetic activity and promote physiological adaptations, including glycemic mobilization and corticosterone release. While it is unclear how brain regions involved in the cognitive appraisal of stress regulate RVLM neural activity, recent studies found that the rodent ventromedial prefrontal cortex (vmPFC) mediates stress appraisal and physiological stress responses. Thus, a vmPFC-RVLM connection could represent a circuit mechanism linking stress appraisal and physiological reactivity. The current study investigated a direct vmPFC-RVLM circuit utilizing genetically-encoded anterograde and retrograde tract tracers. Together, these studies found that stress-reactive vmPFC neurons project to catecholaminergic neurons throughout the ventrolateral medulla in male and female rats. Next, we utilized optogenetic terminal stimulation to evoke vmPFC synaptic glutamate release in the RVLM. Photostimulating the vmPFC-RVLM circuit during restraint stress suppressed glycemic stress responses in males, without altering the female response. However, circuit stimulation decreased corticosterone responses to stress in both sexes. Circuit stimulation did not modulate affective behavior in either sex. Further analysis indicated that circuit stimulation preferentially activated non-catecholaminergic medullary neurons in both sexes. Additionally, vmPFC terminals targeted medullary inhibitory neurons. Thus, both male and female rats have a direct vmPFC projection to the RVLM that reduces endocrine stress responses, likely through the recruitment of local RVLM inhibitory neurons. Ultimately, the excitatory/inhibitory balance of vmPFC synapses in the RVLM may regulate stress reactivity as well as stress-related health outcomes. Significance Statement Stressors stemming from disease outbreaks, political unrest, and racial disparities continue to afflict individuals worldwide. Furthermore, these stressors increase risk for the development of psychiatric and cardiometabolic disorders. This study investigated a neural circuit capable of reducing physiological stress responses in both male and female rodents. Our investigation sheds light on a neural pathway that directly links cortical regions responsible for the cognitive and emotional evaluation of external stimuli with the bodily systems that promote energy mobilization and physiological adaptation. Such a neural circuit identifies biological underpinnings of brain-body connections and suggests that specific circuitry may be leveraged for therapeutic interventions. ![Figure][1] ### Competing Interest Statement The authors have declared no competing interest. [1]: pending:yes
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