Amygdala-liver signaling orchestrates rapid glycemic responses to stress and drives stress-induced metabolic dysfunction.
Sarah A StanleyKavya DevarakondaRichard O'ConnorMaria Jimenez-GonzalezAlexandra AlvarssonRollie F HamptonDiego EspinozaRosemary LiAbigail ShteklerKaetlyn ConnerMitchell BayneDarline GaribayJessie MartinVanessa LehmannLiheng WangPaul J KennyPublished in: Research square (2024)
Behavioral adaptations to environmental threats are crucial for survival and necessitate rapid deployment of energy reserves. The amygdala coordinates behavioral adaptations to threats, but little is known about its involvement in underpinning metabolic adaptations. Here, we show that acute stress activates medial amygdala (MeA) neurons that innervate the ventromedial hypothalamus (MeAVMH neurons), which precipitates hyperglycemia and hypophagia. The glycemic actions of MeAVMH neurons occur independent of adrenal or pancreatic glucoregulatory hormones. Instead, using whole-body virus tracing, we identify a polysynaptic connection from MeA to the liver, which promotes the rapid synthesis of glucose by hepatic gluconeogenesis. Repeated stress exposure disrupts MeA control of blood glucose and appetite, resulting in diabetes-like dysregulation of glucose homeostasis and weight gain. Our findings reveal a novel amygdala-liver axis that regulates rapid glycemic adaptations to stress and links recurrent stress to metabolic dysfunction.
Keyphrases
- stress induced
- blood glucose
- type diabetes
- glycemic control
- functional connectivity
- weight gain
- prefrontal cortex
- spinal cord
- high intensity
- resting state
- body mass index
- cardiovascular disease
- loop mediated isothermal amplification
- weight loss
- blood pressure
- risk assessment
- single cell
- insulin resistance
- dna methylation
- heat stress
- diabetic rats
- preterm birth