4.7 Article

Neural Pathway for Gut Feelings: Vagal Interoceptive Feedback From the Gastrointestinal Tract Is a Critical Modulator of Anxiety-like Behavior

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BIOLOGICAL PSYCHIATRY
卷 92, 期 9, 页码 709-721

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ELSEVIER SCIENCE INC
DOI: 10.1016/j.biopsych.2022.04.020

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资金

  1. Swiss National Science Foundation [183899]
  2. National Institute of Diabetes and Digestive and Kidney Diseases [NIDDK R01 DK116004]
  3. Wallenberg Foundation (WCMTM)
  4. Swedish Research Council [2018-00660, 2021-01549]
  5. Novo Nordisk Foundation Excellence project grant
  6. Ragnar Soderberg Foundation
  7. Harald Jeanssons Stiftelse
  8. Greta Jeanssons Stiftelse
  9. Magnus Bergvalls Stiftelse
  10. Swedish Research Council [2021-01549, 2018-00660] Funding Source: Swedish Research Council

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Anxiety disorders are associated with altered perception of internal body state. Understanding the neuronal basis of interoception through the gastrointestinal tract can lead to novel therapies for anxiety. In rodents, vagal sensory signals from the gut regulate anxiety via the central amygdala, with GABAergic signaling playing a key role in males.
BACKGROUND: Anxiety disorders are associated with an altered perception of the body's internal state. Therefore, understanding the neuronal basis of interoception can foster novel anxiety therapies. In rodents, the feeding status bidirectionally modulates anxiety-like behavior but how the sensing of gastrointestinal state affects anxiety remains unclear.METHODS: We combined chemogenetics, neuropharmacology, and behavioral approaches in male and female rats to test whether vagal afferents terminating in the gastrointestinal tract mediate feeding-induced tuning of anxiety. Using saporin-based lesions and transcriptomics, we investigated the chronic impact of this gut-brain circuit on anxiety-like behavior.RESULTS: Both feeding and selective chemogenetic activation of gut-innervating vagal afferents increased anxiety -like behavior. Conversely, chemogenetic inhibition blocked the increase in anxiety-like behavior induced by feeding. Using a selective saporin-based lesion, we demonstrate that the loss of gut-innervating vagal afferent signaling chronically reduces anxiety-like behavior in male rats but not in female rats. We next identify a vagal circuit that connects the gut to the central nucleus of the amygdala, using anterograde transsynaptic tracing from the nodose ganglia. Lesion of this gut-brain vagal circuit modulated the central amygdala transcriptome in both sexes but selectively affected a network of GABA (gamma-aminobutyric acid)-related genes only in males, suggesting a potentiation of inhibitory control. Blocking GABAergic signaling in the central amygdala re-established normal anxiety levels in male rats. CONCLUSIONS: Vagal sensory signals from the gastrointestinal tract are critical for baseline and feeding-induced tuning of anxiety via the central amygdala in rats. Our results suggest vagal gut-brain signaling as a target to normalize interoception in anxiety disorders.

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