Hiring in life sciences? Share your open positions with our professional community. Read more Close

Advertisement

Cholecystokinin Induces Ca2+ Transients in Brainstem Neurons, Astrocytes and Central Vagal Terminals in Jugular/Nodose Ganglia-Brainstem Slice Cultures.

Created on 11 Sep 2026

Authors

Adam Ujhelyi, Rana Soylu Kucharz, Jens Christian Rekling

Published in

The European journal of neuroscience. Volume 64. Issue 5. Pages e70686.

Abstract

Cholecystokinin is a well-established neuromodulator of brainstem homeostatic circuits, including circuits implicated in satiety and visceral sensation. To better understand the cellular basis of brainstem cholecystokinin signalling, we developed a novel jugular/nodose ganglion-brainstem slice culture, where microdissection isolated bilateral jugular/nodose ganglia attached to a slice of the brainstem via intact vagal rootlets. This preparation preserves the functional vagal afferent pathway to the nucleus of the tractus solitarius and allows for targeted viral transduction of genetically encoded Ca2+ indicators. We show that electrical jugular/nodose ganglion stimulation evokes glutamate-driven Ca2+ transients in second-order brainstem neurons, confirming functional connectivity. Using nuclear-targeted Ca2+ imaging, we demonstrate that cholecystokinin directly activates a specific subpopulation of neurons in the dorsal and ventrolateral medulla, independent of action potential generation. Furthermore, we identify distinct populations of central vagal terminals: those recruited by electrical stimulation of the jugular/nodose ganglion and a separate subpopulation directly activated by cholecystokinin. Multiplex imaging revealed that cholecystokinin and Substance P triggered robust Ca2+ waves in brainstem astrocytes, and muscarine and thyrotropin-releasing hormone selectively activate neuronal populations without recruiting astrocytic networks. Finally, we found that the jugular/nodose ganglion-brainstem slice cultures generate spontaneous respiratory-like rhythmic bursting in the preBötzinger Complex, with a frequency significantly increased by cholecystokinin. Together, these findings establish jugular/nodose ganglion-brainstem slice cultures as a powerful model for dissecting the complex neuro-astrocytic circuitry of cholecystokinin signalling in the brainstem.

PMID:
42723213
Bibliographic data and abstract were imported from PubMed on 11 Sep 2026.

Read full publication at:
Please sign in to see all details.

Advertisement

Stats

  • Community rating n/a 0 votes
  • Reviewers' rating n/a 0 votes
  • Your rating

1-terrible, 9-excellent. How would you rate this publication? Sign in in to submit your rating.

  • Recommendations n/a n/a positive of 0 vote(s)
  • Views 7
  • Comments 0

Recommended by

  • No recommendations yet.

Post a comment

You need to be signed in to post comments. You can sign in here.

Comments

There are no comments yet.

Advertisement