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Urotensin II acts as a modulator of mesopontine cholinergic neurons

  • Stewart D. Clark
  • , Hans Peter Nothacker
  • , Charles D. Blaha
  • , Christopher J. Tyler
  • , Dee M. Duangdao
  • , Stephen L. Grupke
  • , David R. Helton
  • , Christopher S. Leonard
  • , Olivier Civelli

Producción científica: Articlerevisión exhaustiva

20 Citas (Scopus)

Resumen

Urotensin II (UII) is a vasomodulatory peptide that was not predicted to elicit CNS activity. However, because we have recently shown that the urotensin II receptor (UII-R) is selectively expressed in rat mesopontine cholinergic (MPCh) neurons, we hypothesize that UII may have a central function. The present study demonstrates that the UII system is able to modulate MPCh neuron activity. Brain slice experiments demonstrate that UII excites MPCh neurons of the mouse laterodorsal tegmentum (LDTg) by activating a slow inward current. Furthermore, microinfusion of UII into the ventral tegmental area produces a sustained increase in dopamine efflux in the nucleus accumbens, as measured by in vivo chronoamperometry. In agreement with UII activation of MPCh neurons, intracerebroventricular injections of UII significantly modulate ambulatory movements in both rats and mice but do not significantly affect startle habituation or prepulse inhibition. The present study establishes that UII is a neuromodulator that may be exploited to target disorders involving MPCh dysfunction.

Idioma originalEnglish
Páginas (desde-hasta)139-148
Número de páginas10
PublicaciónBrain Research
Volumen1059
N.º2
DOI
EstadoPublished - oct 19 2005

Nota bibliográfica

Funding Information:
We thank our colleagues Rainer Reinscheid, Steven Lin and Zhiwei Wang for advice during the course of this project. This work was supported by grants from NIH (MH60231 (OC), DK63001 (OC), HL64150 (CSL), NS27881 (CSL)) and from the Stanley Research Foundation (03R-415 (OC)).

Financiación

We thank our colleagues Rainer Reinscheid, Steven Lin and Zhiwei Wang for advice during the course of this project. This work was supported by grants from NIH (MH60231 (OC), DK63001 (OC), HL64150 (CSL), NS27881 (CSL)) and from the Stanley Research Foundation (03R-415 (OC)).

FinanciadoresNúmero del financiador
Stanley Research Foundation03R-415
National Institutes of Health (NIH)NS27881, MH60231, DK63001
National Heart, Lung, and Blood Institute (NHLBI)R01HL064150

    ASJC Scopus subject areas

    • General Neuroscience
    • Molecular Biology
    • Clinical Neurology
    • Developmental Biology

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