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Endothelin-3 applied to the brain evokes opposite effects on bile secretion mediated by a central nitric oxide pathway

  • Myrian R. Rodríguez
    ,
  • María E. Sabbatini
    ,
  • Gisela Santella
    ,
  • Paula Dabas
    ,
  • Alberto Villagra
    ,
  • Marcelo S. Vatta
*Corresponding author for this work
  • Universidad de Buenos Aires
Scholary Output:
Contribution to journal
Article
Peer-review

Abstract

We sought to establish Endothelin (ET-3) role in the central regulation of bile secretion in the rat. The intracerebroventricular (icv) injection of ET-3 evoked a cholestatic or a choleretic effect depending on the administered dose. Lower doses increased bile flow and bicarbonate excretion, whereas higher doses decreased bile flow and bile acid output. ET-3 effects were dependent on brain nitric oxide and independent of the autonomic nervous system or hemodynamic variations. A selective ETB antagonist abolished the cholestatic effect, whereas the choleretic effect was totally inhibited by either ET A or ETB selective blockade. These results show that ET-3 applied to the brain modified through a nitric oxide pathway distinct bile flow fractions depending on the administered dose and give further insights into the complexity of brain-liver interaction.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 1219-1227 (9 pages)

Journal (Volume, Issue Number)

Peptides (Volume 26, Issue 7)

Publication milestones

  • Published - 07/2005

Publication status

Published - 07/2005

ISSN

0196-9781

Publication IDs

  • Scopus: 20444391007
  • PubMed: 15949640
  • ORCID: /0000-0001-7100-2482/work/58927569

Publication metrics

Metrics

Scopus
citations
Fractional count
1
Fractional count
0.14
Fractional count
6
Fractional count
0.86
Fractional count
1
Fractional count
1
SciVal
Author count
7
SciVal
citations
4
SciVal
Paper percentile
48

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Captures
15
Citation count
4

Funding Details

This work was supported by grants from the University of Buenos Aires (UBACYT B420 and UBACYT B079).
FundersFunding numbers
UBA
-
UBACyT
B079, B420