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  PGE2 regulates cholecystokinin-octapeptide (CCK-8)-stimulated Cl conductance in isolated zymogen granules from rat pancreas

Plusczyk, T., Piiper, A., & Schulz, I. (1991). PGE2 regulates cholecystokinin-octapeptide (CCK-8)-stimulated Cl conductance in isolated zymogen granules from rat pancreas. FEBS Letters, 295(1), 89-92. doi:10.1016/0014-5793(91)81392-l.

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 Creators:
Plusczyk, Thorsten1, Author           
Piiper, Albrecht1, Author           
Schulz, Irene1, Author           
Affiliations:
1Department of Physiology, Max Planck Institute of Biophysics, Max Planck Society, ou_2068297              

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Free keywords: Signal transduction; Indomethacin; Protein kinase A inhibitor
 Abstract: In this study we have examined the effects of prostaglandin E2 (PGE2), the cyclooxygenase inhibitor, indomethacin, and a protein kinase A inhibitor (PKA‐I) on the Cl conductance in isolated zymogen granules (ZG) from cholecystokinin octapeptide (CCK‐8) pre‐stimulated pancreatic acini. The Cl conductance in isolated ZG from CCK‐8 pre‐stimulated rat pancreatic acini increases with increasing CCK‐8 concentrations and decreases at supramaximal CCK‐8 concentrations. The basal and CCK‐8‐stimulated Cl conductance in ZG is inhibited by pretreatment of acini with PGE2 (10−6 M). This PGE2‐induced inhibition is abolished in the presence of PKA‐I (20 U/ml). Furthermore, pretreatment of acini with indomethacin (10−5 M) or PKA‐I (20 U/ml) abolishes the decrease in the Cl conductance at supramaximal CCK‐8 concentrations (10−9 M). We conclude that the inhibition of the Cl conductance in isolated ZG at high CCK‐8 concentrations is mediated by an enhanced production of PGE2, and that PGE2 operates by stimulating adenylate cyclase (AC) with a consequent rise in cAMP and activation of PKA.

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Language(s): eng - English
 Dates: 1991-10-212002-07-191991-12-16
 Publication Status: Issued
 Pages: 4
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1016/0014-5793(91)81392-l
PMID: 1722467
 Degree: -

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Title: FEBS Letters
  Other : FEBS Lett.
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: Amsterdam : Elsevier
Pages: - Volume / Issue: 295 (1) Sequence Number: - Start / End Page: 89 - 92 Identifier: ISSN: 0014-5793
CoNE: https://pure.mpg.de/cone/journals/resource/954925399501