Direkt zum Inhalt

Kurtz, Armin ; Della Bruna, R. ; Pfeilschifter, J. ; Bauer, Christian

Role of cGMP as second messenger of adenosine in the inhibition of renin release

Kurtz, Armin, Della Bruna, R., Pfeilschifter, J. und Bauer, Christian (1988) Role of cGMP as second messenger of adenosine in the inhibition of renin release. Kidney international 33 (4), S. 798-803.

Veröffentlichungsdatum dieses Volltextes: 08 Jan 2013 08:29
Artikel
DOI zum Zitieren dieses Dokuments: 10.5283/epub.26996


Zusammenfassung

Adenosine is known to be a potent inhibitor of renin release from the kidneys. The aim of this study was to investigate the transmembrane signalling avenue that the second messenger of adenosine causes inhibition of renal renin release. Using short term cultures of juxtaglomerular cells isolated from rat kidneys, we found that adenosine inhibited spontaneous renin release from these cells up to ...

Adenosine is known to be a potent inhibitor of renin release from the kidneys. The aim of this study was to investigate the transmembrane signalling avenue that the second messenger of adenosine causes inhibition of renal renin release. Using short term cultures of juxtaglomerular cells isolated from rat kidneys, we found that adenosine inhibited spontaneous renin release from these cells up to 40% of control, in a dose dependent fashion between 10(-10) M to 10(-6) M. Half maximal inhibition was observed at 2 X 10(-8) M adenosine. The inhibitory effect of adenosine on renin release could be mimicked by the A1-receptor agonist N6-cyclohexyladenosine (CHA) and could be attenuated by the A-receptor antagonist theophylline (5 X 10(-5) M). The A2-receptor agonist 5'-N-ethylcarboxamideadenosine (NECA) had no inhibitory effect on renin release. These findings indicate that the inhibitory effect of adenosine is mediated by A1-receptors on juxtaglomerular cells. Adenosine had no effect on either transmembrane calcium influx or the cytosolic free calcium concentration in the isolated juxtaglomerular cells. Adenosine also did not alter the cellular level of cyclic AMP in the concentration range employed. However, adenosine led to a dose dependent increase of the cellular level of cyclic GMP. Half maximal increase of cGMP was observed at 10(-8) M adenosine. The effect of adenosine on cyclic GMP could be mimicked by the A1-receptor agonist CHA and could be attenuated by the A-receptor antagonist, theophylline.(ABSTRACT TRUNCATED AT 250 WORDS)



Beteiligte Einrichtungen


Details

DokumentenartArtikel
Titel eines Journals oder einer ZeitschriftKidney international
Verlag:Wiley-Blackwell
Band:33
Nummer des Zeitschriftenheftes oder des Kapitels:4
Seitenbereich:S. 798-803
Datum1988
InstitutionenBiologie und Vorklinische Medizin > Institut für Physiologie > Prof. Dr. Armin Kurtz
Identifikationsnummer
WertTyp
2838680PubMed-ID
Klassifikation
NotationArt
Adenosine/physiologyMESH
AnimalsMESH
Calcium/metabolismMESH
Cells, CulturedMESH
Cyclic AMP/metabolismMESH
Cyclic GMP/physiologyMESH
Cytoplasm/metabolismMESH
Juxtaglomerular Apparatus/metabolismMESH
Kidney/metabolismMESH
RatsMESH
Renin/secretionMESH
Dewey-Dezimal-Klassifikation500 Naturwissenschaften und Mathematik > 570 Biowissenschaften, Biologie
600 Technik, Medizin, angewandte Wissenschaften > 610 Medizin
StatusVeröffentlicht
BegutachtetJa, diese Version wurde begutachtet
An der Universität Regensburg entstandenUnbekannt / Keine Angabe
URN der UB Regensburgurn:nbn:de:bvb:355-epub-269969
Dokumenten-ID26996

Bibliographische Daten exportieren

Nur für Besitzer und Autoren: Kontrollseite des Eintrags

nach oben