Intrarenal Renin-Angiotensin-System Dysregulation after Kidney Transplantation.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
05 07 2019
Historique:
received: 21 01 2019
accepted: 17 06 2019
entrez: 7 7 2019
pubmed: 7 7 2019
medline: 23 10 2020
Statut: epublish

Résumé

Angiotensin-converting enzyme inhibitors (ACEis) are beneficial in patients with chronic kidney disease (CKD). Yet, their clinical effects after kidney transplantation (KTx) remain ambiguous and local renin-angiotensin system (RAS) regulation including the 'classical' and 'alternative' RAS has not been studied so far. Here, we investigated both systemic and kidney allograft-specific intrarenal RAS using tandem mass-spectrometry in KTx recipients with or without established ACEi therapy (n = 48). Transplant patients were grouped into early (<2 years), intermediate (2-12 years) or late periods after KTx (>12 years). Patients on ACEi displayed lower angiotensin (Ang) II plasma levels (P < 0.01) and higher levels of Ang I (P < 0.05) and Ang-(1-7) (P < 0.05) compared to those without ACEi independent of graft vintage. Substantial intrarenal Ang II synthesis was observed regardless of ACEi therapy. Further, we detected maximal allograft Ang II synthesis in the late transplant vintage group (P < 0.005) likely as a consequence of increased allograft chymase activity (P < 0.005). Finally, we could identify neprilysin (NEP) as the central enzyme of 'alternative RAS' metabolism in kidney allografts. In summary, a progressive increase of chymase-dependent Ang II synthesis reveals a transplant-specific distortion of RAS regulation after KTx with considerable pathogenic and therapeutic implications.

Identifiants

pubmed: 31278281
doi: 10.1038/s41598-019-46114-x
pii: 10.1038/s41598-019-46114-x
pmc: PMC6611786
doi:

Substances chimiques

Angiotensin-Converting Enzyme Inhibitors 0
Biomarkers 0
Peptide Fragments 0
Angiotensin II 11128-99-7
Angiotensin I 9041-90-1
Renin EC 3.4.23.15
angiotensin I (1-7) IJ3FUK8MOF

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

9762

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Auteurs

Johannes J Kovarik (JJ)

Department of Internal Medicine III, Clinical Division of Nephrology and Dialysis, Medical University of Vienna, Vienna, Austria.

Christopher C Kaltenecker (CC)

Department of Internal Medicine III, Clinical Division of Nephrology and Dialysis, Medical University of Vienna, Vienna, Austria.

Chantal Kopecky (C)

Department of Internal Medicine III, Clinical Division of Nephrology and Dialysis, Medical University of Vienna, Vienna, Austria.
School of Medical Sciences, Faculty of Medicine, University of New South Wales, Sydney, Australia.

Oliver Domenig (O)

Department of Internal Medicine III, Clinical Division of Nephrology and Dialysis, Medical University of Vienna, Vienna, Austria.
Attoquant Diagnostics GmbH, Vienna, Austria.

Marlies Antlanger (M)

Department of Internal Medicine III, Clinical Division of Nephrology and Dialysis, Medical University of Vienna, Vienna, Austria.

Johannes Werzowa (J)

Ludwig Boltzmann Institute of Osteology at the Hanusch Hospital, Vienna, Austria.

Farsad Eskandary (F)

Department of Internal Medicine III, Clinical Division of Nephrology and Dialysis, Medical University of Vienna, Vienna, Austria.

Renate Kain (R)

Clinical Institute of Pathology, Medical University of Vienna, Vienna, Austria.

Marko Poglitsch (M)

Attoquant Diagnostics GmbH, Vienna, Austria.

Sabine Schmaldienst (S)

Department of Internal Medicine I Kaiser-Franz-Josef-Spital, Vienna, Austria.

Georg A Böhmig (GA)

Department of Internal Medicine III, Clinical Division of Nephrology and Dialysis, Medical University of Vienna, Vienna, Austria.

Marcus D Säemann (MD)

Department of Medicine VI with Nephrology and Dialysis, Wilhelminen Hospital, Vienna, Austria. saemannmarcus@gmail.com.
Sigmund Freud University, Medical School, Vienna, Austria. saemannmarcus@gmail.com.

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