Intrarenal Renin-Angiotensin-System Dysregulation after Kidney Transplantation.
Adult
Angiotensin I
/ blood
Angiotensin II
/ blood
Angiotensin-Converting Enzyme Inhibitors
/ pharmacology
Biomarkers
Enzyme Activation
/ drug effects
Female
Gene Expression Regulation, Enzymologic
Humans
Kidney
/ metabolism
Kidney Transplantation
/ adverse effects
Male
Middle Aged
Models, Biological
Peptide Fragments
/ blood
Postoperative Complications
Renin
/ blood
Renin-Angiotensin System
/ drug effects
Journal
Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288
Informations de publication
Date de publication:
05 07 2019
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
9762Références
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