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ACE2 activator diminazene aceturate exerts renoprotective effects in gentamicin-induced acute renal injury in rats.

Authors :
Silva de Almeida, Tatiane Cristine
Lanza, Katharina
da Silva Filha, Roberta
Campos, Leda Maria de Castro C.
Fonseca, Esdras G.
Chagas, Mariana W.
Pessoa Rocha, Natalia
Augusto de Sá, Marcos
Ribeiro Vieira, Maria Aparecida
Vidigal Caliari, Marcelo
Kangussu, Lucas M.
José Ferreira, Anderson
Simões e Silva, Ana Cristina
Source :
Clinical Science. Dec2020, Vol. 134 Issue 23, p3093-3106. 14p.
Publication Year :
2020

Abstract

Acute Kidney Injury (AKI) comprises a rapidly developed renal failure and is associated with high mortality rates. The Renin-Angiotensin System (RAS) plays a pivotal role in AKI, as the over-active RAS axis exerts major deleterious effects in disease progression. In this sense, the conversion of Angiotensin II (Ang II) into Angiotensin-(1-7) (Ang-(1-7)) by the Angiotensin-converting enzyme 2 (ACE2) is of utmost importance to prevent worse clinical outcomes. Previous studies reported the beneficial effects of oral diminazene aceturate (DIZE) administration, an ACE2 activator, in renal diseases models. In the present study, we aimed to evaluate the therapeutic effects of DIZE administration in experimental AKI induced by gentamicin (GM) in rats. Our findings showed that treatment with DIZE improved renal function and tissue damage by increasing Ang-(1-7) and ACE2 activity, and reducing TNF-a. These results corroborate with a raising potential of ACE2 activation as a strategy for treating AKI. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01435221
Volume :
134
Issue :
23
Database :
Academic Search Index
Journal :
Clinical Science
Publication Type :
Academic Journal
Accession number :
147666111
Full Text :
https://doi.org/10.1042/CS20201022