Key result
Treatment with the ACE2 activator diminazene aceturate improved renal function and tissue damage in rats with gentamicin-induced acute kidney injury by increasing Ang-(1-7) and ACE2 activity.
Why the study?
The renin-angiotensin system plays a deleterious role in acute kidney injury progression, prompting evaluation of the therapeutic effects of the ACE2 activator diminazene aceturate in gentamicin-induced acute kidney injury.
Does diminazene aceturate improve renal function and tissue damage in rats with gentamicin-induced acute kidney injury?
Does diminazene aceturate improve renal function and tissue damage in rats with gentamicin-induced acute kidney injury?
ACE2 activation with diminazene aceturate shows potential as a strategy for treating acute kidney injury by improving renal function and reducing tissue damage in a rat model.
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-α. These results corroborate with a raising potential of ACE2 activation as a strategy for treating AKI.
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Almeida et al. (2020) studied Acute Kidney Injury (AKI). Diminazene aceturate (DIZE) was evaluated on Renal function and tissue damage. Treatment with the ACE2 activator diminazene aceturate improved renal function and tissue damage in rats with gentamicin-induced acute kidney injury by increasing Ang-(1-7) and ACE2 activity.
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