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A Novel Aldosterone Antagonist Limits Renal Injury in 5/6 Nephrectomy
Clarice K Fujihara1, M C Kowala2, M D Breyer2
1Faculty of Medicine, University of São Paulo, São Paulo, Brazil.
Abstract:
Aldosterone antagonists slow the progression of chronic kidney disease (CKD), but their use is limited by hyperkalemia, especially when associated with RAS inhibitors. We examined the renoprotective effects of Ly, a novel non-steroidal mineralocorticoid receptor (MR) blocker, through two experimental protocols: In Protocol 1, male Munich-Wistar rats underwent 5/6 renal ablation (Nx), being divided into: Nx+V, receiving vehicle, Nx+Eple, given eplerenone, 150 mg/kg/day, and Nx+Ly, given Ly, 20 mg/kg/day. A group of untreated sham-operated rats was also studied. Ly markedly raised plasma renin activity (PRA) and aldosterone, and exerted more effective anti-albuminuric and renoprotective action than eplerenone. In Protocol 2, Nx rats remained untreated until Day 60, when they were divided into: Nx+V receiving vehicle; Nx+L treated with losartan, 50 mg/kg/day; Nx+L+Eple, given losartan and eplerenone, and Nx+L+Ly, given losartan and Ly. Treatments lasted for 90 days. As an add-on to losartan, Ly normalized blood pressure and albuminuria, and prevented CKD progression more effectively than eplerenone. This effect was associated with strong stimulation of PRA and aldosterone. Despite exhibiting higher affinity for the MR than either eplerenone or spironolactone, Ly caused no hyperkalemia. Ly may become a novel asset in the effort to detain the progression of CKD.
Insights
A novel mineralocorticoid receptor blocker, Ly, effectively reduces chronic kidney disease (CKD) progression and albuminuria in rats without causing hyperkalemia, offering a potential new treatment for kidney disease.
Area of Science:
- Nephrology
- Pharmacology
Background:
- Aldosterone antagonists slow chronic kidney disease (CKD) progression but can cause hyperkalemia, limiting their use with RAS inhibitors.
- A novel non-steroidal mineralocorticoid receptor (MR) blocker, Ly, was investigated for its renoprotective effects.
Purpose of the Study:
- To evaluate the renoprotective efficacy and safety of Ly compared to eplerenone in a rat model of CKD.
- To assess Ly's effects on blood pressure, albuminuria, and kidney function, both as a monotherapy and in combination with losartan.
Main Methods:
- Two protocols using male Munich-Wistar rats with 5/6 renal ablation (Nx).
- Protocol 1: Nx rats treated with vehicle, eplerenone, or Ly.
- Protocol 2: Nx rats treated with losartan alone, or losartan plus eplerenone or Ly.
Main Results:
- Ly demonstrated superior anti-albuminuric and renoprotective effects compared to eplerenone in Protocol 1.
- In Protocol 2, Ly normalized blood pressure and albuminuria when added to losartan, outperforming eplerenone.
- Ly significantly stimulated plasma renin activity (PRA) and aldosterone but did not induce hyperkalemia, despite higher MR affinity than eplerenone or spironolactone.
Conclusions:
- Ly exhibits potent renoprotective effects in a rat CKD model, surpassing eplerenone.
- Ly effectively reduces blood pressure and albuminuria, and prevents CKD progression, even when combined with losartan.
- Ly's ability to block MR without causing hyperkalemia makes it a promising therapeutic candidate for managing CKD.
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