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Renoprotective Effect of Pitavastatin against TAA-Induced Renal Injury: Involvement of the miR-93/PTEN/AKT/mTOR Pathway

This research investigated if pitavastatin (Pita) might protect rats’ kidneys against thioacetamide (TAA). By altering the PTEN/AKT/mTOR pathway, pitavastatin may boost kidney antioxidant capacity and minimize oxidative damage. Statins have several benefits, including antioxidant and anti-inflammato...

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Published in:Advances in pharmacological and pharmaceutical sciences 2024-01, Vol.2024, p.6681873-11
Main Authors: Elbaset, Marawan A., Mohamed, Bassim M. S. A., Moustafa, Passant E., Esatbeyoglu, Tuba, Afifi, Sherif M., Hessin, Alyaa F., Abdelrahman, Sahar S., Fayed, Hany M.
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container_title Advances in pharmacological and pharmaceutical sciences
container_volume 2024
creator Elbaset, Marawan A.
Mohamed, Bassim M. S. A.
Moustafa, Passant E.
Esatbeyoglu, Tuba
Afifi, Sherif M.
Hessin, Alyaa F.
Abdelrahman, Sahar S.
Fayed, Hany M.
description This research investigated if pitavastatin (Pita) might protect rats’ kidneys against thioacetamide (TAA). By altering the PTEN/AKT/mTOR pathway, pitavastatin may boost kidney antioxidant capacity and minimize oxidative damage. Statins have several benefits, including antioxidant and anti-inflammatory characteristics. The principal hypothesis of this study was that Pita can regulate the miR-93/PTEN/AKT/mTOR pathways, which is thought to be responsible for its renoprotective effects. The experiment divided male rats into four groups. Group 1 included untreated rats as the control. Group 2 included rats which received TAA (100 mg/kg intraperitoneally thrice a week for two weeks) to destroy their kidneys. Groups 3 and 4 included rats which received Pita orally at 0.4 and 0.8 mg/kg for 14 days after TAA injections. Renal injury increased BUN, creatinine, and MDA levels and decreased glutathione (GSH) levels. Pitavastatin prevented these alterations. TAA decreased PTEN and increased miR-93, Akt, p-Akt, mTOR, and Stat3 in the kidneys. Pitavastatin also regulated the associated culprit pathway, miR-93/PTEN/Akt/mTOR. In addition, TAA induced adverse effects on the kidney tissue, which were significantly ameliorated by pitavastatin treatment. The findings suggest that pitavastatin can attenuate renal injury, likely by regulating the miR-93/PTEN/Akt/mTOR pathway. This modulation of the pathway appears to contribute to the protective effects of pitavastatin against TAA-induced renal injury, adding to the growing evidence of the pleiotropic benefits of statins in renal health.
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S. A. ; Moustafa, Passant E. ; Esatbeyoglu, Tuba ; Afifi, Sherif M. ; Hessin, Alyaa F. ; Abdelrahman, Sahar S. ; Fayed, Hany M.</creator><contributor>Mirzavi, Farshad ; Farshad Mirzavi</contributor><creatorcontrib>Elbaset, Marawan A. ; Mohamed, Bassim M. S. A. ; Moustafa, Passant E. ; Esatbeyoglu, Tuba ; Afifi, Sherif M. ; Hessin, Alyaa F. ; Abdelrahman, Sahar S. ; Fayed, Hany M. ; Mirzavi, Farshad ; Farshad Mirzavi</creatorcontrib><description>This research investigated if pitavastatin (Pita) might protect rats’ kidneys against thioacetamide (TAA). By altering the PTEN/AKT/mTOR pathway, pitavastatin may boost kidney antioxidant capacity and minimize oxidative damage. Statins have several benefits, including antioxidant and anti-inflammatory characteristics. The principal hypothesis of this study was that Pita can regulate the miR-93/PTEN/AKT/mTOR pathways, which is thought to be responsible for its renoprotective effects. The experiment divided male rats into four groups. Group 1 included untreated rats as the control. Group 2 included rats which received TAA (100 mg/kg intraperitoneally thrice a week for two weeks) to destroy their kidneys. Groups 3 and 4 included rats which received Pita orally at 0.4 and 0.8 mg/kg for 14 days after TAA injections. Renal injury increased BUN, creatinine, and MDA levels and decreased glutathione (GSH) levels. Pitavastatin prevented these alterations. TAA decreased PTEN and increased miR-93, Akt, p-Akt, mTOR, and Stat3 in the kidneys. Pitavastatin also regulated the associated culprit pathway, miR-93/PTEN/Akt/mTOR. In addition, TAA induced adverse effects on the kidney tissue, which were significantly ameliorated by pitavastatin treatment. The findings suggest that pitavastatin can attenuate renal injury, likely by regulating the miR-93/PTEN/Akt/mTOR pathway. 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subjects Animal experimentation
Antioxidants
Apoptosis
Biomarkers
Creatinine
Diabetes
Inflammation
Ischemia
Kidney diseases
Kidneys
Kinases
MicroRNAs
Nitrogen
Oxidative stress
Phosphatase
Phosphorylation
Proteins
Side effects
Statins
Type 2 diabetes
title Renoprotective Effect of Pitavastatin against TAA-Induced Renal Injury: Involvement of the miR-93/PTEN/AKT/mTOR Pathway
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