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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 |
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container_title | Advances in pharmacological and pharmaceutical sciences |
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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. 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.</description><identifier>ISSN: 2633-4682</identifier><identifier>ISSN: 2633-4690</identifier><identifier>EISSN: 2633-4690</identifier><identifier>DOI: 10.1155/2024/6681873</identifier><identifier>PMID: 38293706</identifier><language>eng</language><publisher>England: Hindawi</publisher><subject>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</subject><ispartof>Advances in pharmacological and pharmaceutical sciences, 2024-01, Vol.2024, p.6681873-11</ispartof><rights>Copyright © 2024 Marawan A. Elbaset et al.</rights><rights>COPYRIGHT 2024 John Wiley & Sons, Inc.</rights><rights>Copyright © 2024 Marawan A. Elbaset et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. https://creativecommons.org/licenses/by/4.0</rights><rights>Copyright © 2024 Marawan A. Elbaset et al. 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c573t-ce8fb2357272ebadfce34eade8209dcf271d756e92ee9cb552183ecc311b64813</cites><orcidid>0000-0002-0861-6251 ; 0000-0003-2413-6925 ; 0000-0001-8638-1737 ; 0000-0002-2690-5997 ; 0000-0002-7775-923X ; 0000-0002-3673-5733 ; 0000-0003-0536-8261</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2921793364/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2921793364?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38293706$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Mirzavi, Farshad</contributor><contributor>Farshad Mirzavi</contributor><creatorcontrib>Elbaset, Marawan A.</creatorcontrib><creatorcontrib>Mohamed, Bassim M. S. A.</creatorcontrib><creatorcontrib>Moustafa, Passant E.</creatorcontrib><creatorcontrib>Esatbeyoglu, Tuba</creatorcontrib><creatorcontrib>Afifi, Sherif M.</creatorcontrib><creatorcontrib>Hessin, Alyaa F.</creatorcontrib><creatorcontrib>Abdelrahman, Sahar S.</creatorcontrib><creatorcontrib>Fayed, Hany M.</creatorcontrib><title>Renoprotective Effect of Pitavastatin against TAA-Induced Renal Injury: Involvement of the miR-93/PTEN/AKT/mTOR Pathway</title><title>Advances in pharmacological and pharmaceutical sciences</title><addtitle>Adv Pharmacol Pharm Sci</addtitle><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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S. A.</au><au>Moustafa, Passant E.</au><au>Esatbeyoglu, Tuba</au><au>Afifi, Sherif M.</au><au>Hessin, Alyaa F.</au><au>Abdelrahman, Sahar S.</au><au>Fayed, Hany M.</au><au>Mirzavi, Farshad</au><au>Farshad Mirzavi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Renoprotective Effect of Pitavastatin against TAA-Induced Renal Injury: Involvement of the miR-93/PTEN/AKT/mTOR Pathway</atitle><jtitle>Advances in pharmacological and pharmaceutical sciences</jtitle><addtitle>Adv Pharmacol Pharm Sci</addtitle><date>2024-01-23</date><risdate>2024</risdate><volume>2024</volume><spage>6681873</spage><epage>11</epage><pages>6681873-11</pages><issn>2633-4682</issn><issn>2633-4690</issn><eissn>2633-4690</eissn><abstract>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.</abstract><cop>England</cop><pub>Hindawi</pub><pmid>38293706</pmid><doi>10.1155/2024/6681873</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-0861-6251</orcidid><orcidid>https://orcid.org/0000-0003-2413-6925</orcidid><orcidid>https://orcid.org/0000-0001-8638-1737</orcidid><orcidid>https://orcid.org/0000-0002-2690-5997</orcidid><orcidid>https://orcid.org/0000-0002-7775-923X</orcidid><orcidid>https://orcid.org/0000-0002-3673-5733</orcidid><orcidid>https://orcid.org/0000-0003-0536-8261</orcidid><oa>free_for_read</oa></addata></record> |
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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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