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Protective Effects of Simvastatin on Endotoxin-Induced Acute Kidney Injury through Activation of Tubular Epithelial Cells' Survival and Hindering Cytochrome C-Mediated Apoptosis
L. Nežić, R. Škrbić, L. Amidžić, R. Gajanin, Z. Milovanović, E. Nepovimova, K. Kuča, V. Jaćević
Language English Country Switzerland
Document type Journal Article
Grant support
Faculty of Science VT2019-2021
UHK
CEP Register
MFVMA/04/20-22
Medical Faculty of the Military Medical Academy, the University of Defence in Belgrade, Republic of Serbia
NLK
Free Medical Journals
from 2000
Freely Accessible Science Journals
from 2000
PubMed Central
from 2007
Europe PubMed Central
from 2007
ProQuest Central
from 2000-03-01
Open Access Digital Library
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Open Access Digital Library
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Health & Medicine (ProQuest)
from 2000-03-01
ROAD: Directory of Open Access Scholarly Resources
from 2000
PubMed
33008033
DOI
10.3390/ijms21197236
Knihovny.cz E-resources
- MeSH
- Acute Kidney Injury chemically induced drug therapy genetics pathology MeSH
- Apoptosis drug effects MeSH
- Cytochromes c genetics MeSH
- Endotoxins toxicity MeSH
- Epithelial Cells drug effects pathology MeSH
- Rats MeSH
- Kidney Tubules drug effects pathology MeSH
- Kidney drug effects injuries metabolism pathology MeSH
- Humans MeSH
- Lipopolysaccharides toxicity MeSH
- bcl-X Protein genetics MeSH
- Simvastatin pharmacology MeSH
- Cell Survival drug effects MeSH
- Inflammation chemically induced drug therapy genetics pathology MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
Increasing evidence suggests that apoptosis of tubular cells and renal inflammation mainly determine the outcome of sepsis-associated acute kidney injury (AKI). The study aim was to investigate the molecular mechanism involved in the renoprotective effects of simvastatin in endotoxin (lipopolysaccharide, LSP)-induced AKI. A sepsis model was established by intraperitoneal injection of a single non-lethal LPS dose after short-term simvastatin pretreatment. The severity of the inflammatory injury was expressed as renal damage scores (RDS). Apoptosis of tubular cells was detected by Terminal deoxynucleotidyl transferase-mediated dUTP Nick End Labeling (TUNEL assay) (apoptotic DNA fragmentation, expressed as an apoptotic index, AI) and immunohistochemical staining for cleaved caspase-3, cytochrome C, and anti-apoptotic Bcl-xL and survivin. We found that endotoxin induced severe renal inflammatory injury (RDS = 3.58 ± 0.50), whereas simvastatin dose-dependently prevented structural changes induced by LPS. Furthermore, simvastatin 40 mg/kg most profoundly attenuated tubular apoptosis, determined as a decrease of cytochrome C, caspase-3 expression, and AIs (p < 0.01 vs. LPS). Conversely, simvastatin induced a significant increase of Bcl-XL and survivin, both in the strong inverse correlations with cleaved caspase-3 and cytochrome C. Our study indicates that simvastatin has cytoprotective effects against LPS-induced tubular apoptosis, seemingly mediated by upregulation of cell-survival molecules, such as Bcl-XL and survivin, and inhibition of the mitochondrial cytochrome C and downstream caspase-3 activation.
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