Protocatechuic acid ameliorates lipopolysaccharide‐induced kidney damage in mice via downregulation of TLR‐4‐mediated IKBKB/NF‐κB and MAPK/Erk signaling pathways

Acute kidney injury (AKI) is a very critical cause of death in the whole world. Lipopolysaccharide (LPS) induces kidney damage by activating various deleterious inflammatory and oxidative pathways. Protocatechuic acid, a natural phenolic compound, has shown to exert beneficial effects against oxidat...

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Veröffentlicht in:Journal of applied toxicology 2023-08, Vol.43 (8), p.1119-1129
Hauptverfasser: Salama, Abeer A. A., Elgohary, Rania, Fahmy, Mohamed Ibrahim
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Elgohary, Rania
Fahmy, Mohamed Ibrahim
description Acute kidney injury (AKI) is a very critical cause of death in the whole world. Lipopolysaccharide (LPS) induces kidney damage by activating various deleterious inflammatory and oxidative pathways. Protocatechuic acid, a natural phenolic compound, has shown to exert beneficial effects against oxidative and inflammatory responses. The study aimed to clarify the nephroprotective activity of protocatechuic acid in LPS‐induced acute kidney damage in mice. Forty male Swiss mice were allocated in four groups as follows: normal control group; LPS (250 μg/kg, ip)‐induced kidney injury group; LPS‐injected mice treated with protocatechuic acid (15 mg/kg, po), and LPS‐injected mice treated with protocatechuic acid (30 mg/kg, po). Significant toll‐like receptor 4 (TLR‐4)‐mediated activation of IKBKB/NF‐κB and MAPK/Erk/COX‐2 inflammatory pathways has been observed in kidneys of mice treated with LPS. Oxidative stress was revealed by inhibition of total antioxidant capacity, catalase, nuclear factor erythroid 2‐related factor 2 (Nrf2), and NAD(P)H quinone oxidoreductase (NQO1) enzyme along with increased nitric oxide level. In parallel, focal inflammatory effects were shown in between the tubules and glomeruli as well as in the perivascular dilated blood vessels at the cortex affecting the normal morphology of the kidney tissues of LPS‐treated mice. However, treatment with protocatechuic acid reduced LPS‐induced changes in the aforementioned parameters and restored normal histological features of the affected tissues. In conclusion, our study uncovered that protocatechuic acid has nephroprotective effects in mice with AKI through opposing different inflammatory and oxidative cascades. Acute kidney injury is a major cause of death. The aim of the work is to study the protective effects of protocatechuic acid against oxidative and inflammatory responses in kidneys after lipopolysaccharide treatment using mice. Treatment with both doses of protocatechuic acid attenuated LPS‐induced changes in the aforementioned parameters and restored normal renal morphology. In conclusion, our study uncovered that protocatechuic acid has nephroprotective effects in mice with kidney injury through opposing inflammatory and oxidative cascades.
doi_str_mv 10.1002/jat.4447
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Significant toll‐like receptor 4 (TLR‐4)‐mediated activation of IKBKB/NF‐κB and MAPK/Erk/COX‐2 inflammatory pathways has been observed in kidneys of mice treated with LPS. Oxidative stress was revealed by inhibition of total antioxidant capacity, catalase, nuclear factor erythroid 2‐related factor 2 (Nrf2), and NAD(P)H quinone oxidoreductase (NQO1) enzyme along with increased nitric oxide level. In parallel, focal inflammatory effects were shown in between the tubules and glomeruli as well as in the perivascular dilated blood vessels at the cortex affecting the normal morphology of the kidney tissues of LPS‐treated mice. However, treatment with protocatechuic acid reduced LPS‐induced changes in the aforementioned parameters and restored normal histological features of the affected tissues. In conclusion, our study uncovered that protocatechuic acid has nephroprotective effects in mice with AKI through opposing different inflammatory and oxidative cascades. Acute kidney injury is a major cause of death. The aim of the work is to study the protective effects of protocatechuic acid against oxidative and inflammatory responses in kidneys after lipopolysaccharide treatment using mice. Treatment with both doses of protocatechuic acid attenuated LPS‐induced changes in the aforementioned parameters and restored normal renal morphology. 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A.</creatorcontrib><creatorcontrib>Elgohary, Rania</creatorcontrib><creatorcontrib>Fahmy, Mohamed Ibrahim</creatorcontrib><title>Protocatechuic acid ameliorates lipopolysaccharide‐induced kidney damage in mice via downregulation of TLR‐4‐mediated IKBKB/NF‐κB and MAPK/Erk signaling pathways</title><title>Journal of applied toxicology</title><addtitle>J Appl Toxicol</addtitle><description>Acute kidney injury (AKI) is a very critical cause of death in the whole world. Lipopolysaccharide (LPS) induces kidney damage by activating various deleterious inflammatory and oxidative pathways. Protocatechuic acid, a natural phenolic compound, has shown to exert beneficial effects against oxidative and inflammatory responses. The study aimed to clarify the nephroprotective activity of protocatechuic acid in LPS‐induced acute kidney damage in mice. 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However, treatment with protocatechuic acid reduced LPS‐induced changes in the aforementioned parameters and restored normal histological features of the affected tissues. In conclusion, our study uncovered that protocatechuic acid has nephroprotective effects in mice with AKI through opposing different inflammatory and oxidative cascades. Acute kidney injury is a major cause of death. The aim of the work is to study the protective effects of protocatechuic acid against oxidative and inflammatory responses in kidneys after lipopolysaccharide treatment using mice. Treatment with both doses of protocatechuic acid attenuated LPS‐induced changes in the aforementioned parameters and restored normal renal morphology. 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The study aimed to clarify the nephroprotective activity of protocatechuic acid in LPS‐induced acute kidney damage in mice. Forty male Swiss mice were allocated in four groups as follows: normal control group; LPS (250 μg/kg, ip)‐induced kidney injury group; LPS‐injected mice treated with protocatechuic acid (15 mg/kg, po), and LPS‐injected mice treated with protocatechuic acid (30 mg/kg, po). Significant toll‐like receptor 4 (TLR‐4)‐mediated activation of IKBKB/NF‐κB and MAPK/Erk/COX‐2 inflammatory pathways has been observed in kidneys of mice treated with LPS. Oxidative stress was revealed by inhibition of total antioxidant capacity, catalase, nuclear factor erythroid 2‐related factor 2 (Nrf2), and NAD(P)H quinone oxidoreductase (NQO1) enzyme along with increased nitric oxide level. 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source Wiley Online Library Journals Frontfile Complete
subjects Acids
AKI
Blood vessels
Catalase
Damage
Down-regulation
Inflammation
Kidneys
Lipopolysaccharides
LPS
MAP kinase
MAPK
NADPH quinone oxidoreductase
NF‐ĸB
Nitric oxide
Oxidative stress
Phenols
Protocatechuic acid
Quinone oxidoreductase
Quinones
Tubules
title Protocatechuic acid ameliorates lipopolysaccharide‐induced kidney damage in mice via downregulation of TLR‐4‐mediated IKBKB/NF‐κB and MAPK/Erk signaling pathways
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