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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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. |
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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.</description><identifier>ISSN: 0260-437X</identifier><identifier>EISSN: 1099-1263</identifier><identifier>DOI: 10.1002/jat.4447</identifier><identifier>PMID: 36807594</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>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</subject><ispartof>Journal of applied toxicology, 2023-08, Vol.43 (8), p.1119-1129</ispartof><rights>2023 John Wiley & Sons Ltd.</rights><rights>2023 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2647-d23b227348f8b61196af87fa062d84dfc033199ed77bf6665f31e627ae6e8cdc3</citedby><cites>FETCH-LOGICAL-c2647-d23b227348f8b61196af87fa062d84dfc033199ed77bf6665f31e627ae6e8cdc3</cites><orcidid>0000-0002-2948-5449 ; 0000-0001-9870-5583 ; 0000-0003-3660-3981</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjat.4447$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjat.4447$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36807594$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Salama, Abeer A. 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. 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.</description><subject>Acids</subject><subject>AKI</subject><subject>Blood vessels</subject><subject>Catalase</subject><subject>Damage</subject><subject>Down-regulation</subject><subject>Inflammation</subject><subject>Kidneys</subject><subject>Lipopolysaccharides</subject><subject>LPS</subject><subject>MAP kinase</subject><subject>MAPK</subject><subject>NADPH quinone oxidoreductase</subject><subject>NF‐ĸB</subject><subject>Nitric oxide</subject><subject>Oxidative stress</subject><subject>Phenols</subject><subject>Protocatechuic acid</subject><subject>Quinone oxidoreductase</subject><subject>Quinones</subject><subject>Tubules</subject><issn>0260-437X</issn><issn>1099-1263</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp1kU1uEzEYhi0EoqEgcQJkiQ2bafwzsT3LpGqhJECFgsRu9MX2JE5nxlN7hmh2HIFzcAQOwSE4CS4tICGxsCy9fvzo0_ci9JSSE0oIm-6hP8nzXN5DE0qKIqNM8PtoQpggWc7lxyP0KMY9IemNqYfoiAtF5KzIJ-jrZfC919BbvRucxqCdwdDY2vmQwohr1_nO12MErXcQnLE_Pn9xrRm0NfjKmdaO2EADW4tdixunLf7kABt_aIPdDjX0zrfYV3i9ep9-5uk01rjkNvhiuVgupm_PU_b92wJDa_Cb-eVyehaucHTbFmrXbnEH_e4AY3yMHlRQR_vk7j5GH87P1qevstW7lxen81WmmchlZhjfMCZ5riq1EZQWAiolKyCCGZWbShPOaVFYI-WmEkLMKk6tYBKssEobzY_Ri1tvF_z1YGNfNi5qW9fQWj_EkkmpCikZ5Ql9_g-690NIcydKcUYLwmfqr1AHH2OwVdkF10AYS0rKm_7K1F95019Cn90Jh01a0x_wd2EJyG6Bg6vt-F9R-Xq-_iX8CeFyqhg</recordid><startdate>202308</startdate><enddate>202308</enddate><creator>Salama, Abeer A. A.</creator><creator>Elgohary, Rania</creator><creator>Fahmy, Mohamed Ibrahim</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7ST</scope><scope>7TK</scope><scope>7U7</scope><scope>C1K</scope><scope>K9.</scope><scope>SOI</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-2948-5449</orcidid><orcidid>https://orcid.org/0000-0001-9870-5583</orcidid><orcidid>https://orcid.org/0000-0003-3660-3981</orcidid></search><sort><creationdate>202308</creationdate><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><author>Salama, Abeer A. A. ; Elgohary, Rania ; Fahmy, Mohamed Ibrahim</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2647-d23b227348f8b61196af87fa062d84dfc033199ed77bf6665f31e627ae6e8cdc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Acids</topic><topic>AKI</topic><topic>Blood vessels</topic><topic>Catalase</topic><topic>Damage</topic><topic>Down-regulation</topic><topic>Inflammation</topic><topic>Kidneys</topic><topic>Lipopolysaccharides</topic><topic>LPS</topic><topic>MAP kinase</topic><topic>MAPK</topic><topic>NADPH quinone oxidoreductase</topic><topic>NF‐ĸB</topic><topic>Nitric oxide</topic><topic>Oxidative stress</topic><topic>Phenols</topic><topic>Protocatechuic acid</topic><topic>Quinone oxidoreductase</topic><topic>Quinones</topic><topic>Tubules</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Salama, Abeer A. A.</creatorcontrib><creatorcontrib>Elgohary, Rania</creatorcontrib><creatorcontrib>Fahmy, Mohamed Ibrahim</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Environment Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of applied toxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Salama, Abeer A. A.</au><au>Elgohary, Rania</au><au>Fahmy, Mohamed Ibrahim</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Protocatechuic acid ameliorates lipopolysaccharide‐induced kidney damage in mice via downregulation of TLR‐4‐mediated IKBKB/NF‐κB and MAPK/Erk signaling pathways</atitle><jtitle>Journal of applied toxicology</jtitle><addtitle>J Appl Toxicol</addtitle><date>2023-08</date><risdate>2023</risdate><volume>43</volume><issue>8</issue><spage>1119</spage><epage>1129</epage><pages>1119-1129</pages><issn>0260-437X</issn><eissn>1099-1263</eissn><abstract>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.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>36807594</pmid><doi>10.1002/jat.4447</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-2948-5449</orcidid><orcidid>https://orcid.org/0000-0001-9870-5583</orcidid><orcidid>https://orcid.org/0000-0003-3660-3981</orcidid></addata></record> |
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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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