Ameliorative effect of chrysin on adenine-induced chronic kidney disease in rats
Chrysin (5, 7- dihydroxyflavone) is a flavonoid with several pharmacological properties that include antioxidant, anti-inflammatory and antiapoptotic activities. in this work, we investigated some effects of three graded oral doses of chrysin (10, 50 and 250 mg/kg) on kidney structure and function i...
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description | Chrysin (5, 7- dihydroxyflavone) is a flavonoid with several pharmacological properties that include antioxidant, anti-inflammatory and antiapoptotic activities. in this work, we investigated some effects of three graded oral doses of chrysin (10, 50 and 250 mg/kg) on kidney structure and function in rats with experimental chronic renal disease (CKD) induced by adenine (0.25% w/w in feed for 35 days), which is known to involve inflammation and oxidative stress. Using several indices in plasma, urine and kidney homogenates, adenine was found to impair kidney function as it lowered creatinine clearance and increased plasma concentrations of creatinine, urea, neutrophil gelatinase-associated lipocalin and N-Acetyl-beta-D-glucosaminidase activity. Furthermore, it raised plasma concentrations of the uremic toxin indoxyl sulfate, some inflammatory cytokines and urinary albumin concentration. Renal morphology was severely damaged and histopathological markers of inflammation and fibrosis were especially increased. In renal homogenates, antioxidant indices, including superoxide dismutase and catalase activities, total antioxidant capacity and reduced glutathione were all adversely affected. Most of these adenine - induced actions were moderately and dose -dependently mitigated by chrysin, especially at the highest dose. Chrysin did not cause any overt adverse effect on the treated rats. The results suggest that different doses of chrysin produce variable salutary effects against adenine-induced CKD in rats, and that, pending further pharmacological and toxicological studies, its usability as a possible ameliorative agent in human CKD should be considered. |
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Using several indices in plasma, urine and kidney homogenates, adenine was found to impair kidney function as it lowered creatinine clearance and increased plasma concentrations of creatinine, urea, neutrophil gelatinase-associated lipocalin and N-Acetyl-beta-D-glucosaminidase activity. Furthermore, it raised plasma concentrations of the uremic toxin indoxyl sulfate, some inflammatory cytokines and urinary albumin concentration. Renal morphology was severely damaged and histopathological markers of inflammation and fibrosis were especially increased. In renal homogenates, antioxidant indices, including superoxide dismutase and catalase activities, total antioxidant capacity and reduced glutathione were all adversely affected. Most of these adenine - induced actions were moderately and dose -dependently mitigated by chrysin, especially at the highest dose. Chrysin did not cause any overt adverse effect on the treated rats. The results suggest that different doses of chrysin produce variable salutary effects against adenine-induced CKD in rats, and that, pending further pharmacological and toxicological studies, its usability as a possible ameliorative agent in human CKD should be considered.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0125285</identifier><identifier>PMID: 25909514</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Acetylglucosaminidase - blood ; Adenine ; Adenine - pharmacology ; Animals ; Antioxidants ; Antioxidants (Nutrients) ; Antioxidants - metabolism ; Catalase ; Chronic kidney failure ; Creatinine ; Creatinine - blood ; Cytokines ; Disease Models, Animal ; Fibrosis ; Fibrosis - metabolism ; Fibrosis - pathology ; Flavonoids - pharmacology ; Gelatinase ; Glucosaminidase ; Glutathione ; Inflammation ; Inflammation - metabolism ; Inflammation - pathology ; Kidney - drug effects ; Kidney - metabolism ; Kidney diseases ; Kidney Function Tests - methods ; Kidney transplantation ; Lipocalin ; Lipocalins - blood ; Male ; Neutrophils - drug effects ; Neutrophils - metabolism ; Oxidative stress ; Oxidative Stress - drug effects ; Pharmacology ; Purines ; Rats ; Rats, Wistar ; Renal Insufficiency, Chronic - blood ; Renal Insufficiency, Chronic - chemically induced ; Renal Insufficiency, Chronic - drug therapy ; Renal Insufficiency, Chronic - metabolism ; Structure-function relationships ; Sulfates ; Superoxide dismutase ; Superoxides ; Toxicity testing ; Urea ; Urea - blood ; Urine</subject><ispartof>PloS one, 2015-04, Vol.10 (4), p.e0125285</ispartof><rights>COPYRIGHT 2015 Public Library of Science</rights><rights>2015 Ali et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2015 Ali et al 2015 Ali et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-3de319d9ba49057fbb1cd2e7781cabd4341df657fe8dd39d56a45cbf0eb8f8c73</citedby><cites>FETCH-LOGICAL-c692t-3de319d9ba49057fbb1cd2e7781cabd4341df657fe8dd39d56a45cbf0eb8f8c73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4409384/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4409384/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2096,2915,23845,27901,27902,53766,53768,79343,79344</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25909514$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ali, Badreldin H</creatorcontrib><creatorcontrib>Adham, Sirin A</creatorcontrib><creatorcontrib>Al Za'abi, Mohammed</creatorcontrib><creatorcontrib>Waly, Mostafa I</creatorcontrib><creatorcontrib>Yasin, Javed</creatorcontrib><creatorcontrib>Nemmar, Abderrahim</creatorcontrib><creatorcontrib>Schupp, Nicole</creatorcontrib><title>Ameliorative effect of chrysin on adenine-induced chronic kidney disease in rats</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Chrysin (5, 7- dihydroxyflavone) is a flavonoid with several pharmacological properties that include antioxidant, anti-inflammatory and antiapoptotic activities. in this work, we investigated some effects of three graded oral doses of chrysin (10, 50 and 250 mg/kg) on kidney structure and function in rats with experimental chronic renal disease (CKD) induced by adenine (0.25% w/w in feed for 35 days), which is known to involve inflammation and oxidative stress. Using several indices in plasma, urine and kidney homogenates, adenine was found to impair kidney function as it lowered creatinine clearance and increased plasma concentrations of creatinine, urea, neutrophil gelatinase-associated lipocalin and N-Acetyl-beta-D-glucosaminidase activity. Furthermore, it raised plasma concentrations of the uremic toxin indoxyl sulfate, some inflammatory cytokines and urinary albumin concentration. Renal morphology was severely damaged and histopathological markers of inflammation and fibrosis were especially increased. In renal homogenates, antioxidant indices, including superoxide dismutase and catalase activities, total antioxidant capacity and reduced glutathione were all adversely affected. Most of these adenine - induced actions were moderately and dose -dependently mitigated by chrysin, especially at the highest dose. Chrysin did not cause any overt adverse effect on the treated rats. The results suggest that different doses of chrysin produce variable salutary effects against adenine-induced CKD in rats, and that, pending further pharmacological and toxicological studies, its usability as a possible ameliorative agent in human CKD should be considered.</description><subject>Acetylglucosaminidase - blood</subject><subject>Adenine</subject><subject>Adenine - pharmacology</subject><subject>Animals</subject><subject>Antioxidants</subject><subject>Antioxidants (Nutrients)</subject><subject>Antioxidants - metabolism</subject><subject>Catalase</subject><subject>Chronic kidney failure</subject><subject>Creatinine</subject><subject>Creatinine - blood</subject><subject>Cytokines</subject><subject>Disease Models, Animal</subject><subject>Fibrosis</subject><subject>Fibrosis - metabolism</subject><subject>Fibrosis - pathology</subject><subject>Flavonoids - pharmacology</subject><subject>Gelatinase</subject><subject>Glucosaminidase</subject><subject>Glutathione</subject><subject>Inflammation</subject><subject>Inflammation - metabolism</subject><subject>Inflammation - pathology</subject><subject>Kidney - drug effects</subject><subject>Kidney - metabolism</subject><subject>Kidney diseases</subject><subject>Kidney Function Tests - methods</subject><subject>Kidney transplantation</subject><subject>Lipocalin</subject><subject>Lipocalins - blood</subject><subject>Male</subject><subject>Neutrophils - drug effects</subject><subject>Neutrophils - metabolism</subject><subject>Oxidative stress</subject><subject>Oxidative Stress - drug effects</subject><subject>Pharmacology</subject><subject>Purines</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Renal Insufficiency, Chronic - blood</subject><subject>Renal Insufficiency, Chronic - chemically induced</subject><subject>Renal Insufficiency, Chronic - drug therapy</subject><subject>Renal Insufficiency, Chronic - metabolism</subject><subject>Structure-function relationships</subject><subject>Sulfates</subject><subject>Superoxide dismutase</subject><subject>Superoxides</subject><subject>Toxicity testing</subject><subject>Urea</subject><subject>Urea - blood</subject><subject>Urine</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><sourceid>DOA</sourceid><recordid>eNqNkl2LEzEUhgdR3HX1H4gOCIIXrfmcydwIZfGjsLDi123IJCdt6jTpJjOL_femdnbpgILkIsk5z3kTXt6ieI7RHNMav92EIXrVzXfBwxxhwongD4pz3FAyqwiiD0_OZ8WTlDYIcSqq6nFxRniDGo7ZefF5sYXOhah6dwslWAu6L4Mt9Truk_Nl8KUy4J2HmfNm0GAOreCdLn8642FfGpdAJSgznFXS0-KRVV2CZ-N-UXz_8P7b5afZ1fXH5eXiaqarhvQzaoDixjStYg3itW1brA2BuhZYq9YwyrCxVW6AMIY2hleKcd1aBK2wQtf0onh51N11IcnRjCRxVVeYI0JwJpZHwgS1kbvotiruZVBO_imEuJIq9k53IAGJumq10IJUjOebwVYZy1tiVfbwoPVufG1ot2A0-D6qbiI67Xi3lqtwKxlDDRUsC7waBWK4GSD1__jySK1U_pXzNmQxvXVJywUjhDOBRJOp-V-ovAxsnc5xsC7XJwNvJgOZ6eFXv1JDSnL59cv_s9c_puzrE3YNquvXKXRD74JPU5AdQR1DShHsvXMYyUOa79yQhzTLMc157MWp6_dDd_GlvwFXu_CI</recordid><startdate>20150424</startdate><enddate>20150424</enddate><creator>Ali, Badreldin H</creator><creator>Adham, Sirin A</creator><creator>Al Za'abi, Mohammed</creator><creator>Waly, Mostafa I</creator><creator>Yasin, Javed</creator><creator>Nemmar, Abderrahim</creator><creator>Schupp, Nicole</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20150424</creationdate><title>Ameliorative effect of chrysin on adenine-induced chronic kidney disease in rats</title><author>Ali, Badreldin H ; Adham, Sirin A ; Al Za'abi, Mohammed ; Waly, Mostafa I ; Yasin, Javed ; Nemmar, Abderrahim ; Schupp, Nicole</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c692t-3de319d9ba49057fbb1cd2e7781cabd4341df657fe8dd39d56a45cbf0eb8f8c73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Acetylglucosaminidase - blood</topic><topic>Adenine</topic><topic>Adenine - pharmacology</topic><topic>Animals</topic><topic>Antioxidants</topic><topic>Antioxidants (Nutrients)</topic><topic>Antioxidants - metabolism</topic><topic>Catalase</topic><topic>Chronic kidney failure</topic><topic>Creatinine</topic><topic>Creatinine - blood</topic><topic>Cytokines</topic><topic>Disease Models, Animal</topic><topic>Fibrosis</topic><topic>Fibrosis - metabolism</topic><topic>Fibrosis - pathology</topic><topic>Flavonoids - pharmacology</topic><topic>Gelatinase</topic><topic>Glucosaminidase</topic><topic>Glutathione</topic><topic>Inflammation</topic><topic>Inflammation - metabolism</topic><topic>Inflammation - pathology</topic><topic>Kidney - drug effects</topic><topic>Kidney - metabolism</topic><topic>Kidney diseases</topic><topic>Kidney Function Tests - methods</topic><topic>Kidney transplantation</topic><topic>Lipocalin</topic><topic>Lipocalins - blood</topic><topic>Male</topic><topic>Neutrophils - drug effects</topic><topic>Neutrophils - metabolism</topic><topic>Oxidative stress</topic><topic>Oxidative Stress - drug effects</topic><topic>Pharmacology</topic><topic>Purines</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Renal Insufficiency, Chronic - blood</topic><topic>Renal Insufficiency, Chronic - chemically induced</topic><topic>Renal Insufficiency, Chronic - drug therapy</topic><topic>Renal Insufficiency, Chronic - metabolism</topic><topic>Structure-function relationships</topic><topic>Sulfates</topic><topic>Superoxide dismutase</topic><topic>Superoxides</topic><topic>Toxicity testing</topic><topic>Urea</topic><topic>Urea - blood</topic><topic>Urine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ali, Badreldin H</creatorcontrib><creatorcontrib>Adham, Sirin A</creatorcontrib><creatorcontrib>Al Za'abi, Mohammed</creatorcontrib><creatorcontrib>Waly, Mostafa I</creatorcontrib><creatorcontrib>Yasin, Javed</creatorcontrib><creatorcontrib>Nemmar, Abderrahim</creatorcontrib><creatorcontrib>Schupp, Nicole</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Meteorological & Geoastrophysical Abstracts - 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Using several indices in plasma, urine and kidney homogenates, adenine was found to impair kidney function as it lowered creatinine clearance and increased plasma concentrations of creatinine, urea, neutrophil gelatinase-associated lipocalin and N-Acetyl-beta-D-glucosaminidase activity. Furthermore, it raised plasma concentrations of the uremic toxin indoxyl sulfate, some inflammatory cytokines and urinary albumin concentration. Renal morphology was severely damaged and histopathological markers of inflammation and fibrosis were especially increased. In renal homogenates, antioxidant indices, including superoxide dismutase and catalase activities, total antioxidant capacity and reduced glutathione were all adversely affected. Most of these adenine - induced actions were moderately and dose -dependently mitigated by chrysin, especially at the highest dose. Chrysin did not cause any overt adverse effect on the treated rats. The results suggest that different doses of chrysin produce variable salutary effects against adenine-induced CKD in rats, and that, pending further pharmacological and toxicological studies, its usability as a possible ameliorative agent in human CKD should be considered.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>25909514</pmid><doi>10.1371/journal.pone.0125285</doi><oa>free_for_read</oa></addata></record> |
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subjects | Acetylglucosaminidase - blood Adenine Adenine - pharmacology Animals Antioxidants Antioxidants (Nutrients) Antioxidants - metabolism Catalase Chronic kidney failure Creatinine Creatinine - blood Cytokines Disease Models, Animal Fibrosis Fibrosis - metabolism Fibrosis - pathology Flavonoids - pharmacology Gelatinase Glucosaminidase Glutathione Inflammation Inflammation - metabolism Inflammation - pathology Kidney - drug effects Kidney - metabolism Kidney diseases Kidney Function Tests - methods Kidney transplantation Lipocalin Lipocalins - blood Male Neutrophils - drug effects Neutrophils - metabolism Oxidative stress Oxidative Stress - drug effects Pharmacology Purines Rats Rats, Wistar Renal Insufficiency, Chronic - blood Renal Insufficiency, Chronic - chemically induced Renal Insufficiency, Chronic - drug therapy Renal Insufficiency, Chronic - metabolism Structure-function relationships Sulfates Superoxide dismutase Superoxides Toxicity testing Urea Urea - blood Urine |
title | Ameliorative effect of chrysin on adenine-induced chronic kidney disease in rats |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-02T18%3A03%3A33IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Ameliorative%20effect%20of%20chrysin%20on%20adenine-induced%20chronic%20kidney%20disease%20in%20rats&rft.jtitle=PloS%20one&rft.au=Ali,%20Badreldin%20H&rft.date=2015-04-24&rft.volume=10&rft.issue=4&rft.spage=e0125285&rft.pages=e0125285-&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0125285&rft_dat=%3Cgale_plos_%3EA422548089%3C/gale_plos_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1676150221&rft_id=info:pmid/25909514&rft_galeid=A422548089&rft_doaj_id=oai_doaj_org_article_e0876bc8c82645e08d1fadf5b2fa9321&rfr_iscdi=true |