Quercetin flavonoid and vitamin C recuperate kidney functions in potassium bromate-induced renal dysfunction in Wistar rats
Studies into the functions and mechanisms of action of quercetin may be able to help dispel the negative effects of toxicants on renal toxicity due to its anti-inflammatory potential, as well as provide a simple, low-cost alternative for treating renal toxicity in developing nations. Therefore, the...
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description | Studies into the functions and mechanisms of action of quercetin may be able to help dispel the negative effects of toxicants on renal toxicity due to its anti-inflammatory potential, as well as provide a simple, low-cost alternative for treating renal toxicity in developing nations. Therefore, the present study evaluated the ameliorative and renal protective activities of quercetin dihydrate in potassium bromate-induced, renal-toxic Wistar rats. Forty-five (45) mature female Wistar rats (180–200 g) were randomly grouped into nine (9) (
n
= 5). Group A served as general control. Nephrotoxicity was induced in groups B to I with the administration of potassium bromate. While group B served as a negative control, groups C–E received graded doses of quercetin (40, 60, and 80 mg/kg, respectively). Group F received 2.5 mg/kg/day of vitamin C, while groups G–I received vitamin C (2.5 mg/kg/day) and co-administration of a graded dose of quercetin (40, 60, and 80 mg/kg, respectively). Daily urine levels and final blood samples by retro-orbital techniques were collected for GFR, urea, and creatinine level assessment. The collected data were subjected to ANOVA and Tukey’s post hoc test, and the results were presented as mean SEM with a
p
< 0.05 level considered significant. Body and organ weight and GFR were significantly reduced (
p
< 0.05), while serum and urine creatinine and urea were decreased in renotoxic animals. However, treatment with QCT reversed the renotoxic effects. We, therefore, concluded that quercetin administered alone or with vitamin C conferred renal protection by reversing KBrO
3
-induced renal toxicity in rats. Further studies to corroborate the present findings are recommended. |
doi_str_mv | 10.1007/s00210-023-02571-w |
format | Article |
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n
= 5). Group A served as general control. Nephrotoxicity was induced in groups B to I with the administration of potassium bromate. While group B served as a negative control, groups C–E received graded doses of quercetin (40, 60, and 80 mg/kg, respectively). Group F received 2.5 mg/kg/day of vitamin C, while groups G–I received vitamin C (2.5 mg/kg/day) and co-administration of a graded dose of quercetin (40, 60, and 80 mg/kg, respectively). Daily urine levels and final blood samples by retro-orbital techniques were collected for GFR, urea, and creatinine level assessment. The collected data were subjected to ANOVA and Tukey’s post hoc test, and the results were presented as mean SEM with a
p
< 0.05 level considered significant. Body and organ weight and GFR were significantly reduced (
p
< 0.05), while serum and urine creatinine and urea were decreased in renotoxic animals. However, treatment with QCT reversed the renotoxic effects. We, therefore, concluded that quercetin administered alone or with vitamin C conferred renal protection by reversing KBrO
3
-induced renal toxicity in rats. Further studies to corroborate the present findings are recommended.</description><identifier>ISSN: 0028-1298</identifier><identifier>EISSN: 1432-1912</identifier><identifier>DOI: 10.1007/s00210-023-02571-w</identifier><identifier>PMID: 37341785</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Animals ; Antioxidants - metabolism ; Antioxidants - pharmacology ; Antioxidants - therapeutic use ; Ascorbic acid ; Ascorbic Acid - metabolism ; Ascorbic Acid - pharmacology ; Ascorbic Acid - therapeutic use ; Biomedical and Life Sciences ; Biomedicine ; Creatinine ; Female ; Flavonoids ; Flavonoids - pharmacology ; Inflammation ; Kidney ; Kidney Diseases - chemically induced ; Kidney Diseases - drug therapy ; Kidney Diseases - prevention & control ; Neurosciences ; Oxidative Stress ; Pharmacology/Toxicology ; Potassium ; Potassium bromate ; Quercetin ; Quercetin - pharmacology ; Quercetin - therapeutic use ; Rats ; Rats, Wistar ; Renal function ; Renal Insufficiency ; Toxicants ; Toxicity ; Urea ; Vitamin C</subject><ispartof>Naunyn-Schmiedeberg's archives of pharmacology, 2023-12, Vol.396 (12), p.3789-3796</ispartof><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-61016b0b1478246d9ed2575429bac1fc19e6488d1e8689a6bfd09e70303861903</citedby><cites>FETCH-LOGICAL-c375t-61016b0b1478246d9ed2575429bac1fc19e6488d1e8689a6bfd09e70303861903</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00210-023-02571-w$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00210-023-02571-w$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37341785$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ogagayere, Lucky Omamuzo</creatorcontrib><creatorcontrib>Naiho, Alexander Obidike</creatorcontrib><creatorcontrib>Emojevwe, Victor</creatorcontrib><creatorcontrib>Igweh, John Chukwuka</creatorcontrib><title>Quercetin flavonoid and vitamin C recuperate kidney functions in potassium bromate-induced renal dysfunction in Wistar rats</title><title>Naunyn-Schmiedeberg's archives of pharmacology</title><addtitle>Naunyn-Schmiedeberg's Arch Pharmacol</addtitle><addtitle>Naunyn Schmiedebergs Arch Pharmacol</addtitle><description>Studies into the functions and mechanisms of action of quercetin may be able to help dispel the negative effects of toxicants on renal toxicity due to its anti-inflammatory potential, as well as provide a simple, low-cost alternative for treating renal toxicity in developing nations. Therefore, the present study evaluated the ameliorative and renal protective activities of quercetin dihydrate in potassium bromate-induced, renal-toxic Wistar rats. Forty-five (45) mature female Wistar rats (180–200 g) were randomly grouped into nine (9) (
n
= 5). Group A served as general control. Nephrotoxicity was induced in groups B to I with the administration of potassium bromate. While group B served as a negative control, groups C–E received graded doses of quercetin (40, 60, and 80 mg/kg, respectively). Group F received 2.5 mg/kg/day of vitamin C, while groups G–I received vitamin C (2.5 mg/kg/day) and co-administration of a graded dose of quercetin (40, 60, and 80 mg/kg, respectively). Daily urine levels and final blood samples by retro-orbital techniques were collected for GFR, urea, and creatinine level assessment. The collected data were subjected to ANOVA and Tukey’s post hoc test, and the results were presented as mean SEM with a
p
< 0.05 level considered significant. Body and organ weight and GFR were significantly reduced (
p
< 0.05), while serum and urine creatinine and urea were decreased in renotoxic animals. However, treatment with QCT reversed the renotoxic effects. We, therefore, concluded that quercetin administered alone or with vitamin C conferred renal protection by reversing KBrO
3
-induced renal toxicity in rats. Further studies to corroborate the present findings are recommended.</description><subject>Animals</subject><subject>Antioxidants - metabolism</subject><subject>Antioxidants - pharmacology</subject><subject>Antioxidants - therapeutic use</subject><subject>Ascorbic acid</subject><subject>Ascorbic Acid - metabolism</subject><subject>Ascorbic Acid - pharmacology</subject><subject>Ascorbic Acid - therapeutic use</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Creatinine</subject><subject>Female</subject><subject>Flavonoids</subject><subject>Flavonoids - pharmacology</subject><subject>Inflammation</subject><subject>Kidney</subject><subject>Kidney Diseases - chemically induced</subject><subject>Kidney Diseases - drug therapy</subject><subject>Kidney Diseases - prevention & control</subject><subject>Neurosciences</subject><subject>Oxidative Stress</subject><subject>Pharmacology/Toxicology</subject><subject>Potassium</subject><subject>Potassium bromate</subject><subject>Quercetin</subject><subject>Quercetin - pharmacology</subject><subject>Quercetin - therapeutic use</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Renal function</subject><subject>Renal Insufficiency</subject><subject>Toxicants</subject><subject>Toxicity</subject><subject>Urea</subject><subject>Vitamin C</subject><issn>0028-1298</issn><issn>1432-1912</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp9kcFqFTEUhoMo9lp9ARcScONmNCeZySRLuagVCiJYugyZ5IykzmSuyaTl4ss3t7dVcNFFCOR8_x8OHyGvgb0HxvoPmTEOrGFc1NP10Nw8IRtoBW9AA39KNnWuGuBanZAXOV8xxiR03XNyInrRQq-6DfnzvWByuIZIx8leL3EJntro6XVY7VxftzShKztMdkX6K_iIezqW6NawxEwrsFtWm3MoMx3SMleqCdEXh74Go52o3-cH_oBfhrzaRGtdfkmejXbK-Or-PiUXnz_92J4159--fN1-PG-c6Lu1kcBADmyAtle8lV6jr9t2LdeDdTA60ChbpTygkkpbOYyeaeyZYEJJ0EycknfH3l1afhfMq5lDdjhNNuJSsuGKKyGBqwP69j_0aimprnGglG57KVtRKX6kXFpyTjiaXQqzTXsDzBzUmKMaU9WYOzXmpobe3FeXYUb_N_LgogLiCOQ6ij8x_fv7kdpb7mCatQ</recordid><startdate>20231201</startdate><enddate>20231201</enddate><creator>Ogagayere, Lucky Omamuzo</creator><creator>Naiho, Alexander Obidike</creator><creator>Emojevwe, Victor</creator><creator>Igweh, John Chukwuka</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</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>3V.</scope><scope>7QP</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope></search><sort><creationdate>20231201</creationdate><title>Quercetin flavonoid and vitamin C recuperate kidney functions in potassium bromate-induced renal dysfunction in Wistar rats</title><author>Ogagayere, Lucky Omamuzo ; 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Therefore, the present study evaluated the ameliorative and renal protective activities of quercetin dihydrate in potassium bromate-induced, renal-toxic Wistar rats. Forty-five (45) mature female Wistar rats (180–200 g) were randomly grouped into nine (9) (
n
= 5). Group A served as general control. Nephrotoxicity was induced in groups B to I with the administration of potassium bromate. While group B served as a negative control, groups C–E received graded doses of quercetin (40, 60, and 80 mg/kg, respectively). Group F received 2.5 mg/kg/day of vitamin C, while groups G–I received vitamin C (2.5 mg/kg/day) and co-administration of a graded dose of quercetin (40, 60, and 80 mg/kg, respectively). Daily urine levels and final blood samples by retro-orbital techniques were collected for GFR, urea, and creatinine level assessment. The collected data were subjected to ANOVA and Tukey’s post hoc test, and the results were presented as mean SEM with a
p
< 0.05 level considered significant. Body and organ weight and GFR were significantly reduced (
p
< 0.05), while serum and urine creatinine and urea were decreased in renotoxic animals. However, treatment with QCT reversed the renotoxic effects. We, therefore, concluded that quercetin administered alone or with vitamin C conferred renal protection by reversing KBrO
3
-induced renal toxicity in rats. Further studies to corroborate the present findings are recommended.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>37341785</pmid><doi>10.1007/s00210-023-02571-w</doi><tpages>8</tpages></addata></record> |
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subjects | Animals Antioxidants - metabolism Antioxidants - pharmacology Antioxidants - therapeutic use Ascorbic acid Ascorbic Acid - metabolism Ascorbic Acid - pharmacology Ascorbic Acid - therapeutic use Biomedical and Life Sciences Biomedicine Creatinine Female Flavonoids Flavonoids - pharmacology Inflammation Kidney Kidney Diseases - chemically induced Kidney Diseases - drug therapy Kidney Diseases - prevention & control Neurosciences Oxidative Stress Pharmacology/Toxicology Potassium Potassium bromate Quercetin Quercetin - pharmacology Quercetin - therapeutic use Rats Rats, Wistar Renal function Renal Insufficiency Toxicants Toxicity Urea Vitamin C |
title | Quercetin flavonoid and vitamin C recuperate kidney functions in potassium bromate-induced renal dysfunction in Wistar rats |
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