Effect of Dioscorea tokoro Makino extract on hyperuricemia in mice
Purpose: To investigate the anti-hyperuricemic effect of Dioscorea tokoro Makino extract (DTME) in potassium oxonate-induced hyperuricemic mice. Method: The effect of DTME was investigated in the hyperuricemic mice induced by potassium oxonate. DTME. The extract was administered to the mice daily at...
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creator | Fei, Yang Ye, Dan Fan, XiaoFen Dong, FengQin |
description | Purpose: To investigate the anti-hyperuricemic effect of Dioscorea
tokoro Makino extract (DTME) in potassium oxonate-induced hyperuricemic
mice. Method: The effect of DTME was investigated in the hyperuricemic
mice induced by potassium oxonate. DTME. The extract was administered
to the mice daily at doses of 220, 440 and 880 mg/kg for 10 days;
allopurinol (5 mg/kg) was given as positive control. Serum and urine
levels of uric acid and creatinine were determined by colorimetric
method. Simultaneously, protein levels of urate transporter 1 (URAT1)
and organic anion transporter 1 (OAT1) in the rat kidney were analyzed
by Western blotting. Results: Compared with control, a high dose of
DTME inhibited xanthine oxidase (XOD) activity in both serum (18.12
± 1.33 U/L) and in liver (70.15 ± 5.20 U/g protein) (p <
0.05); decreased levels of serum uric acid (2.04 ± 0.64 mg/L) (p
< 0.05), serum creatinine (0.35 ± 0.18 μmol/L) and blood
urea nitrogen (BUN) (8.83 ± 0.71 mmol/L) (p < 0.05).
Furthermore, the extract increased levels of urine uric acid (38.34
± 8.23 mg/L), urine creatinine (34.38 ± 1.98 mmol/L), down
regulated of URAT1 and up regulated of OAT1 protein expressions (p <
0.05) in the renal tissue of hyperuricemic mice. Conclusion: DTME
improves renal dysfunction in rats by regulating renal urate
transporters in hyperuricemic rats. This may find therapeutic
application in antihypertensive therapy. |
doi_str_mv | 10.4314/tjpr.v15i9.10 |
format | Article |
fullrecord | <record><control><sourceid>bioline_cross</sourceid><recordid>TN_cdi_crossref_primary_10_4314_tjpr_v15i9_10</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>cria_bioline_pr_pr16248</sourcerecordid><originalsourceid>FETCH-LOGICAL-b276t-710ee1eb09119fbc352bfe65947436a9d0f46e7074ae1e0bc333f0b67a12624a3</originalsourceid><addsrcrecordid>eNpFkE1LAzEQhoMoWKtH7_kDu2Y2X81Ra61CxYuel2SdYNrupmRXsf_erC0KA_Py8jADDyHXwErBQdwM610qv0AGUwI7IROQRhVmVunTY5bGqHNy0fdrxqQyBibkbuE9NgONnt6H2DcxoaVD3MQU6bPdhC5S_B6SHZGOfux3mD5TaLANloaOtjlekjNvtz1eHfeUvD0sXuePxepl-TS_XRWu0mooNDBEQMcMgPGu4bJyHpU0QguurHlnXijUTAubMZYBzj1zSluoVCUsn5LicLdJse8T-nqXQmvTvgZWjwLqUUD9KyBXmS8PvAtxGzr8w5sUbP1f5oH8YMZ_ADaNYRQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Effect of Dioscorea tokoro Makino extract on hyperuricemia in mice</title><source>DOAJ Directory of Open Access Journals</source><source>African Journals Online (Open Access)</source><source>Bioline International</source><source>EZB-FREE-00999 freely available EZB journals</source><source>Free Full-Text Journals in Chemistry</source><creator>Fei, Yang ; Ye, Dan ; Fan, XiaoFen ; Dong, FengQin</creator><creatorcontrib>Fei, Yang ; Ye, Dan ; Fan, XiaoFen ; Dong, FengQin</creatorcontrib><description>Purpose: To investigate the anti-hyperuricemic effect of Dioscorea
tokoro Makino extract (DTME) in potassium oxonate-induced hyperuricemic
mice. Method: The effect of DTME was investigated in the hyperuricemic
mice induced by potassium oxonate. DTME. The extract was administered
to the mice daily at doses of 220, 440 and 880 mg/kg for 10 days;
allopurinol (5 mg/kg) was given as positive control. Serum and urine
levels of uric acid and creatinine were determined by colorimetric
method. Simultaneously, protein levels of urate transporter 1 (URAT1)
and organic anion transporter 1 (OAT1) in the rat kidney were analyzed
by Western blotting. Results: Compared with control, a high dose of
DTME inhibited xanthine oxidase (XOD) activity in both serum (18.12
± 1.33 U/L) and in liver (70.15 ± 5.20 U/g protein) (p <
0.05); decreased levels of serum uric acid (2.04 ± 0.64 mg/L) (p
< 0.05), serum creatinine (0.35 ± 0.18 μmol/L) and blood
urea nitrogen (BUN) (8.83 ± 0.71 mmol/L) (p < 0.05).
Furthermore, the extract increased levels of urine uric acid (38.34
± 8.23 mg/L), urine creatinine (34.38 ± 1.98 mmol/L), down
regulated of URAT1 and up regulated of OAT1 protein expressions (p <
0.05) in the renal tissue of hyperuricemic mice. Conclusion: DTME
improves renal dysfunction in rats by regulating renal urate
transporters in hyperuricemic rats. This may find therapeutic
application in antihypertensive therapy.</description><identifier>ISSN: 1596-5996</identifier><identifier>EISSN: 1596-9827</identifier><identifier>DOI: 10.4314/tjpr.v15i9.10</identifier><language>eng</language><publisher>Pharmacotherapy Group, Faculty of Pharmacy, University of Benin, Benin City, Nigeria</publisher><subject>Creatinine ; Dioscorea tokoro Makino ; Hyperuricemic ; Renal urate transporters ; Uric acid</subject><ispartof>Tropical journal of pharmaceutical research, 2016-09, Vol.15 (9), p.1883</ispartof><rights>Copyright 2016 - Tropical Journal of Pharmaceutical Research</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b276t-710ee1eb09119fbc352bfe65947436a9d0f46e7074ae1e0bc333f0b67a12624a3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,864,27924,27925,79426</link.rule.ids></links><search><creatorcontrib>Fei, Yang</creatorcontrib><creatorcontrib>Ye, Dan</creatorcontrib><creatorcontrib>Fan, XiaoFen</creatorcontrib><creatorcontrib>Dong, FengQin</creatorcontrib><title>Effect of Dioscorea tokoro Makino extract on hyperuricemia in mice</title><title>Tropical journal of pharmaceutical research</title><description>Purpose: To investigate the anti-hyperuricemic effect of Dioscorea
tokoro Makino extract (DTME) in potassium oxonate-induced hyperuricemic
mice. Method: The effect of DTME was investigated in the hyperuricemic
mice induced by potassium oxonate. DTME. The extract was administered
to the mice daily at doses of 220, 440 and 880 mg/kg for 10 days;
allopurinol (5 mg/kg) was given as positive control. Serum and urine
levels of uric acid and creatinine were determined by colorimetric
method. Simultaneously, protein levels of urate transporter 1 (URAT1)
and organic anion transporter 1 (OAT1) in the rat kidney were analyzed
by Western blotting. Results: Compared with control, a high dose of
DTME inhibited xanthine oxidase (XOD) activity in both serum (18.12
± 1.33 U/L) and in liver (70.15 ± 5.20 U/g protein) (p <
0.05); decreased levels of serum uric acid (2.04 ± 0.64 mg/L) (p
< 0.05), serum creatinine (0.35 ± 0.18 μmol/L) and blood
urea nitrogen (BUN) (8.83 ± 0.71 mmol/L) (p < 0.05).
Furthermore, the extract increased levels of urine uric acid (38.34
± 8.23 mg/L), urine creatinine (34.38 ± 1.98 mmol/L), down
regulated of URAT1 and up regulated of OAT1 protein expressions (p <
0.05) in the renal tissue of hyperuricemic mice. Conclusion: DTME
improves renal dysfunction in rats by regulating renal urate
transporters in hyperuricemic rats. This may find therapeutic
application in antihypertensive therapy.</description><subject>Creatinine</subject><subject>Dioscorea tokoro Makino</subject><subject>Hyperuricemic</subject><subject>Renal urate transporters</subject><subject>Uric acid</subject><issn>1596-5996</issn><issn>1596-9827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>RBI</sourceid><recordid>eNpFkE1LAzEQhoMoWKtH7_kDu2Y2X81Ra61CxYuel2SdYNrupmRXsf_erC0KA_Py8jADDyHXwErBQdwM610qv0AGUwI7IROQRhVmVunTY5bGqHNy0fdrxqQyBibkbuE9NgONnt6H2DcxoaVD3MQU6bPdhC5S_B6SHZGOfux3mD5TaLANloaOtjlekjNvtz1eHfeUvD0sXuePxepl-TS_XRWu0mooNDBEQMcMgPGu4bJyHpU0QguurHlnXijUTAubMZYBzj1zSluoVCUsn5LicLdJse8T-nqXQmvTvgZWjwLqUUD9KyBXmS8PvAtxGzr8w5sUbP1f5oH8YMZ_ADaNYRQ</recordid><startdate>20160901</startdate><enddate>20160901</enddate><creator>Fei, Yang</creator><creator>Ye, Dan</creator><creator>Fan, XiaoFen</creator><creator>Dong, FengQin</creator><general>Pharmacotherapy Group, Faculty of Pharmacy, University of Benin, Benin City, Nigeria</general><scope>RBI</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20160901</creationdate><title>Effect of Dioscorea tokoro Makino extract on hyperuricemia in mice</title><author>Fei, Yang ; Ye, Dan ; Fan, XiaoFen ; Dong, FengQin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b276t-710ee1eb09119fbc352bfe65947436a9d0f46e7074ae1e0bc333f0b67a12624a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Creatinine</topic><topic>Dioscorea tokoro Makino</topic><topic>Hyperuricemic</topic><topic>Renal urate transporters</topic><topic>Uric acid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fei, Yang</creatorcontrib><creatorcontrib>Ye, Dan</creatorcontrib><creatorcontrib>Fan, XiaoFen</creatorcontrib><creatorcontrib>Dong, FengQin</creatorcontrib><collection>Bioline International</collection><collection>CrossRef</collection><jtitle>Tropical journal of pharmaceutical research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fei, Yang</au><au>Ye, Dan</au><au>Fan, XiaoFen</au><au>Dong, FengQin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of Dioscorea tokoro Makino extract on hyperuricemia in mice</atitle><jtitle>Tropical journal of pharmaceutical research</jtitle><date>2016-09-01</date><risdate>2016</risdate><volume>15</volume><issue>9</issue><spage>1883</spage><pages>1883-</pages><issn>1596-5996</issn><eissn>1596-9827</eissn><abstract>Purpose: To investigate the anti-hyperuricemic effect of Dioscorea
tokoro Makino extract (DTME) in potassium oxonate-induced hyperuricemic
mice. Method: The effect of DTME was investigated in the hyperuricemic
mice induced by potassium oxonate. DTME. The extract was administered
to the mice daily at doses of 220, 440 and 880 mg/kg for 10 days;
allopurinol (5 mg/kg) was given as positive control. Serum and urine
levels of uric acid and creatinine were determined by colorimetric
method. Simultaneously, protein levels of urate transporter 1 (URAT1)
and organic anion transporter 1 (OAT1) in the rat kidney were analyzed
by Western blotting. Results: Compared with control, a high dose of
DTME inhibited xanthine oxidase (XOD) activity in both serum (18.12
± 1.33 U/L) and in liver (70.15 ± 5.20 U/g protein) (p <
0.05); decreased levels of serum uric acid (2.04 ± 0.64 mg/L) (p
< 0.05), serum creatinine (0.35 ± 0.18 μmol/L) and blood
urea nitrogen (BUN) (8.83 ± 0.71 mmol/L) (p < 0.05).
Furthermore, the extract increased levels of urine uric acid (38.34
± 8.23 mg/L), urine creatinine (34.38 ± 1.98 mmol/L), down
regulated of URAT1 and up regulated of OAT1 protein expressions (p <
0.05) in the renal tissue of hyperuricemic mice. Conclusion: DTME
improves renal dysfunction in rats by regulating renal urate
transporters in hyperuricemic rats. This may find therapeutic
application in antihypertensive therapy.</abstract><pub>Pharmacotherapy Group, Faculty of Pharmacy, University of Benin, Benin City, Nigeria</pub><doi>10.4314/tjpr.v15i9.10</doi><oa>free_for_read</oa></addata></record> |
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subjects | Creatinine Dioscorea tokoro Makino Hyperuricemic Renal urate transporters Uric acid |
title | Effect of Dioscorea tokoro Makino extract on hyperuricemia in mice |
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