Antioxidant, antihyperuricemic and xanthine oxidase inhibitory activities of Hyoscyamus reticulatus
Context: Xanthine oxidase (XO) is a key enzyme in the pathophysiological homeostasis of hyperuricemia. It catalyzes the oxidation of hypoxanthine to xanthine and then to uric acid, the reaction involves the formation of free radical intermediates and superoxide byproducts. Objectives: This study was...
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Veröffentlicht in: | Pharmaceutical biology 2010-12, Vol.48 (12), p.1376-1383 |
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creator | Mohammad, Mohammad K. Almasri, Ihab M. Tawaha, Khaled Issa, Ala Al-Nadaf, Afaf Hudaib, Mohammad AlKhatib, Hatim S. Abu-Gharbieh, Eman Bustanji, Yasser |
description | Context: Xanthine oxidase (XO) is a key enzyme in the pathophysiological homeostasis of hyperuricemia. It catalyzes the oxidation of hypoxanthine to xanthine and then to uric acid, the reaction involves the formation of free radical intermediates and superoxide byproducts.
Objectives: This study was undertaken to investigate the antioxidant, antihyperuricemic, and xanthine oxidase inhibitory potentials of Hyoscyamus reticulatus L. (Solanaceae) extract.
Materials and methods: The antioxidant potency was measured using the ABTS*+ scavenging capacity system, which includes Trolox as a standard. The xanthine oxidase inhibitory activity of the extract was quantitated in vitro by measuring the decline in the catalytic rate of xanthine oxidase following incubations with the plant extracts and using xanthine as a substrate. The hypouricemic potential of the extract was evaluated using an in vivo model for hyperuricemia. We tested three different doses of the extract and allopurinol was used as standard antihyperuricemic positive control.
Results: H. reticulatus aqueous extract exhibited significant antioxidant scavenging properties (533.26 μmol TE/g dry extract weight) and inhibitory effect on xanthine oxidase activity (IC50 12.8 μg/mL). Furthermore, oral administration of the aqueous extract significantly reduced serum urate levels in oxonate-induced hyperuricemic mice in a dose-dependent manner.
Discussion and conclusion: Our results suggest that the aqueous extract of H. reticulatus aerial parts might have great potential as an antioxidant and a hypouricemic agent. Our lab is currently identifying the active compounds in the extract to which the biological activities could be attributed. |
doi_str_mv | 10.3109/13880209.2010.483521 |
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Objectives: This study was undertaken to investigate the antioxidant, antihyperuricemic, and xanthine oxidase inhibitory potentials of Hyoscyamus reticulatus L. (Solanaceae) extract.
Materials and methods: The antioxidant potency was measured using the ABTS*+ scavenging capacity system, which includes Trolox as a standard. The xanthine oxidase inhibitory activity of the extract was quantitated in vitro by measuring the decline in the catalytic rate of xanthine oxidase following incubations with the plant extracts and using xanthine as a substrate. The hypouricemic potential of the extract was evaluated using an in vivo model for hyperuricemia. We tested three different doses of the extract and allopurinol was used as standard antihyperuricemic positive control.
Results: H. reticulatus aqueous extract exhibited significant antioxidant scavenging properties (533.26 μmol TE/g dry extract weight) and inhibitory effect on xanthine oxidase activity (IC50 12.8 μg/mL). Furthermore, oral administration of the aqueous extract significantly reduced serum urate levels in oxonate-induced hyperuricemic mice in a dose-dependent manner.
Discussion and conclusion: Our results suggest that the aqueous extract of H. reticulatus aerial parts might have great potential as an antioxidant and a hypouricemic agent. Our lab is currently identifying the active compounds in the extract to which the biological activities could be attributed.</description><identifier>ISSN: 1388-0209</identifier><identifier>EISSN: 1744-5116</identifier><identifier>DOI: 10.3109/13880209.2010.483521</identifier><identifier>PMID: 20738177</identifier><language>eng</language><publisher>England: Informa Healthcare</publisher><subject><![CDATA[Allopurinol - pharmacology ; Animals ; Antioxidants - administration & dosage ; Antioxidants - isolation & purification ; Antioxidants - pharmacology ; BALB/c mice ; Disease Models, Animal ; Dose-Response Relationship, Drug ; free radicals ; gout ; Gout Suppressants - administration & dosage ; Gout Suppressants - isolation & purification ; Gout Suppressants - pharmacology ; Hyoscyamus - chemistry ; Hyperuricemia ; Hyperuricemia - drug therapy ; Inhibitory Concentration 50 ; Male ; Mice ; Mice, Inbred BALB C ; phenolic compounds ; Plant Components, Aerial ; Plant Extracts - administration & dosage ; Plant Extracts - pharmacology ; Xanthine Oxidase - antagonists & inhibitors]]></subject><ispartof>Pharmaceutical biology, 2010-12, Vol.48 (12), p.1376-1383</ispartof><rights>2010 Informa Healthcare USA, Inc. 2010</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c417t-4c1a7407a0d1323495a713d3c6e75233ac7c274c3c7d63eac4d773f20a95013d3</citedby><cites>FETCH-LOGICAL-c417t-4c1a7407a0d1323495a713d3c6e75233ac7c274c3c7d63eac4d773f20a95013d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20738177$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mohammad, Mohammad K.</creatorcontrib><creatorcontrib>Almasri, Ihab M.</creatorcontrib><creatorcontrib>Tawaha, Khaled</creatorcontrib><creatorcontrib>Issa, Ala</creatorcontrib><creatorcontrib>Al-Nadaf, Afaf</creatorcontrib><creatorcontrib>Hudaib, Mohammad</creatorcontrib><creatorcontrib>AlKhatib, Hatim S.</creatorcontrib><creatorcontrib>Abu-Gharbieh, Eman</creatorcontrib><creatorcontrib>Bustanji, Yasser</creatorcontrib><title>Antioxidant, antihyperuricemic and xanthine oxidase inhibitory activities of Hyoscyamus reticulatus</title><title>Pharmaceutical biology</title><addtitle>Pharm Biol</addtitle><description>Context: Xanthine oxidase (XO) is a key enzyme in the pathophysiological homeostasis of hyperuricemia. It catalyzes the oxidation of hypoxanthine to xanthine and then to uric acid, the reaction involves the formation of free radical intermediates and superoxide byproducts.
Objectives: This study was undertaken to investigate the antioxidant, antihyperuricemic, and xanthine oxidase inhibitory potentials of Hyoscyamus reticulatus L. (Solanaceae) extract.
Materials and methods: The antioxidant potency was measured using the ABTS*+ scavenging capacity system, which includes Trolox as a standard. The xanthine oxidase inhibitory activity of the extract was quantitated in vitro by measuring the decline in the catalytic rate of xanthine oxidase following incubations with the plant extracts and using xanthine as a substrate. The hypouricemic potential of the extract was evaluated using an in vivo model for hyperuricemia. We tested three different doses of the extract and allopurinol was used as standard antihyperuricemic positive control.
Results: H. reticulatus aqueous extract exhibited significant antioxidant scavenging properties (533.26 μmol TE/g dry extract weight) and inhibitory effect on xanthine oxidase activity (IC50 12.8 μg/mL). Furthermore, oral administration of the aqueous extract significantly reduced serum urate levels in oxonate-induced hyperuricemic mice in a dose-dependent manner.
Discussion and conclusion: Our results suggest that the aqueous extract of H. reticulatus aerial parts might have great potential as an antioxidant and a hypouricemic agent. Our lab is currently identifying the active compounds in the extract to which the biological activities could be attributed.</description><subject>Allopurinol - pharmacology</subject><subject>Animals</subject><subject>Antioxidants - administration & dosage</subject><subject>Antioxidants - isolation & purification</subject><subject>Antioxidants - pharmacology</subject><subject>BALB/c mice</subject><subject>Disease Models, Animal</subject><subject>Dose-Response Relationship, Drug</subject><subject>free radicals</subject><subject>gout</subject><subject>Gout Suppressants - administration & dosage</subject><subject>Gout Suppressants - isolation & purification</subject><subject>Gout Suppressants - pharmacology</subject><subject>Hyoscyamus - chemistry</subject><subject>Hyperuricemia</subject><subject>Hyperuricemia - drug therapy</subject><subject>Inhibitory Concentration 50</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>phenolic compounds</subject><subject>Plant Components, Aerial</subject><subject>Plant Extracts - administration & dosage</subject><subject>Plant Extracts - pharmacology</subject><subject>Xanthine Oxidase - antagonists & inhibitors</subject><issn>1388-0209</issn><issn>1744-5116</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1P3DAQhq2qVYFt_wFCufVCqO1x1tkLFUJ8VELqBc7WMHEUoyRebKcl_74OC0hcuNjWq2fesR7GDgU_AcE3PwXUNZd8cyJ5jlQNlRSf2L7QSpWVEOvP-Z2RcmH22EGMD5zzCqD6yvYk11ALrfcZnY3J-SfX4JiOi3y4bt7aMAVHdnCUk6Z4ynHnRls8c9EWbuzcvUs-zAVScn9dcjYWvi2uZx9pxmGKRbDJ0dRjmuI39qXFPtrvL_eK3V1e3J5flzd_rn6fn92UpIROpSKBWnGNvBEgQW0q1AIaoLXVlQRA0iS1IiDdrMEiqUZraCXHTcUXcMV-7Hq3wT9ONiYzuEi273G0foqmFlIAyFy1YmpHUvAxBtuabXADhtkIbha75tWuWeyand08dvSyYLofbPM29KozA792gBtbHwb850PfmIRz70MbcCQXl_oPV5y-a-gs9qkjDNY8-CmM2d_Hf_wPMl2d9w</recordid><startdate>201012</startdate><enddate>201012</enddate><creator>Mohammad, Mohammad K.</creator><creator>Almasri, Ihab M.</creator><creator>Tawaha, Khaled</creator><creator>Issa, Ala</creator><creator>Al-Nadaf, Afaf</creator><creator>Hudaib, Mohammad</creator><creator>AlKhatib, Hatim S.</creator><creator>Abu-Gharbieh, Eman</creator><creator>Bustanji, Yasser</creator><general>Informa Healthcare</general><general>Taylor & Francis</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>7X8</scope></search><sort><creationdate>201012</creationdate><title>Antioxidant, antihyperuricemic and xanthine oxidase inhibitory activities of Hyoscyamus reticulatus</title><author>Mohammad, Mohammad K. ; Almasri, Ihab M. ; Tawaha, Khaled ; Issa, Ala ; Al-Nadaf, Afaf ; Hudaib, Mohammad ; AlKhatib, Hatim S. ; Abu-Gharbieh, Eman ; Bustanji, Yasser</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c417t-4c1a7407a0d1323495a713d3c6e75233ac7c274c3c7d63eac4d773f20a95013d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Allopurinol - pharmacology</topic><topic>Animals</topic><topic>Antioxidants - administration & dosage</topic><topic>Antioxidants - isolation & purification</topic><topic>Antioxidants - pharmacology</topic><topic>BALB/c mice</topic><topic>Disease Models, Animal</topic><topic>Dose-Response Relationship, Drug</topic><topic>free radicals</topic><topic>gout</topic><topic>Gout Suppressants - administration & dosage</topic><topic>Gout Suppressants - isolation & purification</topic><topic>Gout Suppressants - pharmacology</topic><topic>Hyoscyamus - chemistry</topic><topic>Hyperuricemia</topic><topic>Hyperuricemia - drug therapy</topic><topic>Inhibitory Concentration 50</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>phenolic compounds</topic><topic>Plant Components, Aerial</topic><topic>Plant Extracts - administration & dosage</topic><topic>Plant Extracts - pharmacology</topic><topic>Xanthine Oxidase - antagonists & inhibitors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mohammad, Mohammad K.</creatorcontrib><creatorcontrib>Almasri, Ihab M.</creatorcontrib><creatorcontrib>Tawaha, Khaled</creatorcontrib><creatorcontrib>Issa, Ala</creatorcontrib><creatorcontrib>Al-Nadaf, Afaf</creatorcontrib><creatorcontrib>Hudaib, Mohammad</creatorcontrib><creatorcontrib>AlKhatib, Hatim S.</creatorcontrib><creatorcontrib>Abu-Gharbieh, Eman</creatorcontrib><creatorcontrib>Bustanji, Yasser</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Pharmaceutical biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mohammad, Mohammad K.</au><au>Almasri, Ihab M.</au><au>Tawaha, Khaled</au><au>Issa, Ala</au><au>Al-Nadaf, Afaf</au><au>Hudaib, Mohammad</au><au>AlKhatib, Hatim S.</au><au>Abu-Gharbieh, Eman</au><au>Bustanji, Yasser</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antioxidant, antihyperuricemic and xanthine oxidase inhibitory activities of Hyoscyamus reticulatus</atitle><jtitle>Pharmaceutical biology</jtitle><addtitle>Pharm Biol</addtitle><date>2010-12</date><risdate>2010</risdate><volume>48</volume><issue>12</issue><spage>1376</spage><epage>1383</epage><pages>1376-1383</pages><issn>1388-0209</issn><eissn>1744-5116</eissn><abstract>Context: Xanthine oxidase (XO) is a key enzyme in the pathophysiological homeostasis of hyperuricemia. It catalyzes the oxidation of hypoxanthine to xanthine and then to uric acid, the reaction involves the formation of free radical intermediates and superoxide byproducts.
Objectives: This study was undertaken to investigate the antioxidant, antihyperuricemic, and xanthine oxidase inhibitory potentials of Hyoscyamus reticulatus L. (Solanaceae) extract.
Materials and methods: The antioxidant potency was measured using the ABTS*+ scavenging capacity system, which includes Trolox as a standard. The xanthine oxidase inhibitory activity of the extract was quantitated in vitro by measuring the decline in the catalytic rate of xanthine oxidase following incubations with the plant extracts and using xanthine as a substrate. The hypouricemic potential of the extract was evaluated using an in vivo model for hyperuricemia. We tested three different doses of the extract and allopurinol was used as standard antihyperuricemic positive control.
Results: H. reticulatus aqueous extract exhibited significant antioxidant scavenging properties (533.26 μmol TE/g dry extract weight) and inhibitory effect on xanthine oxidase activity (IC50 12.8 μg/mL). Furthermore, oral administration of the aqueous extract significantly reduced serum urate levels in oxonate-induced hyperuricemic mice in a dose-dependent manner.
Discussion and conclusion: Our results suggest that the aqueous extract of H. reticulatus aerial parts might have great potential as an antioxidant and a hypouricemic agent. Our lab is currently identifying the active compounds in the extract to which the biological activities could be attributed.</abstract><cop>England</cop><pub>Informa Healthcare</pub><pmid>20738177</pmid><doi>10.3109/13880209.2010.483521</doi><tpages>8</tpages></addata></record> |
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subjects | Allopurinol - pharmacology Animals Antioxidants - administration & dosage Antioxidants - isolation & purification Antioxidants - pharmacology BALB/c mice Disease Models, Animal Dose-Response Relationship, Drug free radicals gout Gout Suppressants - administration & dosage Gout Suppressants - isolation & purification Gout Suppressants - pharmacology Hyoscyamus - chemistry Hyperuricemia Hyperuricemia - drug therapy Inhibitory Concentration 50 Male Mice Mice, Inbred BALB C phenolic compounds Plant Components, Aerial Plant Extracts - administration & dosage Plant Extracts - pharmacology Xanthine Oxidase - antagonists & inhibitors |
title | Antioxidant, antihyperuricemic and xanthine oxidase inhibitory activities of Hyoscyamus reticulatus |
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