Quantitative HPLC analysis of two key flavonoids and inhibitory activities against aldose reductase from different parts of the Korean thistle, Cirsium maackii
Previously, the correlation between antioxidant activity and HPLC profiles of several Korean thistles has been recognized. In our ongoing study of the comparative evaluation of Korean thistles, we chose Cirsium maackii to assess the antioxidant and aldose reductase (AR) inhibitory activities of its...
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description | Previously, the correlation between antioxidant activity and HPLC profiles of several Korean thistles has been recognized. In our ongoing study of the comparative evaluation of Korean thistles, we chose
Cirsium
maackii to assess the antioxidant and aldose reductase (AR) inhibitory activities of its varying parts, including the leaves, roots, stems, and flowers, along with two major components, luteolin 5-
O-β-
d-glucopyranoside (
1) and the aglycone luteolin (
2). In order to determine selective and efficient usage of the individual parts, HPLC quantitative analysis of the two key flavonoids of each
C.
maackii part has been performed for the first time. From the results of the comparative evaluation between the oxidative stress-related diabetic complications and quantitative phytochemical analysis from various parts of
C.
maackii, the content of
1 and
2 might contribute to the antioxidant and AR inhibitory activities of this thistle, clearly suggesting their potential for use in the development of therapeutic or preventive agents for diabetic complications and oxidative stress-related diseases. Furthermore, our present study will pave the way of the guidelines for the efficacy and differentiation and standardization of individual parts of this herbal material, and as such, this bioactive thistle could serve as an alternative source of
1 and
2. |
doi_str_mv | 10.1016/j.fct.2009.08.014 |
format | Article |
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Cirsium
maackii to assess the antioxidant and aldose reductase (AR) inhibitory activities of its varying parts, including the leaves, roots, stems, and flowers, along with two major components, luteolin 5-
O-β-
d-glucopyranoside (
1) and the aglycone luteolin (
2). In order to determine selective and efficient usage of the individual parts, HPLC quantitative analysis of the two key flavonoids of each
C.
maackii part has been performed for the first time. From the results of the comparative evaluation between the oxidative stress-related diabetic complications and quantitative phytochemical analysis from various parts of
C.
maackii, the content of
1 and
2 might contribute to the antioxidant and AR inhibitory activities of this thistle, clearly suggesting their potential for use in the development of therapeutic or preventive agents for diabetic complications and oxidative stress-related diseases. Furthermore, our present study will pave the way of the guidelines for the efficacy and differentiation and standardization of individual parts of this herbal material, and as such, this bioactive thistle could serve as an alternative source of
1 and
2.</description><identifier>ISSN: 0278-6915</identifier><identifier>EISSN: 1873-6351</identifier><identifier>DOI: 10.1016/j.fct.2009.08.014</identifier><identifier>PMID: 19733610</identifier><identifier>CODEN: FCTOD7</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Aldehyde Reductase - antagonists & inhibitors ; aldose reductase ; Antioxidant ; antioxidants ; Biological and medical sciences ; Cirsium ; Cirsium - chemistry ; Cirsium maackii ; diabetes ; Diabetes. Impaired glucose tolerance ; Diabetic complication ; Endocrine pancreas. Apud cells (diseases) ; Endocrinopathies ; enzyme inhibition ; enzyme inhibitors ; enzymes ; Etiopathogenesis. Screening. Investigations. Target tissue resistance ; flavanoids ; Flavones - chemistry ; Flavones - pharmacology ; General pharmacology ; Glucosides - chemistry ; Glucosides - pharmacology ; high performance liquid chromatography ; HPLC quantitative analysis ; Luteolin - chemistry ; Luteolin - pharmacology ; Luteolin 5- O-β- d-glucopyranoside ; Medical sciences ; Molecular Structure ; oxidative stress ; Pharmacognosy. Homeopathy. Health food ; Pharmacology. Drug treatments ; Plant Components, Aerial - chemistry ; Plant Roots - chemistry ; protective effect ; Thistle</subject><ispartof>Food and chemical toxicology, 2009-11, Vol.47 (11), p.2790-2797</ispartof><rights>2009 Elsevier Ltd</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c472t-5b0f329a4607d08e5635c73afaa4aa40c3ab074ea3371523b779ca9c1d221a553</citedby><cites>FETCH-LOGICAL-c472t-5b0f329a4607d08e5635c73afaa4aa40c3ab074ea3371523b779ca9c1d221a553</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0278691509004025$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22103031$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19733610$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jung, Hyun Ah</creatorcontrib><creatorcontrib>Kim, Yeong Shik</creatorcontrib><creatorcontrib>Choi, Jae Sue</creatorcontrib><title>Quantitative HPLC analysis of two key flavonoids and inhibitory activities against aldose reductase from different parts of the Korean thistle, Cirsium maackii</title><title>Food and chemical toxicology</title><addtitle>Food Chem Toxicol</addtitle><description>Previously, the correlation between antioxidant activity and HPLC profiles of several Korean thistles has been recognized. In our ongoing study of the comparative evaluation of Korean thistles, we chose
Cirsium
maackii to assess the antioxidant and aldose reductase (AR) inhibitory activities of its varying parts, including the leaves, roots, stems, and flowers, along with two major components, luteolin 5-
O-β-
d-glucopyranoside (
1) and the aglycone luteolin (
2). In order to determine selective and efficient usage of the individual parts, HPLC quantitative analysis of the two key flavonoids of each
C.
maackii part has been performed for the first time. From the results of the comparative evaluation between the oxidative stress-related diabetic complications and quantitative phytochemical analysis from various parts of
C.
maackii, the content of
1 and
2 might contribute to the antioxidant and AR inhibitory activities of this thistle, clearly suggesting their potential for use in the development of therapeutic or preventive agents for diabetic complications and oxidative stress-related diseases. Furthermore, our present study will pave the way of the guidelines for the efficacy and differentiation and standardization of individual parts of this herbal material, and as such, this bioactive thistle could serve as an alternative source of
1 and
2.</description><subject>Aldehyde Reductase - antagonists & inhibitors</subject><subject>aldose reductase</subject><subject>Antioxidant</subject><subject>antioxidants</subject><subject>Biological and medical sciences</subject><subject>Cirsium</subject><subject>Cirsium - chemistry</subject><subject>Cirsium maackii</subject><subject>diabetes</subject><subject>Diabetes. Impaired glucose tolerance</subject><subject>Diabetic complication</subject><subject>Endocrine pancreas. Apud cells (diseases)</subject><subject>Endocrinopathies</subject><subject>enzyme inhibition</subject><subject>enzyme inhibitors</subject><subject>enzymes</subject><subject>Etiopathogenesis. Screening. Investigations. Target tissue resistance</subject><subject>flavanoids</subject><subject>Flavones - chemistry</subject><subject>Flavones - pharmacology</subject><subject>General pharmacology</subject><subject>Glucosides - chemistry</subject><subject>Glucosides - pharmacology</subject><subject>high performance liquid chromatography</subject><subject>HPLC quantitative analysis</subject><subject>Luteolin - chemistry</subject><subject>Luteolin - pharmacology</subject><subject>Luteolin 5- O-β- d-glucopyranoside</subject><subject>Medical sciences</subject><subject>Molecular Structure</subject><subject>oxidative stress</subject><subject>Pharmacognosy. Homeopathy. Health food</subject><subject>Pharmacology. Drug treatments</subject><subject>Plant Components, Aerial - chemistry</subject><subject>Plant Roots - chemistry</subject><subject>protective effect</subject><subject>Thistle</subject><issn>0278-6915</issn><issn>1873-6351</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kUGP0zAQhSMEYpeFH8AFfEFcaBnHSZyIE6qARVQCBHu2ps54d7pJ3LWdov4a_ipetYIbkiWPNN8bPb1XFM8lLCXI5u126WxalgDdEtolyOpBcS5brRaNquXD4hxK3S6aTtZnxZMYtwCgpW4eF2ey00o1Es6L399nnBInTLwncfltvRI44XCIHIV3Iv3y4pYOwg2495PnPuZ1L3i64Q0nHw4CbVZyYsqba-QpJoFD7yOJQP1sE-bJBT-Knp2jQFMSOwzpeP2GxBcfCKc8ckwDvRErDpHnUYyI9pb5afHI4RDp2em_KK4-fvi5ulysv376vHq_XthKl2lRb8CpssOqAd1DS3VOwGqFDrHKD6zCDeiKUCkt61JttO4sdlb2ZSmxrtVF8fp4dxf83UwxmZGjpWHAifwcjVZVjryTkEl5JG3wMQZyZhd4xHAwEsx9LWZrci3mvhYDrcm1ZM2L0_V5M1L_T3HqIQOvTgBGi4MLOFmOf7lsEhQombmXR86hN3gdMnP1owSpQGpZlq3KxLsjQTmtPVMw0TJNlnoOlG31nv9j9A_kW7ZZ</recordid><startdate>20091101</startdate><enddate>20091101</enddate><creator>Jung, Hyun Ah</creator><creator>Kim, Yeong Shik</creator><creator>Choi, Jae Sue</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>FBQ</scope><scope>IQODW</scope><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>20091101</creationdate><title>Quantitative HPLC analysis of two key flavonoids and inhibitory activities against aldose reductase from different parts of the Korean thistle, Cirsium maackii</title><author>Jung, Hyun Ah ; Kim, Yeong Shik ; Choi, Jae Sue</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c472t-5b0f329a4607d08e5635c73afaa4aa40c3ab074ea3371523b779ca9c1d221a553</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Aldehyde Reductase - antagonists & inhibitors</topic><topic>aldose reductase</topic><topic>Antioxidant</topic><topic>antioxidants</topic><topic>Biological and medical sciences</topic><topic>Cirsium</topic><topic>Cirsium - chemistry</topic><topic>Cirsium maackii</topic><topic>diabetes</topic><topic>Diabetes. Impaired glucose tolerance</topic><topic>Diabetic complication</topic><topic>Endocrine pancreas. Apud cells (diseases)</topic><topic>Endocrinopathies</topic><topic>enzyme inhibition</topic><topic>enzyme inhibitors</topic><topic>enzymes</topic><topic>Etiopathogenesis. Screening. Investigations. Target tissue resistance</topic><topic>flavanoids</topic><topic>Flavones - chemistry</topic><topic>Flavones - pharmacology</topic><topic>General pharmacology</topic><topic>Glucosides - chemistry</topic><topic>Glucosides - pharmacology</topic><topic>high performance liquid chromatography</topic><topic>HPLC quantitative analysis</topic><topic>Luteolin - chemistry</topic><topic>Luteolin - pharmacology</topic><topic>Luteolin 5- O-β- d-glucopyranoside</topic><topic>Medical sciences</topic><topic>Molecular Structure</topic><topic>oxidative stress</topic><topic>Pharmacognosy. Homeopathy. Health food</topic><topic>Pharmacology. Drug treatments</topic><topic>Plant Components, Aerial - chemistry</topic><topic>Plant Roots - chemistry</topic><topic>protective effect</topic><topic>Thistle</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jung, Hyun Ah</creatorcontrib><creatorcontrib>Kim, Yeong Shik</creatorcontrib><creatorcontrib>Choi, Jae Sue</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><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>Food and chemical toxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jung, Hyun Ah</au><au>Kim, Yeong Shik</au><au>Choi, Jae Sue</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Quantitative HPLC analysis of two key flavonoids and inhibitory activities against aldose reductase from different parts of the Korean thistle, Cirsium maackii</atitle><jtitle>Food and chemical toxicology</jtitle><addtitle>Food Chem Toxicol</addtitle><date>2009-11-01</date><risdate>2009</risdate><volume>47</volume><issue>11</issue><spage>2790</spage><epage>2797</epage><pages>2790-2797</pages><issn>0278-6915</issn><eissn>1873-6351</eissn><coden>FCTOD7</coden><abstract>Previously, the correlation between antioxidant activity and HPLC profiles of several Korean thistles has been recognized. In our ongoing study of the comparative evaluation of Korean thistles, we chose
Cirsium
maackii to assess the antioxidant and aldose reductase (AR) inhibitory activities of its varying parts, including the leaves, roots, stems, and flowers, along with two major components, luteolin 5-
O-β-
d-glucopyranoside (
1) and the aglycone luteolin (
2). In order to determine selective and efficient usage of the individual parts, HPLC quantitative analysis of the two key flavonoids of each
C.
maackii part has been performed for the first time. From the results of the comparative evaluation between the oxidative stress-related diabetic complications and quantitative phytochemical analysis from various parts of
C.
maackii, the content of
1 and
2 might contribute to the antioxidant and AR inhibitory activities of this thistle, clearly suggesting their potential for use in the development of therapeutic or preventive agents for diabetic complications and oxidative stress-related diseases. Furthermore, our present study will pave the way of the guidelines for the efficacy and differentiation and standardization of individual parts of this herbal material, and as such, this bioactive thistle could serve as an alternative source of
1 and
2.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>19733610</pmid><doi>10.1016/j.fct.2009.08.014</doi><tpages>8</tpages></addata></record> |
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source | MEDLINE; Elsevier ScienceDirect Journals Complete |
subjects | Aldehyde Reductase - antagonists & inhibitors aldose reductase Antioxidant antioxidants Biological and medical sciences Cirsium Cirsium - chemistry Cirsium maackii diabetes Diabetes. Impaired glucose tolerance Diabetic complication Endocrine pancreas. Apud cells (diseases) Endocrinopathies enzyme inhibition enzyme inhibitors enzymes Etiopathogenesis. Screening. Investigations. Target tissue resistance flavanoids Flavones - chemistry Flavones - pharmacology General pharmacology Glucosides - chemistry Glucosides - pharmacology high performance liquid chromatography HPLC quantitative analysis Luteolin - chemistry Luteolin - pharmacology Luteolin 5- O-β- d-glucopyranoside Medical sciences Molecular Structure oxidative stress Pharmacognosy. Homeopathy. Health food Pharmacology. Drug treatments Plant Components, Aerial - chemistry Plant Roots - chemistry protective effect Thistle |
title | Quantitative HPLC analysis of two key flavonoids and inhibitory activities against aldose reductase from different parts of the Korean thistle, Cirsium maackii |
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