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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Veröffentlicht in:Food and chemical toxicology 2009-11, Vol.47 (11), p.2790-2797
Hauptverfasser: Jung, Hyun Ah, Kim, Yeong Shik, Choi, Jae Sue
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Kim, Yeong Shik
Choi, Jae Sue
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.
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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. 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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. 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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. 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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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