Coptidis Rhizoma: protective effects against peroxynitrite-induced oxidative damage and elucidation of its active components

ABSTRACT We have investigated the protective effects of Coptidis Rhizoma against peroxynitrite (ONOO−)‐induced oxidative damage and have elucidated the active components of this preparation. In an invitro system, Coptidis Rhizoma extract scavenged ONOO− and its precursors, nitric oxide (NO) and supe...

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Veröffentlicht in:Journal of pharmacy and pharmacology 2004-04, Vol.56 (4), p.547-556
Hauptverfasser: Yokozawa, Takako, Ishida, Ai, Cho, Eun Ju, Kim, Hyun Young, Kashiwada, Yoshiki, Ikeshiro, Yasumasa
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container_end_page 556
container_issue 4
container_start_page 547
container_title Journal of pharmacy and pharmacology
container_volume 56
creator Yokozawa, Takako
Ishida, Ai
Cho, Eun Ju
Kim, Hyun Young
Kashiwada, Yoshiki
Ikeshiro, Yasumasa
description ABSTRACT We have investigated the protective effects of Coptidis Rhizoma against peroxynitrite (ONOO−)‐induced oxidative damage and have elucidated the active components of this preparation. In an invitro system, Coptidis Rhizoma extract scavenged ONOO− and its precursors, nitric oxide (NO) and superoxide anion (O2−). This scavenging activity was more marked for ONOO− than its precursors. In addition, against 3‐morpholinosydnonimine‐induced cellular damage, this extract significantly reduced cellular ONOO− formation and increased cell viability. In an in‐vivo lipopolysaccharide plus ischaemia‐reperfusion system that generated ONOO−, the administration of Coptidis Rhizoma extract at 50 and 100 mg kg−1/day for 30 days exerted greater inhibition of ONOO− than NO and O2−. This suggested that it acted as a direct scavenger of ONOO− rather than as a scavenger of its precursors. Moreover, the suppression of the activities of the antioxidative enzymes superoxide dismutase, catalase and glutathione peroxidase was significantly attenuated by the administration of Coptidis Rhizoma extract. Furthermore, the extract ameliorated renal dysfunction judged by decreasing serum urea nitrogen and creatinine levels. To elucidate the active components of Coptidis Rhizoma extract, we evaluated and compared the effects of the phenol plus alkaloid and alkaloid fractions on ONOO−‐induced damage. We found that the alkaloid fraction consisting of berberine, palmatine and coptisine was the most effective at protecting against ONOO−. We confirmed that berberine (10 and 20 mg kg−1/day for 10 days), the main and most active alkaloid in Coptidis Rhizoma extract, was also protective, exerting NO‐, O2−‐ and ONOO−‐scavenging activities. This study suggested that Coptidis Rhizoma could protect against ONOO−‐induced oxidative damage and that this effect was mainly attributable to the constituent alkaloids, especially berberine. This study is the first to demonstrate an antioxidative effect of alkaloids, including berberine, against ONOO−‐induced damage.
doi_str_mv 10.1211/0022357023024
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In an invitro system, Coptidis Rhizoma extract scavenged ONOO− and its precursors, nitric oxide (NO) and superoxide anion (O2−). This scavenging activity was more marked for ONOO− than its precursors. In addition, against 3‐morpholinosydnonimine‐induced cellular damage, this extract significantly reduced cellular ONOO− formation and increased cell viability. In an in‐vivo lipopolysaccharide plus ischaemia‐reperfusion system that generated ONOO−, the administration of Coptidis Rhizoma extract at 50 and 100 mg kg−1/day for 30 days exerted greater inhibition of ONOO− than NO and O2−. This suggested that it acted as a direct scavenger of ONOO− rather than as a scavenger of its precursors. Moreover, the suppression of the activities of the antioxidative enzymes superoxide dismutase, catalase and glutathione peroxidase was significantly attenuated by the administration of Coptidis Rhizoma extract. Furthermore, the extract ameliorated renal dysfunction judged by decreasing serum urea nitrogen and creatinine levels. To elucidate the active components of Coptidis Rhizoma extract, we evaluated and compared the effects of the phenol plus alkaloid and alkaloid fractions on ONOO−‐induced damage. We found that the alkaloid fraction consisting of berberine, palmatine and coptisine was the most effective at protecting against ONOO−. We confirmed that berberine (10 and 20 mg kg−1/day for 10 days), the main and most active alkaloid in Coptidis Rhizoma extract, was also protective, exerting NO‐, O2−‐ and ONOO−‐scavenging activities. This study suggested that Coptidis Rhizoma could protect against ONOO−‐induced oxidative damage and that this effect was mainly attributable to the constituent alkaloids, especially berberine. 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In an invitro system, Coptidis Rhizoma extract scavenged ONOO− and its precursors, nitric oxide (NO) and superoxide anion (O2−). This scavenging activity was more marked for ONOO− than its precursors. In addition, against 3‐morpholinosydnonimine‐induced cellular damage, this extract significantly reduced cellular ONOO− formation and increased cell viability. In an in‐vivo lipopolysaccharide plus ischaemia‐reperfusion system that generated ONOO−, the administration of Coptidis Rhizoma extract at 50 and 100 mg kg−1/day for 30 days exerted greater inhibition of ONOO− than NO and O2−. This suggested that it acted as a direct scavenger of ONOO− rather than as a scavenger of its precursors. Moreover, the suppression of the activities of the antioxidative enzymes superoxide dismutase, catalase and glutathione peroxidase was significantly attenuated by the administration of Coptidis Rhizoma extract. Furthermore, the extract ameliorated renal dysfunction judged by decreasing serum urea nitrogen and creatinine levels. To elucidate the active components of Coptidis Rhizoma extract, we evaluated and compared the effects of the phenol plus alkaloid and alkaloid fractions on ONOO−‐induced damage. We found that the alkaloid fraction consisting of berberine, palmatine and coptisine was the most effective at protecting against ONOO−. We confirmed that berberine (10 and 20 mg kg−1/day for 10 days), the main and most active alkaloid in Coptidis Rhizoma extract, was also protective, exerting NO‐, O2−‐ and ONOO−‐scavenging activities. This study suggested that Coptidis Rhizoma could protect against ONOO−‐induced oxidative damage and that this effect was mainly attributable to the constituent alkaloids, especially berberine. 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inhibitors</topic><topic>Swine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yokozawa, Takako</creatorcontrib><creatorcontrib>Ishida, Ai</creatorcontrib><creatorcontrib>Cho, Eun Ju</creatorcontrib><creatorcontrib>Kim, Hyun Young</creatorcontrib><creatorcontrib>Kashiwada, Yoshiki</creatorcontrib><creatorcontrib>Ikeshiro, Yasumasa</creatorcontrib><collection>Istex</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>Journal of pharmacy and pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yokozawa, Takako</au><au>Ishida, Ai</au><au>Cho, Eun Ju</au><au>Kim, Hyun Young</au><au>Kashiwada, Yoshiki</au><au>Ikeshiro, Yasumasa</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Coptidis Rhizoma: protective effects against peroxynitrite-induced oxidative damage and elucidation of its active components</atitle><jtitle>Journal of pharmacy and pharmacology</jtitle><addtitle>J Pharm Pharmacol</addtitle><date>2004-04</date><risdate>2004</risdate><volume>56</volume><issue>4</issue><spage>547</spage><epage>556</epage><pages>547-556</pages><issn>0022-3573</issn><eissn>2042-7158</eissn><abstract>ABSTRACT We have investigated the protective effects of Coptidis Rhizoma against peroxynitrite (ONOO−)‐induced oxidative damage and have elucidated the active components of this preparation. In an invitro system, Coptidis Rhizoma extract scavenged ONOO− and its precursors, nitric oxide (NO) and superoxide anion (O2−). This scavenging activity was more marked for ONOO− than its precursors. In addition, against 3‐morpholinosydnonimine‐induced cellular damage, this extract significantly reduced cellular ONOO− formation and increased cell viability. In an in‐vivo lipopolysaccharide plus ischaemia‐reperfusion system that generated ONOO−, the administration of Coptidis Rhizoma extract at 50 and 100 mg kg−1/day for 30 days exerted greater inhibition of ONOO− than NO and O2−. This suggested that it acted as a direct scavenger of ONOO− rather than as a scavenger of its precursors. Moreover, the suppression of the activities of the antioxidative enzymes superoxide dismutase, catalase and glutathione peroxidase was significantly attenuated by the administration of Coptidis Rhizoma extract. Furthermore, the extract ameliorated renal dysfunction judged by decreasing serum urea nitrogen and creatinine levels. To elucidate the active components of Coptidis Rhizoma extract, we evaluated and compared the effects of the phenol plus alkaloid and alkaloid fractions on ONOO−‐induced damage. We found that the alkaloid fraction consisting of berberine, palmatine and coptisine was the most effective at protecting against ONOO−. We confirmed that berberine (10 and 20 mg kg−1/day for 10 days), the main and most active alkaloid in Coptidis Rhizoma extract, was also protective, exerting NO‐, O2−‐ and ONOO−‐scavenging activities. This study suggested that Coptidis Rhizoma could protect against ONOO−‐induced oxidative damage and that this effect was mainly attributable to the constituent alkaloids, especially berberine. This study is the first to demonstrate an antioxidative effect of alkaloids, including berberine, against ONOO−‐induced damage.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>15099450</pmid><doi>10.1211/0022357023024</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
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subjects Alkaloids - chemistry
Alkaloids - pharmacology
Animals
Antioxidants - chemistry
Antioxidants - pharmacology
Chromatography, High Pressure Liquid
Drugs, Chinese Herbal - chemistry
Drugs, Chinese Herbal - pharmacology
Free Radical Scavengers - chemistry
Free Radical Scavengers - pharmacology
Ischemia - drug therapy
Ischemia - metabolism
Kidney - blood supply
LLC-PK1 Cells
Male
Nitric Oxide - antagonists & inhibitors
Peroxynitrous Acid
Rats
Rats, Wistar
Reperfusion
Superoxides - antagonists & inhibitors
Swine
title Coptidis Rhizoma: protective effects against peroxynitrite-induced oxidative damage and elucidation of its active components
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