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Article: Paeonol attenuates high-fat-diet-induced atherosclerosis in rabbits by anti-inflammatory activity

TitlePaeonol attenuates high-fat-diet-induced atherosclerosis in rabbits by anti-inflammatory activity
Authors
KeywordsAtherosclerosis
Cortex Moutan
NF-kB
Paeonia suffruticosa Andrews (Ranunculaceae)
Paeonol
Proinflammatory cytokine
Issue Date2009
Citation
Planta Medica, 2009, v. 75, n. 1, p. 7-11 How to Cite?
AbstractCortex Moutan (Paeonia suffruticosa Andrews, Ranunculaceae) has several uses in traditional medicine, such as analgesic, antipyretic, and anti-inflammatory applications and use in the prevention of thromboembolic diseases. Paeonol, a main active component in Cortex Moutan, possesses various pharmacological activities, particularly an anti-atherosclerosis effect. However, so far there have been no reports evaluating the anti-inflammatory action of paeonol in atherosclerosis therapy. The purpose of this study was to investigate the association of the therapeutic effect of paeonol on atherosclerotic rabbits with its anti-inflammatory action. The atherosclerotic model was developed in 24 rabbits fed a high-fat diet for 12 weeks. Twelve rabbits on the high-fat diet then were administered with paeonol (p.o) for a subsequent 6 weeks at the doses of 75 mg/kg and 150 mg/kg. Histological analysis showed significant improvement in atherosclerosis plaque in the paeonol groups. Moreover, the blood levels of TNF-α, IL-1β, and CRP and the translocation of NF-κB to the nucleus were significantly suppressed in paeonol groups, as was the inhibition of lipid peroxidation. In conclusion, these findings suggest that the anti-inflammatory action of paeonol may contribute to its anti-atherosclerosis effect. © Georg Thieme Verlag KG Stuttgart.
Persistent Identifierhttp://hdl.handle.net/10722/342351
ISSN
2021 Impact Factor: 3.007
2020 SCImago Journal Rankings: 0.422
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLi, Houkai-
dc.contributor.authorDai, Min-
dc.contributor.authorJia, Wei-
dc.date.accessioned2024-04-17T07:03:10Z-
dc.date.available2024-04-17T07:03:10Z-
dc.date.issued2009-
dc.identifier.citationPlanta Medica, 2009, v. 75, n. 1, p. 7-11-
dc.identifier.issn0032-0943-
dc.identifier.urihttp://hdl.handle.net/10722/342351-
dc.description.abstractCortex Moutan (Paeonia suffruticosa Andrews, Ranunculaceae) has several uses in traditional medicine, such as analgesic, antipyretic, and anti-inflammatory applications and use in the prevention of thromboembolic diseases. Paeonol, a main active component in Cortex Moutan, possesses various pharmacological activities, particularly an anti-atherosclerosis effect. However, so far there have been no reports evaluating the anti-inflammatory action of paeonol in atherosclerosis therapy. The purpose of this study was to investigate the association of the therapeutic effect of paeonol on atherosclerotic rabbits with its anti-inflammatory action. The atherosclerotic model was developed in 24 rabbits fed a high-fat diet for 12 weeks. Twelve rabbits on the high-fat diet then were administered with paeonol (p.o) for a subsequent 6 weeks at the doses of 75 mg/kg and 150 mg/kg. Histological analysis showed significant improvement in atherosclerosis plaque in the paeonol groups. Moreover, the blood levels of TNF-α, IL-1β, and CRP and the translocation of NF-κB to the nucleus were significantly suppressed in paeonol groups, as was the inhibition of lipid peroxidation. In conclusion, these findings suggest that the anti-inflammatory action of paeonol may contribute to its anti-atherosclerosis effect. © Georg Thieme Verlag KG Stuttgart.-
dc.languageeng-
dc.relation.ispartofPlanta Medica-
dc.subjectAtherosclerosis-
dc.subjectCortex Moutan-
dc.subjectNF-kB-
dc.subjectPaeonia suffruticosa Andrews (Ranunculaceae)-
dc.subjectPaeonol-
dc.subjectProinflammatory cytokine-
dc.titlePaeonol attenuates high-fat-diet-induced atherosclerosis in rabbits by anti-inflammatory activity-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1055/s-0028-1088332-
dc.identifier.pmid19003727-
dc.identifier.scopuseid_2-s2.0-64749100650-
dc.identifier.volume75-
dc.identifier.issue1-
dc.identifier.spage7-
dc.identifier.epage11-
dc.identifier.eissn1439-0221-
dc.identifier.isiWOS:000263032200002-

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