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- Publisher Website: 10.1016/j.phymed.2007.01.007
- Scopus: eid_2-s2.0-35048853562
- PMID: 17298878
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Article: Pharmacological investigations of the anti-diabetic effect of Cortex Moutan and its active component paeonol
Title | Pharmacological investigations of the anti-diabetic effect of Cortex Moutan and its active component paeonol |
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Authors | |
Keywords | Cortex Moutan Diabetes mellitus Paenonia suffruticosa Paeonol Traditional Chinese medicine |
Issue Date | 2007 |
Citation | Phytomedicine, 2007, v. 14, n. 11, p. 778-784 How to Cite? |
Abstract | Cortex Moutan (CM, root bark of Paeonia suffruticosa Andr.) is one of the common herbs found in anti-diabetic traditional Chinese medicine formulae. To study the potential anti-diabetic mechanisms of CM, four in vitro models (intestinal brush border membrane vesicles (BBMV), rat hepatoma cell line H4IIE, human skin fibroblasts cell line Hs68 and mouse adipocytes 3T3-L1) were used. CM showed significant in vitro anti-diabetic effects by inhibiting glucose uptake of BBMV and enhancing glucose uptake into Hs68 and 3T3-L1 cells. Using bioassay-guided fractionation, paeonol was confirmed to be one of the active constituents for inhibiting BBMV glucose uptake. With neonatal-streptozotocin diabetic rats, paeonol (200 and 400 mg/kg body wt.) was found to improve oral glucose tolerance in vivo. To the best of our knowledge, this is the first report on the anti-diabetic effect of paeonol. © 2007 Elsevier GmbH. All rights reserved. |
Persistent Identifier | http://hdl.handle.net/10722/343025 |
ISSN | 2023 Impact Factor: 6.7 2023 SCImago Journal Rankings: 1.267 |
DC Field | Value | Language |
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dc.contributor.author | Lau, C. H. | - |
dc.contributor.author | Chan, C. M. | - |
dc.contributor.author | Chan, Y. W. | - |
dc.contributor.author | Lau, K. M. | - |
dc.contributor.author | Lau, T. W. | - |
dc.contributor.author | Lam, F. C. | - |
dc.contributor.author | Law, W. T. | - |
dc.contributor.author | Che, C. T. | - |
dc.contributor.author | Leung, P. C. | - |
dc.contributor.author | Fung, K. P. | - |
dc.contributor.author | Ho, Y. Y. | - |
dc.contributor.author | Lau, C. B.S. | - |
dc.date.accessioned | 2024-05-10T09:04:52Z | - |
dc.date.available | 2024-05-10T09:04:52Z | - |
dc.date.issued | 2007 | - |
dc.identifier.citation | Phytomedicine, 2007, v. 14, n. 11, p. 778-784 | - |
dc.identifier.issn | 0944-7113 | - |
dc.identifier.uri | http://hdl.handle.net/10722/343025 | - |
dc.description.abstract | Cortex Moutan (CM, root bark of Paeonia suffruticosa Andr.) is one of the common herbs found in anti-diabetic traditional Chinese medicine formulae. To study the potential anti-diabetic mechanisms of CM, four in vitro models (intestinal brush border membrane vesicles (BBMV), rat hepatoma cell line H4IIE, human skin fibroblasts cell line Hs68 and mouse adipocytes 3T3-L1) were used. CM showed significant in vitro anti-diabetic effects by inhibiting glucose uptake of BBMV and enhancing glucose uptake into Hs68 and 3T3-L1 cells. Using bioassay-guided fractionation, paeonol was confirmed to be one of the active constituents for inhibiting BBMV glucose uptake. With neonatal-streptozotocin diabetic rats, paeonol (200 and 400 mg/kg body wt.) was found to improve oral glucose tolerance in vivo. To the best of our knowledge, this is the first report on the anti-diabetic effect of paeonol. © 2007 Elsevier GmbH. All rights reserved. | - |
dc.language | eng | - |
dc.relation.ispartof | Phytomedicine | - |
dc.subject | Cortex Moutan | - |
dc.subject | Diabetes mellitus | - |
dc.subject | Paenonia suffruticosa | - |
dc.subject | Paeonol | - |
dc.subject | Traditional Chinese medicine | - |
dc.title | Pharmacological investigations of the anti-diabetic effect of Cortex Moutan and its active component paeonol | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1016/j.phymed.2007.01.007 | - |
dc.identifier.pmid | 17298878 | - |
dc.identifier.scopus | eid_2-s2.0-35048853562 | - |
dc.identifier.volume | 14 | - |
dc.identifier.issue | 11 | - |
dc.identifier.spage | 778 | - |
dc.identifier.epage | 784 | - |