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- Publisher Website: 10.1016/S0024-3205(00)00994-2
- Scopus: eid_2-s2.0-0035846884
- PMID: 11213366
- WOS: WOS:000166536500012
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Article: Angelica sinensis modulates migration and proliferation of gastric epithelial cells
Title | Angelica sinensis modulates migration and proliferation of gastric epithelial cells |
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Authors | |
Keywords | Angelica sinensis Gastric epithelial cells Migration Proliferation |
Issue Date | 2001 |
Publisher | Elsevier Inc. The Journal's web site is located at http://www.elsevier.com/locate/lifescie |
Citation | Life Sciences, 2001, v. 68 n. 8, p. 961-968 How to Cite? |
Abstract | A crude extract from Angelica sinensis (ASCE), which mainly consists of polysaccharides, prevents ethanol- or indomethacin-induced gastric mucosal damage and promotes ulcer healing. The aim of this study was to test the hypothesis that ASCE has a direct stimulating effect on gastric epithelial cells for wound healing. We found that ASCE significantly promoted the migration of epithelial cells over an artificial wound on the surface of an RGM-1 monolayer. The extract also stimulated DNA synthesis in a dose-dependent manner and concomitantly increased EGF mRNA expression. Co-incubation of ASCE with anti-EGF antibody reduced the speed of migration and the DNA synthesis, which however were still higher than the control without ASCE. These results strongly suggest that ASCE has a direct wound healing effect on gastric mucosa, and this is acting partially through an EGF-mediated pathway. © 2001 Elsevier Science Inc. |
Persistent Identifier | http://hdl.handle.net/10722/80246 |
ISSN | 2023 Impact Factor: 5.2 2023 SCImago Journal Rankings: 1.257 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Ye, YN | en_HK |
dc.contributor.author | Koo, MWL | en_HK |
dc.contributor.author | Li, Y | en_HK |
dc.contributor.author | Matsui, H | en_HK |
dc.contributor.author | Cho, CH | en_HK |
dc.date.accessioned | 2010-09-06T08:04:10Z | - |
dc.date.available | 2010-09-06T08:04:10Z | - |
dc.date.issued | 2001 | en_HK |
dc.identifier.citation | Life Sciences, 2001, v. 68 n. 8, p. 961-968 | en_HK |
dc.identifier.issn | 0024-3205 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/80246 | - |
dc.description.abstract | A crude extract from Angelica sinensis (ASCE), which mainly consists of polysaccharides, prevents ethanol- or indomethacin-induced gastric mucosal damage and promotes ulcer healing. The aim of this study was to test the hypothesis that ASCE has a direct stimulating effect on gastric epithelial cells for wound healing. We found that ASCE significantly promoted the migration of epithelial cells over an artificial wound on the surface of an RGM-1 monolayer. The extract also stimulated DNA synthesis in a dose-dependent manner and concomitantly increased EGF mRNA expression. Co-incubation of ASCE with anti-EGF antibody reduced the speed of migration and the DNA synthesis, which however were still higher than the control without ASCE. These results strongly suggest that ASCE has a direct wound healing effect on gastric mucosa, and this is acting partially through an EGF-mediated pathway. © 2001 Elsevier Science Inc. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Elsevier Inc. The Journal's web site is located at http://www.elsevier.com/locate/lifescie | en_HK |
dc.relation.ispartof | Life Sciences | en_HK |
dc.rights | Life Sciences. Copyright © Elsevier Inc. | en_HK |
dc.subject | Angelica sinensis | en_HK |
dc.subject | Gastric epithelial cells | en_HK |
dc.subject | Migration | en_HK |
dc.subject | Proliferation | en_HK |
dc.title | Angelica sinensis modulates migration and proliferation of gastric epithelial cells | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0024-3205&volume=68&spage=961&epage=968&date=2001&atitle=Angelica+sinensis+modulates+migration+and+proliferation+of+gastric+epithelial+cells | en_HK |
dc.identifier.email | Koo, MWL: wlkoo@hku.hk | en_HK |
dc.identifier.authority | Koo, MWL=rp00233 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1016/S0024-3205(00)00994-2 | en_HK |
dc.identifier.pmid | 11213366 | - |
dc.identifier.scopus | eid_2-s2.0-0035846884 | en_HK |
dc.identifier.hkuros | 61326 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-0035846884&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 68 | en_HK |
dc.identifier.issue | 8 | en_HK |
dc.identifier.spage | 961 | en_HK |
dc.identifier.epage | 968 | en_HK |
dc.identifier.isi | WOS:000166536500012 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Ye, YN=7401627402 | en_HK |
dc.identifier.scopusauthorid | Koo, MWL=7004550899 | en_HK |
dc.identifier.scopusauthorid | Li, Y=54970596900 | en_HK |
dc.identifier.scopusauthorid | Matsui, H=7401527136 | en_HK |
dc.identifier.scopusauthorid | Cho, CH=14067000400 | en_HK |
dc.identifier.issnl | 0024-3205 | - |