Loading…

In vitro and in vivo wound healing-promoting activities of beta-lapachone

Impaired wound healing is a serious problem for diabetic patients. Wound healing is a complex process that requires the cooperation of many cell types, including keratinocytes, fibroblasts, endothelial cells, and macrophages. beta-Lapachone, a natural compound extracted from the bark of the lapacho...

Full description

Saved in:
Bibliographic Details
Published in:American Journal of Physiology: Cell Physiology 2008-10, Vol.295 (4), p.C931-C943
Main Authors: Kung, Hsiu-Ni, Yang, Mei-Jun, Chang, Chi-Fen, Chau, Yat-Pang, Lu, Kuo-Shyan
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c301t-cc3c37311cc411e9915f29c4b34d891f4ac5dc41024f41ea607fd3a1db959bcd3
cites cdi_FETCH-LOGICAL-c301t-cc3c37311cc411e9915f29c4b34d891f4ac5dc41024f41ea607fd3a1db959bcd3
container_end_page C943
container_issue 4
container_start_page C931
container_title American Journal of Physiology: Cell Physiology
container_volume 295
creator Kung, Hsiu-Ni
Yang, Mei-Jun
Chang, Chi-Fen
Chau, Yat-Pang
Lu, Kuo-Shyan
description Impaired wound healing is a serious problem for diabetic patients. Wound healing is a complex process that requires the cooperation of many cell types, including keratinocytes, fibroblasts, endothelial cells, and macrophages. beta-Lapachone, a natural compound extracted from the bark of the lapacho tree (Tabebuia avellanedae), is well known for its antitumor, antiinflammatory, and antineoplastic effects at different concentrations and conditions, but its effects on wound healing have not been studied. The purpose of the present study was to investigate the effects of beta-lapachone on wound healing and its underlying mechanism. In the present study, we demonstrated that a low dose of beta-lapachone enhanced the proliferation in several cells, facilitated the migration of mouse 3T3 fibroblasts and human endothelial EAhy926 cells through different MAPK signaling pathways, and accelerated scrape-wound healing in vitro. Application of ointment with or without beta-lapachone to a punched wound in normal and diabetic (db/db) mice showed that the healing process was faster in beta-lapachone-treated animals than in those treated with vehicle only. In addition, beta-lapachone induced macrophages to release VEGF and EGF, which are beneficial for growth of many cells. Our results showed that beta-lapachone can increase cell proliferation, including keratinocytes, fibroblasts, and endothelial cells, and migration of fibroblasts and endothelial cells and thus accelerate wound healing. Therefore, we suggest that beta-lapachone may have potential for therapeutic use for wound healing.
doi_str_mv 10.1152/ajpcell.00266.2008
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_69649295</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>69649295</sourcerecordid><originalsourceid>FETCH-LOGICAL-c301t-cc3c37311cc411e9915f29c4b34d891f4ac5dc41024f41ea607fd3a1db959bcd3</originalsourceid><addsrcrecordid>eNpFkD1PwzAQhi0EoqXwBxiQJzYXn-249YgqPipVYoHZchyHukriECdF_HscGonp7vR-6PQgdAt0CZCxB3NorauqJaVMyiWjdH2G5klgBDLJz9GccsmJBMFn6CrGA6VUMKku0QzWMkshMUfbbYOPvu8CNk2B_XgcA_4OQ7r2zlS--SRtF-rQpw0b2_vk9i7iUOLc9YZUpjV2Hxp3jS5KU0V3M80F-nh-et-8kt3by3bzuCOWU-iJtdzyFQewVgA4pSArmbIi56JYKyiFsVmRJMpEKcAZSVdlwQ0UucpUbgu-QPen3vTW1-Bir2sfRw6mcWGIWiopFFNZMrKT0XYhxs6Vuu18bbofDVSPAPUEUP8B1CPAFLqb2oe8dsV_ZCLGfwGTyW4Z</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>69649295</pqid></control><display><type>article</type><title>In vitro and in vivo wound healing-promoting activities of beta-lapachone</title><source>American Physiological Society Free</source><creator>Kung, Hsiu-Ni ; Yang, Mei-Jun ; Chang, Chi-Fen ; Chau, Yat-Pang ; Lu, Kuo-Shyan</creator><creatorcontrib>Kung, Hsiu-Ni ; Yang, Mei-Jun ; Chang, Chi-Fen ; Chau, Yat-Pang ; Lu, Kuo-Shyan</creatorcontrib><description>Impaired wound healing is a serious problem for diabetic patients. Wound healing is a complex process that requires the cooperation of many cell types, including keratinocytes, fibroblasts, endothelial cells, and macrophages. beta-Lapachone, a natural compound extracted from the bark of the lapacho tree (Tabebuia avellanedae), is well known for its antitumor, antiinflammatory, and antineoplastic effects at different concentrations and conditions, but its effects on wound healing have not been studied. The purpose of the present study was to investigate the effects of beta-lapachone on wound healing and its underlying mechanism. In the present study, we demonstrated that a low dose of beta-lapachone enhanced the proliferation in several cells, facilitated the migration of mouse 3T3 fibroblasts and human endothelial EAhy926 cells through different MAPK signaling pathways, and accelerated scrape-wound healing in vitro. Application of ointment with or without beta-lapachone to a punched wound in normal and diabetic (db/db) mice showed that the healing process was faster in beta-lapachone-treated animals than in those treated with vehicle only. In addition, beta-lapachone induced macrophages to release VEGF and EGF, which are beneficial for growth of many cells. Our results showed that beta-lapachone can increase cell proliferation, including keratinocytes, fibroblasts, and endothelial cells, and migration of fibroblasts and endothelial cells and thus accelerate wound healing. Therefore, we suggest that beta-lapachone may have potential for therapeutic use for wound healing.</description><identifier>ISSN: 0363-6143</identifier><identifier>EISSN: 1522-1563</identifier><identifier>DOI: 10.1152/ajpcell.00266.2008</identifier><identifier>PMID: 18650264</identifier><language>eng</language><publisher>United States</publisher><subject>Animals ; Anti-Infective Agents - pharmacology ; Cell Cycle - drug effects ; Cell Line ; Cell Movement - drug effects ; Cell Proliferation - drug effects ; Cells, Cultured ; Humans ; Male ; Mice ; Mice, Inbred C57BL ; Mice, Inbred NOD ; Mitogen-Activated Protein Kinase Kinases - antagonists &amp; inhibitors ; Mitogen-Activated Protein Kinase Kinases - metabolism ; Naphthoquinones - pharmacology ; Skin - pathology ; Wound Healing - drug effects</subject><ispartof>American Journal of Physiology: Cell Physiology, 2008-10, Vol.295 (4), p.C931-C943</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c301t-cc3c37311cc411e9915f29c4b34d891f4ac5dc41024f41ea607fd3a1db959bcd3</citedby><cites>FETCH-LOGICAL-c301t-cc3c37311cc411e9915f29c4b34d891f4ac5dc41024f41ea607fd3a1db959bcd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18650264$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kung, Hsiu-Ni</creatorcontrib><creatorcontrib>Yang, Mei-Jun</creatorcontrib><creatorcontrib>Chang, Chi-Fen</creatorcontrib><creatorcontrib>Chau, Yat-Pang</creatorcontrib><creatorcontrib>Lu, Kuo-Shyan</creatorcontrib><title>In vitro and in vivo wound healing-promoting activities of beta-lapachone</title><title>American Journal of Physiology: Cell Physiology</title><addtitle>Am J Physiol Cell Physiol</addtitle><description>Impaired wound healing is a serious problem for diabetic patients. Wound healing is a complex process that requires the cooperation of many cell types, including keratinocytes, fibroblasts, endothelial cells, and macrophages. beta-Lapachone, a natural compound extracted from the bark of the lapacho tree (Tabebuia avellanedae), is well known for its antitumor, antiinflammatory, and antineoplastic effects at different concentrations and conditions, but its effects on wound healing have not been studied. The purpose of the present study was to investigate the effects of beta-lapachone on wound healing and its underlying mechanism. In the present study, we demonstrated that a low dose of beta-lapachone enhanced the proliferation in several cells, facilitated the migration of mouse 3T3 fibroblasts and human endothelial EAhy926 cells through different MAPK signaling pathways, and accelerated scrape-wound healing in vitro. Application of ointment with or without beta-lapachone to a punched wound in normal and diabetic (db/db) mice showed that the healing process was faster in beta-lapachone-treated animals than in those treated with vehicle only. In addition, beta-lapachone induced macrophages to release VEGF and EGF, which are beneficial for growth of many cells. Our results showed that beta-lapachone can increase cell proliferation, including keratinocytes, fibroblasts, and endothelial cells, and migration of fibroblasts and endothelial cells and thus accelerate wound healing. Therefore, we suggest that beta-lapachone may have potential for therapeutic use for wound healing.</description><subject>Animals</subject><subject>Anti-Infective Agents - pharmacology</subject><subject>Cell Cycle - drug effects</subject><subject>Cell Line</subject><subject>Cell Movement - drug effects</subject><subject>Cell Proliferation - drug effects</subject><subject>Cells, Cultured</subject><subject>Humans</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Inbred NOD</subject><subject>Mitogen-Activated Protein Kinase Kinases - antagonists &amp; inhibitors</subject><subject>Mitogen-Activated Protein Kinase Kinases - metabolism</subject><subject>Naphthoquinones - pharmacology</subject><subject>Skin - pathology</subject><subject>Wound Healing - drug effects</subject><issn>0363-6143</issn><issn>1522-1563</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNpFkD1PwzAQhi0EoqXwBxiQJzYXn-249YgqPipVYoHZchyHukriECdF_HscGonp7vR-6PQgdAt0CZCxB3NorauqJaVMyiWjdH2G5klgBDLJz9GccsmJBMFn6CrGA6VUMKku0QzWMkshMUfbbYOPvu8CNk2B_XgcA_4OQ7r2zlS--SRtF-rQpw0b2_vk9i7iUOLc9YZUpjV2Hxp3jS5KU0V3M80F-nh-et-8kt3by3bzuCOWU-iJtdzyFQewVgA4pSArmbIi56JYKyiFsVmRJMpEKcAZSVdlwQ0UucpUbgu-QPen3vTW1-Bir2sfRw6mcWGIWiopFFNZMrKT0XYhxs6Vuu18bbofDVSPAPUEUP8B1CPAFLqb2oe8dsV_ZCLGfwGTyW4Z</recordid><startdate>200810</startdate><enddate>200810</enddate><creator>Kung, Hsiu-Ni</creator><creator>Yang, Mei-Jun</creator><creator>Chang, Chi-Fen</creator><creator>Chau, Yat-Pang</creator><creator>Lu, Kuo-Shyan</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>200810</creationdate><title>In vitro and in vivo wound healing-promoting activities of beta-lapachone</title><author>Kung, Hsiu-Ni ; Yang, Mei-Jun ; Chang, Chi-Fen ; Chau, Yat-Pang ; Lu, Kuo-Shyan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c301t-cc3c37311cc411e9915f29c4b34d891f4ac5dc41024f41ea607fd3a1db959bcd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Animals</topic><topic>Anti-Infective Agents - pharmacology</topic><topic>Cell Cycle - drug effects</topic><topic>Cell Line</topic><topic>Cell Movement - drug effects</topic><topic>Cell Proliferation - drug effects</topic><topic>Cells, Cultured</topic><topic>Humans</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Inbred NOD</topic><topic>Mitogen-Activated Protein Kinase Kinases - antagonists &amp; inhibitors</topic><topic>Mitogen-Activated Protein Kinase Kinases - metabolism</topic><topic>Naphthoquinones - pharmacology</topic><topic>Skin - pathology</topic><topic>Wound Healing - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kung, Hsiu-Ni</creatorcontrib><creatorcontrib>Yang, Mei-Jun</creatorcontrib><creatorcontrib>Chang, Chi-Fen</creatorcontrib><creatorcontrib>Chau, Yat-Pang</creatorcontrib><creatorcontrib>Lu, Kuo-Shyan</creatorcontrib><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>American Journal of Physiology: Cell Physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kung, Hsiu-Ni</au><au>Yang, Mei-Jun</au><au>Chang, Chi-Fen</au><au>Chau, Yat-Pang</au><au>Lu, Kuo-Shyan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In vitro and in vivo wound healing-promoting activities of beta-lapachone</atitle><jtitle>American Journal of Physiology: Cell Physiology</jtitle><addtitle>Am J Physiol Cell Physiol</addtitle><date>2008-10</date><risdate>2008</risdate><volume>295</volume><issue>4</issue><spage>C931</spage><epage>C943</epage><pages>C931-C943</pages><issn>0363-6143</issn><eissn>1522-1563</eissn><abstract>Impaired wound healing is a serious problem for diabetic patients. Wound healing is a complex process that requires the cooperation of many cell types, including keratinocytes, fibroblasts, endothelial cells, and macrophages. beta-Lapachone, a natural compound extracted from the bark of the lapacho tree (Tabebuia avellanedae), is well known for its antitumor, antiinflammatory, and antineoplastic effects at different concentrations and conditions, but its effects on wound healing have not been studied. The purpose of the present study was to investigate the effects of beta-lapachone on wound healing and its underlying mechanism. In the present study, we demonstrated that a low dose of beta-lapachone enhanced the proliferation in several cells, facilitated the migration of mouse 3T3 fibroblasts and human endothelial EAhy926 cells through different MAPK signaling pathways, and accelerated scrape-wound healing in vitro. Application of ointment with or without beta-lapachone to a punched wound in normal and diabetic (db/db) mice showed that the healing process was faster in beta-lapachone-treated animals than in those treated with vehicle only. In addition, beta-lapachone induced macrophages to release VEGF and EGF, which are beneficial for growth of many cells. Our results showed that beta-lapachone can increase cell proliferation, including keratinocytes, fibroblasts, and endothelial cells, and migration of fibroblasts and endothelial cells and thus accelerate wound healing. Therefore, we suggest that beta-lapachone may have potential for therapeutic use for wound healing.</abstract><cop>United States</cop><pmid>18650264</pmid><doi>10.1152/ajpcell.00266.2008</doi></addata></record>
fulltext fulltext
identifier ISSN: 0363-6143
ispartof American Journal of Physiology: Cell Physiology, 2008-10, Vol.295 (4), p.C931-C943
issn 0363-6143
1522-1563
language eng
recordid cdi_proquest_miscellaneous_69649295
source American Physiological Society Free
subjects Animals
Anti-Infective Agents - pharmacology
Cell Cycle - drug effects
Cell Line
Cell Movement - drug effects
Cell Proliferation - drug effects
Cells, Cultured
Humans
Male
Mice
Mice, Inbred C57BL
Mice, Inbred NOD
Mitogen-Activated Protein Kinase Kinases - antagonists & inhibitors
Mitogen-Activated Protein Kinase Kinases - metabolism
Naphthoquinones - pharmacology
Skin - pathology
Wound Healing - drug effects
title In vitro and in vivo wound healing-promoting activities of beta-lapachone
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-21T03%3A49%3A57IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=In%20vitro%20and%20in%20vivo%20wound%20healing-promoting%20activities%20of%20beta-lapachone&rft.jtitle=American%20Journal%20of%20Physiology:%20Cell%20Physiology&rft.au=Kung,%20Hsiu-Ni&rft.date=2008-10&rft.volume=295&rft.issue=4&rft.spage=C931&rft.epage=C943&rft.pages=C931-C943&rft.issn=0363-6143&rft.eissn=1522-1563&rft_id=info:doi/10.1152/ajpcell.00266.2008&rft_dat=%3Cproquest_cross%3E69649295%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c301t-cc3c37311cc411e9915f29c4b34d891f4ac5dc41024f41ea607fd3a1db959bcd3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=69649295&rft_id=info:pmid/18650264&rfr_iscdi=true