Document Detail


Impaired wound healing after local soft x-ray irradiation in rat skin: time course study of pathology, proliferation, cell cycle, and apoptosis.
MedLine Citation:
PMID:  16361913     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
BACKGROUND: Soft x-ray irradiation is usually used to treat skin-related disease in the clinic, but its effect on wound healing has not been well elucidated. The purpose of our study was to develop a wound-healing model of local soft x-ray irradiation on rats and to clarify the possible cellular mechanisms through which radiation may influence healing. METHODS: Full-thickness, 2-cm-diameter, dorsal cutaneous tissue was excised after local irradiation in rats. The dose-effect curve was recorded, and five animals irradiated with doses of 521 rad were killed at postwound days 3, 6, 9, and 15 and five were healed for histologic examination (hematoxylin and eosin staining), cell proliferation (5-bromo-2'-deoxyuridine [BrdU] incorporation), apoptosis (and terminal deoxynucleotidyl transferase biotin-dUTP nick end-labeling [TUNEL] method), and the cell cycle (flow cytometry). RESULTS: Soft x-ray irradiation delayed wound-healing time with an S-like curve, and the wounds that received doses in excess of 700 rad failed to heal within 40 days. This dose-effect range is far below that of gamma and hard x-ray irradiation. Relative to control wounds, which contained prominent BrdU-positive labeling at days 3 through 9 and minimal TUNEL-positive labeling during the entire healing, the irradiated wounds had less BrdU-positive labeling and significant TUNEL-positive labeling at days 3 through 9 but more BrdU-positive labeling and similar TUNEL-positive labeling at day 15. Flow cytometry studies found a higher proportion of G0/G1 phase cells (days 3-9), a lower (days 3-9) then higher (days 13-22) proportion of S phase cells, and a persistent lower proportion of G2/M phase cells (during the entire healing process) in the irradiated wounds compared with the controls. CONCLUSION: Local soft x-ray irradiation could delay wound healing in a dose-dependent manner and shows a more effective biological effect than that of gamma and hard x-ray irradiation. Radiation-induced inactive cell proliferation, active cell apoptosis, and arrested cell cycle at days 3 through 9 may be one of the cellular mechanism responsible for delayed wound healing.
Authors:
Xia Liu; Jian-Zhong Liu; En Zhang; Ping Li; Ping Zhou; Tian-Min Cheng; Yuan-Guo Zhou
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Publication Detail:
Type:  Evaluation Studies; Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  The Journal of trauma     Volume:  59     ISSN:  0022-5282     ISO Abbreviation:  -     Publication Date:  2005 Sep 
Date Detail:
Created Date:  2005-12-19     Completed Date:  2006-02-23     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  0376373     Medline TA:  J Trauma     Country:  United States    
Other Details:
Languages:  eng     Pagination:  682-90     Citation Subset:  AIM; IM    
Affiliation:
Molecular Biologic Center, Research Institute of Surgery, Third Military Medical University, Chongqing, China.
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MeSH Terms
Descriptor/Qualifier:
Animals
Apoptosis / radiation effects
Cell Cycle / radiation effects
Cell Proliferation / radiation effects
Dose-Response Relationship, Radiation
Female
Male
Rats
Rats, Wistar
Skin Diseases / radiotherapy*
Wound Healing / radiation effects*
Wounds and Injuries / pathology

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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