Subglottic injury, gastric juice, corticosteroids, and peptide growth factors in a porcine model

被引:13
作者
Yellon, RF
Szeremeta, W
Grandis, JR
Diguisseppe, P
Dickman, PS
机构
[1] Univ Pittsburgh, Childrens Hosp Pittsburgh, Sch Med, Dept Pediat Otolaryngol, Pittsburgh, PA 15213 USA
[2] Univ Pittsburgh, Sch Med, Dept Otolaryngol, Pittsburgh, PA USA
[3] Univ Pittsburgh, Sch Med, Dept Pathol, Pittsburgh, PA USA
关键词
D O I
10.1097/00005537-199806000-00014
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Objectives: To study the effects of mucosal injury, gastric juice, and corticosteroids and to determine the presence of peptide growth factors in the subglottic mucosa in a porcine model. Study Design: Prospective cohort animal study. Methods: in this model of subglottic injury, five groups (n = 5 each) of piglets were used. injury was induced by electrocautery (acute), electrocautery plus repeated saline application (chronic), electrocautery plus repeated gastric juice application (chronic plus gastric juice), or repeated gastric juice application (gastric). Control piglets had normal saline applied repeatedly, Results: Histopathologic findings for the gastric juice group included basal cell hyperplasia (80%), squamous metaplasia (80%), and mucosal ulceration (40%). Control piglets showed squamous metaplasia (80%) but mo basilar hyperplasia or ulceration. Immunohistochemistry detected peptide growth factors and epidermal growth factor receptor (EGFR) in all groups, Decreased staining was most frequent ha the acute injury group. Quantitative reverse transcriptase polymerase chain reaction (RT-PCR) documented lower expression of EGFR in the gastric juice group (P =.01). Conclusions: These findings suggest that peptide growth factors and EGFR are part of normal subglottic mucosal turnover, Noxious stimuli decrease production of these factors. Gastric juice had adverse effects documented by histopathology and molecular techniques.
引用
收藏
页码:854 / 862
页数:9
相关论文
共 25 条
[1]  
ARONOW E, 1983, PEDIAT GASTROENTEROL, P214
[2]   EXPERIMENTAL ANIMAL-MODEL OF SUBGLOTTIC STENOSIS [J].
BOROWIECKI, B ;
CROFT, CB .
ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY, 1977, 86 (06) :835-840
[3]  
BRENNER CA, 1989, BIOTECHNIQUES, V7, P1096
[4]   ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE [J].
CHIRGWIN, JM ;
PRZYBYLA, AE ;
MACDONALD, RJ ;
RUTTER, WJ .
BIOCHEMISTRY, 1979, 18 (24) :5294-5299
[5]  
CONTENCIN P, 1992, ARCH OTOLARYNGOL, V118, P1028
[6]   EXPERIMENTALLY PRODUCED VOCAL CORD GRANULOMAS [J].
DELAHUNTY, JE ;
CHERRY, J .
LARYNGOSCOPE, 1968, 78 (11) :1941-+
[7]   ANGIOGENIC FACTORS [J].
FOLKMAN, J ;
KLAGSBRUN, M .
SCIENCE, 1987, 235 (4787) :442-447
[8]  
GRANDIS JR, 1993, CANCER RES, V53, P3579
[9]  
HANSSON HA, 1991, ARCH OTOLARYNGOL, V117, P1368
[10]   IMMUNOHISTOCHEMICAL DEMONSTRATION OF INSULIN-LIKE GROWTH FACTOR-I IN INFLAMMATORY LESIONS IN WEGENERS GRANULOMATOSIS AND IDIOPATHIC MIDLINE DESTRUCTIVE DISEASE [J].
HANSSON, HA ;
PETRUSON, B ;
PETRUSON, K .
SCANDINAVIAN JOURNAL OF RHEUMATOLOGY, 1989, 18 (03) :133-141