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DOI 10.1159/000201463

Медицинская библиотека · Digestion · 1997

Kinetics of fibroblasts in ulcer healing in rats: interference with indomethacin.

Hirose Y, Goto H, Arisawa T, Hase S, Niwa Y, Hayakawa T, Asai J, Tsukamoto Y

Сравнительное исследованиеСтатьяПеревод пока не подготовлен

Аннотация

OBJECTIVE

The authors reported that the repair of submucosal tissue is important in ulcer healing. The kinetics of fibroblasts have not been well known in gastric ulcer healing. The effect of subcutaneous administration of indomethacin (1 mg/kg) to submucosal tissue was also examined.

METHOD: Immunohistological staining was done using the antibodies for the proliferating cell nuclear antigen prolyl 4-hydroxylase and alpha-smooth muscle actin in acetic acid induced gastric ulcers in rats. The terminal deoxynucleotidyl transferase mediated deoxyuridine triphosphate-biotin nick end labeling method was also employed.

RESULTS

The granulation tissue consisted predominantly of lymphocytes in indomethacin-treated rats. In the control group, proliferative cell nuclear antigen positive cells were at their peak 5 days after ulcer formation (day 5). Prolyl 4-hydroxylase positive fibroblasts were maximal on day 10. Alpha-smooth muscle actin positive myofibroblasts were few on day 5 and increased on day 15. In terminal deoxynucleotidyl transferase mediated deoxyuridine triphosphate-biotin nick end labeling, positive cells were sporadically seen on days 20 and 30. In indomethacin-administered rats, the fibroblasts proliferated weakly. The numbers of prolyl 4-hydroxylase and alpha-smooth muscle actin positive spindle-shaped cells were fewer and their appearance delayed. Nick end labeling positive cells were few before day 30 and sporadically observed on days 50 and 80.

CONCLUSION

The results indicate that fibroblasts differentiated into several phenotypes and finally underwent apoptosis.

Для цитирования: Hirose Y, Goto H, Arisawa T, Hase S, Niwa Y, Hayakawa T, Asai J, Tsukamoto Y. Kinetics of fibroblasts in ulcer healing in rats: interference with indomethacin.. Digestion. 1997. DOI: 10.1159/000201463.

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