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Dive into the research topics where Yoshinobu Fuse is active.

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Featured researches published by Yoshinobu Fuse.


Scandinavian Journal of Gastroenterology | 1990

Thickness of Brunner's Glands and Its Clinical Significance in Duodenal Ulcer Disease

Yoshinobu Fuse; Yasunari Tsuchihashi; Masahiko Takamasu; T. Kodama; Setsuya Fujita; Kei Kashima

The thickness of Brunners glands was measured with an ocular micrometer in 75 cases of surgically resected duodenal ulcer and in 75 autopsy cases (control group). Endoscopic findings before operation were also studied. Maximum mean thickness of Brunners glands in the control group was 1.54 +/- 0.38 mm (mean +/- SD), and no regional difference in thickness was noted. The thickness of Brunners glands in the duodenal ulcer group was widely distributed, from 0.5 mm to 5.0 mm, and the average value was 3.0 +/- 1.0 mm, with a statistically significant difference from that of the control group. In most duodenal ulcer cases Brunners glands were thickest within 1 cm from the center of an ulcer. Only six cases of duodenal ulcer (8.0%) showed a diffusely thin layer of Brunners glands, less than 1.5 mm thick. These results show that the Brunners glands become hyperplastic in duodenal ulcer patients, especially near the ulcer. In the healed ulcer Brunners glands were thin at the center of an ulcer scar, and the average thickness was 0.42 +/- 0.26 mm. This histologic finding corresponded to the depressed scarred area observed endoscopically, suggesting a decreased mucosal resistance at this area.


Scandinavian Journal of Gastroenterology | 1989

Healing Process of Experimental Esophageal Ulcers Induced by Acetic Acid in Rats

Hideharu Tsuji; Yoshinobu Fuse; Katsuhisa Kawamoto; Hiroya Fujino; T. Kodama

We studied the healing of acetic acid-induced esophageal ulcers in rats with respect to the cellular kinetics. Esophageal ulcers were induced by topical application of acetic acid to the serosal surface. Well-demarcated circular or elliptical ulcers had developed by day 3 after the acid treatment. These ulcers began to decrease in size from day 7 and had healed by day 14. Histological and cellular kinetic findings, with bromodeoxyuridine (BrdU), were degeneration of the esophageal mucosa on day 1 and ulcer formation on day 3, with an increase in the number of BrdU-labeled cells in the esophageal mucosa around the ulcer. On day 7, regenerated epithelium was found to extend towards the ulcer base and the regenerated epithelium had become thicker, with papilla formation, by day 10. On day 14, the ulcer base was covered with thickened regenerated mucosa, with a decrease in the number of BrdU-labeled cells. Marked proliferative activity of the regenerated mucosa and thickening of the esophageal mucosa, with papilla formation, were observed during the healing process.


Digestive Diseases and Sciences | 1988

Autoradiographic study on healing process of cysteamine-induced duodenal ulcer in rat. Possible importance of Brunner's glands in ulcer healing

Yoshinobu Fuse; Yasunari Tsuchihashi; Hiroyuki Sugihara; Tadashi Kodama; Tatsuro Takino; Setsuya Fujita

The healing process of cysteamine-induced duodenal ulcer was studied by [3H]thymidine autoradiography. After the development of ulcer in the duodenum, cell proliferation was markedly activated not only in the crypts but also in the Brunners glands near the ulcer. In the initial stages of ulcer healing, they both contributed to form the surface covering regenerating epithelium. Granulation tissue also proliferated at the base of the ulcer. In later stages of ulcer healing, new crypts were formed in the floor of the ulcer. New villi regenerated from these crypts and Brunners glands regenerated by proliferationin situ. The ulcer base then was completely covered with new villi and granulation tissue was replaced by dense fibrous connective tissue. The present study suggested that the Brunners glands, together with the crypts of Lieberkühn, play an important role in the healing process of cysteamine-induced duodenal ulcer.


Gastroenterologia Japonica | 1989

Thickness of Brunner’s glands and its clinical significance in peptic ulcer diseases

Yoshinobu Fuse; Yasunari Tsuchihashi; Masahiko Takamasu; Katsuhisa Kawamoto; Tadashi Kodama; Setsuya Fujita; Kei Kashima

SummaryThe thickness of Brunner’s glands was measured using an ocular micrometer in 297 cases of surgically resected peptic ulcer and in 120 autopsy cases (control group). The mean maximum thickness of Brunner’s glands in the control group was 1.55±0.37mm (mean±SD) and no difference in thickness was noted for each decade of age. The mean maximum thickness of Brunner’s glands in patients with gastric ulcer, duodenal ulcer and gastroduodenal ulcer was 2.34±1.06, 3.18±1.07 and 3.24±1.05mm, respectively. When an ulcer is within the duodenum, Brunner’s glands near the ulcer were thicker than those contralateral to it. In patients with gastric ulcer, Brunner’s glands were the thickest in the pyloric ulcer group and negative correlation was noted between the thickness of Brunner’s glands and the distance to the ulcer from the pyloric ring. Since gastric acidity is supposed to be lower when an ulcer is located more proximally, these results suggest that Brunner’s glands become hyperplastic not only with the presence of an ulcer in the duodenum but also by acid hypersecretion of the stomach.


Scandinavian Journal of Gastroenterology | 1989

Possible Mechanisms of Diethyldithiocarbamate-Induced Gastro-Duodenal Mucosal Damage in Rats

Masahiko Takamasu; Yoshinobu Fuse; Katsuhisa Kawamoto; T. Kodama; Toru Ohishi

A single s.c. injection of diethyldithiocarbamate (DDC, 1 g/kg) induced not only gastric but also duodenal mucosal damage in rats. DDC induced marked decreases in gastric acid output, gastro-duodenal mucosal blood flow and transmucosal potential difference prior to the development of mucosal lesions. Superoxide dismutase activity in the gastro-duodenal mucosa was also inhibited, while catalase and glutathione peroxidase activities gradually increased after the administration of DDC. These results suggest that a decrease in mucosal defensive mechanisms plays an important role in the development of DDC-induced gastro-duodenal mucosal damage and that oxygen-derived free radicals may also participate in the development of this mucosal damage.


Acta Gastro-Enterologica Belgica | 1990

CLINICAL STUDY OF 51 CASES OF ISCHEMIC COLITIS

Satoshi Ebisui; Katsuhisa Kawamoto; Naoki Teramae; Shinji Fukumitsu; Chiemi Michinaka; Shinichi Furuya; Masahiko Takamasu; Hiroshi Nishida; Tatsuyuki Satoh; Yoshinobu Fuse; Tadashi Kodama; Kei Kashima


Acta Gastro-Enterologica Belgica | 1988

EVALUATION OF ENDOSCOPIC POLYPECTOMY FOR THE DUODENAL POLYPOID LESIONS

Shinichi Furuya; Katsuhisa Kawamoto; Masahide Atsumi; Satoshi Ebisui; Kazushi Isetani; Hiroyuki Ogasawara; Takashi Ohara; Hitoshi Koso; Junpei Takaaki; Hiroshi Akagi; Yoshinobu Fuse; T. Kodama; Tatsuro Takino


Acta Gastro-Enterologica Belgica | 1984

ENDOSCOPIC STUDIES OF POLYPOID LESIONS ON THE DUODENAL BULB

Toru Ohishi; Yoshinobu Fuse; Hitoshi Okano; Tatsuyuki Satoh; Kyohei Maruyama; Shozo Yorioka; Shinichiro Fukuda; Eiji Naitoh; Tadashi Kodama; Tatsuro Takino


Acta Gastro-Enterologica Belgica | 1987

CLINICAL EVALUATION OF ENDOSCOPIC INJECTION SCLEROTHERAPY FOR BLEEDING VARICES OF THE GASTRIC CARDIA

Hitoshi Okano; Tadashi Kodama; Hideharu Tsuji; Masahiko Takamasu; Shoji Mitsufuji; Shinichi Furuy; Hiroshi Nishida; Tatsuyuki Satoh; Kyohei Maruyama; Shozo Yorioka; Sinichiro Fukuda; Yoshinobu Fuse; Tatsuro Takino


Acta Gastro-Enterologica Belgica | 1990

A CLINICAL STUDY OF 8 CASES OF RECTAL CARCINOID

Masahide Atsumi; Katsuhisa Kawamoto; Chiemi Michinaka; Naoki Teramae; Shinji Fukumitsu; Kazuhiko Tokita; Hideharu Tsuji; Shinichiro Fukuda; Yoshinobu Fuse; Tadashi Kodama; Kei Kashima

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Tadashi Kodama

Kyoto Prefectural University of Medicine

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Tatsuro Takino

Kyoto Prefectural University of Medicine

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Masahiko Takamasu

Kyoto Prefectural University of Medicine

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Hideharu Tsuji

Kyoto Prefectural University of Medicine

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Shinichiro Fukuda

Kyoto Prefectural University of Medicine

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Katsuhisa Kawamoto

Kyoto Prefectural University of Medicine

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Shinichi Furuya

Kyoto Prefectural University of Medicine

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Hiroshi Nishida

Kyoto Prefectural University of Medicine

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Hitoshi Okano

Kyoto Prefectural University of Medicine

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Shoji Mitsufuji

Kyoto Prefectural University of Medicine

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