Shigekazu Hayashi
Nagoya University
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Featured researches published by Shigekazu Hayashi.
DNA and Cell Biology | 2009
Toshihito Kosaka; Junji Yoshino; Kazuo Inui; Takao Wakabayashi; Takashi Kobayashi; Shinya Watanabe; Shigekazu Hayashi; Yoshifumi Hirokawa; Taizo Shiraishi; Takayuki Yamamoto; Mayumi Tsuji; Takahiko Katoh; Masatoshi Watanabe
Inflammatory bowel disease is a multifactorial disease. Oxidative stress has been thought to be one of etiologic factor for inflammatory bowel disease. The genes superoxide dismutase (SOD2) and NAD(P)H:quinone oxidoreductase 1 (NQO1) are involved in inflammation and oxidative stress. The purpose of the present case-control study with 134 patients with ulcerative colitis (UC) and 125 healthy controls was to determine whether polymorphisms of these genes, the NQO1 C609T and the SOD2 Ala-9Val, are associated with the risk of UC and influence the clinical characteristics. These polymorphisms were examined by polymerase chain reaction-restriction fragment length polymorphisms and direct sequencing. In patients showing steroid resistance, the number with the NQO1 T/T genotype was significantly higher than other genotypes (odds ratio 9.45, 95% confidence interval 2.46-41.6, p = 0.002). In the patients whose onset of UC was age 20 years or younger, more patients had SOD2 T/T genotype than the other genotypes (odds ratio 6.46, 95% confidence interval 0.82-51.0). No association between these polymorphisms and UC risk was apparent. The NQO1 C609T polymorphism may influence steroid resistance of UC patients, while the SOD2 Ala-9Val polymorphism may influence age of onset of UC. Oxidative stress may influence the clinical features of UC.
Gastroenterologia Japonica | 1977
Saburo Nakazawa; Yasuo Naito; Yoshiki Yamamoto; Hiroshiko Yamase; Kunio Sobue; Kenichi Yamada; Terumasa Yamamoto; Masahumi Ichikawa; Hitoshi Hidano; Tsuneaki Kachi; Shigekazu Hayashi; Manabu Kazikawa; Toshiyuki Hattori
SummaryThe present study was designed to produce the experimental carcinoma of the biliary tract in dogs. Tube cholecystostomy was constructed in 8 mongrel dogs and 5–10 ml of 0.7–1.0 mg/ml solution of N-ethyl-N’-nitro-N-nitrosoguanidine (ENNG) was administered through the tube every day for the maximum period of 180 days. As the results: The experiment had to be cut off in 7 dogs (5 dogs: The tube was inadvertently pulled out. 2 dogs: died of general weakness). Pathological changes were observed in one dog given ENNG for 180 days and sacrificed at 372 days after the beginning of the experiment. Macroscopically, scattered foci of flat elevation of the mucosa were observed in the entire mucosal surface of common bile duct and a tiny polypoid lesion at the terminal portion. A tiny polypoid projection was adenocarcinoma confined to the mucosa, and areas of flat elevation showed marked hyperplasia of mucosa with partial atypical proliferation. No remarkable findings were noted in other organs.
Gastroenterologia Japonica | 1977
Kose Segawa; Saburo Nakazawa; Yasuo Naito; Kenji Imai; Hirohiko Yamase; Kenichi Yamada; Teruyoshi Yamamoto; Masahumi Ichikawa; Hitoshi Hidano; Tsuneaki Kachi; Shigekazu Hayashi; Shinpei Kawaguchi; Yoshihisa Tsukamoto; Manabu Kajikawa; Eizo Kimoto; Tomohiro Ichikawa
SummaryThe gastric acid output was studied in the 11 patients of hyperparathyroidism before and after parathyroidectomy. The gastric acid output before operation was almost equal to the normal control in our hospital. After the correction of serum calcium by parathyroidectomy, the gastric acid output and serum gastrin were decreased. The decreased gastric acid output was recovered as the days passed since operation and approached to the preoperative level. The acid output in hyperparathyroidism was less in the case whose activity of alkaline phosphatase was more, which suggested that the calcium deposition on gastric mucosa might damage the parietal cell as the result of long lasting hypercalcemia.
World Journal of Gastroenterology | 2006
Toshihito Kosaka; Junji Yoshino; Kazuo Inui; Takao Wakabayashi; Kazumu Okushima; Takashi Kobayashi; Hironao Miyoshi; Yuta Nakamura; Shigekazu Hayashi; Taizou Shiraishi; Masatoshi Watanabe; Takayuki Yamamoto; Ai Nakahara; Takahiko Katoh
Acta Gastro-Enterologica Belgica | 1989
Tsuneya Nakamura; Shigekazu Hayashi; Yasumitsu Kurita; Junichi Kano; Tsuyoshi Furukawa; Tatsunari Satake; Saburo Nakazawa; Kenji Yamao
Jpn J Gastroenterol Surg, Nihon Shokaki Geka Gakkai zasshi | 1987
Takehito Katoh; Takao Nakai; Kiyoshi Ohba; Takeo Okumura; Yutaka Matsuura; Yoshiki Miyazaki; Tatsurou Satoh; Ikuo Nagano; Norihiro Yuasa; Kunihiko Uwatoko; Shigekazu Hayashi; Masanori Esaki; Masahiro Yamada; Youji Kojima; Tatsunari Satake
Jpn J Gastroenterol Surg, Nihon Shokaki Geka Gakkai zasshi | 1987
Norihiro Yuasa; Takao Nakai; Kiyoshi Ohba; Takeo Okumura; Yutaka Matsuura; Yoshiki Miyazaki; Takehito Katoh; Tatsuro Satoh; Kunihiko Uwatoko; Shigekazu Hayashi; Masanori Esaki; Yôji Kojima; Masahiro Yamada; Tatsunari Satake
Nihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine | 1989
Shigekazu Hayashi; Tsuneya Nakamura; Yasumitsu Kurita; Jun-ichi Kanoh; Saiji Yoshii
Acta Gastro-Enterologica Belgica | 2005
Shigekazu Hayashi; Takayoshi Kanbe; Wataru Honda; Masaki Sasaki
Acta Gastro-Enterologica Belgica | 2001
Shigekazu Hayashi; Takayoshi Kanbe; Hideaki Ieda; Hiroshi Nishio; Akihiko Oguri