1988
DOI: 10.1111/j.1440-1827.1988.tb02356.x
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Alteration of Gastrin‐producing Cells in Rat Antral Mucosa After Truncal Vagotomy

Abstract: Gastrin‐producing cells (G cells) were studied in the rat antral mucosa after truncal vagotomy. Significant elevation of circulating gastrin levels was observed from 12 hours after the operation and this was sustained throughout the entire experimental period. Upon light microscopic observation, G cells showing positive immunostaining for G17 were significantly increased in number at 2 days, 1, 2 and 3 weeks after the operation and were a more prominent cell type than G cells containing positive reaction produ… Show more

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Cited by 5 publications
(2 citation statements)
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“…19 Primary antibodies used were anti-alpha-1-antitrypsin (AAT) (prediluted, Dako, Carpinteria, California, U.S.A.) polyclonal and anti-neuron specific enolase (NSE) (prediluted, Biomeda, Foster City, California, U.S.A.) monoclonal antibody. Furthermore, antichromogranin A (1:100), antiinsulin (1:300), antisomatostatin (1:300), antiglucagon (1:600) and antipancreatic polypeptides (1:600) polyclonal antibodies (Dako), antigastrin polyclonal antibody produced in our laboratory, 14 and antiserotonin monoclonal antibody (Dako, 1:10) were used for the tissue sections of all cases of SCT to eliminate the possibility of islet cell tumor. As a negative control, nonimmunized rabbit or mouse immunoglobulins were used instead of the primary antibodies, and negative results were obtained.…”
Section: Methodsmentioning
confidence: 99%
“…19 Primary antibodies used were anti-alpha-1-antitrypsin (AAT) (prediluted, Dako, Carpinteria, California, U.S.A.) polyclonal and anti-neuron specific enolase (NSE) (prediluted, Biomeda, Foster City, California, U.S.A.) monoclonal antibody. Furthermore, antichromogranin A (1:100), antiinsulin (1:300), antisomatostatin (1:300), antiglucagon (1:600) and antipancreatic polypeptides (1:600) polyclonal antibodies (Dako), antigastrin polyclonal antibody produced in our laboratory, 14 and antiserotonin monoclonal antibody (Dako, 1:10) were used for the tissue sections of all cases of SCT to eliminate the possibility of islet cell tumor. As a negative control, nonimmunized rabbit or mouse immunoglobulins were used instead of the primary antibodies, and negative results were obtained.…”
Section: Methodsmentioning
confidence: 99%
“…Several reports have shown an elevation in serum gastrin levels and hyperplasia of gastrin-producing cells (G-cells) following vagotomy in both experimental models and humans. [1][2][3][4][5][6][7][8][9][10][11][12][13][14][15][16] In association with high serum gastrin levels, hyperplasia of certain cell organelles within G-cells has also been described in a few Reprint requests to: H. Shimoda (Received for publication on Feb. 7,1991; accepted on May 1, 1992) reports. 2-4 The mechanism of G-cell hyperplasia in the rat antral mucosa after truncal vagotomy was reported in our previous study using double immunostaining for bromodeoxyuridine (BrdU) and little gastrin (G17).…”
Section: Introductionmentioning
confidence: 99%