Premium
α 1 ‐adrenoceptor stimulation enhances experimental gastric carcinogenesis induced by N ‐methyl‐ N′ ‐nitro‐ N ‐nitrosoguanidine in Wistar rats
Author(s) -
Tatsuta Masaharu,
Iishi Hiroyasu,
Baba Miyako,
Yano Hiroyuki,
Sakai Noriko,
Uehara Hiroyuki,
Hirasawa Ryuto,
Nakaizumi Akihiko
Publication year - 1998
Publication title -
international journal of cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.475
H-Index - 234
eISSN - 1097-0215
pISSN - 0020-7136
DOI - 10.1002/(sici)1097-0215(19980729)77:3<467::aid-ijc25>3.0.co;2-3
Subject(s) - phenylephrine , endocrinology , medicine , metaraminol , stimulation , agonist , gastric mucosa , clonidine , methylnitronitrosoguanidine , stomach , chemistry , receptor , blood pressure , biochemistry , mutant , gene
The effect of prolonged administration of the norepinephrine‐mimicking agent metaraminol, the α 1 ‐adrenergic agonist phenylephrine and the α 2 ‐adrenergic agonist clonidine on the incidence of gastric cancers induced by N ‐methyl‐ N′ ‐nitro‐ N ‐nitrosoguanidine (MNNG), the ornithine decarboxylase activity of the gastric cancer and the labeling index of the gastric mucosa were investigated in Wistar rats. Rats received s.c. injections of metaraminol, phenylephrine or clonidine every other day after 20 weeks of oral treatment with MNNG. At week 52, administration of metaraminol and phenylephrine at the higher dose significantly increased the incidence of gastric cancers, the ornithine decarboxylase activity of the gastric cancers and the labeling index of the antral epithelial cells. Administration of phenylephrine at the lower dose and clonidine at both doses had no significant effect on the incidence of gastric cancers, the ornithine decarboxylase activity of the gastric cancers or the labeling index of the gastric mucosa. Our results suggest that adrenoreceptor stimulation enhances gastric carcinogenesis and that such enhancement is mediated through α 1 ‐adrenoceptors without α 2 ‐adrenoceptor involvement. Int. J. Cancer 77:467–469, 1998. © 1998 Wiley‐Liss, Inc.