The effect of cimetidine and hypoxia on the gastric macromolecular glycoprotein in rat.

In an experimental study in rats, cimetidine, a potent gastric-acid inhibitor (50 mg/kg, .p.o.) reduced the macromolecular glycoprotein level of glandular stomach. The administration of cimeti­ dine at a dose of 50 mg/kg, which inhibited the gastric lesions induced by hypoxia (13% O2 for 6 hours), reduced the glandular stomach level of high molecular glycoproteins in animals receiving a low oxygen load as well as in those receiving no load. It was assumed that the reduction of macro­ molecular glycoprotein accelerated the gastric lesion induced by hypoxia load in rats and that cimeti­ dine inhibited the lesions through a process other than that of recovering the glycoprotein level in the glandular stomach.

[1]  S. Nakazawa,et al.  [Localization and determination of macromolecular glycoproteins of the glandular stomach in rats]. , 1983, Nihon Shokakibyo Gakkai zasshi = The Japanese journal of gastro-enterology.

[2]  S. Nakazawa,et al.  Studies on the localization and the measurement of macromolecular glycoproteins of the glandular stomach in rats , 1983 .

[3]  S. E. Williams,et al.  Studies of the protective properties of gastric mucus. , 1982, Advances in experimental medicine and biology.

[4]  G. Kauffman,et al.  Gastric gel mucus thickness: effect of distention, 16,16-dimethyl prostaglandin e2, and carbenoxolone. , 1981, Gastroenterology.

[5]  H. S. Himal,et al.  Prevention of Sepsis-Induced Gastric Lesions in Dogs by Cimetidine via Inhibition of Gastric Secretion and by Prostaglandin via Cytoprotection , 1981 .

[6]  H. S. Himal,et al.  Prevention of sepsis-induced gastric lesions in dogs by cimetidine via inhibition of gastric secretion and by prostaglandin via cytoprotection. , 1981, Gastroenterology.

[7]  K. Hotta,et al.  Correlation of quantitative changes of gastric mucosal glycoproteins with aspirin-induced gastric damage in rats. , 1980, Gut.

[8]  I. Samloff,et al.  Actions of histamine, secretin, and PGE2 on cyclic AMP production by isolated canine fundic mucosal cells. , 1979, The American journal of physiology.

[9]  F. Moody,et al.  Mechanisms of mucus release in exposed canine gastric mucosa. , 1979, Gastroenterology.

[10]  Y. Mikuni‐Takagaki,et al.  Characterization of peptic inhibitory activity associated with sulfated glycoprotein isolated from gastric mucosa. , 1979, Biochimica et biophysica acta.

[11]  K. Sirinek,et al.  The role of cimetidine in the prevention of stress induced gastric mucosal injury. , 1979, Surgery, gynecology & obstetrics.

[12]  A. Allen Structure of gastrointestinal mucus glycoproteins and the viscous and gel-forming properties of mucus. , 1978, British medical bulletin.

[13]  T. Dousa,et al.  Interrelationships between histamine, prostaglandins, and cyclic AMP in gastric secretion: a hypothesis. , 1977, Gastroenterology.

[14]  E. D. Jacobson,et al.  Cyclic AMP and gastric secretion: the illusive second messenger. , 1976, Advances in cyclic nucleotide research.

[15]  R. Cathcart,et al.  Histochemical Patients Changes in Gastric M ucosubstances in with Acute and Chronic Ulcer Disease , 1974 .

[16]  R. Cathcart,et al.  Histochemical changes in gastric mucosubstances in patients with acute and chronic ulcer disease. , 1974, Annals of surgery.

[17]  P. Whiteman The quantitative determination of glycosaminoglycans in urine with Alcian Blue 8GX. , 1973, The Biochemical journal.

[18]  K TAKAGI,et al.  STUDIES ON THE DRUGS FOR PEPTIC ULCER. A RELIABLE METHOD FOR PRODUCING STRESS ULCER IN RATS. , 1964, Chemical & pharmaceutical bulletin.

[19]  F. Smith,et al.  COLORIMETRIC METHOD FOR DETER-MINATION OF SUGAR AND RELATED SUBSTANCE , 1956 .

[20]  F. Hollander The two-component mucous barrier; its activity in protecting the gastroduodenal mucosa against peptic ulceration. , 1954, A.M.A. archives of internal medicine.