STUDIES ON PHARMACOLOGICAL ACTIVATION OF HUMAN SERUM IgG BY CHEMICAL MODIFICATION AND ACTIVE SUBFRAGMENTS. II. INHIBITORY EFFECTS OF CARBOXAMIDEMETHYLATED L CHAIN FROM HUMAN SERUM IgG ON VARIOUS ULCER MODELS AND ITS INHIBITION MECHANISM

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In view of the strong inhibitory effects of the carboxamide-methylated Lchain (Fr.I-L) from human IgGon gastric ulceration and juice secretion, we carried out various experiments to clarify the mechanism of its action and obtained the following results. Fr. I-L inhibited the gastric ulceration induced by phenylbutazone or aspirin in rats, but no appreciable effect was observed on stress or acetic acid ulceration. The distribution of ^<14>Clabelled Fr. I-L increased particularly in the stomach mucous membrane of rats after the intravenous or intraperitoneal administraion. The hexosamine content in the gastric mucous membrane, reduced by the treatment with phenylbutazone, aspirin or pylorus-ligation, was recovered by the administration of Fr.I-L to an intact level. The high total of hexosamine levels found in the gastric juice after aspirin treatment or pylorus-ligation were decreased by the injection of Fr.I-L or cimetidine. The histochmical observation revealed that the concomitant administration of Fr. I-L with phenylbutazone or aspirin prevented the abolishment of Hematoxylin-Eosin, Periodic Acid Schiff and Alcian Blue staining polysaccharides from the stomach epithelial cells.
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