Biochemical Studies on Oral Toxicity of Ricin. I. Ricin Administered Orally Can Impair Sugar Absorption by Rat Small Intestine

Rats intoxicated orally with ricin (30mg/kg) showed clear signs of sickness and all died within 36 h. Dying animals shivered and lost body weight. The animals suffered from severe diarrhea within 5-10 h and profuse watery purging. In all intoxicated animals, large amounts of watery fluid were seen i...

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Published inChemical & pharmaceutical bulletin Vol. 31; no. 9; pp. 3222 - 3227
Main Authors ISHIGURO, MASATSUNE, MITARAI, MASAKO, HARADA, HIROMICHI, SEKINE, ICHIRO, NISHIMORI, ISSEI, KIKUTANI, MOTOSUKE
Format Journal Article
LanguageEnglish
Published Tokyo The Pharmaceutical Society of Japan 1983
Maruzen
Japan Science and Technology Agency
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Summary:Rats intoxicated orally with ricin (30mg/kg) showed clear signs of sickness and all died within 36 h. Dying animals shivered and lost body weight. The animals suffered from severe diarrhea within 5-10 h and profuse watery purging. In all intoxicated animals, large amounts of watery fluid were seen in the small intestine, but no significant changes in other organs were observed on gross examination. The effect of oral administration of ricin (30 mg/kg) on D-glucose absorption by rat small intestine was examined by the in vitro everted sac method. The amount of D-glucose absorbed by the small intestine derived from ricin-treated rats was 61.8 μg per 100 mg of tissue per hour or 30% of that of normal rats (206 μg/100 mg of tissue/h) at 5 h after intoxication. Absorptions of D-galactose, D-mannose, and 3-O-methylglucose by the small intestine of ricin-treated rats were 66, 46, and 80% of those of the normal intestine, respectively. Light microscopic examination revealed significant changes such as loss of villi and delay of the regeneration of absorptive epithelials of the small intestine at 5 h after administration. From these results, it was inferred that ricin acts primarily on the intestinal mucosa and impairs sugar absorption.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
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content type line 23
ISSN:0009-2363
1347-5223
DOI:10.1248/cpb.31.3222