Metabolism of pyrrolizidine alkaloids in the ovine rumen. I. Formation of 7-α-hydroxy-1-α-methyl-8-α pyrrolizidine from heliotrine and lasiocarpine

Australian Journal of Agricultural Research
1970.0

Abstract

When the pyrrolizidine alkaloids heliotrine and lasiocarpine were incubated in vitro with sheep’s rumen contents, a common metabolic product was formed. Thiscompound was also found as an end-product of metabolism in the rumen contents of sheep fed on a ration containing the plant Heliotropium europaeum. Previously described rumen metabolites of the Heliotropium alkaloids were 1-methylenepyrrolizidine derivatives, e.g. I-goreensine. The newly found product represents a further stage of reduction of 1-goreensine in which the 1-methylene group has been replaced by a 1-methyl group. This compound has been identified as 7α-hydroxy-1α- methyl-8α-pyrrolizidine, a previously unknown pyrrolizidine derivative. © 1970, CSIRO Publishing.

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