ISOMERIZATION OF 11-cis VITAMIN A IN VIVO

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Abstract
Single oral doses of all-trans and 11-cis vitamin A acetate were given to young, vitamin A deficient rats and the proportion of cis isomer in the intestinal tract and liver measured. Some conversion of 11-cis to all-trans occurred in the stomach and intestine, and a mixture of the two isomers was absorbed and stored in the liver. The high proportion of cis isomer found in the liver stores 5 hours after a dose of 11-cis vitamin A disappeared completely in 23 days. Oral doses of both all-trans and 11-cis vitamin A produced greater liver stores than the same doses given subcutaneously. The relative biological potency of the 11-cis isomer was the same by either route, which indicated that the low potency of this isomer was not due only to poor absorption from the intestine.

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