4.2 Article

Biotransformation and disposition of testosterone in the eastern mud snail Ilyanassa obsoleta

Journal

GENERAL AND COMPARATIVE ENDOCRINOLOGY
Volume 122, Issue 2, Pages 172-180

Publisher

ACADEMIC PRESS INC
DOI: 10.1006/gcen.2001.7630

Keywords

Ilyanassa obsoleta; mud snail; fatty acid conjugates; testosterone; imposex; invertebrate endocrinology; tributyltin

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Elevated testosterone levels have been reported to be associated with imposer (pseudohermaphroditism), the superimposition of male characteristics such as a penis and vas deferens on female gonachoristic snails. Tributyltin (TBT), a marine biocide in anti-fouling paints, is a known causal agent of imposer. Evidence suggests that imposer is elicited by TBT-mediated changes in the biotransformation and disposition of testosterone. To identify potential targets of TBT in gastropod species susceptible to imposer, biotransformation and disposition of testosterone in normal individuals must first be characterized. Nonimposex mud snail, Ilyanassa obsoleta, readily extracted [C-14] testosterone, added to aqueous media, and converted the testosterone to at least five apolar conjugates designated AP1 through APS. All were retained by the organisms. No significant amount of [C-14]testosterone was retained or eliminated as polar metabolites. Following enzymatic hydrolysis of the most abundant metabolite (AP1), free fatty acids and [C-14] testosterone were liberated. Furthermore, AP1 was produced when homogenized snail tissue was incubated with [C-14]testosterone and oleoyl coenzyme A or palmitoyl coenzyme A. These results indicate that AP1, which represents over 70% of the testosterone biotransformation products, is a fatty acid ester of testosterone. Apolar metabolites AP2-AP5 might represent testosterone derivatives that are multiply conjugated to fatty acid molecules. Fatty acid conjugates of testosterone have not been previously described in the gastropods. The esterification of testosterone to fatty acids might be a mechanism where by steroid titers are regulated and could represent a target of TBT toxicity. (C) 2001 Academic Press.

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