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Biology of Reproduction 63, 1024-1033 (2000)
© 2000 Society for the Study of Reproduction, Inc.


ARTICLES

Effects of Lindane on Steroidogenesis and Steroidogenic Acute Regulatory Protein Expression1

Lance P. Walsha, and Douglas M. Stocco2,a

a Department of Cell Biology and Biochemistry, Texas Tech University Health Sciences Center, Lubbock, Texas 79430

Lindane, the {gamma} isomer of hexachlorocyclohexane (HCH), is one of the oldest synthetic pesticides still in use worldwide. Numerous reports have shown that this pesticide adversely affects reproductive function in animals. Although the pathogenesis of reproductive dysfunction is not yet fully understood, recent reports indicate that lindane can directly inhibit adrenal and gonadal steroidogenesis. Because Leydig cells play a pivotal role in male reproductive function through the production of testosterone, the mouse MA-10 Leydig tumor cell line was used to assess the potential effects of {gamma}-HCH and its isomers, {alpha}-HCH and {delta}-HCH, on steroid production, steroidogenic enzyme expression and activity, and steroidogenic acute regulatory (StAR) protein expression. StAR mediates the rate-limiting and acutely regulated step in hormone-stimulated steroidogenesis, the intramitochondrial transfer of cholesterol to the P450scc enzyme. Our studies demonstrate that {alpha}-, {delta}-, and {gamma}-HCH inhibited dibutyryl ([Bu]2) cAMP-stimulated progesterone production in MA-10 cells in a dosage-dependent manner without affecting general protein synthesis; and protein kinase A or steroidogenic enzyme expression, activity, or both. In contrast, each of these isomers dramatically reduced (Bu)2cAMP-stimulated StAR protein levels. Therefore, our results are consistent with the hypothesis that {alpha}-, {delta}-, and {gamma}-HCH inhibited steroidogenesis by reducing StAR protein expression, an action that may contribute to the pathogenesis of lindane-induced reproductive dysfunction.

First decision: 22 March 2000.

1 Supported by NIH grant HD17481 to D.M.S. L.P.W was supported by NIH grant T32-HD07271 and a scholarship from the Lubbock Achievement Rewards for College Scientists chapter.

2 Correspondence. FAX: 806 743 2990; doug.stocco{at}ttmc.ttuhsc.edu




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