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    Please use this identifier to cite or link to this item: http://asiair.asia.edu.tw/ir/handle/310904400/16070


    Title: Alteration of FSH-stimulated progesterone production and calcium homeostasis in primarily cultured human leteinizing-granulosa cells induced by Fenvalerate
    Authors: 張竣維;Hebron, C.Chang
    Contributors: 生物科技學系
    Keywords: Endocrine disruptor;Pyrethroids;Granulosa cell;Progesterone;Calcium homeostasis
    Date: 2004
    Issue Date: 2012-11-23 17:08:12 (UTC+8)
    Abstract: Fenvalerate, a synthetic pyrethroid, is widely used in agriculture and other domestic applications in China. Recently, Fenvalerate has been suspected to be one of the endocrine-disrupting chemicals (EDC). In this study, we investigated the effects of fenvalerate on follicle-stimulating hormone (FSH)-stimulated progesterone (P4) production by human ovarian luteinizing-granulosa cells (hGLCs). After 24 h incubation, fenvalerate inhibited FSH-stimulated P4 production. At the same time, FSH-stimulated cAMP also decreased. Due to calcium and Ca2+–calmodulin (CaM) system involving gonadotropin-stimulated steroidogenesis by granulosa cells, we then evaluated the effects of fenvalerate on trifluoperazine (TFP)- and verapamil-driven FSH-stimulated P4 production. The results showed that calcium or calmodulin might play a role in fenvalerate-induced alterations in FSH-stimulated P4 biosysthesis. Then, the effects of fenvalerate on calcium homeostasis in hGLCs were studied. The result showed that 5 μM fenvalerate induced a slow increase in [Ca2+]i in hGLCs by using a fluorescent Ca2+ indicator fluo-3/AM. The changes in total concentration of CaM in hGLCs induced by fenvalerate were evaluated by a method of immunofluorescence. There is a significant increase in all treated groups. In summary, fenvalerate could inhibit FSH-stimulated P4 production. Also, fenvalerate interferes with calcium homeostasis in hGLCs. The effects of fenvalerate on FSH-stimulated ovarian steroidogenesis may be mediated partly through calcium signal.
    Relation: TOXICOLOGY,V.203(1–3):61–68.
    Appears in Collections:[生物科技學系] 期刊論文

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