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The aim of the study was to examine the action of green tea polyphenols (GTPP) and their main constituent, epigallocatechin-3-gallate (EGCG), on porcine ovarian granulosa cells. For this purpose, the effect of GTPP and EGCG on cultured porcine ovarian granulosa cell functions, including proliferation, apoptosis, steroidogenesis and response to insulin-like growth factor I (IGF-I) was examined. Proliferation (the accumulation of proliferating cell nuclear antigen (PCNA) and cyclin B1), apoptosis (the accumulation of bax and caspase 3) and the release of steroid hormones (progesterone and testosterone) were evaluated by using immunocytochemistry and enzyme immunoassay. The addition of both GTPP and EGCG reduced the percentage of both PCNA- and cyclin B1-positive cells, increased the proportion of cells containing bax and caspase 3 and stimulated progesterone release. GTPP had a biphasic effect on testosterone output – stimulating at dose 1 μg/ml and inhibiting at doses 10 and 100 μg/ml, whilst EGCG did not affect testosterone secretion. IGF-I, when administered alone, promoted % of cells containing PCNA, suppressed bax accumulation, and stimulated progesterone release (only at dose 100 ng/ml). Testosterone release increased after the addition of IGF-I at 1 ng/ml, but decreased after IGF-I addition at 10 or 100 ng/ml. Both GTPP and EGCG suppressed or even reversed the effects of IGF-I on percentage of PCNA-positive cells, bax, testosterone output, and promoted IGF-I action on progesterone release. These observations suggested the inhibitory actions of green tea constituents on porcine ovarian granulosa cell functions were mediated through various regulatory mechanisms: suppression of the ovarian cell cycle in the S and G2 phases; promotion of cytoplasmic apoptosis; alteration of steroid hormone release; and, predominantly, prevention of the action of the hormonal stimulator IGF-I on ovarian cells. It can be also suggested that the major GTPP effects may result from the presence of EGCG.
It was supposed, that xylene as environmental contaminant and chia (Salvia hispanica L.) as a medicinal plant may affect ovarian cell functions, and that chia seed extract could modify the potentially adverse effect of xylene. So, the aim of our investigation was to study the effect of xylene, extract of chia seed and their combination on bovine ovarian cell functions (proliferation, apoptosis and secretory activity) in vitro. Proliferation, apoptosis and the release of hormones (insulin-like growth factor 1 (IGF-1), progesterone and testosterone) were analysed with the use of either immunocytochemistry or EIA/RIA. It was observed, that xylene when given alone stimulated proliferation and did not influence the apoptosis. Furthermore, xylene inhibited release of progesterone and testosterone but did not change the release of IGF-1. Chia seed extract inhibited proliferation, apoptosis and the release of IGF-1, progesterone and testosterone. Moreover, chia seed extract suppressed the stimulatory effect of xylene on proliferation, and added together stimulated apoptosis. The simultaneous addition of chia seed extract and xylene stimulated IGF-1 release and inhibited the release of progesterone, but not testosterone. The obtained results prove a direct effect of both xylene and chia seed extract on bovine ovarian cell proliferation, apoptosis and secretory activity. Moreover, it is the first study in which chia seed extract was able to suppress xylene effect on ovarian cell proliferation. However, it prevented only from one xylene effect among five analysed suggesting that chia seed extract could not be potentially useful for natural prevention of all negative effects of xylene on reproduction.
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