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    請使用永久網址來引用或連結此文件: http://libir.tmu.edu.tw/handle/987654321/4617


    題名: 17beta-estradiol抑制血小板凝集作用之機轉探討
    Mechanisms involved in the antiplatelet activity of 17beta-estradiol
    作者: 陳威帆
    Wei-Fan Chen
    貢獻者: 藥學研究所
    關鍵詞: 血小板
    女性荷爾蒙
    platelet
    estradiol
    日期: 2007
    上傳時間: 2009-09-09 12:28:20 (UTC+8)
    摘要: 近幾年來的研究發現停經後婦女長期使用賀爾蒙療法會增加靜脈血栓以及增加心肌梗塞和缺血性中風這些疾病的危險性。然而賀爾蒙補充療法和加成性的賀爾蒙補充療法已經廣泛的被用來預防心血管疾病和血栓產生。這和目前的發現是互相矛盾的，所以我們對於17beta-estradiol如何調節血小板的活性感到興趣。
    經由一系列實驗後，我們發現17beta-estradiol (50-80 micro M)明顯的抑制collagen所引起的人類血小板凝集反應，但對於thrombin和U46619所引起的血小板凝集並沒有抑制的效果；17beta-estradiol (50-80 micro M)可以抑制由collagen所刺激細胞內鈣離子的流動和thromboxane A2的形成；17beta-estradiol (50-80 micro M)能抑制由collagen所引起的PLC2的磷酸化，進而去影響47 kD磷酸化，但對於由PDBu所引起47 kD磷酸化卻沒有影響，同時它也能增加NO的形成以及VASP的磷酸化，進而抑制血小板的凝集；再者17beta-estradiol (50-80 micro M)並不會對collagen所引起的p38 MAPK、ERK1/2的磷酸化造成影響。在我們的實驗中發現，17beta-estradiol抑制collagen所引起的的血小板活化，這個血小板凝集的機轉，主要是透過抑制PLC2 的活性，進而抑制PKC的磷酸化，接著抑制TxA2的形成，最後導致細胞內減少鈣離子，所以抑制血小板的凝集；另一方面17beta-estradiol會增加NO的產生，使cGMP產生，且17beta-estradiol也會使cAMP產生，進而抑制血小板的凝集，其他更詳細的機轉將會更清楚的說明。
    Post-menopausal hormone therapy increases the risk of venous thrombosis, and possibly myocardial infarction and ischemic stroke. However, estrogen replacement therapy or combined hormone replacement therapy has been widely used to protect against development of both cardiovascular diseases and other thrombotic diseases. Therefore, we are interested to evaluate whether 17beat-estradiol can regulate platelet activities. In this study, we found that 17beta-estradiol (50-80 micro M) significantly inhibited collagen (1 micro g/ml) but not thrombin (0.02 U/ml) or U46619 (0.1 micro M)-induced platelet aggregation in washed human platelets; 17beta-estradiol (50-80 micro M) markedly inhibited collagen (1 micro g /ml)-triggered calcium mobilization and thromboxane A2 (TxA2) formation in washed human platelets; 17beta-estradiol (50-80 micro M) significantly inhibited collagen- but not PDBu-induced 47-kDa protein phosphorylation; 17beta-estradiol also inhibited collagen-induced PLC2 phosphorylation; in addition 17beta-estradiol (50-80 micro M) also increased NO formation and induced phosphorylation of vasodilator-stimulated phosphoprotein(VASP). In conclusion, we showed that estradiol inhibited collagen-induced platelet aggregation. The anti-aggregatory mechanism of 17beta-estradiol occurs via reducing PLC2 phosphorylation, TxA2 formation, calcium mobilization and increasing NO, cGMP and cAMP in washed human platelets. However, the more detailed anti-aggregatory mechanism of 17beta-estradiol will be elucidated in the future.
    資料類型: thesis
    顯示於類別:[藥學系] 博碩士論文

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