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首页> 外文期刊>Osteoporosis international: a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA >Additive effects of estrogen and mechanical stress on nitric oxide and prostaglandin E2 production by bone cells from osteoporotic donors.
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Additive effects of estrogen and mechanical stress on nitric oxide and prostaglandin E2 production by bone cells from osteoporotic donors.

机译:雌激素和机械应力对骨质疏松性供体骨细胞产生的一氧化氮和前列腺素E2的累加作用。

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Mechanical loading is thought to provoke a cellular response via loading-induced flow of interstitial fluid through the lacuno-canalicular network of osteocytes. This response supposedly leads to an adaptation of local bone mass and architecture. It has been suggested that loss of estrogen during menopause alters the sensitivity of bone tissue to mechanical load, thereby contributing to the rapid loss of bone. The present study aimed to determine whether estrogen modulates the mechanoresponsiveness of bone cells from osteoporotic women. Bone cell cultures from nine osteoporotic women (aged 62-90 years) were pre-cultured for 24 h with 10(-11) mol/l 17beta-estradiol (E2) or vehicle, and subjected to 1 h of pulsating fluid flow (PFF) or static culture. E2 alone enhanced prostaglandin E(2) (PGE(2)) and nitric oxide (NO) production by 2.8-fold and 2.0-fold, respectively, and stimulated endothelial nitric oxide synthase protein expression by 2.5-fold. PFF, in the absence of E2, stimulated PGE(2) production by 3.1-fold and NO production by 3.9-fold. Combined treatment with E2 and PFF increased PGE(2) and NO production in an additive manner. When expressed as PFF-treatment-over-control ratio, the response to fluid shear stress was similar in the absence or presence of E2. These results suggest that E2 does not affect the early response to stress in bone cells. Rather, E2 and shear stress both promote the production of paracrine factors such as NO and PGE(2) in an additive manner.
机译:人们认为机械负荷是通过负荷诱导的间质液流经骨细胞的腔管网络而引起细胞反应。据推测,这种反应导致局部骨量和结构的适应。已经提出,绝经期间雌激素的损失改变了骨组织对机械负荷的敏感性,从而促进了骨的迅速损失。本研究旨在确定雌激素是否调节骨质疏松妇女骨细胞的机械反应性。将来自9名骨质疏松妇女(年龄62-90岁)的骨细胞培养物与10(-11)mol / l17β-雌二醇(E2)或溶媒预培养24小时,并进行1小时的脉动液流(PFF) )或静态文化。单独的E2增强前列腺素E(2)(PGE(2))和一氧化氮(NO)的产生分别为2.8倍和2.0倍,并刺激内皮一氧化氮合酶蛋白质表达为2.5倍。在没有E2的情况下,PFF刺激PGE(2)的产量提高了3.1倍,而NO的产量却提高了3.9倍。 E2和PFF的联合处理以累加的方式增加了PGE(2)和NO的产生。当表示为PFF-处理-控制比时,在不存在或存在E2的情况下,对流体剪切应力的响应相似。这些结果表明,E2不会影响骨细胞对压力的早期反应。相反,E2和剪切应力都以加性方式促进旁分泌因子(如NO和PGE(2))的产生。

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