首页> 外文期刊>Journal of neurobiology >Effects of progesterone and its reduced metabolites, dihydroprogesterone and tetrahydroprogesterone, on the expression and phosphorylation of glycogen synthase kinase-3 and the microtubule-associated protein tau in the rat cerebellum.
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Effects of progesterone and its reduced metabolites, dihydroprogesterone and tetrahydroprogesterone, on the expression and phosphorylation of glycogen synthase kinase-3 and the microtubule-associated protein tau in the rat cerebellum.

机译:孕酮及其还原代谢产物二氢孕酮和四氢孕酮对大鼠小脑糖原合酶激酶3和微管相关蛋白tau的表达和磷酸化的影响。

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Progesterone exerts a variety of actions in the brain, where it is rapidly metabolized to 5alpha-dihydroprogesterone (DHP) and 3alpha,5alpha-tetrahydroprogesterone (THP). The effect of progesterone and its metabolites on the expression and phosphorylation of the microtubule-associated protein Tau and glycogen synthase kinase 3beta (GSK3beta), a kinase involved in Tau phosphorylation, were assessed in two progesterone-sensitive brain areas: the hypothalamus and the cerebellum. Administration of progesterone, DHP, and THP to ovariectomized rats did not affect Tau and GSK3beta assessed in whole hypothalamic homogenates. In contrast, progesterone and its metabolites resulted in a significant decrease in the expression of Tau and GSK3beta in the cerebellum. Furthermore, progesterone administration resulted in an increase in the phosphorylation of two epitopes of Tau (Tau-1 and PHF-1) phosphorylated by GSK3beta, but did not affect the phosphorylation of an epitope of Tau (Ser262) that is GSK3beta insensitive. These effects were accompanied by a decrease in the phosphorylation of GSK3beta in serine, which is associated to an increase in its activity, suggesting that the effect of progesterone on Tau-1 and PHF-1 phosphorylation in the cerebellum is mediated by GSK3beta. The regulation of Tau expression and phosphorylation by progesterone may contribute to the hormonal regulation of cerebellar function by the modification of neuronal cytoskeleton.
机译:孕酮在大脑中发挥多种作用,并迅速代谢为5α-二氢孕酮(DHP)和3α,5α-四氢孕酮(THP)。在两个对孕激素敏感的大脑区域(下丘脑和小脑)中评估了孕酮及其代谢物对微管相关蛋白Tau和糖原合酶激酶3beta(GSK3beta)(一种参与Tau磷酸化的激酶)的表达和磷酸化的影响。 。给卵巢切除的大鼠施用孕酮,DHP和THP不会影响在整个下丘脑匀浆中评估的Tau和GSK3beta。相反,孕酮及其代谢产物导致小脑中Tau和GSK3beta的表达显着下降。此外,黄体酮的给药导致被GSK3beta磷酸化的Tau的两个表位(Tau-1和PHF-1)的磷酸化增加,但不影响GSK3beta不敏感的Tau的表位(Ser262)的磷酸化。这些作用伴随着丝氨酸中GSK3β磷酸化的减少,这与其活性的增加有关,这表明孕酮对小脑中Tau-1和PHF-1磷酸化的影响是由GSK3beta介导的。孕酮调节Tau表达和磷酸化可能通过修饰神经元细胞骨架来促进小脑功能的激素调节。

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