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Phosphorylation State of Tyrosine Hydroxylase in the Stalk-Median Eminence Is Decreased by Progesterone in Cycling Female Rats

机译:孕酮降低骑行雌性大鼠茎中位酪氨酸羟化酶的磷酸化状态

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摘要

Progesterone has the capacity to suppress hypothalamic dopaminergic neuronal activity on proestrous afternoon and prolong or amplify the preovulatory prolactin surge in rats. In the present study, we examined enzyme activity and phosphorylation state of tyrosine hydroxylase (TH) in the stalk-median eminence of cycling female rats on proestrus and estrus and related these to circulating progesterone levels. Phospho-TH levels were evaluated by Western blot analysis. TH activity was determined from the rate of 3,4-dihydroxyphenylalanine (DOPA) accumulation. Phospho-TH levels at Ser-19, Ser-31, and Ser-40 were similar at 1100, 1300, and 1500 h on proestrus but declined at 1700, 1900, and 2200 h, coincident with rising serum progesterone levels. Similarly, DOPA accumulation was 30–50% lower at 1700, 1900, and 2200 h as compared with 1100–1500 h on proestrus. Ser-31 and Ser-40 phosphorylation states were increased by 1100 h on estrus to a level similar to 1100 h on proestrus, whereas DOPA accumulation was 30% greater on estrous as compared with proestrous morning. There were no significant differences among the several time points on proestrus and estrus with regard to TH protein or β-tubulin levels. Exogenous progesterone administration (7.5 mg/kg, sc) before the preovulatory progesterone surge decreased TH activity and phospho-TH at Ser-19, Ser-31, and Ser-40, accompanied by premature increased serum prolactin. Our study suggests that decreased TH phosphorylation at Ser-19, Ser-31, and Ser-40 contributes to the decline in TH activity in the stalk-median eminence on proestrous afternoon and that progesterone may cause this initial cytoplasmic response of TH dephosphorylation.
机译:孕酮具有在下午发情时抑制下丘脑多巴胺能神经元活动并延长或扩大大鼠排卵前催乳素激增的能力。在本研究中,我们检查了雌性单车前发和发情的茎中位突起中酪氨酸羟化酶(TH)的酶活性和磷酸化状态,并将其与循环孕酮水平相关联。通过蛋白质印迹分析评估磷酸-TH水平。由3,4-二羟基苯丙氨酸(DOPA)积累的速率确定TH活性。 Ser-19,Ser-31和Ser-40的磷TH水平在发情期的1100、1300和1500 h相似,但在1700、1900和2200 h下降,这与血清孕酮水平升高相吻合。同样,DOPA积累在1700、1900和2200 h时比发情期的1100–1500 h低30–50%。 Ser-31和Ser-40的磷酸化状态在发情期增加了1100 h,达到与发情期1100 h相似的水平,而发情期的DOPA积累则比发情上午增加了30%。在TH蛋白或β-微管蛋白水平方面,在发情和发情的几个时间点之间没有显着差异。在排卵前孕酮激增之前,外源孕激素给药(7.5 mg / kg,皮下注射)降低了Ser-19,Ser-31和Ser-40的TH活性和磷酸化TH,并伴有血清催乳素过早升高。我们的研究表明,Ser-19,Ser-31和Ser-40处的TH磷酸化水平下降,导致下午发情时茎中部突起的TH活性下降,而孕酮可能引起TH脱磷酸作用的这种初始细胞质反应。

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