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雌性小鼠特定脑区和垂体中[3h]雌二醇的区域及亚细胞定位:未标记雌二醇和各种抗激素的影响。

Regional and subcellular [3h]estradiol localization in selected brain regions and pituitary of female mice: effects of unlabeled estradiol and various anti-hormones.

作者信息

Luttge W G, Gray H E, Hughes J R

出版信息

Brain Res. 1976 Mar 12;104(2):273-81. doi: 10.1016/0006-8993(76)90619-3.

Abstract

Groups of ovariectomized mice were pretreated for 30 min with either vehicle, unlabeled estradiol benzoate or one of the following anti-hormones: cyproterone acetate, CI-628 or CN-69, 725-27. One hour after an I.V. injection of [3H]estradiol the levels of toluence extractable radioactivity retained in the crude nuclear and cytosol fractions of selected brain regions, pituitary and plasma were determined by liquid scintillation spectrometry. The major findings were: (1) In vehicle treated animals [3H]estradiol uptake in the pituitary greatly exceeded that in all brain regions. Within the brain uptake was greatest in the preoptic anterior hypothalamus (POA-AH) and medial basal hypothalamus (MBH) samples. Nuclear uptake exceeded cytosol uptake only in the pituitary and POA-AH and MBH samples. (2) Estradiol benzoate pretreatment greatly reduced nuclear, and to a lesser extent cytosol [3H]estradiol uptake in pituitary, POA-AH and MBH samples. Estradiol benzoate pretreatment also reduced nuclear uptake in the dorsal middle hypothalamus (DMH). (3) The anti-androgen cyproterone acetate, previously shown to have anti-estrogenic effects in female sexual behavior tests, was found to have no effect on nuclear or cytosol [3H]estradiol uptake in brain and pituitary. (4) The anti-estrogen CI-628 was found to reduce nuclear [3H]estradiol uptake in the POA-AH and pituitary samples. It also reduced cytosol [3H]estradiol uptake in the pituitary sample. The anti-estrogen CN-69, 725-27 produced a much greater inhibition of nuclear [3H]estradiol uptake than CI-628 in the POA-AH, MBH, DMH, dorsal posterior hypothalamus and pituitary samples. This anti-estrogen also reduced cytosol [3H]estradiol uptake in the POA-AH, MBH and pituitary samples. (5) A preliminary chromatographic analysis of vehicle control samples indicated that 70-98% of the nuclear radioactivity in target regions such as POA-AH, MBH and pituitary was iso-polar with authentic estradiol, while less than 50% of the radioactivity in plasma and cortex behaved as estradiol.

摘要

将去卵巢小鼠分组,分别用赋形剂、未标记的苯甲酸雌二醇或以下抗激素之一进行30分钟的预处理:醋酸环丙孕酮、CI - 628或CN - 69,725 - 27。静脉注射[3H]雌二醇1小时后,通过液体闪烁光谱法测定选定脑区、垂体和血浆的粗核和胞质溶胶部分中甲苯可提取放射性的水平。主要发现如下:(1) 在赋形剂处理的动物中,垂体对[3H]雌二醇的摄取大大超过所有脑区。在脑内,视前区下丘脑前部(POA - AH)和内侧基底下丘脑(MBH)样本中的摄取量最大。仅在垂体以及POA - AH和MBH样本中,核摄取超过胞质溶胶摄取。(2) 苯甲酸雌二醇预处理大大降低了垂体、POA - AH和MBH样本中的核[3H]雌二醇摄取,对胞质溶胶摄取的降低程度较小。苯甲酸雌二醇预处理还降低了背侧下丘脑中部(DMH)的核摄取。(3) 抗雄激素醋酸环丙孕酮先前在雌性性行为测试中显示具有抗雌激素作用,现发现其对脑和垂体中的核或胞质溶胶[3H]雌二醇摄取无影响。(4) 抗雌激素CI - 628被发现可降低POA - AH和垂体样本中的核[3H]雌二醇摄取。它还降低了垂体样本中的胞质溶胶[3H]雌二醇摄取。抗雌激素CN - 69,725 - 27在POA - AH、MBH、DMH、背侧下丘脑后部和垂体样本中对核[3H]雌二醇摄取的抑制作用比CI - 628大得多。这种抗雌激素还降低了POA - AH、MBH和垂体样本中的胞质溶胶[3H]雌二醇摄取。(5) 对赋形剂对照样本的初步色谱分析表明,在POA - AH、MBH和垂体等靶区域中,70 - 98%的核放射性与纯雌二醇具有同极性,而血浆和皮质中的放射性只有不到50%表现为雌二醇。

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