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在表达牛生长激素基因的转基因小鼠肝脏中,体内特定的促生长激素和催乳激素摄取情况。

Specific somatotropic and lactogenic uptake in vivo in the livers of transgenic mice expressing bovine growth hormone gene.

作者信息

Turyn D, Yun J S, Wagner T E, Bartke A

机构信息

Instituto de Quimica y Fisicoquimica Biológicas (UBA-CONICET), Facultad de Farmacia y Bioquimica, Buenos Aires, Argentina.

出版信息

Growth Regul. 1993 Sep;3(3):190-7.

PMID:8220111
Abstract

The distribution of labeled hGH, oGH and mPRL in different tissues of MT-bGH transgenic and normal mice was investigated using an in vivo technique. This technique allows comparisons of tissue uptake of radioactivity after the labeled hormone was injected alone (20 ng/50 g BW) or together with an excess (300 micrograms/50 g BW) of unlabeled hormone. Liver, kidney and spleen are the organs that concentrate a significant amount of radioactivity 20 min after the injection of labeled hormones, but the uptake of radioactivity decreased in the presence of unlabeled hormones only in the liver. Graphical analysis showed that the disappearance curves were described by the sum of 3 compartments alpha, beta and gamma. The first two are similar in transgenic and in normal mice but the third had a t1/2 of 56 +/- 9 min in transgenic and 71 +/- 8 min in normal mice. The inhibition of liver uptake was related to the dose of unlabeled hormone injected and a half maximal displacement was obtained with 4 micrograms and 10 micrograms of hGH per 50 g of body weight for normal and transgenic mice, respectively. The 125I-hGH taken up in vivo by the liver of transgenic mice was bound to a molecular species with Stokes radius of approximately 64 A (which is consistent with the molecular size reported for the hormone-receptor complex).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

采用体内技术研究了MT-bGH转基因小鼠和正常小鼠不同组织中标记的人生长激素(hGH)、牛生长激素(oGH)和鼠催乳素(mPRL)的分布。该技术可比较单独注射标记激素(20 ng/50 g体重)或与过量(300 μg/50 g体重)未标记激素一起注射后组织对放射性的摄取情况。注射标记激素20分钟后,肝脏、肾脏和脾脏是摄取大量放射性的器官,但仅在肝脏中,未标记激素存在时放射性摄取会降低。图形分析表明,消失曲线由α、β和γ三个区室的总和描述。前两个区室在转基因小鼠和正常小鼠中相似,但第三个区室在转基因小鼠中的半衰期为56±9分钟,在正常小鼠中为71±8分钟。肝脏摄取的抑制与注射的未标记激素剂量有关,正常小鼠和转基因小鼠每50 g体重分别用4 μg和10 μg hGH可获得半数最大置换。转基因小鼠肝脏在体内摄取的125I-hGH与斯托克斯半径约为64 Å的分子物种结合(这与报道的激素-受体复合物的分子大小一致)。(摘要截短于250字)

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