Pardridge W M, Mietus L J
Am J Physiol. 1979 Oct;237(4):E367-72. doi: 10.1152/ajpendo.1979.237.4.E367.
The unidirectional influx of 3H-gonadal (progesterone, dihydrotestosterone, testosterone, estradiol) and adrenal (aldosterone, cortisol) steroid hormones into liver was studied with a tissue-sampling single-injection technique in barbiturate-anesthetized rats. Liver uptake of the steroid hormone was measured relative to [14C]butanol, a highly diffusible reference, after a single pass through the liver. Portal flow (1.4 ml.min-1.g-1) under the experimental conditions was measured with 3H2O. The extraction of unidirectional influx of all six steroid hormones was 70-100% after a bolus portal injection of labeled steroid in Ringer solution (0.1% albumin). Steroid transport was nonsaturable because 35 muM concentrations of unlabeled hormone resulted in no inhibition of liver transport. The plasma proteins (albumin and specific globulins) in serum from human (male, female, pregnancy), rat (male), and guinea pig (pregnancy) sources inhibited the liver clearance of the respective steroid hormones to a variable extent. In all cases albumin-bound steroid hormone was freely cleared by liver and, in the case of cortisol or estradiol, the fraction bound to a specific globulin was also transported into liver.
采用组织采样单次注射技术,在巴比妥麻醉的大鼠中研究了3H标记的性腺(孕酮、二氢睾酮、睾酮、雌二醇)和肾上腺(醛固酮、皮质醇)类固醇激素向肝脏的单向流入。在单次通过肝脏后,相对于[14C]丁醇(一种高扩散性参比物)测量肝脏对类固醇激素的摄取。在实验条件下,用3H2O测量门静脉血流量(1.4 ml·min-1·g-1)。在林格溶液(含0.1%白蛋白)中经门静脉推注标记类固醇后,所有六种类固醇激素的单向流入提取率为70-100%。类固醇转运不饱和,因为35 μM浓度的未标记激素不会抑制肝脏转运。来自人(男性、女性、妊娠)、大鼠(雄性)和豚鼠(妊娠)血清中的血浆蛋白(白蛋白和特异性球蛋白)在不同程度上抑制了相应类固醇激素的肝脏清除率。在所有情况下,与白蛋白结合的类固醇激素可被肝脏自由清除,对于皮质醇或雌二醇,与特异性球蛋白结合的部分也被转运至肝脏。