Wang M D, Wahlström G, Bäckström T
Department of Physiology, Umeå, Sweden.
J Steroid Biochem Mol Biol. 1997 Jul;62(4):299-306. doi: 10.1016/s0960-0760(97)00041-1.
We have studied the distribution of the neurosteroids pregnenolone (Pe) and pregnenolone sulfate (PeS) in seven brain regions, and plasma and fat tissues in male adult rats following the intravenous infusion of 14 mg/kg Pe and 18 mg/kg PeS, respectively. After chromatographic separation of steroid sulfate esters and non-conjugated steroids by solid phase octadecyl C18 columns and celite column chromatographic separation of Pe from cross-reacted steroids, the concentrations of Pe and PeS were determined by radioimmunoassay. We found that both Pe and PeS concentrations were significantly increased in plasma, fat and brain compared to the vehicle controls after i.v. infusion of Pe and PeS. In the controls, Pe concentrations were highly correlated within brain regions and between fat and brain regions. Most correlations were lost after Pe and PeS infusions. The content of Pe and PeS was not uniformly distributed in the brain. The hypothalamus contained the highest level of Pe in controls, Pe-infused and PeS-infused rats (12 +/- 3.1, 3500 +/- 180 and 590 +/- 54 ng/g, respectively). The highest concentration of PeS was detected in the hypothalamus (26 +/- 8.2 ng/g) and striatum (17 +/- 4.1 ng/g) in controls, in the hypothalamus (200 +/- 24 ng/g) after PeS infusion as well as in the hypothalamus and medulla oblongata (57 +/- 9.6 and 55 +/- 7.6 ng/g, respectively) after Pe infusion. This study has yielded evidence that PeS injected i.v. can cross the blood-brain barrier without being hydrolysed to the more lipophilic Pe, and can thus be taken up by the brain.
我们分别向成年雄性大鼠静脉注射14mg/kg孕烯醇酮(Pe)和18mg/kg硫酸孕烯醇酮(PeS)后,研究了这两种神经甾体在七个脑区、血浆及脂肪组织中的分布情况。通过十八烷基C18固相柱对硫酸酯类甾体和非共轭甾体进行色谱分离,并用硅藻土柱色谱法从交叉反应的甾体中分离出Pe后,采用放射免疫分析法测定Pe和PeS的浓度。我们发现,静脉注射Pe和PeS后,与注射赋形剂的对照组相比,血浆、脂肪及脑内的Pe和PeS浓度均显著升高。在对照组中,脑区内以及脂肪与脑区之间的Pe浓度高度相关。注射Pe和PeS后,多数相关性消失。Pe和PeS在脑内的分布并不均匀。在对照组、注射Pe组及注射PeS组的大鼠中,下丘脑的Pe含量最高(分别为12±3.1、3500±180和590±54ng/g)。对照组中,下丘脑(26±8.2ng/g)和纹状体(17±4.1ng/g)的PeS浓度最高;注射PeS后,下丘脑的PeS浓度最高(200±24ng/g);注射Pe后,下丘脑和延髓的PeS浓度最高(分别为57±9.6和55±7.6ng/g)。本研究提供了证据,静脉注射的PeS能够穿过血脑屏障,且不会水解为亲脂性更强的Pe,因此能够被脑摄取。