Jadot M, Wattiaux-De Coninck S, Wattiaux R
Laboratoire de Chimie Physiologique, Facultés Universitaires Notre Dame de la Paix, Namur, Belgium.
Biochem J. 1989 Sep 15;262(3):981-4. doi: 10.1042/bj2620981.
We have investigated the effect on the osmotic activation of rat liver lysosomes, by glucose penetration, of different substances known to inhibit the glucose transport through the plasma membrane. Diethylstilbestrol is the most efficient, particularly when purified lysosomes are used. It has no effect on osmotic activation induced by hypo-osmotic sucrose or by iso-osmotic KCl. It is proposed that diethylstilbestrol reacts with specific sites involved in the glucose translocation through the lysosomal membrane. These sites could not be identified by binding experiments, presumably owing to the considerable unspecific binding of the compound to the membrane.
我们研究了已知可抑制葡萄糖通过质膜转运的不同物质,通过葡萄糖渗透对大鼠肝脏溶酶体渗透激活的影响。己烯雌酚最为有效,尤其是在使用纯化的溶酶体时。它对低渗蔗糖或等渗氯化钾诱导的渗透激活没有影响。有人提出,己烯雌酚与参与葡萄糖通过溶酶体膜转运的特定位点发生反应。这些位点无法通过结合实验确定,可能是由于该化合物与膜存在大量非特异性结合。