Mukherjee S, Mohammad A R, Das S K
Department of Biochemistry, Meharry Medical College, Nashville, TN 37208.
Biochem Pharmacol. 1990 Oct 1;40(7):1589-94. doi: 10.1016/0006-2952(90)90459-x.
The binding of [3H]Ro 5-4864 to peripheral benzodiazepine receptors (PBRs) was studied in normal and malignant submandibular glands of rats. The carcinoma was induced by implantation of 7,12-dimethylbenz[a]anthracene (DMBA) into the glands. [3H]Ro 5-4864 binding to normal and malignant submandibular glands indicated one population of binding sites with high affinity (KD of 3.4 and 4.4 nM for normal and malignant respectively) and saturability (Bmax) of 487 and 321 pmol/g tissue for normal and malignant respectively). Subcellular localization of PBRs indicates that mitochondria was the primary locale of the receptor in both cases and the decrease in Bmax was due primarily to a decrease in the binding capacity of PBRs in mitochondria.
在大鼠正常和恶性下颌下腺中研究了[3H]Ro 5-4864与外周苯二氮䓬受体(PBRs)的结合情况。通过将7,12-二甲基苯并[a]蒽(DMBA)植入腺体诱导产生癌。[3H]Ro 5-4864与正常和恶性下颌下腺的结合表明存在一类具有高亲和力的结合位点(正常和恶性的解离常数KD分别为3.4和4.4 nM)以及可饱和性(最大结合量Bmax),正常和恶性的分别为487和321 pmol/g组织)。PBRs的亚细胞定位表明,在两种情况下线粒体都是受体的主要所在部位,Bmax的降低主要是由于线粒体中PBRs结合能力的下降。