Migani P, Ciani E, Virgili M, Barnabei O
Faculty Center for Biological Sciences, University of Ancona, Italy.
Comp Biochem Physiol Pharmacol Toxicol Endocrinol. 1994 Jul;108(2):205-14. doi: 10.1016/1367-8280(94)90032-9.
Extracts from the rat brain were screened to identify a putative endogenous ligand for the binding sites of the neuroexcitant kainic acid (KA). The extracted substances were separated by chromatographic techniques and tested for their ability to inhibit KA binding to fish synaptosomes and to membranes from rat brain. A substance isolated in this way (rat kainate-binding inhibitor, RKBI) display a competitive interaction with KA for the low-affinity binding sites in rat brain membranes. According to the separation behavior in the purification step, RKBI is distinct from an inhibitor formerly isolated from fish nervous tissue (KBI). The substance exhibits positive co-operativity with KA for a very-low-affinity site population, particularly concentrated in the cerebellum, and could play a physiological role in this area.
对大鼠脑提取物进行筛选,以鉴定一种假定的内源性配体,该配体可与神经兴奋性红藻氨酸(KA)的结合位点相结合。通过色谱技术分离提取的物质,并测试它们抑制KA与鱼突触体以及大鼠脑膜结合的能力。以这种方式分离出的一种物质(大鼠红藻氨酸结合抑制剂,RKBI)在大鼠脑膜中与KA对低亲和力结合位点表现出竞争性相互作用。根据纯化步骤中的分离行为,RKBI与先前从鱼神经组织中分离出的一种抑制剂(KBI)不同。该物质在一个极低亲和力的位点群体中与KA表现出正协同作用,该位点群体尤其集中在小脑中,并且可能在该区域发挥生理作用。