Tsai V W-W, Dodd P R, Lewis R J
School of Molecular and Microbial Sciences, University of Queensland, Brisbane 4072, Australia.
Neuroscience. 2005;130(2):457-64. doi: 10.1016/j.neuroscience.2004.09.039.
We evaluated the effects of Ala-7-conantokin-G (Con-G(A7)) and ifenprodil on the modulation by spermine of [(3)H]MK801 binding to human cortical membranes. Human cortical tissue was obtained at autopsy and stored at -80 degrees C until assay. Both Con-G(A7) and ifenprodil inhibited [(3)H]MK801 binding, but spermine affected these inhibitions differently. Con-G(A7) IC(50) changed little with spermine concentration, indicative of a non-competitive interaction, whereas the rightward shift in ifenprodil IC(50) with increasing spermine concentration suggested partial competition. When the two agents were tested against the biphasic activation of [(3)H]MK801 binding by spermine, they again differed in their effects. In the activation phase Con-G(A7) was a non-competitive inhibitor of spermine activation, and may even enhance the spermine EC(50), while the ifenprodil data indicated a partially competitive interaction. Both agents were non-competitive in the inhibitory phase. Overall, the data suggest that Con-G(A7) and ifenprodil interact differently with the polyamine modulation of the glutamate-N-methyl-D-aspartate receptor.
我们评估了丙氨酸 -7-芋螺毒素 -G(Con -G(A7))和艾芬地尔对精胺调节[³H]MK801与人脑皮质膜结合的影响。人脑皮质组织在尸检时获取,并储存于 -80℃直至检测。Con -G(A7)和艾芬地尔均抑制[³H]MK801结合,但精胺对这些抑制作用的影响不同。Con -G(A7)的半数抑制浓度(IC₅₀)随精胺浓度变化不大,表明存在非竞争性相互作用,而随着精胺浓度增加,艾芬地尔的IC₅₀向右移动,提示存在部分竞争性。当测试这两种药物对精胺引起的[³H]MK801结合双相激活的影响时,它们的作用再次不同。在激活阶段,Con -G(A7)是精胺激活的非竞争性抑制剂,甚至可能提高精胺的半数有效浓度(EC₅₀),而艾芬地尔的数据表明存在部分竞争性相互作用。在抑制阶段,两种药物均为非竞争性。总体而言,数据表明Con -G(A7)和艾芬地尔与谷氨酸 -N-甲基 -D-天冬氨酸受体的多胺调节相互作用不同。