Weissman B A, Cott J, Jackson J A, Bolger G T, Weber K H, Horst W D, Paul S M, Skolnick P
J Neurochem. 1985 May;44(5):1494-9. doi: 10.1111/j.1471-4159.1985.tb08787.x.
Previous studies have shown that Ro 5-4864 is a potent convulsant and increases the firing rate of substantia nigra zona reticulata neurons. The pharmacologic profile of compounds that antagonize these actions suggested that the effects of Ro 5-4864 were not mediated by "brain-type" benzodiazepine receptors. We examined a number of compounds that are structurally related to Ro 5-4864 for their capacities to displace [3H]Ro 5-4864 from "peripheral-type" binding sites and their potencies as convulsants (or as antagonists of Ro 5-4864-induced convulsions). It was observed that compounds such as KW 3600 (the N-desmethyl analog of Ro 5-4864), which have very low affinities for "peripheral-type" sites, are convulsants with a potency nearly equal to that of Ro 5-4864. In contrast, compounds such as Ro 5-6900 and PK 11195, which bind with very high affinities to "peripheral-type" binding sites, are neither convulsants nor do they antagonize the convulsant actions of Ro 5-4864. Within a series of compounds that are structurally related to Ro 5-4864 there is a good correlation (r = 0.93; p less than 0.01) between their potencies as convulsants and their capacities to displace [35S]t-butylbicyclophosphorothionate from sites that may be associated with the chloride ionophore. Thus, it appears that occupation of "peripheral-type" binding sites by high-affinity ligands may not be directly involved in the convulsant actions of Ro 5-4864 and related compounds.
先前的研究表明,Ro 5-4864是一种强效惊厥剂,可提高黑质网状带神经元的放电频率。拮抗这些作用的化合物的药理学特征表明,Ro 5-4864的作用不是由“脑型”苯二氮䓬受体介导的。我们研究了许多与Ro 5-4864结构相关的化合物,考察它们从“外周型”结合位点置换[3H]Ro 5-4864的能力以及作为惊厥剂(或Ro 5-4864诱导惊厥的拮抗剂)的效力。据观察,诸如KW 3600(Ro 5-4864的N-去甲基类似物)等对“外周型”位点亲和力非常低的化合物是惊厥剂,其效力几乎与Ro 5-4864相当。相反,诸如Ro 5-6900和PK 11195等与“外周型”结合位点具有非常高亲和力的化合物,既不是惊厥剂,也不拮抗Ro 5-4864的惊厥作用。在一系列与Ro 5-4864结构相关的化合物中,它们作为惊厥剂的效力与其从可能与氯离子载体相关的位点置换[35S]叔丁基双环磷硫代酸盐的能力之间存在良好的相关性(r = 0.93;p小于0.01)。因此,似乎高亲和力配体占据“外周型”结合位点可能与Ro 5-4864及相关化合物的惊厥作用没有直接关系。