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BmK IT2, a site-4-specific modulator of VGSCs, significantly suppressed the formalin-induced rat spontaneous flinches and spinal c-Fos expression in a dose-dependent manner.Binding assay of 125I-BmK IT2 showed two non-interacting binding sites on insect neuronal membranes: a high affinity (Kd1=0.65±0.20 nM) and low capacity (Bmax1=0.46±0.13 pmol/mg protein) binding site, as well as a low-affinity (Kd2=78.7±16.4 nM) and high capacity (Bmax2=33.1±8.5 pmol/mg protein) binding site.