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. Author manuscript; available in PMC: 2015 Feb 23.
Published in final edited form as: J Neurosci. 2011 Dec 7;31(49):18185–18194. doi: 10.1523/JNEUROSCI.4936-11.2011

Fig. 2.

Fig. 2

Voltage-gated sodium channel distribution is rapidly disrupted by hypoperfusion. (A) Nav1.6 sodium channels, which outline the node of Ranvier, are normally bounded by the paranodal protein CASPR as shown in the sham. In response to hypoperfusion, after 3 days and 1 month, the distribution of the Nav1.6 sodium channels is markedly altered and laterally spreads along the axon, corpus callosum, scale bar = 1 μm. (B) There is a significant increase in the length of the Nav1.6 clusters after 3 days of hypoperfusion in the corpus callosum and additionally after 1 month in the internal capsule and optic tract. 40 nodes per animal were analysed and these 240 to 400 nodes are plotted as cumulative frequency distribution, tabulated as relative frequencies as percent (Two-sample Kolmogorov-Smirnov test). Number of nodes of Ranvier remains unchanged after 3 day or 1 month of hypoperfusion. (C) Confocal stack of nodes of Ranvier in the corpus callosum, double labelled with Nav1.6 and CASPR, left sham, right 1 month of hypoperfusion, scale bar = 1 μm. (D) Numbers of nodes of Ranvier are not altered in response to hypoperfusion. After 3 days and 1 month the number of Nav1.6 immuno-positive nodes was not changed between the sham and hypoperfused groups. Analysis was conducted by confocal laser microscopy in the corpus callosum, internal capsule and optic tract in a 47×47×5 μm3 confocal stack (Mann-Whitney, two-tailed).