Invited reviewCalcium permeability of ligand-gated channels
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2021, International Review of Cell and Molecular BiologyQuantifying Ca<sup>2+</sup> current and permeability in ATP-gated P2X7 receptors
2015, Journal of Biological ChemistryVinpocetine regulates cation channel permeability of inner retinal neurons in the ischaemic retina
2014, Neurochemistry InternationalCitation Excerpt :Vinpocetine does not prevent binding of NMDA agonists to the NMDA receptor suggesting it’s actions to reduce cation channel permeability do not involve blocking the receptor itself (Kaneko et al., 1991; Kiss et al., 1991). Vinpocetine however could selectively affect NMDA activated neurons via Ca2+ as NMDA receptors but not kainate receptors are highly permeable to Ca2+ (Burnashev, 1998). We established that cation channel permeability and calcium binding protein immunoreactivity of inner retinal neurons was altered following hypoglycaemia and ischaemia.
The astrocyte excitability brief: From receptors to gliotransmission
2012, Neurochemistry InternationalCitation Excerpt :It should be noted that the presence of the GluR2 subunit in the AMPA receptors determines its lack of permeability for Ca2+ (Hollmann et al., 1991). Thus, in astrocytes lacking GluR2 subunits, AMPA receptors flux Na+, K+ and Ca2+ (Burnashev, 1998), although the fractional Ca2+ current does not exceed ∼4% (Table 1). Kainate receptors, composed from the five subunits (KA1, KA2 and GluR5–7), were identified, at transcription and protein levels, in some astrocytes (Garcia-Barcina and Matute, 1996; Brand-Schieber et al., 2004).
(-)Clausenamide facilitates synaptic transmission at hippocampal Schaffer collateral-CA1 synapses
2012, European Journal of Pharmacology