Figure 1 - Neuronal-Specific Inhibition of Endoplasmic Reticulum Mg2+ /Ca2+ ATPase Ca2+ Uptake in a Mixed Primary Hippocampal Culture Model of Status Epilepticus

Electrophysiological monitoring of SE in hippocampal neurons. Culture dishes were incubated in control or low Mg 2+ solutions and neurons were patch clamped using the whole-cell current-clamp mode as described in Materials and Methods. Scale bar described in part B is applicable to all traces. (A) Representative recording of a neuron incubated in control solution. (B) Representative trace of a neuron incubated in low Mg 2+ solution for approximately 1 h. (C) Representative recording of a neuron incubated in low Mg 2+ solution for approximately 3 h.

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Reference

Neuronal-Specific Inhibition of Endoplasmic Reticulum Mg2+ /Ca2+ ATPase Ca2+ Uptake in a Mixed Primary Hippocampal Culture Model of Status Epilepticus - Scientific Figure on ResearchGate. Available from: https://www.researchgate.net/figure/Electrophysiological-monitoring-of-SE-in-hippocampal-neurons-Culture-dishes-were_fig1_342923494 [accessed 30 Jun, 2024]

Caption

Figure 1. Electrophysiological monitoring of SE in hippocampal neurons. Culture dishes were incubated in control or low Mg 2+ solutions and neurons were patch clamped using the whole-cell current-clamp mode as described in Materials and Methods. Scale bar described in part B is applicable to all traces. (A) Representative recording of a neuron incubated in control solution. (B) Representative trace of a neuron incubated in low Mg 2+ solution for approximately 1 h. (C) Representative recording of a neuron incubated in low Mg 2+ solution for approximately 3 h.

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<a href="https://www.researchgate.net/figure/Electrophysiological-monitoring-of-SE-in-hippocampal-neurons-Culture-dishes-were_fig1_342923494"><img src="https://www.researchgate.net/profile/Laxmikant-Deshpande/publication/342923494/figure/fig1/AS:913205773737984@1594736631777/Electrophysiological-monitoring-of-SE-in-hippocampal-neurons-Culture-dishes-were.png" alt="Electrophysiological monitoring of SE in hippocampal neurons. Culture dishes were incubated in control or low Mg 2+ solutions and neurons were patch clamped using the whole-cell current-clamp mode as described in Materials and Methods. Scale bar described in part B is applicable to all traces. (A) Representative recording of a neuron incubated in control solution. (B) Representative trace of a neuron incubated in low Mg 2+ solution for approximately 1 h. (C) Representative recording of a neuron incubated in low Mg 2+ solution for approximately 3 h."/></a>