The results are shown in Table 2. 3657L cells, lung fibroblasts derived from wild-type CD47/IAP-expressing mice, showed a membrane depolarisation response when mechanically stimulated at 0.33 Hz.
The same cells, however, showed a membrane hyperpolarisation response when mechanically stimulated at 0.083 Hz. 3656 1/Sra cells, CD47/IAP-/ mouse lung fibroblasts derived from CD47/IAP knockout mice transfected with vector control, showed no change in cell membrane potential when mechanically stimulated at both 0.33 and 0.083 Hz.
This acceleration was qualitatively similar to that found in toad rod membrane voltage responses when 2 mM CsCl was introduced [16].
The open-ended PSi microcavity membrane exhibited a fourfold faster response when exposed to the large, 247.5-kDa CAT protein, as the flow-through scheme facilitated improved mass transport.
In all cases, |ΔZRF| consisted of an initial onset response when the rate of change of TEVC membrane potential was large (o, |ΔZRF|o, dVm*/dt>0) and a steady-state response when TEVC membrane potential was approximately constant (s, |ΔZRF|s, dVm*/dt ≅ 0).
(a) Simulations of the membrane response at different input current levels revealed absent action potential generation in the WT at high currents, even when A1273V neurons continue to fire.
Age-related deficits in retention of the classically conditioned nictitating membrane response in rabbits.
The hippocampus and the classically conditioned nicitating membrane response: A real-time attentional-associative network.
They are as follows: (1) depression of the excitatory end-plate potential and the postsynaptic membrane response to applied glutamate, and (2) a hyperpolarization of the postsynaptic resting membrane potential associated with a decrease in effective membrane resistance.
When we applied repeated single PP stimuli of a constant strength near the threshold for eliciting somatic APs, the CA2 PN membrane response often fluctuated between a full-blown AP response and a spikelet.
