Summary: | Thiel and colleagues demonstrated that the all-or-none nature of <em>Chara</em> action potential(AP) is determined by formation of a second messenger, probably inositol triphosphate (IP<sub>3</sub>), whichin turn releases Ca<sup>2+</sup> from internal stores. The Ca<sup>2+</sup>-activated Cl<sup>–</sup> channels are the main agent of thedepolarization phase of the AP. Once the Ca<sup>2+</sup> is re-sequestered by the calcium pumps, the chlorideconductance drops and depolarization-activated outward rectifier current, the background current andthe proton pump current return the membrane potential difference (PD) to resting level. Departingfrom the Thiel model of transient increase of Ca<sup>2+</sup> concentration, we set up membrane PD rate ofchange equation to calculate the AP form by numerical integration. Compared to data, this model APdepolarized more gradually. We introduced a prompt Ca<sup>2+</sup> transient from the outside, achieving agood correspondence with the experimental AP. In <em>Chara</em> cells subjected to 50 mM NaCl/0.1 mMCa<sup>2+</sup> medium, the AP duration increased from 2 s to up to 50 s and the APs were often spontaneous.The lack of stimulating pulse revealed a sharp positive spike at the beginning of each AP, confirmingthat <em>Chara</em> plasma membrane may contain transient receptor potential (TRP)-like channels, possiblyactivated by another second messenger diacylglycerol (DAG) formed at the same time as IP<sub>3</sub>. Thelong duration of the saline AP can be modeled by decreasing the coefficients in the Hill equationdescribing the Ca<sup>2+</sup> pumps on the internal stores. The model provides new insights into the characeanAP and suggests a range of experiments.
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