Analysis of Mechanisms of Spiking in Normally 'Non-Spiking' Motoneurone Somata in Crayfish (original) (raw)
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Journal of Experimental Biology, 1995
Ionic currents from freshly isolated and identified swimmeret motor neurones were characterized using a whole-cell patch-clamp technique. Two outward currents could be distinguished. A transient outward current was elicited by delivering depolarizing voltage steps from a holding potential of -80 mV. This current was inactivated by holding the cells at a potential of -40 mV and was also blocked completely by 4-aminopyridine. A second current had a sustained time course and continued to be activated at a holding potential of -40 mV. This current was partially blocked by tetraethylammonium. These outward currents resembled two previously described potassium currents: the K+ A-current and the delayed K+ rectifier current respectively. Two inward currents were also detected. A fast transient current was blocked by tetrodotoxin and inactivated at holding potential of -40 mV, suggesting that this is an inward Na+ current. A second inward current had a sustained time course and was affected...
Journal of Comparative Physiology A, 1995
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The Journal of experimental biology, 1999
Inward Ca2+ current through voltage-gated Ca2+ channels was recorded from freshly dissociated crayfish X-organ (XO) neurones using the whole-cell voltage-clamp technique. Changing the holding potential from -50 to -90 mV had little effect on the characteristics of the current-voltage relationship: neither the time course nor the amplitude of the Ca2+ current was affected. Inactivation of the Ca2+ current was observed over a small voltage range, between -35 and -10 mV, with half-inactivation at -20 mV. The activation of the Ca2+ current was modelled using Hodgkin-Huxley kinetics. The time constant of activation, &tgr; m, was 568+/-66 micros at -20 mV and decreased gradually to 171+/-23 micros at 40 mV (means +/- s.e.m., N=5). The steady-state activation, m(infinity), was fitted with a Boltzmann function, with a half-activation voltage of -7.45 mV and an apparent threshold at -40 mV. The instantaneous current-voltage relationship was adjusted using the Goldman-Hodgkin-Katz constant-fi...
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The Journal of physiology, 1986
Arsenazo III was used to investigate Ca2+ transients in the normally non-excitable soma of the motor giant neurones of the crayfish Procambarus clarkii. Two kinds of regenerative potentials could be obtained depending on membrane potential conditioning: a fast spike after a pre-hyperpolarization to -90 mV and a slow action potential after a pre-depolarization to -50 mV. Only the second of these was accompanied by an Arsenazo III transient. In voltage-clamped, somata injected, with tetraethylammonium chloride, an absorbance change could be obtained by pulsing the membrane potential above -44 mV. The relationship between absorbance change and potential peaked between 0 and +10 mV then fell off to zero at ca. +150 mV. Changes in light absorbance studied using double-pulse protocols suggested that the inactivation of Ca2+ entry was predominantly mediated by the intracellular free Ca2+ concentration. External application of 1 mM-CdCl2 abolished both the absorbance changes and the (Ca2+) ...
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NeuroReport, 1999
CURRENTS from the slowly adapting stretch receptor neuron of the cray®sh (Pacifastacus leniusculus) were studied in a cell attached con®guration using patch pipettes with an opening diameter of 2±10 ìm. The neuronal membrane was enzymatically freed from the glial layer. The voltage gated Na and K channels seemed to be more concentrated in the lower part of soma close to the axon hillock. The Na and K currents could be analysed by ®tting the currents to a fourth-order exponential function for Na current and a second-order exponential function for the K current. The macropatch recordings of enzymatically treated neurons are superior to two electrode voltage clamp recordings when analyzing voltage gated Na and K currents. NeuroReport 10:2503±2507 # 1999 Lippincott Williams & Wilkins.
Journal of Neurophysiology, 1998
Purali, Nuhan and Bo Rydqvist. Action potential and sodium current in the slowly and rapidly adapting stretch receptor neurons of the crayfish ( Astacus astacus). J. Neurophysiol. 80: 2121–2132, 1998. Action potentials (APs) and sodium current from the slowly and the rapidly adapting stretch receptor neurons in the crayfish ( Astacus astacus) were recorded with a two microelectrode voltage- and current-clamp technique. In the rapidly adapting neuron the APs had a duration of 3.2 ± 0.2 ms (means ± SE) and an amplitude of 55.2 ± 1.5 mV. In the slowly adapting receptor neuron APs had a duration of 4.1 ± 0.2 ms and an amplitude 79.9 ± 2.0 mV. APs in the rapidly adapting neuron had a larger amplitude if they were recorded from the axon. In the rapidly adapting neuron adaptation of the impulse response was prolonged by hyperpolarization or by exposure to scorpion venom. Also, sinusoidal current stimulation added to the current steps prevented impulse adaptation. Block of the potassium cur...