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Membrane Conductances Involved in Amplification of Small Signals by Sodium Channels in Photoreceptors of Drone Honey Bee

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Journal J Physiol
Specialty Physiology
Date 1992 Oct 1
PMID 1338099
Citations 6
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Abstract

1. Voltage signals of about 1 mV evoked in photoreceptors of the drone honey bee by shallow modulation of a background illumination of an intensity useful for behaviour are thought to be amplified by voltage-dependent Na+ channels. To elucidate the roles of the various membrane conductances in this amplification we have studied the effects of the Na+ channel blocker tetrodotoxin (TTX) and various putative K+ channel blockers on the membrane potential, Vm. 2. Superfusion of a slice of retina with 0.5-10 mM-4-aminopyridine (4-AP) depolarized the membrane and, in fifty of sixty-three cells induced repetitive action potentials. Ionophoretic injection of tetraethylammonium produced similar effects. 3. In order to measure the depolarization caused by 4-AP, action potentials were prevented by application of TTX: 4-AP was applied when the membrane was depolarized to different levels by light. 4-AP induced an additional depolarization at all membrane potentials tested (-64 to -27 mV). We conclude that there are 4-AP-sensitive K+ channels that are open at constant voltage over this range. 4. 4-AP slowed down the recovery phase of the action potential induced by a light flash by a factor that ranged from 0.51 to 0.16. This reduction could be accounted for by the reduction in a voltage-independent K+ conductance estimated from the steady-state depolarization. 5. After the voltage-gated Na+ channels had been blocked by TTX, exposure to 4-AP further changed the amplitude of the response to a small (approximately 10%) decremental light stimulus. The change was an increase when the background illumination brought Vm to potentials more negative than about -40 mV; it was a decrease when Vm > -40 mV. The data could be fitted by a circuit representation of the membrane with a light-activated conductance and a K+ conductance (EK = -66 mV) that was partly blocked by 4-AP. The voltage range studied was from -52 to -27 mV; neither conductance in the model was voltage dependent. 6. The responses to small changes in light intensity in the absence of TTX were mimicked by a model. We conclude that a voltage-dependent Na+ conductance described by the Hodgkin-Huxley equations can amplify small voltage changes in a cell membrane that is also capable of generating action potentials; the magnitude of the K+ conductance is critical for optimization of signals while avoiding membrane instability.

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References
1.
Okabe K, Kitamura K, Kuriyama H . The existence of a highly tetrodotoxin sensitive Na channel in freshly dispersed smooth muscle cells of the rabbit main pulmonary artery. Pflugers Arch. 1988; 411(4):423-8. DOI: 10.1007/BF00587722. View

2.
Luk H, Carmeliet E . Na(+)-activated K+ current in cardiac cells: rectification, open probability, block and role in digitalis toxicity. Pflugers Arch. 1990; 416(6):766-8. DOI: 10.1007/BF00370627. View

3.
Castle N, Haylett D, JENKINSON D . Toxins in the characterization of potassium channels. Trends Neurosci. 1989; 12(2):59-65. DOI: 10.1016/0166-2236(89)90137-9. View

4.
Szatkowski M . The effect of extracellular weak acids and bases on the intracellular buffering power of snail neurones. J Physiol. 1989; 409:103-20. PMC: 1190434. DOI: 10.1113/jphysiol.1989.sp017487. View

5.
Llinas R . The intrinsic electrophysiological properties of mammalian neurons: insights into central nervous system function. Science. 1988; 242(4886):1654-64. DOI: 10.1126/science.3059497. View