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J Neurophysiol 83: 1181-1187, 2000;
0022-3077/00 $5.00
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The Journal of Neurophysiology Vol. 83 No. 3 March 2000, pp. 1181-1187
Copyright ©2000 by the American Physiological Society

Modification of Synaptic Transmission and Sodium Channel Inactivation by the Insect-Selective Scorpion Toxin Lqhalpha IT

Daewoo Lee,1 Michael Gurevitz,2 and Michael E. Adams1

 1Departments of Entomology and Neuroscience, University of California at Riverside, Riverside, California 92521; and  2Department of Botany, Faculty of Life Sciences, Tel-Aviv University, Ramat-Aviv 69978, Tel-Aviv, Israel

Lee, Daewoo, Michael Gurevitz, and Michael E. Adams. Modification of Synaptic Transmission and Sodium Channel Inactivation by the Insect-Selective Scorpion Toxin Lqhalpha IT. J. Neurophysiol. 83: 1181-1187, 2000. The peptide Lqhalpha IT is an alpha -scorpion toxin that shows significant selectivity for insect sodium channels over mammalian channels. We examined the symptoms of Lqhalpha IT-induced paralysis and its neurophysiological correlates in the house fly (Musca domestica). Injection of Lqhalpha IT into fly larvae produced hyperactivity characterized by continuous, irregular muscle twitching throughout the body. These symptoms were correlated with elevated excitability in motor units caused by two physiological effects of the toxin: 1) increased transmitter release and 2) repetitive action potentials in motor nerves. Increased transmitter release was evident as augmentation of neurally evoked synaptic current, and this was correlated with an increased duration of action potential-associated current (APAC) in loose patch recordings from nerve terminals. Repetitive APACs were observed to invade nerve endings. The toxin produced marked inhibition of sodium current inactivation in fly central neurons, which can account for increased duration of the APAC and elevated neurotransmitter release at the neuromuscular junction. Steady-state inactivation was shifted significantly to more positive potentials, whereas voltage-dependent activation of the channels was not affected. The shift in steady-state inactivation provides a mechanism for inducing repetitive activity in motoneurons. The effects of Lqhalpha IT on sodium channel inactivation in motor nerve endings can account both for increased transmitter release and repetitive activity leading to hyperactivity in affected insects.




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