Journal
JOURNAL OF NEUROPHYSIOLOGY
Volume 103, Issue 4, Pages 2085-2094Publisher
AMER PHYSIOLOGICAL SOC
DOI: 10.1152/jn.01010.2009
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Funding
- National Institutes of Health [C06 RR-015481-01, NS-051668]
- NATIONAL CENTER FOR RESEARCH RESOURCES [C06RR015481] Funding Source: NIH RePORTER
- NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [R01NS051668] Funding Source: NIH RePORTER
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Wang Y, Duan JH, Hingtgen CM, Nicol GD. Augmented sodium currents contribute to the enhanced excitability of small diameter capsaicin-sensitive sensory neurons isolated from Nf1+/- mice. J Neurophysiol 103: 2085-2094, 2010. First published February 17, 2010; doi: 10.1152/jn.01010.2009. Neurofibromin, the product of the Nf1 gene, is a guanosine triphosphatase activating protein ( GAP) for p21ras (Ras) that accelerates conversion of active Ras-GTP to inactive Ras-GDP. Sensory neurons with reduced levels of neurofibromin likely have augmented Ras-GTP activity. We reported previously that sensory neurons isolated from a mouse model with a heterozygous mutation of the Nf1 gene (Nf1+/-) exhibited greater excitability compared with wild-type mice. To determine the mechanism giving rise to the augmented excitability, differences in specific membrane currents were examined. Consistent with the enhanced excitability of Nf1+/- neurons, peak current densities of both tetrodotoxin-resistant sodium current (TTX-R I-Na) and TTX-sensitive (TTX-S) I-Na were significantly larger in Nf1+/- than in wild-type neurons. Although the voltages for half-maximal activation (V-0.5) were not different, there was a significant depolarizing shift in the V-0.5 for steady-state inactivation of both TTX-R and TTX-S I-Na in Nf1+/- neurons. In addition, levels of persistent I-Na were significantly larger in Nf1+/- neurons. Neither delayed rectifier nor A-type potassium currents were altered in Nf1+/- neurons. These results demonstrate that enhanced production of action potentials in Nf1+/- neurons results, in part, from larger current densities and a depolarized voltage dependence of steady-state inactivation for I-Na that potentially leads to a greater availability of sodium channels at voltages near the firing threshold for the action potential.
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