A novel slow-inactivation-specific ion channel modulator attenuates neuropathic pain. [electronic resource]
Producer: 20110726Description: 833-843 p. digitalISSN:- 1872-6623
- Acetanilides -- chemical synthesis
- Acrylates -- chemical synthesis
- Analysis of Variance
- Animals
- Animals, Newborn
- Biophysics
- Calcium Channels, T-Type -- genetics
- Cell Line, Transformed
- Disease Models, Animal
- Electric Stimulation
- Ganglia, Spinal -- pathology
- Heart -- drug effects
- Humans
- Hyperalgesia -- drug therapy
- In Vitro Techniques
- Ion Channels -- genetics
- Male
- Membrane Transport Modulators -- chemical synthesis
- NAV1.7 Voltage-Gated Sodium Channel
- NAV1.8 Voltage-Gated Sodium Channel
- Neural Inhibition -- drug effects
- Neuralgia -- drug therapy
- Pain Measurement -- methods
- Patch-Clamp Techniques
- Piperazines -- chemical synthesis
- Rabbits
- Rats
- Rats, Wistar
- Sensory Receptor Cells -- drug effects
- Sodium Channel Blockers -- pharmacology
- Sodium Channels -- genetics
- Spinal Cord -- pathology
- Spinal Nerves -- pathology
- Tetrodotoxin -- pharmacology
- Transfection -- methods
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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