Sensory nerve terminal mitochondrial dysfunction induces hyperexcitability in airway nociceptors via protein kinase C

Molecular Pharmacology

Volumn 85, Issue 6, 2014, Pages 839-848

  Hadley, Stephen H ^a   Bahia, Parmvir K ^a   Taylor Clark, Thomas E ^a  

^a UNIVERSITY OF SOUTH FLORIDA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIMYCIN A1; BISINDOLYLMALEIMIDE; MYXOTHIAZOL; OLIGOMYCIN; PROTEIN KINASE C; TRANSIENT RECEPTOR POTENTIAL CHANNEL A1; VANILLOID RECEPTOR 1;

ACTION POTENTIAL; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; CONTROLLED STUDY; ENZYME ACTIVATION; MALE; MITOCHONDRIAL DNA DISORDER; MOUSE; NERVE CELL; NERVE ENDING; NERVE EXCITABILITY; NERVE FIBER; NONHUMAN; PAIN RECEPTOR; PRIORITY JOURNAL; RECEPTOR POTENTIAL; SENSORY NERVE;

ACTION POTENTIALS; ANIMALS; ANTIMYCIN A; BRONCHI; MALE; MICE; MICE, INBRED C57BL; MICE, KNOCKOUT; MITOCHONDRIA; NERVE ENDINGS; NOCICEPTORS; PROTEIN KINASE C; REACTIVE OXYGEN SPECIES; SENSORY THRESHOLDS; TRPV CATION CHANNELS;

EID: 84899512386     PISSN: 0026895X     EISSN: 15210111     Source Type: Journal    
DOI: 10.1124/mol.113.091272     Document Type: Article

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