The K channel blocker, tetraethylammonium, displaces beta-endorphin and naloxone from T-cell binding sites

Journal of Neuroimmunology

Volumn 78, Issue 1-2, 1997, Pages 8-18

  Millar, David B ^a,b   Mazorow, Denise L ^a   Hough, Chris ^c  

^a New Ideas Co   (United States)

^b NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES   (United States)

^c Sect Clin and Exp Neuropsychol   (United States)

Author keywords

endorphin; Channel blocker; K channel; Naloxone; Neuroimmunomodulation; Opioid receptor; T cell

Indexed keywords

BETA ENDORPHIN; CHARYBDOTOXIN; NALOXONE; POTASSIUM CHANNEL BLOCKING AGENT; TETRYLAMMONIUM;

ANIMAL CELL; ARTICLE; BINDING SITE; CALCIUM TRANSPORT; COMPETITIVE INHIBITION; DATA ANALYSIS; DRUG RECEPTOR BINDING; ELECTROPHYSIOLOGY; IMMUNOMODULATION; ION TRANSPORT; MEMBRANE BINDING; NONHUMAN; ONCOGENE C MYC; PATCH CLAMP; PRIORITY JOURNAL; PROTEIN DOMAIN; T LYMPHOCYTE ACTIVATION;

BETA-ENDORPHIN; BINDING SITES; BINDING, COMPETITIVE; CALCIUM CHANNEL BLOCKERS; CHARYBDOTOXIN; ELECTROPHYSIOLOGY; MITOGENS; NALOXONE; NARCOTIC ANTAGONISTS; POTASSIUM CHANNEL BLOCKERS; POTASSIUM CHANNELS; PROTO-ONCOGENE PROTEINS C-MYC; QUATERNARY AMMONIUM COMPOUNDS; T-LYMPHOCYTES; TETRAETHYLAMMONIUM; TETRAETHYLAMMONIUM COMPOUNDS; TUMOR CELLS, CULTURED;

EID: 0030868849     PISSN: 01655728     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-5728(97)00078-7     Document Type: Article

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