Monoterpenoids induce agonist-specific desensitization of transient receptor potential vanilloid-3 ion channels

Journal of Pharmacy and Pharmaceutical Sciences

Volumn 12, Issue 1, 2009, Pages 116-128

  Sherkheli, Muhammad Azhar ^a,b   Benecke, Heike ^a   Doerner, Julia Franca ^a   Kletke, Olaf ^a   Vogt Eisele, A K ^a   Gisselmann, Guenter ^a   Hatt, Hanns ^a  

^a RUHR UNIVERSITY BOCHUM   (Germany)

^b IMPRS CB c/o MPI for Molecular Physiology   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CAMPHOR; CINEOLE; COMPLEMENTARY RNA; DIHYDROCARVEOL; MENTHOL; TERPENOID; UNCLASSIFIED DRUG; VANILLOID RECEPTOR 3; TERPENE; VANILLOID RECEPTOR;

ANIMAL CELL; ARTICLE; CONTROLLED STUDY; DRUG MECHANISM; DRUG SENSITIZATION; HUMAN; HUMAN CELL; KERATINOCYTE; LONG TERM EXPOSURE; MOLECULAR DYNAMICS; NONHUMAN; PROTEIN EXPRESSION; VOLTAGE CLAMP; XENOPUS; ANIMAL; CELL MEMBRANE POTENTIAL; DRUG EFFECT; DRUG POTENTIATION; METABOLISM; OOCYTE; XENOPUS LAEVIS;

ANIMALS; HUMANS; MEMBRANE POTENTIALS; MONOTERPENES; OOCYTES; TRPV CATION CHANNELS; XENOPUS LAEVIS;

EID: 70349311418     PISSN: None     EISSN: 14821826     Source Type: Journal    
DOI: 10.18433/j37c7k     Document Type: Article

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