Literature DB >> 2416578

Desensitization of substance P-induced K+ release in rat parotid.

Z Y Friedman, U Wormser, E Rubini, M Chorev, C Gilon, Z Selinger.   

Abstract

Challenge of rat parotid slices with substance P or its analogs, at concentrations which cause less than maximal response resulted in the transient release of K+ into the medium. Reuptake of the released K+ into the cell was accompanied by a parallel decrease in the biologically active concentration of the peptide in the medium, indicating that at low concentrations inactivation of the peptide is a mechanism for termination of the substance P response. At concentrations of substance P and its analogs which are higher than needed for a maximal response, a second mechanism for the termination of the response enters into play, resulting in desensitization of the response to substance P. Desensitization was specific for substance P and was not influenced by activation of the cholinergic or alpha-adrenoceptors. Inactivation of the peptide by proteolytic breakdown does not take part in the development of desensitization to substance P.

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Year:  1985        PMID: 2416578     DOI: 10.1016/0014-2999(85)90005-6

Source DB:  PubMed          Journal:  Eur J Pharmacol        ISSN: 0014-2999            Impact factor:   4.432


  3 in total

1.  Effects of muscarinic, alpha-adrenergic, and substance P agonists and ionomycin on ion transport mechanisms in the rat parotid acinar cell. The dependence of ion transport on intracellular calcium.

Authors:  S P Soltoff; M K McMillian; L C Cantley; E J Cragoe; B R Talamo
Journal:  J Gen Physiol       Date:  1989-02       Impact factor: 4.086

2.  Agonist-induced substance P receptor down-regulation in rat central nervous system.

Authors:  A Inoue; R Takeda; T Fukuyasu; Y Nakata; T Segawa
Journal:  Pharm Res       Date:  1988-12       Impact factor: 4.200

3.  Homologous desensitization of substance-P-induced inositol polyphosphate formation in rat parotid acinar cells.

Authors:  H Sugiya; K A Tennes; J W Putney
Journal:  Biochem J       Date:  1987-06-15       Impact factor: 3.857

  3 in total

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