Caesium ions: A glycine-activated channel agonist in rat spinal cord neurones grown in cell culture

Stephen Smith, R. N. McBurney

Research output: Contribution to journalArticle

4 Scopus citations

Abstract

1. The chloride (Cl -) currents activated by caesium ions (Cs +), glycine and γ-aminobutyric acid (GABA) were compared following their application to rat neurones that had been grown in cell culture. Recordings were made using the whole-cell patch clamp technique under voltage clamp conditions. 2. In spinal cord neurones, bicuculline methiodide antagonized GABA-activated currents more effectively than Cs +- or glycine-activated currents. However, strychnine was more effective at blocking the currents activated by Cs + or glycine than those activated by GABA. 3. Of the 3 agonists, only GABA activated currents in cells from the intermediate lobe of the rat pituitary. 4. In spinal neurones the size of the currents activated by 70 mM Cs + was correlated to the size of the currents activated by 15 μM glycine (P < 0.005; n = 10, Spearman's rank correlation), but there was no significant correlation between the size of the currents activated by these agents and 10 μM GABA. 5. The joint application of glycine and Cs + activated currents that were approximately twice as big as the sums of the currents activated by separate applications of the same doses. This synergism was consistent with Cs + acting at the same receptor as glycine (7 μM glycine being equivalent to 31 ± 7 mM Cs +). 6. It was concluded that Cs + activates the same Cl - channel as the inhibitory neurotransmitter glycine.

Original languageEnglish (US)
Pages (from-to)940-948
Number of pages9
JournalBritish Journal of Pharmacology
Volume96
Issue number4
Publication statusPublished - 1989
Externally publishedYes

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ASJC Scopus subject areas

  • Pharmacology

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