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The 1.3 isoform of Na+–Ca2+ exchanger expressed in guinea pig tracheal smooth muscle is less sensitive to KB-R7943
Algara-Suárez, Paola o; Espinosa-Tanguma, Ricardo; Mejía-Elizondo, Rebeca; Saavedra-Alanis, Victor M; Sims , Stephen M.
Affiliation
  • Algara-Suárez, Paola o; Universidad Autónoma de San Luis Potosí. Facultad de Medicina. Department of Physiology. San Luis Potosí. México
  • Espinosa-Tanguma, Ricardo; Universidad Autónoma de San Luis Potosí. Facultad de Medicina. Department of Physiology. San Luis Potosí. México
  • Mejía-Elizondo, Rebeca; Universidad Autónoma de San Luis Potosí. Facultad de Medicina. Department of Biochemistry. San Luis Potosí. México
  • Saavedra-Alanis, Victor M; Universidad Autónoma de San Luis Potosí. Facultad de Medicina. Department of Biochemistry. San Luis Potosí. México
  • Sims , Stephen M; University of Western Ontario. Schulich School of Medicine & Dentistry. London. Canada
J. physiol. biochem ; 66(2): 117-125, jun. 2010.
Article in English | IBECS | ID: ibc-122835
Responsible library: ES1.1
Localization: BNCS
RESUMEN
No disponible
ABSTRACT
The sodium–calcium exchanger (NCX) plays a major role in the regulation of cytosolic Ca2+ in muscle cells. In this work, we performed force experiments to explore the role of NCX during contraction and relaxation of Cch-stimulated guinea pig tracheal smooth muscle strips. This tissue showed low sensitivity to NCX inhibitor KB-R7943 (IC50, 57 ± 2 µM), although a complete relaxation was obtained by NCX inhibition at 100 µM. Interestingly, relaxation after washing the agonist was prolonged in the absence of external Na+, whereas washing without Na+ and in the presence of KB-R7943 resembled control conditions with physiological solution. Altogether, this suggests the reversal of NCX to a Ca2+ influx mode by the manipulation on the Na+ gradient, which can be inhibited by KB-R7943. In order to understand the low sensitivity to KB-R7943, we studied the molecular aspects of the NCX expressed in this tissue and found that the isoform of NCX expressed is 1.3, similar to that described in human tracheal smooth muscle. Sequencing revealed that amino acid 19 in exon B is phenylalanine, whereas in its human counterpart is leucine, and that the first amino acid after exon D is aspartate instead of glutamate in humans. Results herein presented are discussed in term of their possible functional implications in the exchanger activity and thus in airway physiology (AU)
Subject(s)
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Collection: National databases / Spain Database: IBECS Main subject: Phenylalanine / Aspartate Kinase / Glutamic Acid / Sodium-Calcium Exchanger / Leucine Type of study: Diagnostic study Limits: Animals / Humans Language: English Journal: J. physiol. biochem Year: 2010 Document type: Article Institution/Affiliation country: Universidad Autónoma de San Luis Potosí/México / University of Western Ontario/Canada
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Collection: National databases / Spain Database: IBECS Main subject: Phenylalanine / Aspartate Kinase / Glutamic Acid / Sodium-Calcium Exchanger / Leucine Type of study: Diagnostic study Limits: Animals / Humans Language: English Journal: J. physiol. biochem Year: 2010 Document type: Article Institution/Affiliation country: Universidad Autónoma de San Luis Potosí/México / University of Western Ontario/Canada
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