Ca 2+ signals evoked by histamine H 1 receptors are attenuated by activation of prostaglandin EP 2 and EP 4 receptors in human aortic smooth muscle cells
Autor: | Colin W. Taylor, William G. Bernard, Evangelia Pantazaka, Emily J. A. Taylor |
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Rok vydání: | 2013 |
Předmět: |
Pharmacology
0303 health sciences medicine.medical_specialty Vascular smooth muscle Chemistry Prostaglandin E2 receptor Histamine H1 receptor 030204 cardiovascular system & hematology Cell biology 03 medical and health sciences chemistry.chemical_compound Histamine receptor 0302 clinical medicine Endocrinology Histamine H2 receptor Internal medicine medicine lipids (amino acids peptides and proteins) Histamine H4 receptor Receptor Histamine 030304 developmental biology |
Zdroj: | British Journal of Pharmacology. 169:1624-1634 |
ISSN: | 1476-5381 0007-1188 |
DOI: | 10.1111/bph.12239 |
Popis: | Background and Purpose Histamine and prostaglandin E2 (PGE2), directly and via their effects on other cells, regulate the behaviour of vascular smooth muscle (VSM), but their effects on human VSM are incompletely resolved. Experimental Approach The effects of PGE2 on histamine-evoked changes in intracellular free Ca2+ concentration ([Ca2+]i) and adenylyl cyclase activity were measured in populations of cultured human aortic smooth muscle cells (ASMCs). Selective ligands of histamine and EP receptors were used to identify the receptors that mediate the responses. Key Results Histamine, via H1 receptors, stimulates an increase in [Ca2+]i that is entirely mediated by activation of inositol 1,4,5-trisphosphate receptors. Selective stimulation of EP2 or EP4 receptors attenuates histamine-evoked Ca2+ signals, but the effects of PGE2 on both Ca2+ signals and AC activity are largely mediated by EP2 receptors. Conclusions and Implications Two important inflammatory mediators, histamine via H1 receptors and PGE2 acting largely via EP2 receptors, exert opposing effects on [Ca2+]i in human ASMCs. |
Databáze: | OpenAIRE |
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