TXA2 agonists inhibit high-voltage-activated calcium channels in rat hippocampal CA1 neurons

研究成果: Article同行評審

16 引文 斯高帕斯(Scopus)

摘要

Whole cell voltage clamp recordings were used to investigate the effects of thromboxane A2 (TXA2) agonists on the voltage-dependent Ca2+ currents in rat hippocampal CA1 neurons. TXA2 agonists, |1S-|1α, 2β(5Z), 3α(1E, 3S*)4α]|-7-|3-|3-hydroxy-4-(4'-iodophenoxy)-1-butenyl]-7- oxabicyclo[2,2,1]heptan-2-yl|-5-heptenoic acid (I-BOP) and U-46619, reversibly suppressed the whole cell Ca2+ currents in a concentration- dependent manner. The effect was blocked by specific TXA2 receptor antagonist, SQ-29548. I-BOP as well as U-46619 inhibited both ω-conotoxin GVIA (CgTx)-sensitive and nimodipine-sensitive Ca2+ currents but had no effect on CgTx/nimodipine-insensitive Ca2+ currents. The I-BOP and U-46619 inhibition of Ca2+ currents was blocked by internal dialysis of hippocampal neurons with specific protein kinase C (PKC) inhibitors, NPC-15437 and PKC inhibitor-(19-36). Pretreatment of hippocampal neurons with either 5 μg/ml pertussis toxin (PTX) or 5 μg/ml cholera toxin (CTX) did not significantly affect the suppression of the Ca2+ currents by I-BOP and U-46619. Dialyzing with 1 mM guanosine 5'-O-(3-thiotriphosphate) or 1 mM GDP significantly attenuated the I-BOP or U-46619 action. These results demonstrate that TXA2 agonists inhibit both CgTx- and nimodipine-sensitive Ca2+ currents but not CgTx/nimodipine-insensitive currents in rat hippocampal CA1 neurons via a PTX- and CTX-insensitive G protein-coupled activation of the PKC pathway.

原文English
頁(從 - 到)C1269-C1277
期刊American Journal of Physiology - Cell Physiology
271
發行號4 40-4
DOIs
出版狀態Published - 1996 十月

All Science Journal Classification (ASJC) codes

  • Physiology
  • Cell Biology

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