FEBS Letters · 1986 · 162 citations · 16 references
In the guinea pig myometrium prelabelled with myo-[2-3H]inositol, carbachol and oxytocin enhanced a concentration-dependent and rapid release of IP3 which preceded that of IP2 and IP1. The specific receptor-mediated phospholipase C activation degrading PIP2 to IP3 did not require the presence of extracellular Ca2+. The ionophore A23187 as well as K+ depolarization failed to increase inositol phosphate accumulation. It is proposed that IP3 could have a role in the contraction of uterine smooth muscle elicited by the activation of muscarinic as well as of oxytocin receptors.
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Eiichi Suematsu, Masato Hirata, Toshihiko Hashimoto et al. · Biochemical and Biophysical Research Communications · 1984 · 394 citations
Cell Physiology, Cardiac Muscle, Intracellular Store Sites +13