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- W58993610 abstract "An attempt was made in this brief review first to recount some of our early studies which culminated in the characterization of the polyphosphoinositide (phosphatidylinositol 4-monophosphate, PIP and phosphatidylinositol 4,5-bisphosphate, PIP2) effect in the iris smooth muscle, and second to present more recent data on the rapid breakdown of 32 P-prelabeled polyphosphoinositide (PPI) and release of [3H]myo-inositol phosphates by carbachol (CCh) in this tissue. The PPI effect is defined as the agonist-stimulated breakdown of PIP2 into diacylglycerol, measured as labeled phosphatidate, and inositol trisphosphate (IP3). These early findings included: (1) the demonstration of an agonist-stimulated breakdown of PIP2 which occurred at relatively short time intervals (2.5–10 min), when compared to the phosphatidylinositol (PI) effect reported in a variety of tissues; (2) the demonstration of the PPI effect in vivo, in response to electrical stimulation of the sympathetic nerve of the eye; (3) the demonstration, through pharmacologic and adrenergic denervation supersensitivity studies that PIP2 breakdown is linked to muscarinic cholinergic and aladrenergic receptors; (4) the demonstration that phosphodiesteratic cleavage of PIP2 into diacylglycerol and I P3, by PIP2 phosphodiesterase, is the molecular mechanism underlying the PPI effect; (5) the demonstration of some requirement for (C{{a}^{{{{2}^{ + }}}}}), derived mainly from studies on the inhibitory effects of EGTA and (C{{a}^{{{{2}^{ + }}}}}) ionophore A23187 on this phenomenon; however, the recent finding that the cationophore-stimulated breakdown of PIP2 is blocked by prazosin leads us now to conclude that while the PPI effect in the iris needs some (C{{a}^{{{{2}^{ + }}}}}), it is not regulated by intracellular (C{{a}^{{{{2}^{ + }}}}}); (6) the demonstration of a close correlation between agonist-stimulated PIP2 breakdown and agonist-induced muscle contraction, which led us to suggest that the agonist-stimulated PIP2 breakdown is an early event in the pathway which leads from receptor activation to muscle response. Data are also presented which demonstrate that in the iris, the breakdown of labeled PIP2 and release of IP3 by CCh occur within 15 s; in contrast the release of IP occurred at longer time intervals (>1 min). Thus after incubation for 15 s with CCh there was 48% loss of 32P radioactivity from PIP2 in 32P-labeled iris, 81% increase in IP3 release and no change in the release of IP in iris prelabeled with [3H]inositol. These data suggest that agonist-stimulated PIP2 breakdown is probably involved in the mechanism of both the phasic (fast) and tonic (slow) components of the contractile response. Neither 2-deoxyglucose nor Li+, when added for short time intervals (10 min), had any influence on the PPI effect. In accord with our previous studies we conclude that the phosphodiesteratic cleavage of PIP2 is an early (initial) event in the pathway which leads from activation of (C{{a}^{{{{2}^{ + }}}}})-mobilizing receptors to muscle response." @default.
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- W58993610 date "1985-01-01" @default.
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- W58993610 title "Polyphosphoinositides and Muscarinic Cholinergic and α1-Adrenergic Receptors in the Iris Smooth Muscle" @default.
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