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. 1984 Nov 15;224(1):291–300. doi: 10.1042/bj2240291

Carbachol causes rapid phosphodiesteratic cleavage of phosphatidylinositol 4,5-bisphosphate and accumulation of inositol phosphates in rabbit iris smooth muscle; prazosin inhibits noradrenaline- and ionophore A23187-stimulated accumulation of inositol phosphates.

R A Akhtar, A A Abdel-Latif
PMCID: PMC1144426  PMID: 6095818

Abstract

Rabbit iris smooth muscle was prelabelled with myo-[3H]inositol for 90 min and the effect of carbachol on the accumulation of inositol phosphates from phosphatidylinositol 4,5-bisphosphate [PtdIns(4,5)P2], phosphatidylinositol 4-phosphate (PtdIns4P) and phosphatidylinositol (PtdIns) was monitored with anion-exchange chromatography. Carbachol stimulated the accumulation of inositol phosphates and this was blocked by atropine, a muscarinic antagonist, and it was unaffected by 2-deoxyglucose. The data presented demonstrate that, in the iris, carbachol (50 microM) stimulates the rapid breakdown of PtdIns(4,5)P2 into [3H]inositol trisphosphate (InsP3) and diacylglycerol, measured as phosphatidate, and that the accumulation of InsP3 precedes that of [3H]inositol bisphosphate (InsP2) and [3H]inositol phosphate (InsP). This conclusion is based on the following findings. Time course experiments with myo-[3H]inositol revealed that carbachol increased the accumulation of InsP3 by 12% in 15s and by 23% in 30s; in contrast, a significant increase in InsP release was not observed until about 2 min. Time-course experiments with 32P revealed a 10% loss of radioactivity from PtdIns(4,5)P2 and a corresponding 10% increase in phosphatidate labelling by carbachol in 15s; in contrast a significant increase in PtdIns labelling occurred in 5 min. Dose-response studies revealed that 5 microM-carbachol significantly increased (16%) the accumulation of InsP3 whereas a significant increase in accumulation of InsP2 and InsP was observed only at agonist concentrations greater than 10 microM. Studies on the involvement of Ca2+ in the agonist-stimulated breakdown of PtdIns(4,5)P2 in the iris revealed the following. Marked stimulation (58-78%) of inositol phosphates accumulation by carbachol in 10 min was observed in the absence of extracellular Ca2+. Like the stimulatory effect of noradrenaline, the ionophore A23187-stimulated accumulation of InsP3 was inhibited by prazosin, an alpha 1-adrenergic blocker, thus suggesting that the ionophore stimulation of PtdIns(4,5)P2 breakdown we reported previously [Akhtar & Abdel-Latif (1978) J. Pharmacol. Exp. Ther. 204, 655-688; Akhtar & Abdel-Latif (1980) Biochem. J. 192, 783-791] was secondary to the release of noradrenaline by the ionophore. The carbachol-stimulated accumulation of inositol phosphates was inhibited by EGTA (0.25 mM) and this inhibition was reversed by excess Ca2+ (1.5 mM), suggesting that EGTA treatment of the tissue chelates extracellular Ca2+ required for polyphosphoinositide phosphodiesterase activity. K+ depolarization, which causes influx of extracellular Ca2+ in smooth muscle, did not change the level of InsP3.(ABSTRACT TRUNCATED AT 400 WORDS)

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Selected References

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  1. Abdel-Latif A. A., Akhtar R. A. Acetylcholine causes an increase in the hydrolysis of triphosphoinositide pre-labelled with [32P]phosphate or [3H]myo-inositol and a corresponding increase in the labelling of phosphatidylinositol and phosphatidic acid in rabbit iris muscle. Biochem Soc Trans. 1976;4(2):317–321. doi: 10.1042/bst0040317. [DOI] [PubMed] [Google Scholar]
  2. Abdel-Latif A. A., Akhtar R. A., Hawthorne J. N. Acetylcholine increases the breakdown of triphosphoinositide of rabbit iris muscle prelabelled with [32P] phosphate. Biochem J. 1977 Jan 15;162(1):61–73. doi: 10.1042/bj1620061. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Abdel-Latif A. A., Green K., Smith J. P. Sympathetic denervation and the triphosphoinositide effect in the iris smooth muscle: a biochemical method for the determination of alpha-adrenergic receptor denervation supersensitivity. J Neurochem. 1979 Jan;32(1):225–228. doi: 10.1111/j.1471-4159.1979.tb04532.x. [DOI] [PubMed] [Google Scholar]
  4. Agranoff B. W., Murthy P., Seguin E. B. Thrombin-induced phosphodiesteratic cleavage of phosphatidylinositol bisphosphate in human platelets. J Biol Chem. 1983 Feb 25;258(4):2076–2078. [PubMed] [Google Scholar]
  5. Akhtar R. A., Abdel-Latif A. A. Calcium ion requirement for acetylcholine-stimulated breakdown of triphosphoinositide in rabbit iris smooth muscle. J Pharmacol Exp Ther. 1978 Mar;204(3):655–668. [PubMed] [Google Scholar]
  6. Akhtar R. A., Abdel-Latif A. A. Effects of Na+, Ca2+, and acetylcholine on phosphoinositide- and ATP-phosphate turnover in 32P-labeled rabbit iris smooth muscle. J Neurochem. 1982 Nov;39(5):1374–1380. doi: 10.1111/j.1471-4159.1982.tb12580.x. [DOI] [PubMed] [Google Scholar]
  7. Akhtar R. A., Abdel-Latif A. A. Requirement for calcium ions in acetylcholine-stimulated phosphodiesteratic cleavage of phosphatidyl-myo-inositol 4,5-bisphosphate in rabbit iris smooth muscle. Biochem J. 1980 Dec 15;192(3):783–791. doi: 10.1042/bj1920783. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Akhtar R. A., Taft W. C., Abdel-Latif A. A. Effects of corticotropin-(1-24)-tetracosapeptide on polyphosphoinositide metabolism and protein phosphorylation in rabbit iris subcellular fractions. J Neurochem. 1983 Nov;41(5):1460–1468. doi: 10.1111/j.1471-4159.1983.tb00846.x. [DOI] [PubMed] [Google Scholar]
  9. Berridge M. J., Dawson R. M., Downes C. P., Heslop J. P., Irvine R. F. Changes in the levels of inositol phosphates after agonist-dependent hydrolysis of membrane phosphoinositides. Biochem J. 1983 May 15;212(2):473–482. doi: 10.1042/bj2120473. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Berridge M. J. Inositol trisphosphate and diacylglycerol as second messengers. Biochem J. 1984 Jun 1;220(2):345–360. doi: 10.1042/bj2200345. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Berridge M. J. Rapid accumulation of inositol trisphosphate reveals that agonists hydrolyse polyphosphoinositides instead of phosphatidylinositol. Biochem J. 1983 Jun 15;212(3):849–858. doi: 10.1042/bj2120849. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Berridge M. J. The interaction of cyclic nucleotides and calcium in the control of cellular activity. Adv Cyclic Nucleotide Res. 1975;6:1–98. [PubMed] [Google Scholar]
  13. Billah M. M., Lapetina E. G. Evidence for multiple metabolic pools of phosphatidylinositol in stimulated platelets. J Biol Chem. 1982 Oct 25;257(20):11856–11859. [PubMed] [Google Scholar]
  14. Bradford P. G., Marinetti G. V., Abood L. G. Stimulation of phospholipase A2 and secretion of catecholamines from brain synaptosomes by potassium and A23187. J Neurochem. 1983 Dec;41(6):1684–1693. doi: 10.1111/j.1471-4159.1983.tb00881.x. [DOI] [PubMed] [Google Scholar]
  15. Cohen M. L., Landry A. S., Perry K. W., Fuller R. W. Ionophore (A23187)-induced efflux of [3H]norepinephrine and endogenous norepinephrine in the rat vas deferens. Eur J Pharmacol. 1981 Sep 11;74(2-3):157–165. doi: 10.1016/0014-2999(81)90526-4. [DOI] [PubMed] [Google Scholar]
  16. Creba J. A., Downes C. P., Hawkins P. T., Brewster G., Michell R. H., Kirk C. J. Rapid breakdown of phosphatidylinositol 4-phosphate and phosphatidylinositol 4,5-bisphosphate in rat hepatocytes stimulated by vasopressin and other Ca2+-mobilizing hormones. Biochem J. 1983 Jun 15;212(3):733–747. doi: 10.1042/bj2120733. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Downes P., Michell R. H. Phosphatidylinositol 4-phosphate and phosphatidylinositol 4,5-bisphosphate: lipids in search of a function. Cell Calcium. 1982 Oct;3(4-5):467–502. doi: 10.1016/0143-4160(82)90031-8. [DOI] [PubMed] [Google Scholar]
  18. HENDRICKSON H. S., BALLOU C. E. ION EXCHANGE CHROMATOGRAPHY OF INTACT BRAIN PHOSPHOINOSITIDES ON DIETHYLAMINOETHYL CELLULOSE BY GRADIENT SALT ELUTION IN A MIXED SOLVENT SYSTEM. J Biol Chem. 1964 May;239:1369–1373. [PubMed] [Google Scholar]
  19. Hawthorne J. N. Polyphosphoinositide metabolism in excitable membranes. Review. Biosci Rep. 1983 Oct;3(10):887–904. doi: 10.1007/BF01140658. [DOI] [PubMed] [Google Scholar]
  20. Joseph S. K., Thomas A. P., Williams R. J., Irvine R. F., Williamson J. R. myo-Inositol 1,4,5-trisphosphate. A second messenger for the hormonal mobilization of intracellular Ca2+ in liver. J Biol Chem. 1984 Mar 10;259(5):3077–3081. [PubMed] [Google Scholar]
  21. Kirk C. J., Creba J. A., Downes C. P., Michell R. H. Hormone-stimulated metabolism of inositol lipids and its relationship to hepatic receptor function. Biochem Soc Trans. 1981 Oct;9(5):377–379. doi: 10.1042/bst0090377. [DOI] [PubMed] [Google Scholar]
  22. Mangel A. W., Nelson D. O., Rabovsky J. L., Prosser C. L., Connor J. A. Depolarization-induced contractile activity of smooth muscle in calcium-free solution. Am J Physiol. 1982 Jan;242(1):C36–C40. doi: 10.1152/ajpcell.1982.242.1.C36. [DOI] [PubMed] [Google Scholar]
  23. Marx J. L. A new view of receptor action. Science. 1984 Apr 20;224(4646):271–274. doi: 10.1126/science.6143399. [DOI] [PubMed] [Google Scholar]
  24. Michell R. H., Kirk C. J., Jones L. M., Downes C. P., Creba J. A. The stimulation of inositol lipid metabolism that accompanies calcium mobilization in stimulated cells: defined characteristics and unanswered questions. Philos Trans R Soc Lond B Biol Sci. 1981 Dec 18;296(1080):123–138. doi: 10.1098/rstb.1981.0177. [DOI] [PubMed] [Google Scholar]
  25. Nishizuka Y. The role of protein kinase C in cell surface signal transduction and tumour promotion. Nature. 1984 Apr 19;308(5961):693–698. doi: 10.1038/308693a0. [DOI] [PubMed] [Google Scholar]
  26. Rosenberger L. B., Triggle D. J. The mechanism of action of ionophore A 23187 on guinea pig intestinal smooth muscle. Can J Physiol Pharmacol. 1979 Apr;57(4):348–358. doi: 10.1139/y79-053. [DOI] [PubMed] [Google Scholar]
  27. Streb H., Irvine R. F., Berridge M. J., Schulz I. Release of Ca2+ from a nonmitochondrial intracellular store in pancreatic acinar cells by inositol-1,4,5-trisphosphate. Nature. 1983 Nov 3;306(5938):67–69. doi: 10.1038/306067a0. [DOI] [PubMed] [Google Scholar]
  28. Warenycia M. W., Vohra M. M. The effects of the ionophore A-23187 on the rat vas deferens. Can J Physiol Pharmacol. 1983 Jan;61(1):97–101. doi: 10.1139/y83-012. [DOI] [PubMed] [Google Scholar]
  29. Weiss S. J., McKinney J. S., Putney J. W., Jr Receptor-mediated net breakdown of phosphatidylinositol 4,5-bisphosphate in parotid acinar cells. Biochem J. 1982 Sep 15;206(3):555–560. doi: 10.1042/bj2060555. [DOI] [PMC free article] [PubMed] [Google Scholar]

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