Inositol Trisphosphate and Excitation-contraction Coupling in Skeletal Muscle

Overview

Journal J Bioenerg Biomembr

Publisher Springer

Specialties Biochemistry
Biology
Endocrinology

Date 1989 Apr 1

PMID 2546932

Citations 10

Authors

C Hidalgo

E Jaimovich

Affiliations

Soon will be listed here.

Abstract

The role of inositol trisphosphate as a chemical messenger in excitation-contraction coupling is discussed, both in terms of positive and negative results. The evidence presented includes experiments on the effect of inositol trisphosphate in intact and skinned fibers, in calcium release from isolated sarcoplasmic reticulum vesicles, in activation of single calcium release channels incorporated in planar bilayers, and biochemical experiments that have established the presence of all the intermediate steps involved in the metabolism of phosphoinositides, both in intact muscle and in isolated membranes. From these results, it is clear that a role for inositol triphosphate in skeletal muscle function is highly likely; whether this molecule is the physiological messenger in excitation-contraction coupling remains to be established.

Citing Articles

Nerve-dependent distribution of subsynaptic type 1 inositol 1,4,5-trisphosphate receptor at the neuromuscular junction.

Volpe P, Bosutti A, Nori A, Filadi R, Gherardi G, Trautmann G J Gen Physiol. 2022; 154(11).

PMID: 36149386 PMC: 9513380. DOI: 10.1085/jgp.202213128.

Inositol 1,4,5-trisphosphate-induced Ca2+ release is regulated by cytosolic Ca2+ in intact skeletal muscle.

Lopez J, Terzic A Pflugers Arch. 1996; 432(5):782-90.

PMID: 8772127 DOI: 10.1007/s004240050199.

Hypersensitive response of malignant hyperthermia-susceptible skeletal muscle to inositol 1,4,5-triphosphate induced release of calcium.

Lopez J, Perez C, Linares N, Allen P, Terzic A Naunyn Schmiedebergs Arch Pharmacol. 1995; 352(4):442-6.

PMID: 8532074 DOI: 10.1007/BF00172783.

Kinetic analysis of excitation-contraction coupling.

Ikemoto N, Ronjat M, Meszaros L J Bioenerg Biomembr. 1989; 21(2):247-66.

PMID: 2666410 DOI: 10.1007/BF00812071.

Calcium release modulated by inositol trisphosphate in ruptured fibers from frog skeletal muscle.

Rojas C, Jaimovich E Pflugers Arch. 1990; 416(3):296-304.

PMID: 2381765 DOI: 10.1007/BF00392066.

References

Suarez-Isla B, Irribarra V, Oberhauser A, LARRALDE L, Bull R, Hidalgo C . Inositol (1,4,5)-trisphosphate activates a calcium channel in isolated sarcoplasmic reticulum membranes. Biophys J. 1988; 54(4):737-41. PMC: 1330378. DOI: 10.1016/S0006-3495(88)83009-1. View

Berridge M . Inositol trisphosphate and diacylglycerol: two interacting second messengers. Annu Rev Biochem. 1987; 56:159-93. DOI: 10.1146/annurev.bi.56.070187.001111. View

Sanchez J, Stefani E . Inward calcium current in twitch muscle fibres of the frog. J Physiol. 1978; 283:197-209. PMC: 1282773. DOI: 10.1113/jphysiol.1978.sp012496. View

Rousseau E, Smith J, Henderson J, Meissner G . Single channel and 45Ca2+ flux measurements of the cardiac sarcoplasmic reticulum calcium channel. Biophys J. 1986; 50(5):1009-14. PMC: 1329827. DOI: 10.1016/S0006-3495(86)83543-3. View

Smith J, Coronado R, Meissner G . Sarcoplasmic reticulum contains adenine nucleotide-activated calcium channels. Nature. 1985; 316(6027):446-9. DOI: 10.1038/316446a0. View

Franzini-Armstrong C . STUDIES OF THE TRIAD : I. Structure of the Junction in Frog Twitch Fibers. J Cell Biol. 2009; 47(2):488-99. PMC: 2108094. DOI: 10.1083/jcb.47.2.488. View

Novotny I, Saleh F, Novotna R . K+ depolarization and phospholipid metabolism in frog sartorius muscle. Gen Physiol Biophys. 1983; 2(5):329-37. View

Vergara J, Tsien R, Delay M . Inositol 1,4,5-trisphosphate: a possible chemical link in excitation-contraction coupling in muscle. Proc Natl Acad Sci U S A. 1985; 82(18):6352-6. PMC: 391052. DOI: 10.1073/pnas.82.18.6352. View

Somlyo A, Walker J, Goldman Y, Trentham D, Kobayashi S, Kitazawa T . Inositol trisphosphate, calcium and muscle contraction. Philos Trans R Soc Lond B Biol Sci. 1988; 320(1199):399-414. DOI: 10.1098/rstb.1988.0084. View

10.

Inui M, Saito A, Fleischer S . Purification of the ryanodine receptor and identity with feet structures of junctional terminal cisternae of sarcoplasmic reticulum from fast skeletal muscle. J Biol Chem. 1987; 262(4):1740-7. View

11.

Janiak M, Small D, Shipley G . Temperature and compositional dependence of the structure of hydrated dimyristoyl lecithin. J Biol Chem. 1979; 254(13):6068-78. View

12.

Novotny I, Zivny A, Saleh F . The effect of potassium depolarization on 32P-labelling of phosphatidylinositol and phosphatidylserine in frog sartorius muscle. Physiol Bohemoslov. 1978; 27(5):477-83. View

13.

Volpe P, Salviati G, Di Virgilio F, Pozzan T . Inositol 1,4,5-trisphosphate induces calcium release from sarcoplasmic reticulum of skeletal muscle. Nature. 1985; 316(6026):347-9. DOI: 10.1038/316347a0. View

14.

Nosek T, Williams M, Zeigler S, Godt R . Inositol trisphosphate enhances calcium release in skinned cardiac and skeletal muscle. Am J Physiol. 1986; 250(5 Pt 1):C807-11. DOI: 10.1152/ajpcell.1986.250.5.C807. View

15.

Berridge M, Irvine R . Inositol trisphosphate, a novel second messenger in cellular signal transduction. Nature. 1984; 312(5992):315-21. DOI: 10.1038/312315a0. View

16.

MAJERUS P, Connolly T, Deckmyn H, Ross T, Bross T, Ishii H . The metabolism of phosphoinositide-derived messenger molecules. Science. 1986; 234(4783):1519-26. DOI: 10.1126/science.3024320. View

17.

Carrasco M, Magendzo K, Jaimovich E, Hidalgo C . Calcium modulation of phosphoinositide kinases in transverse tubule vesicles from frog skeletal muscle. Arch Biochem Biophys. 1988; 262(1):360-6. DOI: 10.1016/0003-9861(88)90199-3. View

18.

Volpe P, Di Virgilio F, Pozzan T, Salviati G . Role of inositol 1,4,5-trisphosphate in excitation-contraction coupling in skeletal muscle. FEBS Lett. 1986; 197(1-2):1-4. DOI: 10.1016/0014-5793(86)80285-x. View

19.

Adunyah S, Dean W . Ca2+ transport in human platelet membranes. Kinetics of active transport and passive release. J Biol Chem. 1986; 261(7):3122-7. View

20.

Hymel L, Inui M, Fleischer S, Schindler H . Purified ryanodine receptor of skeletal muscle sarcoplasmic reticulum forms Ca2+-activated oligomeric Ca2+ channels in planar bilayers. Proc Natl Acad Sci U S A. 1988; 85(2):441-5. PMC: 279565. DOI: 10.1073/pnas.85.2.441. View