Streptomycin reduces stretch-induced membrane permeability in muscles from mdx mice

Neuromuscular Disorders

Volumn 16, Issue 12, 2006, Pages 845-854

  Whitehead, Nicholas P ^a   Streamer, Margaret ^a   Lusambili, Lynn I ^a   Sachs, Frederick ^b   Allen, David G ^a  

^a UNIVERSITY OF SYDNEY   (Australia)

^b UNIVERSITY AT BUFFALO   (United States)

Author keywords

mdx mouse; Membrane permeability; Stretch activated channels

Indexed keywords

CALCIUM; EVANS BLUE; STREPTOMYCIN;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CALCIUM CELL LEVEL; CALCIUM TRANSPORT; CELL MEMBRANE PERMEABILITY; CONTROLLED STUDY; DUCHENNE MUSCULAR DYSTROPHY; ECCENTRIC MUSCLE CONTRACTION; MALE; MOUSE; MUSCLE FORCE; MUSCLE STRETCHING; NONHUMAN; PRIORITY JOURNAL; TREADMILL EXERCISE; WILD TYPE;

ANIMALS; CALCIUM; CALCIUM SIGNALING; CELL MEMBRANE; CELL MEMBRANE PERMEABILITY; COLORING AGENTS; DISEASE MODELS, ANIMAL; ION CHANNELS; LARGE-CONDUCTANCE CALCIUM-ACTIVATED POTASSIUM CHANNEL ALPHA SUBUNITS; MALE; MICE; MICE, INBRED C57BL; MICE, INBRED MDX; MUSCLE CONTRACTION; MUSCLE PROTEINS; MUSCLE, SKELETAL; MUSCULAR DYSTROPHY, DUCHENNE; PEPTIDES; PHYSICAL CONDITIONING, ANIMAL; POTASSIUM CHANNEL BLOCKERS; SPIDER VENOMS; STREPTOMYCIN;

EID: 33845221218     PISSN: 09608966     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.nmd.2006.07.024     Document Type: Article

References (52)

1. Hoffman E.P., Brown Jr. R.H., and Kunkel L.M. Dystrophin: the protein product of the Duchenne muscular dystrophy locus. Cell 51 (1987) 919-928
2. Khurana T.S., and Davies K.E. Pharmacological strategies for muscular dystrophy. Nat Rev Drug Discov 2 (2003) 379-390
3. Lansman J.B., and Franco A. What does dystrophin do in normal muscle?. J Muscle Res Cell Motil 12 (1991) 409-411
4. Petrof B.J., Shrager J.B., Stedman H.H., Kelly A.M., and Sweeney H.L. Dystrophin protects the sarcolemma from stresses developed during muscle contraction. Proc Natl Acad Sci USA 90 (1993) 3710-3714
5. Allen D.G., Whitehead N.P., and Yeung E.W. Mechanisms of stretch-induced muscle damage in normal and dystrophic muscle: role of ionic changes. J Physiol 567 (2005) 723-735
6. Disatnik M.H., Dhawan J., Yu Y., Beal M.F., Whirl M.M., Franco A.A., et al. Evidence of oxidative stress in mdx mouse muscle: studies of the pre-necrotic state. J Neurol Sci 161 (1998) 77-84
7. 2 activity in dystrophinopathies. Neuromuscul Disord 5 (1995) 193-199
8. Spencer M.J., Croall D.E., and Tidball J.G. Calpains are activated in necrotic fibers from mdx dystrophic mice. J Biol Chem 270 (1995) 10909-10914
9. Barton-Davis E.R., Cordier L., Shoturma D.I., Leland S.E., and Sweeney H.L. Aminoglycoside antibiotics restore dystrophin function to skeletal muscles of mdx mice. J Clin Invest 104 (1999) 375-381
10. Moens P., Baatsen P.H., and Marechal G. Increased susceptibility of EDL muscles from mdx mice to damage induced by contractions with stretch. J Muscle Res Cell Motil 14 (1993) 446-451
11. Hamer P.W., McGeachie J.M., Davies M.J., and Grounds M.D. Evans Blue Dye as an in vivo marker of myofibre damage: optimising parameters for detecting initial myofibre membrane permeability. J Anat 200 (2002) 69-79
12. McArdle A., Edwards R.H., and Jackson M.J. Time course of changes in plasma membrane permeability in the dystrophin-deficient mdx mouse. Muscle Nerve 17 (1994) 1378-1384
13. Clarke M.S., Khakee R., and McNeil P.L. Loss of cytoplasmic basic fibroblast growth factor from physiologically wounded myofibers of normal and dystrophic muscle. J Cell Sci 106 (1993) 121-133
14. Pasternak C., Wong S., and Elson E.L. Mechanical function of dystrophin in muscle cells. J Cell Biol 128 (1995) 355-361
15. Franco Jr. A., and Lansman J.B. Calcium entry through stretch-inactivated ion channels in mdx myotubes. Nature 344 (1990) 670-673
16. Hutter O.F., Burton F.L., and Bovell D.L. Mechanical properties of normal and mdx mouse sarcolemma: bearing on function of dystrophin. J Muscle Res Cell Motil 12 (1991) 585-589
17. i and muscle damage in the mdx mouse. J Physiol 562 (2005) 367-380
18. Hamill O.P., and McBride Jr. D.W. The pharmacology of mechanogated membrane ion channels. Pharmacol Rev 48 (1996) 231-252
19. Suchyna T.M., Tape S.E., Koeppe R.E., Andersen O.S., Sachs F., and Gottlieb P.A. Bilayer-dependent inhibition of mechanosensitive channels by neuroactive peptide enantiomers. Nature 430 (2004) 235-240
20. 2+ and effects of enzyme inhibitors. Acta Neuropathol 79 (1990) 438-443
21. Jackson M.J., Jones D.A., and Edwards R.H. Experimental skeletal muscle damage: the nature of the calcium-activated degenerative processes. Eur J Clin Invest 14 (1984) 369-374
22. Suchyna T.M., Johnson J.H., Hamer K., et al. Identification of a peptide toxin from Grammostola spatulata spider venom that blocks cation-selective stretch-activated channels. J Gen Physiol 115 (2000) 583-598
23. Durbin P.W., Jeung N., Kullgren B., and Clemons G.K. Gross composition and plasma and extracellular water volumes of tissues of a reference mouse. Health Phys 63 (1992) 427-442
24. i following acute and long-term downhill running exercise in mice. Cell Calcium 22 (1997) 373-383
25. Chleboun G.S., Patel T.J., and Lieber R.L. Skeletal muscle architecture and fiber-type distribution with the multiple bellies of the mouse extensor digitorum longus muscle. Acta Anat 159 (1997) 147-155
26. Brussee V., Tardif F., and Tremblay J.P. Muscle fibers of mdx mice are more vulnerable to exercise than those of normal mice. Neuromuscul Disord 7 (1997) 487-492
27. Bansal D., Miyake K., Vogel S.S., et al. Defective membrane repair in dysferlin-deficient muscular dystrophy. Nature 423 (2003) 168-172
28. Yeung E.W., Head S.I., and Allen D.G. Gadolinium reduces short-term stretch-induced muscle damage in isolated mdx mouse muscle fibres. J Physiol 552 (2003) 449-458
29. McBride T.A., Stockert B.W., Gorin F.A., and Carlsen R.C. Stretch-activated ion channels contribute to membrane depolarization after eccentric contractions. J Appl Physiol 88 (2000) 91-101
30. 2+-activated proteases in toad muscle fibres. J Physiol 564 (2005) 775-790
31. Papadimitriou J.M., Robertson T.A., Mitchell C.A., and Grounds M.D. The process of new plasmalemma formation in focally injured skeletal muscle fibers. J Struct Biol 103 (1990) 124-134
32. Matsuda R., Nishikawa A., and Tanaka H. Visualization of dystrophic muscle fibers in mdx mouse by vital staining with Evans blue: evidence of apoptosis in dystrophin-deficient muscle. J Biochem (Tokyo) 118 (1995) 959-964
33. Wehling M., Spencer M.J., and Tidball J.G. A nitric oxide synthase transgene ameliorates muscular dystrophy in mdx mice. J Cell Biol 155 (2001) 123-131
34. Gailly P. New aspects of calcium signaling in skeletal muscle cells: implications in Duchenne muscular dystrophy. Biochim Biophys Acta 1600 (2002) 38-44
35. Gillis J.M. Understanding dystrophinopathies: an inventory of the structural and functional consequences of the absence of dystrophin in muscles of the mdx mouse. J Muscle Res Cell Motil 20 (1999) 605-625
36. + channels. Proc Natl Acad Sci USA 97 (2000) 4950-4955
37. Oberc M.A., and Engel W.K. Ultrastructural localization of calcium in normal and abnormal skeletal muscle. Lab Invest 36 (1977) 566-577
38. Robert V., Massimino M.L., Tosello V., et al. Alteration in calcium handling at the subcellular level in mdx myotubes. J Biol Chem 276 (2001) 4647-4651
39. Sokabe M., Hasegawa N., and Yamamori K. Blockers and activators for stretch-activated ion channels of chick skeletal muscle. Ann N Y Acad Sci 707 (1993) 417-420
40. Goll D.E., Thompson V.F., Li H., Wei W., and Cong J. The calpain system. Physiol Rev 83 (2003) 731-801
41. Badalamente M.A., and Stracher A. Delay of muscle degeneration and necrosis in mdx mice by calpain inhibition. Muscle Nerve 23 (2000) 106-111
42. Turner P.R., Schultz R., Ganguly B., and Steinhardt R.A. Proteolysis results in altered leak channel kinetics and elevated free calcium in mdx muscle. J Membr Biol 133 (1993) 243-251
43. Spencer M.J., and Mellgren R.L. Overexpression of a calpastatin transgene in mdx muscle reduces dystrophic pathology. Hum Mol Genet 11 (2002) 2645-2655
44. Brookes P.S., Yoon Y., Robotham J.L., Anders M.W., and Sheu S.S. Calcium, ATP, and ROS: a mitochondrial love-hate triangle. Am J Physiol Cell Physiol 287 (2004) C817-C833
45. Rando T.A., Disatnik M.H., Yu Y., and Franco A. Muscle cells from mdx mice have an increased susceptibility to oxidative stress. Neuromuscul Disord 8 (1998) 14-21
46. 2 dependent release of fatty acids from peroxidized membranes. J Free Radic Biol Med 1 (1985) 263-271
47. Nethery D., Callahan L.A., Stofan D., Mattera R., DiMarco A., and Supinski G. PLA(2) dependence of diaphragm mitochondrial formation of reactive oxygen species. J Appl Physiol 89 (2000) 72-80
48. 2 activity in dystrophinopathies. Neuromuscul Disord 5 (1995) 193-199
49. Wagner K.R., Hamed S., Hadley D.W., Gropman A.L., Burstein A.H., Escolar D.M., et al. Gentamicin treatment of Duchenne and Becker muscular dystrophy due to nonsense mutations. Ann Neurol 49 (2001) 706-711
50. Gottlieb P.A., Suchyna T.M., Ostrow L.W., and Sachs F. Mechanosensitive ion channels as drug targets. Curr Drug Targets CNS Neurol Disord 3 (2004) 287-295
51. Maroto R., Raso A., Wood T.G., Kurosky A., Martinac B., and Hamill O.P. TRPC1 forms the stretch-activated cation channel in vertebrate cells. Nat Cell Biol 7 (2005) 179-185
52. Vandebrouck C., Martin D., Colson-Van Schoor M., Debaix H., and Gailly P. Involvement of TRPC in the abnormal calcium influx observed in dystrophic (mdx) mouse skeletal muscle fibers. J Cell Biol 158 (2002) 1089-1096