Formation of Neuromuscular Junctions in Transplanted Peroneus Longus Muscles in the Rat: A Quantitative Comparison with Reinnervation of the Muscle in situ

References

• Anderl H., Mühlbauer W. Surgery of facial palsy. Recent advances in plastic surgery 2, I. T. Jackson. Churchill Livingstone, Edinburgh, London, Melbourne and New York 1981; 181
   Google Scholar
• Bennett M. R., Pettigrew A. G. The formation of synapses in striated muscle during development. J Physiol 1974a; 241: 515
   PubMed Web of Science ®Google Scholar
• Bennett M. R., Pettigrew A. G. The formation of synapses in reinnervated and cross-innervated striated muscle during development. J Physiol 1974b; 241: 547
   PubMedGoogle Scholar
• Brown M. C., Goodwin G. M., Ironton R. Prevention of motor nerve sprouting in botulinum toxin poisoned mouse, soleus muscles by direct stimulation of the muscle. J Physiol (Lond) 1977; 267: 42
   Google Scholar
• Brown M. C., Ironton R. Motor neurone sprouting induced by prolonged tetrodotoxin block of nerve action potentials. Nature 1977; 265: 459
   PubMed Web of Science ®Google Scholar
• Brown M. C., Jansen J. K. S., Van Essen D. Polyneuronal innervation of skeletal muscle in new born rats and its elimination during maturation. J Physiol 1976; 261: 387
   PubMedGoogle Scholar
• Brzin M., Zajicek J. Quantitative determination of cholinesterase activity in individual end-plates of normal and denervated gastrocnemius muscle. Nature 1958; 181: 624
   Google Scholar
• Carlson B. M. The regeneration of skeletal muscle—a review. Am J Anat 1973; 137: 119
   PubMedGoogle Scholar
• Carlson B. M. A Quantitative study of muscle fiber survival and regeneration in normal, predenervated and mar cain-treated free muscle grafts in the rat. Exp Neurol 1976; 52: 421
   PubMedGoogle Scholar
• Carlson B. M., Gutmann E. Development of contractile properties of minced muscle regenerates in the rat. Experimental. Neurology 1972; 36: 239
   Google Scholar
• Carlson B. M., Gutmann E. Regeneration in grafts of normal and denervated rat muscles. Pflügers Arch 1973; 353: 215
   Google Scholar
• Caugiano A., Lomo T., Lutzenberger L., Sveen O. Effects of chronic nerve conduction block on formation of neuromuscular junctions and junctional AChE in the rat. Acta Physiol Scand 1980; 109: 283
   PubMedGoogle Scholar
• Coërs C. Etude histochimique des variations de I'activite cholinesterasique au niveau de la jonction neuromusculaire apres section nerveuse. Bull Acad Belg Sci 1953; 39: 447
   Google Scholar
• Reske-Coërs C., Niesen E., Harmsen A. The pattern of terminal motor innervation in healthy young adults. J Neurol Sci 1973; 19: 351
   PubMedGoogle Scholar
• Coërs C., Telerman-Toppet N., Gerard J.-M. Terminal innervation ratio in neuromuscular disease. Arch Neurol 1973a; 29: 210
   PubMedGoogle Scholar
• Coërs C., Telerman-Toppet N., Gerard J.-M. Terminal innervation ratio in neuromuscular disease. Arch Neurol 1973b; 29: 215
   PubMedGoogle Scholar
• Coërs C., Woolf A. L. The innervation of muscle. Blackwell, Oxford 1959; 12–41
   Google Scholar
• Dryden W. F. Development of acetylcholine sensitivity in cultured skeletal muscie. Experientia 1970; 26: 984
   PubMedGoogle Scholar
• Dryden W. F., Erulkar S. D., De la Haba G. Properties of the cell membrane of development skeletal muscle fibers in culture and it's sensitivity to acetylcholine. Clin Exp Pharmacol Physiol 1974; 1: 369
   Google Scholar
• Duchen L. W. Changes in motor innervation and cholinesterase localization induced by botulinum toxin in skeletal muscle of the mouse: Differences between fast and slow muscles. J Neurol Neurosurg Psychiatry 1970; 33: 40
   PubMed Web of Science ®Google Scholar
• Duchen L. W., Rogers M., Stolkin C., Tonge D. A. Suppression of botulinum toxin-induced axonal sprouting in skeletal muscle by implantation of an extra nerve. J Physiol (Lond) 1975; 248: 1
   Google Scholar
• Duchen L. W., Strich S. J. The effects of botulinum toxin on the pattern of innervation of skeletal muscle in the mouse. Q J Exp Physiol 1968; 53: 84
   PubMed Web of Science ®Google Scholar
• Edds M. Collateral regeneration of residual motor axons in partially denervated muscles. J Exp Zool 1950; 113: 517
   Google Scholar
• Ernäko O., Teraväinen H. Cholinesterase and esenne-resistant carboxylic esterases in degenerating and regenerating motor end-plates of the rat. J Neuro-chem 1967; 14: 947
   PubMedGoogle Scholar
• Fatt P., Katz B. An analysis of the end-plate potential recorded with an intracellular electrode. J Physiol 1951; 115: 320
   PubMed Web of Science ®Google Scholar
• Faulkner J. A., Maxwell L. C., Mufti S. A., Carlson B. M. Skeletal muscle fiber regeneration following heterotopic autotransplantation in cats. Life Sci 1976; 19: 289
   PubMedGoogle Scholar
• Gruber H., Freilinger G., Holle J., Mayr R. Motor end-plates in autologous muscle transplants. Experientia 1974; 30: 1191
   PubMedGoogle Scholar
• Gutmann E., Young J. Z. The reinnervation of muscle after various periods of atrophy. J Anat 1944; 78: 15
   PubMedGoogle Scholar
• Hakelius L. Transplantation of free autogenous muscle in the treatment of facial paralysis. Scand J Plast Reconstr Surg 1974; 8: 220
   PubMed Web of Science ®Google Scholar
• Hakelius L. Free muscle grafting. Clin Plast Surg 1979; 6: 301
   PubMed Web of Science ®Google Scholar
• Hakelius L., Gierup J., Grotte G., Jorulf H. Further experience with free autogenous muscle transplantation in children with anal incontinence. Z Kinderchir 1980; 31, Heft 2
   Google Scholar
• Hakelius L., Nyström B. Histochemical studies of end-plate formation in free autologous muscle transplants in cats. Scand J Plast Reconstr Surg 1975; 9: 9
   PubMed Web of Science ®Google Scholar
• Hakelius L., Nyström B., Stålberg E. Histochemical and neurophysiological studies of autotransplanted cat muscle. Scand J Plast Reconstr Surg 1975; 9: 15
   PubMed Web of Science ®Google Scholar
• Hoffman H. Local reinnervation in partially denervated muscle: A histophysiological study. Aust J Exp Biol Med Sci 1950; 28: 383
   PubMedGoogle Scholar
• Ip M. C., Vrbova G. Motor and sensory reinnervation of fast and slow mammalian muscles. Z Zellforsch Mikrosk Anat 1973; 146: 261
   PubMedGoogle Scholar
• Karpati G., Engel W. K. Type grouping in skeletal muscles after experimental reinnervation. Neurology 1968; 18: 447
   PubMedGoogle Scholar
• Karnovsky M. J., Roots L. A. A direct-coloring thiocholine method for cholinesterases. J Histochem Cytochem 1964; 12: 219
   PubMed Web of Science ®Google Scholar
• Kuftler S. W., Vaughan-Williams E. M. Properties of the “slow” skeletal muscle fibres of the frog. J Physiol 1953a; 121: 318
   PubMedGoogle Scholar
• Kuftler S. W., Vaughan-Williams E. M. Small nerve junction potentials. The distribution of small motor nerves to frog skeletal muscles, and the membrane characteristics of the fibres they innervate. J Physiol 1953b; 121: 298
   Google Scholar
• Lømo T. What controls the developments of neuromuscular junctions. Trends in Neurosciences May, 1980; 126, 1980
   Google Scholar
• McArdle J. J. Complex end-plate potentials of the regenerating neuromuscular junction of the rat. Exp Neurology 1975; 49: 629
   PubMed Web of Science ®Google Scholar
• Miledi R. Properties of regenerating neuromuscular synapses in the frog. J Physiol 1960; 154: 190
   PubMedGoogle Scholar
• Nyström B. Postnatal development of motor nerve terminals in “slow-red” and “fast-white” cat muscles. Acta Neurol Scand 1968a; 44: 363
   PubMedGoogle Scholar
• Nyström B. Histochemistry of developing cat muscles. Acta Neurol Scand 1968b; 44: 405
   PubMed Web of Science ®Google Scholar
• O'Brien R., Purves R., Vrbová G. Effect of activity on the elimination of multiple innervation in soleus muscles of rats. J Physiol 1977; 271: 54
   Google Scholar
• Padykula H. A., Gauthier G. F. The ulstrastructure of the neuromuscular junctions of mammalian red, white and intermediate skeletal muscle fibres. J Cell Biol 1970; 46: 27
   PubMedGoogle Scholar
• Pestronk A., Drachman D. B. A new stain for quantitative measurement of sprouting at neuromuscular junctions. Muscle Nerve 1978; 1: 70
   PubMedGoogle Scholar
• Pestronk A., Drachman B., Griffin J. W. Effects of aging on nerve sprouting and regeneration. Exp Neurology 1980; 70: 65
   PubMed Web of Science ®Google Scholar
• Redfern P. Neuromuscular transmission in newborn rats. J Physiol 1970; 209: 701
   PubMedGoogle Scholar
• Rothshenker S., McMahan V. J. Altered patterns of innervation in frog muscle after denervation. J Neurocytol 1976; 5: 719
   PubMedGoogle Scholar
• Sávay G., Csillik B. The effect of denervation on the cholinesterase activity of motor end-plates. Acta Morph Acad Sci Hung 1956; 6: 289
   Google Scholar
• Schiaffino S., Sjöström M., Thornell L. E., Hakelius L. The process of survival of denervated and freely autotransplanted skeletal muscle. Experientia 1975; 31: 1328
   PubMedGoogle Scholar
• Studitsky A. N. Free auto-and homografts of muscle tissue in experiments on animals. Ann NY Acad Sci 1964; 120: 789
   PubMed Web of Science ®Google Scholar
• Thompson N. Treatment of facial paralysis by free skeletal muscle grafts. Trans Fifth World Congr Plast Reconstr Surg, Australia. Butterworths, London 1972a; 66, 1971
   Google Scholar
• Thompson N. Autogenous free grafts of skeletal muscle. Plast Reconstr Surg 1971b; 48: 11
   PubMed Web of Science ®Google Scholar
• Thompson N. Investigation of autogenous skeletal muscle free grafts in the dog. Transplantation 1971c; 12: 353
   PubMedGoogle Scholar
• Vedung S., Olsson Y. Light and electron microscopic findings in the distal end of human cross-face sural nerve grafts. Scand J Plast Reconstr Surg 1982; 16: 478
   Google Scholar