Ultrastructural and Histochemical Study of the Neuromuscular Junctions in the Denervated Intrinsic Laryngeal Muscle of the Cat

References

• Matzel D, Vosteen KH. Electronoptische und enzymatische Untersuchungen des menschlicher Kehlkopf-muskulatur. Arch Ohren Nasen Kehlkopfheilkd 1963; 181: 447–57
   PubMedGoogle Scholar
• Shagal V, Hast MH. Histochemistry of primate laryngeal muscles. Acta Otolaryngol (Stockh) 1974; 78: 277–81
   PubMedGoogle Scholar
• Malmgren L T, Gacek RR. Histochemical characteristics of muscle fiber types in the posterior cricoarytenoid muscle. Ann Otol 1981; 90: 423–9
   Google Scholar
• Rossi G, Cortestina G. Morphological study of the laryngeal muscle of man. Acta Otolaryngol (Stockh) 1964; 59: 575–92
   Google Scholar
• Abo E. Significance of the pattern of motor innervation of the intrinsic laryngeal muscles of cat. Acta Anat 1975; 93: 543–53
   PubMedGoogle Scholar
• Morales J R, Rama J, Gayoso M. Some aspects of the nerve endings and synapses in the vocalis muscle. J Laryngol Otol 1980; 94: 1047–3
   PubMed Web of Science ®Google Scholar
• Rosen M, Malmgren L T, Gacek RR. Three-dimensional computer reconstruction of the distribution of neuromuscular junctions is the thyroarytenoid muscle. Ann Otol Rhinol Laryngol 1983; 92: 424–9
   PubMedGoogle Scholar
• Michael A DV, Malmgren L T, Gacek RR. Three-dimensional distribution of neuromuscular junctions in human cricothyroid. Arch Otolaryngol 1985; 111: 110–3
   PubMedGoogle Scholar
• Gambino D R, Malmgren L T, Gacek RR. Three-dimensional computer reconstruction of the neuromuscular junction distribution in the human posterior cricoarytenoid muscle. Laryngoscope 1985; 95: 556–90
   PubMedGoogle Scholar
• Freije J, Malmgren L T, Gacek RR. Motor end-plate distribution in the human interarytenoid muscle. Arch Otolaryngol Head Neck Surg 1987; 113: 63–8
   PubMedGoogle Scholar
• Kanda T, Yoshihara T, Miyazaki M, Kaneko T. Neuromuscular junctions of the posterior cricoarytenoid muscle in the cat. Fluorescent staining and autoradiography of acetylcholine receptors and histochemical staining of cholinesterase. Acta Otolaryngol (Stockh) 1983; 25–32, Suppl 393
   Google Scholar
• Yoshihara T, Kanda T, Yaku Y, Kaneko T. Neuromuscular junctions of the posterior cricoarytenoid muscle in the human adult, human fetus and cat. Histochemical and electron microscopic study. Acta Otolaryngol (Stockh) 1984; 97: 161–8
   PubMed Web of Science ®Google Scholar
• Chan-Palay V, Engel A G, Wu J-Y, Palay SL. Coexistence in human and primate neuromuscular junctions of enzymes synthesizing acetylcholine, catecholamine, taurine, and y-aminobutyric acid. Proc Natl Acad Sci USA 1982; 79: 7027–30
   PubMedGoogle Scholar
• Takami K, Kawai Y, Uchida S. Effect of calcitonin gene-related peptide on contraction of striated muscle in the mouse. Neurosci Lett 1985; 60: 227–30
   PubMed Web of Science ®Google Scholar
• Karnovsky M J, Root SL. A “direct-coloring” thiocholine method for cholinesterase. J Histo-chem Cytochem 1964; 12: 219–21
   PubMed Web of Science ®Google Scholar
• Sternberger L A, Hardy PH, Jr., Cuculis J J, Meyer HG. The unlabeled antibody-enzyme method of immunohistochemistry. Preparation and properties of soluble antigen-antibody complex (horseradish peroxidase-antihorseradish peroxidase) and its use in identification of spirochetes. J Histochem Cytochem 1970; 18: 315–33
   PubMed Web of Science ®Google Scholar
• Birks R, Katz B, Miledi R. Physiological and structural changes at the amphibian myoneural junction in the course of nerve degeneration. J Physiol 1960; 150: 145–68
   PubMedGoogle Scholar
• Miledi R, Slater R. On the degeneration of rat neuromuscular junctions after nerve section. J Physiol 1970; 207: 507–28
   PubMed Web of Science ®Google Scholar
• Saito A, Zacks SI. Fine structure observations of denervation and reinnervation of neuromuscular junctions in mouse foot muscle. J Bone Joint Surg 1969; 51 A: 1163–78
   Google Scholar
• Linkhart T A, Wilson BW. Acetylcholinesterase in singly and multiply innervated muscles of normal and dystrophic chickens. II. Effects of denervation. J Exp Zool 1970; 193: 191–200
   Google Scholar
• Steinbach JH. Neuromuscular junctions and α-bungurotoxin-binding sites in denervated and contralateral cat skeletal muscles. J Physiol 1981; 313: 513–28
   PubMedGoogle Scholar
• McMahan U J, Sanes J R, Marshall IM. Cholinesterase is associated with the basal lamina at the neuromuscular junction. Nature 1978; 271: 172–4
   PubMed Web of Science ®Google Scholar
• Rotundo RL. Biogenesis and regulation of acetylcholinesterase. The vertebrate neuromuscular junction. Vol 23. Neurology and neurobiology, MM Salpeter. Alan R. Liss Inc., New York 1987; 247–84
   Google Scholar
• Hartzell H C, Fambrough DM. Acetylcholine receptors. Distribution and extrajunctional density in rat diaphragm after denervation correlated with acetylcholine sensitivity. J Gen Physiol 1972; 60: 248–62
   PubMed Web of Science ®Google Scholar
• New H V, Mudge AW. Calcitonin gene-related peptide regulates muscle acetylcholine receptor synthesis. Nature 1986; 323: 809–11
   PubMed Web of Science ®Google Scholar