Skip to main content
Log in

Effects of vagotomy on the ultrastructure of the atrial myocardium in the monkey (Macaca fascicularis)

  • Published:
Anatomy and Embryology Aims and scope Submit manuscript

Summary

The ultrastructure of the atrial myocardium in the monkey (Macaca fascicularis) was studied after bilateral cervical vagotomy and survival times of 1, 3, 5, 7, 10, 21 and 28 days. During the first week after vagotomy, a few atrial cells showed a reduction in the sarcoplasm, crowding of the myofibrils, peripheral dispersion and reduced intercristal density of the mitochondria and increased sarcoplasmic reticulum and glycogen particles. In some profiles, there was increased electron density and granularity at the I bands and the intercalated discs. The number of such affected cells increased in the subsequent days such that by 21 to 28 days about 50% of the cells were estimated to be affected. During the latter stages further changes included, the degradation of the myofilaments and increased electron density, disorganisation and disintegration of the digital extensions at the intercalated discs. Throughout the experiments there was a leucocytic infiltration, more evident in the longer survival times.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Ayettey AS, Navaratnam V (1978) The T-tubule system in the specialized and general myocardium of the rat. J Anat 127:125–140

    Google Scholar 

  • Ayettey AS, Navaratnam V (1981) The ultrastructure of myocardial cells in the golden hamsterCriatus auratus. J Anat 132:519–524

    Google Scholar 

  • Bullock GR (1986) Structural changes at cardiac cell junctions during ischaemia. J Mol Cell Cardiol 18 [Suppl 4]:1–5

    Google Scholar 

  • Cantin M, Benchimol S, Castonguay Y, Berlinguet J-C, Huet M (1975) Ultrastructural cytochemistry of atrial muscle cells. V. Characterization of specific granules in the human left atrium. J Ultrastruct Res 52:179–192

    Google Scholar 

  • Chernukh AM, Chernysheva GV, Kopteva LA (1974) Certain biochemical and ultrastructural features of the ventricular myocardium following cardiac denervation. Circ Res 34–35 [Suppl III]: 99–107

    Google Scholar 

  • Chiba T, Yamauchi A (1970) On the fine structure of the nerve terminals in the human myocardium. Z Zellforsch 108:324–338

    Google Scholar 

  • Feigl EO (1984) Parasympathetic control of coronary blood flow. Fed Proc 43:2881–2883

    Google Scholar 

  • Forbes MS, Hawkey LA, Jirge SR, Sperkelakis N (1985) The sarcoplasmic reticulum of mouse heart: its divisions, configurations and distribution. J Ultrastruct Res 93:1–16

    Google Scholar 

  • Forssman WG, Girardier L (1970) A study of the T system in rat heart. J Cell Biol 44:1–19

    Google Scholar 

  • Hayat MA (1981) Fixation for electron microscopy. Academic Press, New York

    Google Scholar 

  • Hibbs RG, Ferrans VJ (1969) An ultrastructural and histochemical study of rat atrial myocardium. Am J Anat 124:251–280

    Google Scholar 

  • Jamieson JD, Palade GE (1964) Specific granules in atrial muscle cells. J Cell Biol 23:151–172

    Google Scholar 

  • Korr IM, Appeltauer GSL (1974) The time course of axonal transport of neuronal proteins to muscle. Exptl Neurol 43:452–463

    Google Scholar 

  • Korr IM, Wilkinson PN, Chornock FW (1967) Axonal delivery of neuroplasmic components to muscle cells. Science 155:342–345

    Google Scholar 

  • Kuhn H, Richards JG, Tranzer JP (1975) The nature of rat “specific heart granules” with regard to catecholamines: an investigation by ultrastructural cytochemistry. J Ultrastruct Res 50:159–166

    Google Scholar 

  • Löffenholz K, Pappano A (1985) The parasympathetic neuroeffector junction of the heart. Pharmacol Rev 37:1–24

    Google Scholar 

  • MacCanon DM, Horvath SM (1957) Effect of bilateral cervical vagotomy in the dog. Am J Physiol 189:569–572

    Google Scholar 

  • McNutt NS, Fawcett DW (1969) The ultrastructure of the cat myocardium. II. Atrial muscle. J Cell Biol 42:46–67

    Google Scholar 

  • Metz J, Mutt V, Forssman WG (1984) Immunohistochemical localization of cardiodilatin in myoendocrine cells of the cardiac atria. Anat Embryol 170:123–127

    Google Scholar 

  • Miledi R, Slater CR (1969) Electron-microscopic structure of denervated skeletal muscle. Proc R Soc (Lond) 174:253–269

    Google Scholar 

  • Palmer JW, Tandler B, Hoppel CL (1977) Biochemical properties of subsarcolemmal and interfibrillar mitochondria isolated from rat cardiac muscle. J Biol Chem 252:8731–8739

    Google Scholar 

  • Schrodt GR, Walker SM (1966) Ultrastructure of membranes in denervation atrophy. Am J Pathol 49:33–51

    Google Scholar 

  • Tchervova IA (1960) On structural and functional alterations in heart caused by section of vagal nerves (in Russian). Arch Anat 39:13–22

    Google Scholar 

  • Wanson J-C, Drochmans P (1972) Role of the sarcoplasmic reticulum in glycogen metabolism: binding of phosphorylase, phosphorylase kinase, and primer complexes to sarcovesicles of rabbit skeletal muscle. J Cell Biol 54:206–224

    Google Scholar 

  • Wong WC, Ling EA, Yick TY, Tay SSW (1987) Effects of bilateral vagotomy on the ultrastructure of the cardiac ganglia in the monkey (Macaca fascicularis). J Anat 150:75–88

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Wong, W.C., Yick, T.Y. & Ling, E.A. Effects of vagotomy on the ultrastructure of the atrial myocardium in the monkey (Macaca fascicularis). Anat Embryol 177, 147–152 (1987). https://doi.org/10.1007/BF00572539

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00572539

Key words

Navigation