Skip to main content
Log in

Microphotometric analysis of NADH-tetrazolium reductase and α-glycerophosphate dehydrogenase in human quadriceps muscle

  • Papers
  • Published:
The Histochemical Journal Aims and scope Submit manuscript

Synopsis

In serial cross-sections of human skeletal muscles stained for either NADH-tetrazolium reductase (NADH-TR) or α-glycerophosphate dehydrogenase (α-GPD), a linear relation was found between the total content of enzyme in a cell (expressed as the thickness of the section) and the absorbance of the formazan reaction product formed. Little variation (<4.8%) was found in the concentration of formazan (absorbance per unit thickness) when the same cell was measured in serial cross-sections of various thicknesses (2–10 μm) along a longitudinal distance of at least 200 μm along the cell. The reduction in enzyme activity was found to be negligible after aqueous preincubation. A maximum of 10–12% of the formazan produced in the NADH-TR reaction might be the result of ‘nothing dehydrogenase’ activity, whereas this unspecific reaction might account for up to 20% of the formazan deposited in the α-GPD reactions after 30 min incubation. The diffusion of Nitro BT into the tissue during the incubation period was found to be unhindered. The rates of formazan production decreased with increasing incubation time, especially in the α-GPD reaction in both fibre types. The ratio of the mean absorbance of the formazan in type I fibres to that in type II fibres (in the same section) was 1.41 (coefficient of variation, 2.5%) in the NADH-TR reaction and 0.68 (coefficient of variation, 3.8%) in the α-GPD reaction. These values were not affected either by variations in the incubation time (5–40 min) or by the thickness of the section (2–8 μm). The concentrations of NADH-TR and α-GPD seem to be constant along the length of the muscle fibre. The histochemical reactions reported, together with measurements of the thickness of the sections, seem suitable for the microphotometric quantification of the two enzymes in single fibres of human skeletal muscles.

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

  • Altman, F. P. (1975). Quantitation in histochemistry: A review of some commercially available microdensitometers.Histochem. J. 7, 375–95.

    Google Scholar 

  • Andersen, H. &Høyer, P. E. (1974). Simplified control experiments in the histochemical study of coenzyme-linked dehydrogenases.Histochemistry 38, 71–83.

    Google Scholar 

  • Bergström, J. (1962). Muscle electrolytes in man.Scand. J. Clin. Lab. Invest. 14, suppl. 68.

    Google Scholar 

  • Dubowitz, V. &Brooke, M. H. (1973).Muscle Biopsy: A Modern Approach. London, Philadelphia, Toronto: Saunders.

    Google Scholar 

  • Edström, L. (1970). Selective changes in the sizes of red and white muscle fibers in upper motor lesions and parkinsonism.J. neurol. Sci. 11, 537–50.

    Google Scholar 

  • Edström, L. &Nordemar, R. (1974). Differential changes in type I and type II muscle fibers in rheumatoid arthritis.Scand. J. Rheum. 3, 155–60.

    Google Scholar 

  • Engel, W. K. (1974). Fiber type nomenclature of human skeletal muscle for histochemical purposes.Neurology 24, 344–8.

    Google Scholar 

  • Essen, B., Jansson, E., Henriksson, J., Tayler, A. W. &Saltin, B. (1975). Metabolic characteristics of fiber types in human skeletal muscle.Acta physiol. scand. 95, 153–65.

    Google Scholar 

  • Gollnick, P. D., Piehl, K. &Saltin, B. (1974). Selective glycogen depletion pattern in human muscle fibers after exercise of varying intensity and at varying pedalling rates.J. Physiol. 241, 45–57.

    Google Scholar 

  • Guth, L. &Samaha, F. J. (1969). Qualitative differences between actomyosin ATPase of slow and fast mammalian muscle.Expl. Neurol. 25, 138–52.

    Google Scholar 

  • Halkjaer-Kristensen, J. &Ingemann-Hansen, T. (1977). Microphotometry of single fibers from the quadriceps muscle in man.Scand. J. Clin. Lab. Invest. 37, 461–8.

    Google Scholar 

  • Halkjaer-Kristensen, J. &Ingemann-Hansen, T.(1978). Thickness measurements of skeletal muscle sections using the light microscope.Histochem. J. 10, 497–504.

    Google Scholar 

  • Lowry, O. H. &Passonneau, J. V. (1972).A Flexible System of Enzymatic Analysis. New York, London: Academic Press.

    Google Scholar 

  • Lundsteen, C. &Philip, J. (1974). Microphotometry of banded human chromosomes. High resolving power by direct scanning of the specimen compared with scanning on microphotographs.J. Med. Genetics 11, 196–200.

    Google Scholar 

  • Nolte, J. &Pette, D. (1972a). Microsphotometric determination of enzyme activity in single cells in cryostat sections. I. Application of the gel film technique to microphotometry and studies on the intralobular distribution of succinate dehydrogenase and lactate dehydrogenase activities in rat liver.J. Histochem. Cytochem. 20, 567–76.

    Google Scholar 

  • Nolte, J. &Pette, D. (1972b). Microphotometric determination of enzyme activity in single cells in cryostat sections. II. Succinate dehydrogenase, lactate dehydrogenase and triosephosphate dehydrogenase activities in red, intermediate and white fibers of soleus and rectus femoris muscles of rat.J. Histochem. Cytochem. 20, 577–82.

    Google Scholar 

  • Novikoff, A. B., Shin, W.-Y. &Drucker, J. (1961). Mitochondrial localization of oxidative enzymes: Staining results with two tetrazolium salts.J. biophys. biochem. Cytol. 9, 47–61.

    Google Scholar 

  • Padykula, H. A. &Herman, E. (1955). The specificity of the histochemical method for adenosine triphosphatase.J. Histochem. Cytochem. 3, 170–95.

    Google Scholar 

  • Pearse, A. G. E. (1968).Histochemistry, Theoretical and Applied, Vol. 1, 3rd edn. Edinburgh, London and New York: Churchill Livingstone.

    Google Scholar 

  • Pearse, A. G. E. (1972).Histochemistry, Theoretical and Applied, Vol. 2, 3rd edn. Edinburgh and London: Churchill Livingstone.

    Google Scholar 

  • Wattenberg, L. W. &Leong, J. L. (1960). Effects of coenzyme Q10 and menadione on succinic dehydrogenase activity as measured by tetrazolium salt reduction.J. Histochem. Cytochem. 8, 296–303.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Halkjaer-Kristensen, J., Ingemann-Hansen, T. Microphotometric analysis of NADH-tetrazolium reductase and α-glycerophosphate dehydrogenase in human quadriceps muscle. Histochem J 11, 127–136 (1979). https://doi.org/10.1007/BF01002990

Download citation

  • Received:

  • Revised:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01002990

Keywords

Navigation