Archives of Microbiology

, Volume 102, Issue 1, pp 129–137 | Cite as

Effects of diazepam on photosynthesis, respiration, rubidium uptake, and finestructure of Scenedesmus obliquus in synchronous cultures

  • Kurt Ober
Short Communications

Abstract

Effects of diazepam (Valium) on photosynthesis, chlorophyll/photosynthesis ratios, respiration, uptake of rubidium ions, and ultrastructure of Scenedesmus obliquus synchronized by a light-dark regimen of \(14:\overline {10}\) hrs were determined.

80 and 160 μM diazepam, added to the nutrient medium at the start of the light-dark change (i.e., start of the cell cycle) gradually reduced rates of photosynthesis below the initial rates from the beginning of the experiment. Contents of chlorophyll, however, remained nearly unaffected. Consequently, the diazepam-treated cells had a higher chlorophyll/photosynthesis ratio—also with regard to respiration in order to calculate the gross photosynthesis. The occurrence of photorespiration cannot be assumed. The net influx or rubidium was slightly reduced by 100 μM diazepam 0.5 and 2.0 hrs after the start of the cell cycle and was strongly inhibited after 5 to 14 hrs. 80 and 160 μM diazepam caused separation of thylakoids, formation of giant mitochondria and enlargement of vacuoles.

The results are discussed and it is finally suggested that diazepam acts on different membrane systems. Furthermore an ATP deficiency cannot be excluded.

Key words

Diazepam Benzodiazepines Scenedesmus Ultrastructure Photosynthesis Respiration Rubidium Uptake 

Non-Standard Abbreviations

LDR

light-dark regimen

Glut

glutaraldehyde fixation

Os-Cr

osmium-dichromate post-fixation

Mn

permanganate post-fixation

Pb

lead citrate stain of thin sections

D

dictyosome

M

mitochondrion

N

nucleus

St

starch deposit in the chloroplast

Sp

space between cell wall and plasma-(lemma)

V

vacuole. The scale line indicates 10 μm in low magnification micrographs (Figs. 6 and 9) and 1 μm in the other micrographs

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References

  1. Arnold, C. G., Schimmer, O., Schötz, F., Bathelt, H.: Die Mitochondrien von Chlamydomonas reinhardii. Arch. Mikrobiol. 81, 50–67 (1972)Google Scholar
  2. Beyer, R. E., Ernster, L., Löw, H., Beyer, T.: Correlation of optical density and oxidative phosphorylation in reconstructed mitochondrial systems. Exp. Cell Res. 8, 586–588 (1955)Google Scholar
  3. Böger, P.: Das Strukturproteid aus Chloroplasten einzelliger Grünalgen und seine Beziehung zum Chlorophyll. Flora (Jena) 154, 174–211 (1964)Google Scholar
  4. Brackett, F. S., Olson, R. A., Crickard, R. G.: Respiration and intensity dependence of photosynthesis in Chlorella. J. gen. Physiol. 36, 528–561 (1953)Google Scholar
  5. Bunt, J. S., Heeb, M. A.: Consumption of O2 in the light by Chlorella pyrenoidosa and Chlamydomonas reinhardii. Biochim. biophys. Acta (Amst.) 226, 354–359 (1971)Google Scholar
  6. Cheng, K. H., Colman, B.: Measurements of photorespiration in some microscopic algae. Planta (Berl.) 115, 207–212 (1974)Google Scholar
  7. Damaschke, K.: Messung von Sauerstoffumsätzen an Grünalgen. In: Elektrochemische Sauerstoffmessungen, F. Tödt, ed., pp. 58–70. Berlin: de Gruyter 1958Google Scholar
  8. Essman, W. B.: Subcellular action of benzodiazepines. In: Monographs of the Mario Negri Institute for Pharmacological Research. The benzodiazepines. Symposium, S. Garattini, E. Mussini, L. O. Randall, eds., pp. 177–190. New York: Raven Press 1973Google Scholar
  9. Everhart, L. R., Jr., Rubin, R. W.: Cyclic changes in the cell surface. I. Change in thymidine transport and its inhibition by cytochalasin B in chinese hamster ovary cells. J. Cell Biol. 60, 434–441 (1974)Google Scholar
  10. Hoch, G., Owens, O. v. H., Kok, B.: Photosynthesis and respiration. Arch. Biochem. Biophys. 101, 171–180 (1963)Google Scholar
  11. Kadenbach, B., Lührs, W.: Effects of 7-chloro-2-methyl-amino-5-phenyl-3 H-1,4-benzodiazepen-4-oxide on mitochondria from rat liver and brain. Nature (Lond.) 192, 174–176 (1961)Google Scholar
  12. deLaat, S. W., Bluemink, J. G.: New membrane formation during cytokinesis in normal and cytochalasin B-treated eggs of Xenopus laevis. II. Electrophysiological observations. J. Cell Biol. 60, 529–540 (1974)Google Scholar
  13. Luft, J. H.: Improvements in epoxy resin embedding methods. J. Biophys. Biochem. 9, 409–414 (1961)Google Scholar
  14. Nilshammar, M., Walles, B.: Electron microscope studies on cell differentiation in synchronized cultures of the green alga Scenedesmus. Protoplasma (Wien) 79, 317–332 (1974)Google Scholar
  15. Noonan, K. D., Levine, A. J., Burger, M. M.: Cell cycle-dependent changes in the surface membrane as detected with (3H) concanavalin A. J. Cell Biol. 58, 491–497 (1973)Google Scholar
  16. Ober, K.: Wirkungen von Diazepam auf Scenedesmus obliquus (Gaffron) Stamm D 3. Diss., Universität Göttingen 1973Google Scholar
  17. Ober, K.: Effects of diazepam on cell division rates and productivity of Scenedesmus obliquus in synchronous cultures. Arch. Microbiol. 99, 369–378 (1974)Google Scholar
  18. Paschke, M., Schwanitz, F.: Zum Problem der Vortestung von Arzneimitteln mit Hilfe niederer und höherer Pflanzen. I. Über die Wirkung von Phthalylglutaminsäureimid (Thalidomid) und anderen Schlafmitteln auf Teilungsgeschwindigkeit, Formgestaltung und Sexualität einiger Desmidiaceen. Arzneimittel-Forsch. 18, 1338–1341 (1968)Google Scholar
  19. Paschke, M., Schwanitz, F.: Zum Problem der Vortestung von Arzneimitteln mit Hilfe niederer und höherer Pflanzen. III. Bestimmung der teilungsfördernden oder cytostatischen Wirkung von Medikamenten mit der Grünalge Haematococcus pluvialis Flotow. Arzneimittel-Forsch. 21, 1419–1422 (1971)Google Scholar
  20. Reynolds, E. S.: The use of lead citrate at high pH as an electron opaque stain in electron microscopy. J. Cell Biol. 17, 208–212 (1963)Google Scholar
  21. Scott, R. E., Carter, R. L., Kidwell, W. R.: Structural changes in membranes of synchronized cells demonstrated by freeze cleavage. Nature New Biol. 233, 219–220 (1971)Google Scholar
  22. Stabenau, H.: Untersuchungen über die Aufnahme von Glycolat bei Chlorogonium. Planta (Berl.) 109, 177–183 (1973)Google Scholar
  23. Truesdale, G. A., Downing, A. L., Lowden, G. F.: The solubility of oxygen in pure water and sea-water. J. appl. Chem. 5, 53–62 (1955)Google Scholar
  24. Venable, J. H., Coggeshall, R.: A simplified lead citrate stain for use in electron microscopy. J. Cell Biol. 25, 407–408 (1965)Google Scholar
  25. Zelitch, I.: Photosynthesis, photorespiration, and plant productivity. New York-London: Academic Press 1971Google Scholar
  26. Zubovskaya, A. M., Ostrovskaya, R. U.: Effect of diazepam on oxidative metabolism of mouse brain tissue. Bull. exp. Biol. Med. 73, 649–650 (1972)Google Scholar

Copyright information

© Springer-Verlag 1975

Authors and Affiliations

  • Kurt Ober
    • 1
    • 2
  1. 1.Pflanzenphysiologisches Institut der Universität GöttingenGöttingenGermany
  2. 2.Lehrstuhl für Biologie IXFachbereich Biologie der UniversitätRegensburgFederal Republic of Germany

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