Summary
Whereas dehydroepiandrosterone sulfate or glucuronoside exerted no effects upon the activity of glueose-6-phosphate dehydrogenase in human erythrocytes, a 10-7 M concentration of free dehydroepiandrosterone and synthetic dehydroepiandrosterone sulfatide produced a 9% and 19% resp. inhibition of said enzyme. On the basis of endogenous plasma levels of the later compounds the assumed regulation of the enzyme under physiological conditions may be effected rather through the lipophile sulfoconjugate.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Literatur
Marks, P. A., and J. Banks: Proc. natl. Acad. Sci. (Wash.) 46, 447 (1960).
Brandau, EL, u. W. Luh: Geburtsh. u. Frauenheilk. 28, 1074 (1968).
Tsutsui, E. A., P. A. Marks, and P. Reich: J. biol. Chem. 237, 3009 (1962).
Sonka, J., I. Gregorova, M. Jiranek, P. Kölbel u. Z. Matys: Endokrinologie 45, 115 (1965).
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 1969 Springer-Verlag Berlin · Heidelberg
About this chapter
Cite this chapter
Oertel, G.W., Rebelein, I. (1969). Einwirkung von Dehydroepiandrosteron und seinen Conjugaten auf die Glucose-6-Phosphat-Dehydrogenase in menschlichen Erythrocyten. In: Kracht, J. (eds) Oestrogene Hypophysentumoren. Oestrogene Hypophysentumoren, vol 15. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-95126-8_37
Download citation
DOI: https://doi.org/10.1007/978-3-642-95126-8_37
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-642-95127-5
Online ISBN: 978-3-642-95126-8
eBook Packages: Springer Book Archive