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The metabolism of 17α-methylandrostenediol by the rat adrenal and its effects on the biosynthesis of corticosterone by the cortical tissue in vitro.

The suppression of the formation of corticosterone by the rat adrenal tissue in vivo and in vitro by androgens is reported. There is some evidence that androgens can be converted to more polar compounds by the incubated glands. Two such metabolites of 17α-methyl-Δ5-androstene-3β, 17β-diol (MAD) have been investigated. One is methyltestosterone, probably formed by the oxidation of MAD by the enzyme, 3β-hydroxydehydrogenase. The other may, in addition, contain one or more extra hydroxyl groups. Even more polar compounds have been observed. Whether these originate from the exogenous androgens or arise as a consequence of diversion of corticoid synthesis from corticosterone is not known.

Identiferoai:union.ndltd.org:LACETR/oai:collectionscanada.gc.ca:QMM.115324
Date January 1963
CreatorsYoung, Peter. C.
ContributorsSaffran, M. (Supervisor)
PublisherMcGill University
Source SetsLibrary and Archives Canada ETDs Repository / Centre d'archives des thèses électroniques de Bibliothèque et Archives Canada
LanguageEnglish
Detected LanguageEnglish
TypeElectronic Thesis or Dissertation
Formatapplication/pdf
CoverageMaster of Science. (Department of Chemistry.)
RightsAll items in eScholarship@McGill are protected by copyright with all rights reserved unless otherwise indicated.
Relationalephsysno: NNNNNNNNN, Theses scanned by McGill Library.

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