JOE
HOME HELP CONTACT US SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Journal of Endocrinology (1965) 32, 259-260       DOI: 10.1677/joe.0.0320259
© 1965 Society for Endocrinology
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by YAMASHITA, K.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by YAMASHITA, K.

EFFECT OF FLAVONOID COMPOUNDS ON PROGESTERONE IN PROGESTATIONAL DEVELOPMENT

K. YAMASHITA

The results of a previous study (Yamashita, 1965) indicated that rutin antagonizes the action of progesterone on the endometrium of the rabbit. This was demonstrated by quantitative measurement of endometrial carbonic anhydrase activity (Miyake & Pincus, 1958 b; Yamashita & Kurouji, 1961 a, b). Since rutin is a flavonoid glucoside, it seemed desirable to investigate the antagonistic action of other flavonoid compounds. The following compounds were used: hesperidin (3',5,7-trihydroxy-4'-methoxyflavanone-7-rutinoside), morin (2',3,4',5,7-pentahydroxyflavone) and quercetin (3,3',4',5,7-pentahydroxyflavone).

The methods used were identical with those described previously (Kurouji, 1963; Yamashita, 1965). Using a modified Clauberg method (1930), rabbits (weighing approximately 1·5 kg.) were primed with oestrogen and received a standard dose of 2 mg. progesterone; simultaneously one of the test compounds was administered either subcutaneously or orally in logarithmically spaced doses of 0·001–100 mg./animal to groups of five rabbits.







HOME HELP CONTACT US SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1965 by the Society for Endocrinology.