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Sökning: id:"swepub:oai:DiVA.org:uu-3313" > Regulation of Ovari...

Regulation of Ovarian Aromatase: Studies by Aromatase Assays in vitro and in vivo

Kirilovas, Dmitrijus, 1962- (författare)
Uppsala universitet,Institutionen för kvinnors och barns hälsa
Brännström, Mats, professor (opponent)
Department of Women's and Children's Health, Göteborg
 (creator_code:org_t)
ISBN 9155455409
Uppsala : Acta Universitatis Upsaliensis, 2003
Engelska 160 s.
Serie: Comprehensive Summaries of Uppsala Dissertations from the Faculty of Medicine, 0282-7476 ; 1226
  • Doktorsavhandling (övrigt vetenskapligt/konstnärligt)
Abstract Ämnesord
Stäng  
  • An in vitro method was developed for measuring aromatase, based on binding of competitive aromatase inhibitor [11C]vorozole to the active site of the enzyme. [11C]Vorozole displayed high, specific binding in vitro to human placenta and human granulosa cells (GC), both fresh and frozen/thawed cells, provided correct procedures were used. High, specific binding was also observed in pig and rat ovaries, whereas binding in other tissues was unspecific and usually low. Aromatase concentrations measured by [11C]vorozole binding correlated well to aromatase activity measured by [3H]water release from 1β[3H]androstenedione. In human GC in vitro, low concentrations of 5α-dihydrotestosterone (DHT), but not of other androgens, stimulated aromatase activity measured by [3H]water release but had no effects on aromatase concentration measured by [11C]vorozole binding. DHT may interact with aromatase differently than other androgens, perhaps by changing aromatase affinity to precursor. In the rat estrous cycle, aromatase activity in ovarian homogenate, measured by [3H]water release, together with serum androstenedione and estradiol-17β, peaked between 6 and 13 h after onset of the light period of proestrus, the former activity being independent of radioactive substrate concentration. [11C]Vorozole binding characteristics changed more rapidly than de novo synthesis of the enzyme. [11C]Vorozole binding Kd showed close inverse correlation to aromatase activity in ovarian homogenate and to serum estradiol-17β. Rapid changes in substrate affinity rather than changes in substrate concentration or de novo synthesis of the enzyme may thus be important for regulation of ovarian aromatase. The [11C]vorozole in vivo technique yields additional information compared with traditional in vitro techniques.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Reproduktionsmedicin och gynekologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Obstetrics, Gynaecology and Reproductive Medicine (hsv//eng)

Nyckelord

Obstetrics and gynaecology
aromatase
human
granulosa cells
11C-vorozole
active site
allosteric configuration
in vitro
in vivo
PET
androgens
rat
estrous cycle.
Obstetrik och kvinnosjukdomar
Obstetrics and women's diseases
Obstetrik och kvinnosjukdomar
Obstetrics and Gynaecology
obstetrik och gynekologi

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