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Regulation of Ovarian Aromatase: Studies by Aromatase Assays in <i>vitro</i> and in<i> vivo</i>

<p>An <i>in vitro</i> method was developed for measuring aromatase, based on binding of competitive aromatase inhibitor [<sup>11</sup>C]vorozole to the active site of the enzyme. [<sup>11</sup>C]Vorozole displayed high, specific binding <i>in vitro</i> 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 [<sup>11</sup>C]vorozole binding correlated well to aromatase activity measured by [<sup>3</sup>H]water release from 1β[<sup>3</sup>H]androstenedione. </p><p>In human GC <i>in vitro</i>, low concentrations of 5α-dihydrotestosterone (DHT), but not of other androgens, stimulated aromatase activity measured by [<sup>3</sup>H]water release but had no effects on aromatase concentration measured by [<sup>11</sup>C]vorozole binding. DHT may interact with aromatase differently than other androgens, perhaps by changing aromatase affinity to precursor. </p><p>In the rat estrous cycle, aromatase activity in ovarian homogenate, measured by [<sup>3</sup>H]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. [<sup>11</sup>C]Vorozole binding characteristics changed more rapidly than <i>de novo</i> synthesis of the enzyme. [<sup>11</sup>C]Vorozole binding K<sub>d </sub>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 <i>de novo</i> synthesis of the enzyme may thus be important for regulation of ovarian aromatase. </p><p>The [<sup>11</sup>C]vorozole <i>in vivo</i> technique yields additional information compared with traditional in vitro techniques. </p>

Identiferoai:union.ndltd.org:UPSALLA/oai:DiVA.org:uu-3313
Date January 2003
CreatorsKirilovas, Dmitrijus
PublisherUppsala University, Department of Women's and Children's Health, Uppsala : Acta Universitatis Upsaliensis
Source SetsDiVA Archive at Upsalla University
LanguageEnglish
Detected LanguageEnglish
TypeDoctoral thesis, comprehensive summary, text
RelationComprehensive Summaries of Uppsala Dissertations from the Faculty of Medicine, 0282-7476 ; 1226

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