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Dehydroepiandrosterone Supplementation Results in Varying Tissue-specific Levels of Dihydrotestosterone in Male Mice

Colldén Hannah; Nilsson Maria E; Norlén Anna-Karin; Landin Andreas; Windahl Sara H; Wu Jianyao; Horkeby Karin; Lagerquist Marie K; Ryberg Henrik; Poutanen Matti; Vandenput Liesbeth; Ohlsson Claes

Dehydroepiandrosterone Supplementation Results in Varying Tissue-specific Levels of Dihydrotestosterone in Male Mice

Colldén Hannah
Nilsson Maria E
Norlén Anna-Karin
Landin Andreas
Windahl Sara H
Wu Jianyao
Horkeby Karin
Lagerquist Marie K
Ryberg Henrik
Poutanen Matti
Vandenput Liesbeth
Ohlsson Claes
Katso/Avaa
bqac163.pdf (557.1Kb)
Lataukset: 

ENDOCRINE SOC
doi:10.1210/endocr/bqac163
URI
http://dx.doi.org/10.1210%2Fendocr%2Fbqac163
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Julkaisun pysyvä osoite on:
https://urn.fi/URN:NBN:fi-fe202301255500
Tiivistelmä
Dehydroepiandrosterone (DHEA), an adrenal androgen precursor, can be metabolized in target tissues into active sex steroids. It has been proposed that DHEA supplementation might result in restoration of physiological local sex steroid levels, but knowledge on the effect of DHEA treatment on local sex steroid levels in multiple tissues is lacking. To determine the effects of DHEA on tissue-specific levels of sex steroids, we treated orchiectomized (ORX) male mice with DHEA for 3 weeks and compared them with vehicle-treated ORX mice and gonadal intact mice. Intra-tissue levels of sex steroids were analyzed in reproductive organs (seminal vesicles, prostate, m. levator ani), major body compartments (white adipose tissue, skeletal muscle, and brain), adrenals, liver, and serum using a sensitive and validated gas chromatography-mass spectrometry method. DHEA treatment restored levels of both testosterone (T) and dihydrotestosterone (DHT) to approximately physiological levels in male reproductive organs. In contrast, this treatment did not increase DHT levels in skeletal muscle or brain. In the liver, DHEA treatment substantially increased levels of T (at least 4-fold) and DHT (+536%, P < 0.01) compared with vehicle-treated ORX mice. In conclusion, we provide a comprehensive map of the effect of DHEA treatment on intra-tissue sex steroid levels in ORX mice with a restoration of physiological levels of androgens in male reproductive organs while DHT levels were not restored in the skeletal muscle or brain. This, and the unexpected supraphysiological androgen levels in the liver, may be a cause for concern considering the uncontrolled use of DHEA.
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