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

Author:

Colldén Hannah12ORCID,Nilsson Maria E13,Norlén Anna-Karin3,Landin Andreas2,Windahl Sara H4ORCID,Wu Jianyao1ORCID,Horkeby Karin1,Lagerquist Marie K1ORCID,Ryberg Henrik3,Poutanen Matti15,Vandenput Liesbeth1ORCID,Ohlsson Claes12ORCID

Affiliation:

1. Sahlgrenska Osteoporosis Centre, Centre for Bone and Arthritis Research, Department of Internal Medicine and Clinical Nutrition, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg , SE-413 45 Gothenburg , Sweden

2. Department of Drug Treatment, Sahlgrenska University Hospital , Region Västra Götaland, SE-413 45 Gothenburg , Sweden

3. Department of Clinical Chemistry, Sahlgrenska University Hospital , Region Västra Götaland, SE-413 45 Gothenburg , Sweden

4. Department of Laboratory Medicine, Division of Pathology, Karolinska Institutet , 141 86 Huddinge , Sweden

5. Research Centre for Integrative Physiology and Pharmacology, Institute of Biomedicine and Turku Center for Disease Modeling, University of Turku , FI-20014 Turku , Finland

Abstract

Abstract 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.

Funder

Swedish Research Council

IngaBritt and Arne Lundberg Foundation

Novo Nordisk Foundation

Knut and Alice Wallenberg Foundation

Publisher

The Endocrine Society

Subject

Endocrinology

Reference40 articles.

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3. Supplemental materials for: Dehydroepiandrosterone supplementation results in varying tissue-specific levels of dihydrotestosterone in male mice;Collden

4. Dehydroepiandrosterone research: past, current, and future;Klinge;Vitam Horm,2018

5. Proteomics. Tissue-based map of the human proteome;Uhlén;Science,2015

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