A Novel Tissue-Specific Insight into Sex Steroid Fluctuations Throughout the Murine Estrous Cycle

Author:

Unger Christian A1,Hope Marion C1,Aladhami Ahmed K1,Cotham William E2,Socia Cassidy E1,Rice Barton C1,Clegg Deborah J3,Velázquez Kandy T1,LaVoie Holly A4,Hollis Fiona5,Enos Reilly T1ORCID

Affiliation:

1. Department of Pathology, Microbiology, and Immunology, University of South Carolina-School of Medicine , Columbia, SC 29209 , USA

2. Department of Chemistry and Biochemistry, College of Arts and Science, University of South Carolina , Columbia, SC 29208 , USA

3. Department of Internal Medicine, Texas Tech Health Sciences Center , El Paso, TX 7995 , USA

4. Department of Cell Biology and Anatomy, University of South Carolina, School of Medicine , Columbia, SC 29209 , USA

5. Department of Pharmacology, Physiology, and Neuroscience, School of Medicine , Columbia, SC 29209 , USA

Abstract

Abstract Serum sex steroid levels fluctuate throughout the reproductive cycle. However, the degree to which sex steroid tissue content mimics circulating content is unknown. Understanding the flux and physiological quantity of tissue steroid content is imperative for targeted hormonal therapy development. Utilizing a gold-standard ultrasensitive liquid chromatography–mass spectrometry (LC/MS) method we determined sex steroid (17β-estradiol [E2], testosterone, androstenedione, and progesterone) fluctuations in serum and in 15 tissues throughout the murine estrous cycle (proestrus, estrus, and diestrus I) and in ovariectomized (OVX) mice. We observed dynamic fluctuations in serum and tissue steroid content throughout the estrous cycle with proestrus generally presenting the highest content of E2, testosterone, and androstenedione, and lowest content of progesterone. In general, the trend in circulating steroid content between the stages of the estrous cycle was mimicked in tissue. However, the absolute amounts of steroid levels when normalized to tissue weight were found to be significantly different between the tissues with the serum steroid quantity often being significantly lower than the tissue quantity. Additionally, we found that OVX mice generally displayed a depletion of all steroids in the various tissues assessed, except in the adrenal glands which were determined to be the main site of peripheral E2 production after ovary removal. This investigation provides a comprehensive analysis of steroid content throughout the estrous cycle in a multitude of tissues and serum. We believe this information will help serve as the basis for the development of physiologically relevant, tissue-specific hormonal therapies.

Publisher

The Endocrine Society

Subject

Endocrinology

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