» Articles » PMID: 34827890

The Uptake and Deconjugation of Androstenone Sulfate in the Adipose Tissue of the Boar

Overview
Journal Animals (Basel)
Date 2021 Nov 27
PMID 34827890
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

Boars express high testicular levels of sulfotransferase enzymes, and consequently, the boar taint causing compound androstenone predominantly circulates as a steroid sulfate. Androstenone sulfate is suspected to function as a steroid reservoir that can be deconjugated to provide a source of free androstenone for accumulation. Therefore, the purpose of this study was to characterize the uptake and deconjugation of androstenone sulfate in the adipose tissue of the boar. Real-time PCR was used to quantify the expression of steroid sulfatase (STS) and several organic anion transporting polypeptides (OATPs) in the adipose tissue. Additionally, [H]-androstenone sulfate was incubated with adipocytes or supernatant from homogenized fat to assess steroid uptake and conversion, respectively. A positive correlation existed between OATP-B expression and androstenone sulfate uptake (r = 0.86, = 0.03), as well as between STS expression and androstenone sulfate conversion (r = 0.76, < 0.001). Moreover, fat androstenone concentrations were positively correlated (r = 0.85, < 0.001) with androstenone sulfate conversion and tended to increase with STS expression in early maturing boars. This suggests that androstenone sulfate uptake and deconjugation are mediated by OATP-B and STS, respectively, which may influence the development of boar taint in early maturing animals.

Citing Articles

Hepatic Gene Expression and Metabolite Profiles of Androstenone and Skatole Relative to Plasma Estrone Sulfate Levels in Boars.

Bone C, Squires E Biomolecules. 2024; 14(7).

PMID: 39062564 PMC: 11274532. DOI: 10.3390/biom14070850.


The Effect of the Boar Taint Masking Strategy (Adding Dried or on Sensory Characteristics.

Zadinova K, Sochor A, citek J, Okrouhla M, Pokorna K, Sprysl M Animals (Basel). 2024; 14(11).

PMID: 38891591 PMC: 11171060. DOI: 10.3390/ani14111544.


Nuclear Receptor Pathways Mediating the Development of Boar Taint.

Bone C, Squires E Metabolites. 2022; 12(9).

PMID: 36144190 PMC: 9503508. DOI: 10.3390/metabo12090785.

References
1.
Alexandersson I, Harms M, Boucher J . Isolation and Culture of Human Mature Adipocytes Using Membrane Mature Adipocyte Aggregate Cultures (MAAC). J Vis Exp. 2020; (156). DOI: 10.3791/60485. View

2.
Bone C, Anderson C, Lou Y, Squires E . The characterization of androstenone transport in boar plasma. J Steroid Biochem Mol Biol. 2018; 185:218-224. DOI: 10.1016/j.jsbmb.2018.09.006. View

3.
Ruder H, Loriaux L, LIPSETT M . Estrone sulfate: production rate and metabolism in man. J Clin Invest. 1972; 51(4):1020-33. PMC: 302214. DOI: 10.1172/JCI106862. View

4.
Laderoute H, Bone C, Squires E . The sulfoconjugation of androstenone and dehydroepiandrosterone by human and porcine sulfotransferase enzymes. Steroids. 2018; 136:8-16. DOI: 10.1016/j.steroids.2018.05.010. View

5.
Raeside J, Renaud R . Estrogen and androgen production by purified Leydig cells of mature boars. Biol Reprod. 1983; 28(3):727-33. DOI: 10.1095/biolreprod28.3.727. View