Back to Search
Start Over
Mechanism of testosterone deficiency in the transgenic sickle cell mouse.
- Source :
-
PloS one [PLoS One] 2015 May 29; Vol. 10 (5), pp. e0128694. Date of Electronic Publication: 2015 May 29 (Print Publication: 2015). - Publication Year :
- 2015
-
Abstract
- Testosterone deficiency is associated with sickle cell disease (SCD), but its underlying mechanism is not known. We investigated the possible occurrence and mechanism of testosterone deficiency in a mouse model of human SCD. Transgenic sickle male mice (Sickle) exhibited decreased serum and intratesticular testosterone and increased luteinizing hormone (LH) levels compared with wild type (WT) mice, indicating primary hypogonadism in Sickle mice. LH-, dbcAMP-, and pregnenolone- (but not 22-hydroxycholesterol)- stimulated testosterone production by Leydig cells isolated from the Sickle mouse testis was decreased compared to that of WT mice, implying defective Leydig cell steroidogenesis. There also was reduced protein expression of steroidogenic acute regulatory protein (STAR), but not cholesterol side-chain cleavage enzyme (P450scc), in the Sickle mouse testis. These data suggest that the capacity of P450scc to support testosterone production may be limited by the supply of cholesterol to the mitochondria in Sickle mice. The sickle mouse testis exhibited upregulated NADPH oxidase subunit gp91phox and increased oxidative stress, measured as 4-hydroxy-2-nonenal, and unchanged protein expression of an antioxidant glutathione peroxidase-1. Mice heterozygous for the human sickle globin (Hemi) exhibited intermediate hypogonadal changes between those of WT and Sickle mice. These results demonstrate that testosterone deficiency occurs in Sickle mice, mimicking the human condition. The defects in the Leydig cell steroidogenic pathway in Sickle mice, mainly due to reduced availability of cholesterol for testosterone production, may be related to NADPH oxidase-derived oxidative stress. Our findings suggest that targeting testicular oxidative stress or steroidogenesis mechanisms in SCD offers a potential treatment for improving phenotypic changes associated with testosterone deficiency in this disease.
- Subjects :
- Anemia, Sickle Cell genetics
Anemia, Sickle Cell pathology
Animals
Disease Models, Animal
Glutathione Peroxidase genetics
Glutathione Peroxidase metabolism
Humans
Leydig Cells pathology
Male
Membrane Glycoproteins genetics
Membrane Glycoproteins metabolism
Mice
Mice, Transgenic
NADPH Oxidase 2
NADPH Oxidases genetics
NADPH Oxidases metabolism
Phosphoproteins genetics
Phosphoproteins metabolism
Glutathione Peroxidase GPX1
Steroidogenic Acute Regulatory Protein
Anemia, Sickle Cell metabolism
Leydig Cells metabolism
Luteinizing Hormone metabolism
Oxidative Stress
Testosterone deficiency
Subjects
Details
- Language :
- English
- ISSN :
- 1932-6203
- Volume :
- 10
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- PloS one
- Publication Type :
- Academic Journal
- Accession number :
- 26023917
- Full Text :
- https://doi.org/10.1371/journal.pone.0128694