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Phosphopeptide Analysis of Rodent Epididymal Spermatozoa
Published on: December 30, 2014
Quantitative proteomic profile analysis of thyroid dysfunction effects on seminal vesicles and repercussions on male
Deborah Elzita do Carmo Corrêa1, Paula Bargi-Souza2, Isabela Medeiros Oliveira1
1Department of Medicine, State University of Central-West (UNICENTRO), Guarapuava, Parana, Brazil.
Abstract:
Hypothyroidism and thyrotoxicosis are associated with male reproductive disorders, but little is known about the influence of the thyroid hormone milieu on seminal vesicle (SV) function and metabolism. In this sense, we investigated the effects of hypothyroidism and thyrotoxicosis induced in adulthood Wistar male rats on SV function and identified new thyroid hormone targets on male reproduction regulation using novel proteomic approaches. Hypothyroidism reduces SV size and seminal fluid volume, which are directly associated with low testosterone and estradiol levels, while thyrotoxicosis increases Esr2 and Dio1 expression in the SV. We found 116 differentially expressed proteins. Hypothyroidism reduces the expression of molecular protein markers related to sperm viability, capacitation and fertilization, protection against oxidative stress and energetic metabolism in SV, while it increases the expression of proteins related to tissue damage. In conclusion, thyroid dysfunction in the adult phase impairs several morphological, molecular and functional characteristics of SV.
Insights
Thyroid dysfunction in adult male rats impairs seminal vesicle function, affecting sperm quality and reproductive health. This study reveals key molecular changes in seminal vesicles due to hypothyroidism and thyrotoxicosis.
Area of Science:
- Endocrinology and Reproductive Biology
- Proteomics and Molecular Biology
Background:
- Thyroid hormones significantly impact male reproductive health, yet their specific effects on seminal vesicle (SV) function remain largely unexplored.
- Existing knowledge links hypothyroidism and thyrotoxicosis to male reproductive disorders, but the precise mechanisms involving SV metabolism and function are unclear.
Purpose of the Study:
- To investigate the impact of experimentally induced hypothyroidism and thyrotoxicosis on seminal vesicle function and metabolism in adult male rats.
- To identify novel molecular targets regulated by thyroid hormones within the male reproductive system using advanced proteomic techniques.
Main Methods:
- Induction of hypothyroidism and thyrotoxicosis in adult Wistar male rats.
- Analysis of seminal vesicle morphology, seminal fluid volume, and key gene expression (Esr2, Dio1).
- Quantitative proteomic analysis to identify differentially expressed proteins (116 identified).
Main Results:
- Hypothyroidism led to reduced SV size, seminal fluid volume, and decreased expression of proteins crucial for sperm viability, capacitation, fertilization, antioxidant defense, and energy metabolism.
- Thyrotoxicosis was associated with increased expression of Esr2 and Dio1 in the SV.
- Hypothyroidism increased the expression of proteins linked to tissue damage in the SV.
Conclusions:
- Thyroid hormone imbalance during adulthood significantly impairs seminal vesicle morphology, molecular profiles, and overall function.
- The study identifies specific molecular pathways in the SV affected by thyroid dysfunction, highlighting potential targets for reproductive health interventions.
- Thyroid dysfunction negatively impacts critical aspects of male fertility, including sperm quality and seminal fluid composition.
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