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Advances in Research on Models of Oligoasthenozoospermia
Feng Yang1, Yongyong Ren1, Junpeng Zhang2,3
1College of Pharmacy, Shaanxi University of Chinese Medicine, Xian, 712046, China.
Abstract:
Oligoasthenozoospermia (OAT) is a major cause of declining male fertility worldwide, characterized by reduced sperm count and motility. Its pathogenesis involves multiple factors including genetics, hormones, environment, and lifestyle. Due to ethical and practical limitations in human studies, animal models have become essential tools for elucidating OAT mechanisms and evaluating therapeutic strategies. This review aims to systematically organize and evaluate existing OAT animal models, including those established through chemical agents, heavy metals, endocrine disruptors, physical stress, genetic modification, and nutritional imbalance. It summarizes these models based on their mechanistic foundations, phenotypic characteristics, advantages, and limitations. Results indicate that despite significant research advances, existing models remain limited in standardization, depth of mechanism elucidation, and clinical translational value. Therefore, future efforts should focus on developing more comprehensive and clinically relevant animal models to deepen understanding of OAT pathophysiology and advance the development of effective and personalized therapeutic strategies.
Insights
Oligoasthenozoospermia (OAT), a key factor in male infertility, is studied using animal models. Current models have limitations, necessitating development of more clinically relevant options for better understanding and treatment.
Area of Science:
- Reproductive Biology
- Toxicology
- Animal Models
Background:
- Oligoasthenozoospermia (OAT) significantly impacts global male fertility.
- Pathogenesis of OAT involves complex genetic, hormonal, environmental, and lifestyle factors.
- Animal models are crucial for studying OAT due to human study limitations.
Purpose of the Study:
- To systematically review and evaluate existing animal models for OAT research.
- To assess models based on their mechanistic basis, phenotypes, strengths, and weaknesses.
- To identify gaps and guide future development of OAT animal models.
Main Methods:
- Review of animal models induced by chemical agents, heavy metals, endocrine disruptors, physical stress, genetic modification, and nutritional imbalance.
- Analysis of models concerning their underlying mechanisms and observed phenotypic characteristics.
- Evaluation of model advantages and limitations for OAT research.
Main Results:
- A diverse range of OAT animal models have been established.
- Existing models show variability in standardization and mechanistic detail.
- Current models exhibit limitations in clinical translational value for human OAT.
Conclusions:
- Significant progress has been made in developing OAT animal models.
- There is a critical need for more standardized and mechanistically deep models.
- Future research should prioritize clinically relevant animal models for OAT pathophysiology and personalized therapies.
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