Evidence map›Paper›PMID 41530648›Full record

ReviewReproductive sciences (Thousand Oaks, Calif.)2026

Advances in Research on Models of Oligoasthenozoospermia.

Feng Yang, Yongyong Ren, Junpeng Zhang, Changli Wang, Meng Sun, Jin Li, Anqi Geng

Abstract readReview
PubMed Publisher
In one paragraph

Review in Reproductive sciences (Thousand Oaks, Calif.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Feng YangCollege of Pharmacy, Shaanxi University of Chinese Medicine, Xian, 712046, China.
Yongyong RenCollege of Pharmacy, Shaanxi University of Chinese Medicine, Xian, 712046, China.
Junpeng ZhangSanhang Institute for Brain Science and Technology, Institute of Medical Research, Northwestern Polytechnical University, Xian, 710072, China.
Changli WangShaanxi Haitian Pharmaceutical Co., Ltd, Xian, 712000, China.
Meng SunCollege of Pharmacy, Shaanxi University of Chinese Medicine, Xian, 712046, China.
Jin LiCollege of Pharmacy, Shaanxi University of Chinese Medicine, Xian, 712046, China. 2051014@sntcm.edu.cn.ORCID 0009-0007-9044-5829
Anqi GengSanhang Institute for Brain Science and Technology, Institute of Medical Research, Northwestern Polytechnical University, Xian, 710072, China. anqi@nwpu.edu.cn.

Funding

Innovation Consortium Technology Research Cluster Project 23CXLHTJS-GG0004-2023Key Research and Development Program of Shaanxi 2024SF-YBXM-050Key Research and Development Program of Shaanxi Province 2024SF-GJHX-14Key Research and Development Projects of Shaanxi Province 2024SF-YBXM-492Shaanxi Provincial Natural Science Basic Research Program 2024JC-YBMS-647Shenzhen Science and Technology Program JCYJ20220530161604009Xi 'an Science and Technology Program 2024JH-XTHG-0026
6 · The paper itself

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.

Indexed as

AsthenozoospermiaDisease Models, AnimalOligospermiaAnimalsHumansMaleSpermatogenesisChemical-induced modelsLaboratory animal modelsMale infertilityOligoasthenozoospermiaSpermatogenesis

Identifiers

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.