Back

Distinct HPO axis responses and ovarian aging trajectories to chronic unpredictable mild stress in reproductively young versus middle-aged female mice

Yang, T.; Zhang, S.; Liu, D.; LI, L.; Zhou, K.; Han, Y.; Wang, J.; Zhang, H.; Ma, Y.; Liu, S.; Ma, B.; Jin, F.; Li, J.; Wang, Y.; Hu, Z.

2026-04-28 physiology
10.64898/2026.04.24.720585 bioRxiv
Show abstract

Psychosocial stressors are key contributors to ovarian functional decline. Chronic unpredictable mild stress (CUMS) is widely used to model stress-induced premature ovarian insufficiency (POI) in mice; however, current animal models do not adequately reflect middle-aged women, who represent a key population exposed to chronic psychosocial stress, nor do they capture the dynamic progression toward POI. Here, female C57BL/6 mice aged 2 or 6 months were subjected to CUMS for 8 or 12 weeks. Estrous cyclicity, endocrine profiles, ovarian histology, and transcriptomic changes in HPO axis-related tissues were systematically analyzed. After 8 weeks of exposure, 2-month-old mice exhibited impaired pituitary responsiveness to estradiol negative feedback, as evidenced by dysregulated FSH secretion, indicating reduced stress tolerance compared with 6-month-old mice. Following 12 weeks of CUMS exposure, both age groups showed significant reductions in ovarian size and follicle numbers across all developmental stages. These findings demonstrate that CUMS induces an age-dependent progression toward POI, with short-term exposure eliciting compensatory phases preceding overt ovarian insufficiency, accompanied by distinct endocrine and reproductive alterations and differential responsiveness of the HPO axis. Transcriptomic analyses revealed age-dependent stress responses: ovaries of 2-month-old mice displayed marked activation of inflammatory and immune-related pathways, whereas 6-month-old mice showed sustained upregulation of protein kinase-related signaling networks. Notably, the 6-month-old CUMS model more closely recapitulates stress-associated reproductive aging in adult women. In briefCUMS has been widely used to establish mouse models of psychosocial stress-induced POI. However, current animal models do not adequately reflect middle-aged women, who represent a key population exposed to chronic psychosocial stress, nor do they capture the dynamic progression toward premature ovarian insufficiency (POI). In this study, we demonstrate that different durations of CUMS exposure induce distinct stages of ovarian dysfunction in both young and middle-aged mice, with short-term exposure driving age-dependent compensatory phases and prolonged exposure leading to overt POI, both accompanied by divergent endocrine and reproductive alterations, alongside age-dependent changes in HPO axis responsiveness to CUMS. Notably, the 6-month-old CUMS model shows greater clinical relevance in recapitulating chronic psychosocial stress and stress-related reproductive aging in adult women.

Matching journals

The top 9 journals account for 50% of the predicted probability mass.

1
Endocrinology
38 papers in training set
Top 0.1%
18.9%
2
Aging Cell
144 papers in training set
Top 0.8%
8.3%
3
The Journal of Clinical Endocrinology & Metabolism
35 papers in training set
Top 0.3%
4.0%
4
Cell Reports
1338 papers in training set
Top 13%
4.0%
5
Aging
69 papers in training set
Top 0.6%
3.7%
6
GeroScience
97 papers in training set
Top 0.5%
3.6%
7
Biology of Sex Differences
29 papers in training set
Top 0.1%
3.1%
8
Human Reproduction
18 papers in training set
Top 0.2%
2.9%
9
Scientific Reports
3102 papers in training set
Top 42%
2.9%
50% of probability mass above
10
Reproduction
11 papers in training set
Top 0.1%
2.8%
11
eLife
5422 papers in training set
Top 31%
2.8%
12
Neurobiology of Stress
42 papers in training set
Top 0.2%
2.1%
13
Frontiers in Cell and Developmental Biology
218 papers in training set
Top 3%
1.9%
14
iScience
1063 papers in training set
Top 13%
1.8%
15
Frontiers in Physiology
93 papers in training set
Top 3%
1.7%
16
PLOS ONE
4510 papers in training set
Top 53%
1.7%
17
The FASEB Journal
175 papers in training set
Top 1%
1.7%
18
American Journal of Physiology-Heart and Circulatory Physiology
32 papers in training set
Top 0.6%
1.7%
19
The Journals of Gerontology: Series A
25 papers in training set
Top 0.6%
1.3%
20
Disease Models & Mechanisms
119 papers in training set
Top 2%
1.2%
21
JCI Insight
241 papers in training set
Top 5%
1.1%
22
The Journals of Gerontology, Series A: Biological Sciences and Medical Sciences
22 papers in training set
Top 0.3%
1.1%
23
Journal of the Endocrine Society
11 papers in training set
Top 0.2%
0.9%
24
PNAS Nexus
147 papers in training set
Top 1%
0.9%
25
Molecular Psychiatry
242 papers in training set
Top 3%
0.9%
26
International Journal of Molecular Sciences
453 papers in training set
Top 12%
0.9%
27
Nature Communications
4913 papers in training set
Top 60%
0.9%
28
Cells
232 papers in training set
Top 5%
0.8%
29
Neurobiology of Aging
95 papers in training set
Top 2%
0.8%
30
Science Advances
1098 papers in training set
Top 30%
0.8%