Effect of ferric citrate on hippocampal iron accumulation and widespread molecular alterations associated with cognitive disorder in an ovariectomized mice model
- Lingling Cui 1, Huijun Zhou 1, Yudan Hao 1, Xiaoli Yang 1, Zhiqian Li 1, Yuting Gao 1, Zhengya Zhang 1, Lina Ren 1, Linpu Ji 1, Ruijie Sun 1, Yibo Wang 1, Xian Wang 1
- Lingling Cui 1, Huijun Zhou 1, Yudan Hao 1
- 1College of Public Health, Zhengzhou University, Zhengzhou, Henan, China.
- 0College of Public Health, Zhengzhou University, Zhengzhou, Henan, China.
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View abstract on PubMed
Summary
This summary is machine-generated.Iron accumulation in ovariectomized mice impairs cognitive function and causes hippocampal damage. This study reveals iron metabolism protein alterations, providing insights into postmenopausal cognitive decline.
Area Of Science
- Neuroscience
- Endocrinology
- Toxicology
Background
- Cognitive impairment is increasingly prevalent in women, particularly postmenopause.
- Limited research exists on the neurotoxic mechanisms of iron exposure in postmenopausal women.
- Ovariectomy in mice serves as a model for postmenopausal changes.
Purpose Of The Study
- To investigate the impact of iron accumulation on cognitive function in ovariectomized mice.
- To elucidate the underlying mechanisms of iron-induced neurotoxicity in this model.
- To provide a scientific basis for preventing cognitive dysfunction in postmenopausal women.
Main Methods
- Ovariectomized (Ovx) mice were administered ferric citrate (FAC) at varying doses.
- Cognitive and motor functions were assessed using behavioral tests.
- Serum iron parameters, oxidative stress markers, hippocampal ultrastructure, and proteomic profiles were analyzed.
Main Results
- Iron exposure significantly decreased motor and cognitive function in Ovx mice.
- Histopathological changes were observed in the hippocampus following iron exposure.
- Proteomic analysis revealed differential expression of hippocampal proteins, including increased transferrin receptor protein 1 (TFR1) and divalent metal transporter 1 (DMT1).
Conclusions
- Iron exposure induces histopathological damage in the hippocampus of ovariectomized mice.
- Altered hippocampal proteomics, particularly iron metabolism proteins, contributes to cognitive impairment.
- Findings suggest a link between iron accumulation and postmenopausal cognitive dysfunction.
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