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Updated: Apr 4, 2026

Using Chicken Embryo as a Powerful Tool in Assessment of Developmental Cardiotoxicities
Published on: March 21, 2021
Citalopram and sertraline exposure compromises embryonic bone development.
D Fraher1,2, J M Hodge2,3, F M Collier2
1Metabolic Genetic Diseases Laboratory, Metabolic Research Unit, School of Medicine, Deakin University, Geelong, VIC, Australia.
Selective serotonin reuptake inhibitors (SSRIs) may negatively impact fetal bone development. Studies show SSRIs can inhibit osteoblast activity and decrease bone mineralization in zebrafish and human cells.
Area of Science:
- Pharmacology
- Developmental Biology
- Orthopedics
Background:
- Selective serotonin reuptake inhibitors (SSRIs) are widely used for depression.
- Emerging evidence suggests potential risks of SSRI use during pregnancy, including birth defects.
- Serotonin receptors are present in bone cells, indicating a possible role in skeletal development.
Purpose of the Study:
- To investigate the effects of SSRI exposure on embryonic bone development.
- To determine if SSRIs impact osteoblast differentiation and activity.
Main Methods:
- Zebrafish embryos and human mesenchymal stem cells (MSCs) were treated with citalopram and sertraline.
- Bone mineralization was assessed using alizarin red staining.
- Osteoblast gene expression and apoptosis markers were analyzed via qRT-PCR.
Main Results:
- SSRI treatment in zebrafish led to decreased bone mineralization and reduced expression of mature osteoblast markers.
- In human MSCs, SSRIs decreased osteoblast activity and downregulated key osteoblast-specific genes (Runx2, Sparc, Spp1).
- No significant increase in apoptosis was observed in either model.
Conclusions:
- SSRIs appear to inhibit bone development by impairing osteoblast maturation during embryonic stages and MSC differentiation.
- These findings suggest potential risks of skeletal abnormalities in infants exposed to SSRIs in utero.
- Further research is warranted to fully understand SSRI risks during pregnancy.
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