# Animal models for the study of depressive disorder

**Authors:** Juhyun Song, Young‐Kook Kim

PMC · DOI: 10.1111/cns.13622 · CNS Neuroscience & Therapeutics · 2021-03-01

## TL;DR

This paper reviews animal models of depression to better understand the disorder and improve research methods.

## Contribution

The paper compares and analyzes various animal models of depression using transcriptomic profiles.

## Key findings

- Different animal models show distinct patterns of depressive behavior and pathology.
- Transcriptomic analysis helps in understanding the underlying mechanisms of depression.
- Comparing models is essential for selecting the most suitable ones for depression research.

## Abstract

Depressive disorder is one of the most widespread forms of psychiatric pathology, worldwide. According to a report by the World Health Organization, the number of people with depression, globally, is increasing dramatically with each year. Previous studies have demonstrated that various factors, including genetics and environmental stress, contribute to the risk of depression. As such, it is crucial to develop a detailed understanding of the pathogenesis of depressive disorder and animal studies are essential for identifying the mechanisms and genetic disorders underlying depression. Recently, many researchers have reported on the pathology of depression via various models of depressive disorder. Given that different animal models of depression show differences in terms of patterns of depressive behavior and pathology, the comparison between depressive animal models is necessary for progress in the field of the depression study. However, the various animal models of depression have not been fully compared or evaluated until now. In this paper, we reviewed the pathophysiology of the depressive disorder and its current animal models with the analysis of their transcriptomic profiles. We provide insights for selecting different animal models for the study of depression.

Experimental models for the study of depression.

## Linked entities

- **Diseases:** depressive disorder (MONDO:0002050), depression (MONDO:0002050)

## Full-text entities

- **Genes:** Gprin1 (G protein-regulated inducer of neurite outgrowth 1) [NCBI Gene 26913] {aka Z16}, Sparc (secreted acidic cysteine rich glycoprotein) [NCBI Gene 20692] {aka BM-40, ON}, Tipin (timeless interacting protein) [NCBI Gene 66131] {aka 1110005A05Rik, 1110018P21Rik}, IFT25 (intraflagellar transport 25) [NCBI Gene 51668] {aka C1orf41, CFAP232, FAP232, HSPB11, HSPCO34, PP25}, Ythdf2 (YTH N6-methyladenosine RNA binding protein 2) [NCBI Gene 213541] {aka 9430020E02Rik, HGRG8, NY-REN-2}, Atp5mc1 (ATP synthase membrane subunit c locus 1) [NCBI Gene 11951] {aka Atp5g1}, Npas4 (neuronal PAS domain protein 4) [NCBI Gene 225872] {aka LE-PAS, Nxf}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, Xbp1 (X-box binding protein 1) [NCBI Gene 22433] {aka D11Ertd39e, TREB-5, TREB5, XBP-1}
- **Diseases:** Chronic social defeat (MESH:D002908), social stress (MESH:D000079225), neuropsychiatric features (MESH:C564678), chronic pain (MESH:D059350), traumatic stress (MESH:D040921), and nociceptive pain (MESH:D059226), inflammation (MESH:D007249), anhedonia (MESH:D059445), aggressive (MESH:D010554), appetite pattern change (MESH:D001068), fatigue (MESH:D005221), PUBLICATION (MESH:C000719203), pain (MESH:D010146), anxiety (MESH:D001007), Sleep disturbance (MESH:D012893), loss of pleasure (MESH:D016388), Major depressive disorder (MESH:D003865), Depressive disorder (MESH:D003866), insomnia (MESH:D007319), Neuropathic and nociceptive pain (MESH:D009437), nerve injury (MESH:D000080902), genetic disorders (MESH:D030342), neuroinflammation (MESH:D000090862), Synaptic dysfunction (MESH:C536122), memory deficits (MESH:D008569), continuous involuntary movement (MESH:D014202), behavior motor retardation (MESH:D001523), psychomotor retardation (MESH:D011596), neuronal disorders (MESH:D009410), ANIMAL MODELS (MESH:D004195), Learned helplessness (MESH:D007859)
- **Chemicals:** reactive oxygen species (MESH:D017382), lipid (MESH:D008055), saccharin (MESH:D012439), corticosterone (MESH:D003345), sucrose (MESH:D013395), norepinephrine (MESH:D009638), GABA (MESH:D005680), cortisol (MESH:D006854), Congener (-), Dopamine (MESH:D004298), Serotonin (MESH:D012701), Glu (MESH:D018698)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** S2 — Drosophila melanogaster (Fruit fly), Spontaneously immortalized cell line (CVCL_Z232)

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC8111503/full.md

## References

117 references — full list in the complete paper: https://tomesphere.com/paper/PMC8111503/full.md

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Source: https://tomesphere.com/paper/PMC8111503