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Article

Alterations in cyclin D1 and cyclin‑dependent kinase 4 expression in the amygdalae of post‑traumatic stress disorder rats

  • Authors:
    • Ming Cong
    • Lili Wen
    • Fang Han
    • Yanhao Xu
    • Yuxiu Shi
  • View Affiliations / Copyright

    Affiliations: PTSD Laboratory, Department of Histology and Embryology, China Medical University, Shenyang, Liaoning 110122, P.R. China
  • Pages: 8351-8358
    |
    Published online on: September 26, 2017
       https://doi.org/10.3892/mmr.2017.7613
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Abstract

The amygdalae are an important component of the human limbic system and exhibit a key role in emotional and behavioral reactions. Previous studies have demonstrated abnormal function and morphology in the amygdalae of post‑traumatic stress disorder (PTSD)‑like animal models, however the underlying molecular mechanisms remain elusive. The authors have previously demonstrated that PTSD induced increased apoptosis in the amygdala of PTSD‑like animals. Cyclin D1 and cyclin‑dependent kinase 4 (CDK4) are two important regulators of the cell cycle. The study explored the expression of cyclin D1 and CDK4 in the amygdala in PTSD. The single‑prolonged stress (SPS) rat model was used as a PTSD‑like model. Ultrastructural alterations of cells in the amygdala were observed using transmission electron microscopy (TEM). 4',6‑Diamidino‑2‑phenylindole (DAPI) fluorescence was employed to detect nuclear pycnosis. Cyclin D1 and CDK4 expression in the amygdala cells was examined using immunofluorescence, Western blotting and reverse transcription‑quantitative polymerase chain reaction. TEM revealed morphological alterations to the amygdala cells of the SPS rats. DAPI‑stained nuclear brightness levels differed between the control and SPS groups. Expression of cyclin D1 and CDK4 in the amygdala increased gradually 1 day and 4 days following SPS stimulation, and peaked 7 days following SPS stimulation at the protein and mRNA levels, in comparison with the control rats. These findings suggest that SPS resulted in increased cyclin D1 and CDK4 expression, which may accelerate cell apoptosis. This may be associated with SPS‑induced abnormal function and structure of the amygdala.
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Copy and paste a formatted citation
Spandidos Publications style
Cong M, Wen L, Han F, Xu Y and Shi Y: Alterations in cyclin D1 and cyclin‑dependent kinase 4 expression in the amygdalae of post‑traumatic stress disorder rats. Mol Med Rep 16: 8351-8358, 2017.
APA
Cong, M., Wen, L., Han, F., Xu, Y., & Shi, Y. (2017). Alterations in cyclin D1 and cyclin‑dependent kinase 4 expression in the amygdalae of post‑traumatic stress disorder rats. Molecular Medicine Reports, 16, 8351-8358. https://doi.org/10.3892/mmr.2017.7613
MLA
Cong, M., Wen, L., Han, F., Xu, Y., Shi, Y."Alterations in cyclin D1 and cyclin‑dependent kinase 4 expression in the amygdalae of post‑traumatic stress disorder rats". Molecular Medicine Reports 16.6 (2017): 8351-8358.
Chicago
Cong, M., Wen, L., Han, F., Xu, Y., Shi, Y."Alterations in cyclin D1 and cyclin‑dependent kinase 4 expression in the amygdalae of post‑traumatic stress disorder rats". Molecular Medicine Reports 16, no. 6 (2017): 8351-8358. https://doi.org/10.3892/mmr.2017.7613
Copy and paste a formatted citation
x
Spandidos Publications style
Cong M, Wen L, Han F, Xu Y and Shi Y: Alterations in cyclin D1 and cyclin‑dependent kinase 4 expression in the amygdalae of post‑traumatic stress disorder rats. Mol Med Rep 16: 8351-8358, 2017.
APA
Cong, M., Wen, L., Han, F., Xu, Y., & Shi, Y. (2017). Alterations in cyclin D1 and cyclin‑dependent kinase 4 expression in the amygdalae of post‑traumatic stress disorder rats. Molecular Medicine Reports, 16, 8351-8358. https://doi.org/10.3892/mmr.2017.7613
MLA
Cong, M., Wen, L., Han, F., Xu, Y., Shi, Y."Alterations in cyclin D1 and cyclin‑dependent kinase 4 expression in the amygdalae of post‑traumatic stress disorder rats". Molecular Medicine Reports 16.6 (2017): 8351-8358.
Chicago
Cong, M., Wen, L., Han, F., Xu, Y., Shi, Y."Alterations in cyclin D1 and cyclin‑dependent kinase 4 expression in the amygdalae of post‑traumatic stress disorder rats". Molecular Medicine Reports 16, no. 6 (2017): 8351-8358. https://doi.org/10.3892/mmr.2017.7613
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