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Article

Expression of NR1 and apoptosis levels in the hippocampal cells of mice treated with MK‑801

  • Authors:
    • Juan Ding
    • Hui‑Hui Zhou
    • Quan‑Rui Ma
    • Zhong‑Yi He
    • Jiang‑Bo Ma
    • Yin‑Ming Liu
    • Yi‑Wei Zhang
    • Yu‑Qing He
    • Juan Liu
  • View Affiliations / Copyright

    Affiliations: Ningxia Key Laboratory of Cerebrocranial Diseases, School of Basic Medical Sciences, Ningxia Medical University, Yinchuan, Ningxia 750004, P.R. China
  • Pages: 8359-8364
    |
    Published online on: September 29, 2017
       https://doi.org/10.3892/mmr.2017.7674
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Abstract

The aim of the present study was to investigate the characteristics of N‑methyl‑D‑aspartate receptor R1 (NR1) expression and apoptosis in the nerve cells of the hippocampus in schizophrenia‑like mice. C57BL/6 mice were randomly allocated to the following groups: i) Blank group; ii) MK‑801 group; iii) MK‑801+NMDA group, according to body weight. The NMDAR antagonist, MK‑801 (0.6 mg/kg/d) was intraperitoneally injected daily for 14 days to induce a schizophrenia‑like phenotype mouse model, and the effect of the NMDA injection via the lateral ventricle was observed. The results demonstrated that the number of NR1 positive cells in the MK‑801 group increased in the CA1 and DG regions, indicating that NMDA may reverse this change. The level of damage decreased in the MK‑801 treated group when compared with the blank group in the CA3 region. The protein expression of NR1 increased however, at the mRNA expression level, NR1 was lower in the MK‑801 treated group when compared to the blank group; NMDA also reversed this change. In addition, early and total apoptosis detected in the hippocampal nerve cells was significantly increased in the MK‑801 group when compared with the blank group, which was reversible following treatment with NMDA. These results indicated that NMDA may regulate the expression of NR1 and suppress apoptosis in hippocampal nerve cells in schizophrenia‑like mice. Thus, NR1 may be a promising therapeutic target for the treatment of schizophrenia.
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Copy and paste a formatted citation
Spandidos Publications style
Ding J, Zhou HH, Ma QR, He ZY, Ma JB, Liu YM, Zhang YW, He YQ and Liu J: Expression of NR1 and apoptosis levels in the hippocampal cells of mice treated with MK‑801. Mol Med Rep 16: 8359-8364, 2017.
APA
Ding, J., Zhou, H., Ma, Q., He, Z., Ma, J., Liu, Y. ... Liu, J. (2017). Expression of NR1 and apoptosis levels in the hippocampal cells of mice treated with MK‑801. Molecular Medicine Reports, 16, 8359-8364. https://doi.org/10.3892/mmr.2017.7674
MLA
Ding, J., Zhou, H., Ma, Q., He, Z., Ma, J., Liu, Y., Zhang, Y., He, Y., Liu, J."Expression of NR1 and apoptosis levels in the hippocampal cells of mice treated with MK‑801". Molecular Medicine Reports 16.6 (2017): 8359-8364.
Chicago
Ding, J., Zhou, H., Ma, Q., He, Z., Ma, J., Liu, Y., Zhang, Y., He, Y., Liu, J."Expression of NR1 and apoptosis levels in the hippocampal cells of mice treated with MK‑801". Molecular Medicine Reports 16, no. 6 (2017): 8359-8364. https://doi.org/10.3892/mmr.2017.7674
Copy and paste a formatted citation
x
Spandidos Publications style
Ding J, Zhou HH, Ma QR, He ZY, Ma JB, Liu YM, Zhang YW, He YQ and Liu J: Expression of NR1 and apoptosis levels in the hippocampal cells of mice treated with MK‑801. Mol Med Rep 16: 8359-8364, 2017.
APA
Ding, J., Zhou, H., Ma, Q., He, Z., Ma, J., Liu, Y. ... Liu, J. (2017). Expression of NR1 and apoptosis levels in the hippocampal cells of mice treated with MK‑801. Molecular Medicine Reports, 16, 8359-8364. https://doi.org/10.3892/mmr.2017.7674
MLA
Ding, J., Zhou, H., Ma, Q., He, Z., Ma, J., Liu, Y., Zhang, Y., He, Y., Liu, J."Expression of NR1 and apoptosis levels in the hippocampal cells of mice treated with MK‑801". Molecular Medicine Reports 16.6 (2017): 8359-8364.
Chicago
Ding, J., Zhou, H., Ma, Q., He, Z., Ma, J., Liu, Y., Zhang, Y., He, Y., Liu, J."Expression of NR1 and apoptosis levels in the hippocampal cells of mice treated with MK‑801". Molecular Medicine Reports 16, no. 6 (2017): 8359-8364. https://doi.org/10.3892/mmr.2017.7674
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