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Grape Seed Proanthocyanidin Extract Adjusts NeuN/GFAP in a Murine Model of Neonatal Hypoxic-ischemic Brain Injury

Received: 20 March 2019    Accepted: 22 April 2019    Published: 10 May 2019
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Abstract

Objective: To investigate the neuroprotective effects of grape seed proanthocyanidin extract(GSPE)on a model of neonatal hypoxic ischemic encephalopathy (HIE), we investigated the changes in neuronal cells and astrocytes after pre-treatment with GSPE. Methods: Seven-day-old pups were randomly divided into sham, HI, and GSPE+HI groups. The HIE model was established using a modified Rice-Vannucci method. GSPE was injected intraperitoneally 20 min before surgery. The change in markers of neuronal cells and astrocytes (NeuN/GFAP) were detected by immunofluorescence and Western blot. Results: Compared with the sham group, the expression of NeuN in the HI group was significantly reduced, and the expression of NeuN was significantly increased after GSPE pre-treatment. The expression of GFAP was opposite to NeuN. Conclusion: Our study showed that GSPE pre-treatment significantly protected neurons and inhibited astrocyte over-proliferation. Therefore, we believe that GSPE is a potential drug for the treatment of HIE and can prevent brain damage caused by hypoxia and ischemia.

Published in American Journal of Pediatrics (Volume 5, Issue 2)
DOI 10.11648/j.ajp.20190502.13
Page(s) 51-55
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This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2024. Published by Science Publishing Group

Keywords

Grape Seed Proanthocyanidin Extract, NeuN, GFAP, Neonatal Hypoxic-Ischemic Brain Injury

References
[1] Liu G, Li Z G, Gao J S. Hypothermia in neonatal hypoxic-ischemic encephalopathy (HIE) [J]. Euro Review Medi Pharmacological Sci, 2017, 21: 50-53.
[2] Rao R, Trivedi S, Distler A, et al. Neurodevelopmental Outcomes in Neonates with Mild Hypoxic Ischemic Encephalopathy Treated with Therapeutic Hypothermia [J]. Am J Perinatol, 2019.
[3] Zhou X M, Liu J, Wang Y, et al. Silencing of long noncoding RNA MEG3 enhances cerebral protection of dexmedetomidine against hypoxic-ischemic brain damage in neonatal mice by binding to miR-129-5p [J]. J Cell Biochem, 2018.
[4] Xu B, Xiao A J, Chen W, et al. Neuroprotective effects of a PSD-95 inhibitor in neonatal hypoxic-ischemic brain injury [J]. Molecular Neurobi, 2016, 53: 5962-5970.
[5] Luo Z, Zhang M, Niu X, et al. Inhibition of the PI3K/Akt signaling pathway impedes the restoration of neurological function following hypoxic-ischemic brain damage in a neonatal rabbit model [J]. J Cell Biochem, 2019.
[6] Devi A, Jolitha A B, Ishii N. Grape Seed Proanthocyanidin Extract (GSPE) and antioxidant defense in the brain of adult rats [J]. Medi Sci Mo, 2006, 12: BR124-BR129.
[7] Liu B, Zhang H, Tan X, et al. GSPE reduces lead-induced oxidative stress by activating the Nrf2 pathway and suppressing miR153 and GSK-3β in rat kidney [J]. Oncotarget, 2017, 8: 42226-42237.
[8] Rajput S, Sun L, Zhang N Y, et al. Grape Seed Proanthocyanidin Extract Alleviates AflatoxinB1-Induced Immunotoxicity and Oxidative Stress via Modulation of NF-κB and Nrf2 Signaling Pathways in Broilers [J]. Toxins, 2019, 11: 23.
[9] Guo F, Hu Y, Niu Q, et al. Grape Seed Proanthocyanidin Extract Inhibits Human Esophageal Squamous Cancerous Cell Line ECA109 via the NF-κB Signaling Pathway [J]. Mediators Inflamm, 2018, 22: 6999-7012.
[10] Hao J P, Shi H, Zhang J, et al. Role of GSPE in improving early cerebral vascular damage by inhibition of Profilin-1 expression in a ouabain-induced hypertension model [J]. Euro Review Medi Pharmacol Sci, 2018, 22: 6999-7012.
[11] Sanna R S, Muthangi S, BK C S, et al. Grape seed proanthocyanidin extract and insulin prevents cognitive decline in type 1 diabetic rat by impacting Bcl-2 and Bax in the prefrontal cortex [J]. Metab Brain Dis, 2018: 1-15.
[12] Fang M, Jiang H, Ye L, et al. Metformin treatment after the hypoxia-ischemia attenuates brain injury in newborn rats [J]. Oncotarget, 2017, 8: 75308-75325.
[13] Al Mamun A, Yu H, Romana S, et al. Inflammatory Responses are Sex Specific in Chronic Hypoxic–Ischemic Encephalopathy [J]. Cell Trans, 2018.
[14] Ye L, Feng Z, Doycheva D, et al. CpG-ODN exerts a neuroprotective effect via the TLR9/pAMPK signaling pathway by activation of autophagy in a neonatal HIE rat model [J]. Experi Neuro, 2018, 301: 70-80.
[15] Jiang W, Guo M, Gong M, et al. Vitamin A bio-modulates apoptosis via the mitochondrial pathway after hypoxic-ischemic brain damage [J]. Mole Brain, 2018, 11: 14.
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Cite This Article
  • APA Style

    Li Luo, Xing Tu, Xuexia Zhang, Jing Liu, Yilin Liu, et al. (2019). Grape Seed Proanthocyanidin Extract Adjusts NeuN/GFAP in a Murine Model of Neonatal Hypoxic-ischemic Brain Injury. American Journal of Pediatrics, 5(2), 51-55. https://doi.org/10.11648/j.ajp.20190502.13

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    ACS Style

    Li Luo; Xing Tu; Xuexia Zhang; Jing Liu; Yilin Liu, et al. Grape Seed Proanthocyanidin Extract Adjusts NeuN/GFAP in a Murine Model of Neonatal Hypoxic-ischemic Brain Injury. Am. J. Pediatr. 2019, 5(2), 51-55. doi: 10.11648/j.ajp.20190502.13

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    AMA Style

    Li Luo, Xing Tu, Xuexia Zhang, Jing Liu, Yilin Liu, et al. Grape Seed Proanthocyanidin Extract Adjusts NeuN/GFAP in a Murine Model of Neonatal Hypoxic-ischemic Brain Injury. Am J Pediatr. 2019;5(2):51-55. doi: 10.11648/j.ajp.20190502.13

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  • @article{10.11648/j.ajp.20190502.13,
      author = {Li Luo and Xing Tu and Xuexia Zhang and Jing Liu and Yilin Liu and Wenyan Zhao and Ke Niu and Junhua Yang and Guoying Li and Mengxia Wang},
      title = {Grape Seed Proanthocyanidin Extract Adjusts NeuN/GFAP in a Murine Model of Neonatal Hypoxic-ischemic Brain Injury},
      journal = {American Journal of Pediatrics},
      volume = {5},
      number = {2},
      pages = {51-55},
      doi = {10.11648/j.ajp.20190502.13},
      url = {https://doi.org/10.11648/j.ajp.20190502.13},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ajp.20190502.13},
      abstract = {Objective: To investigate the neuroprotective effects of grape seed proanthocyanidin extract(GSPE)on a model of neonatal hypoxic ischemic encephalopathy (HIE), we investigated the changes in neuronal cells and astrocytes after pre-treatment with GSPE. Methods: Seven-day-old pups were randomly divided into sham, HI, and GSPE+HI groups. The HIE model was established using a modified Rice-Vannucci method. GSPE was injected intraperitoneally 20 min before surgery. The change in markers of neuronal cells and astrocytes (NeuN/GFAP) were detected by immunofluorescence and Western blot. Results: Compared with the sham group, the expression of NeuN in the HI group was significantly reduced, and the expression of NeuN was significantly increased after GSPE pre-treatment. The expression of GFAP was opposite to NeuN. Conclusion: Our study showed that GSPE pre-treatment significantly protected neurons and inhibited astrocyte over-proliferation. Therefore, we believe that GSPE is a potential drug for the treatment of HIE and can prevent brain damage caused by hypoxia and ischemia.},
     year = {2019}
    }
    

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  • TY  - JOUR
    T1  - Grape Seed Proanthocyanidin Extract Adjusts NeuN/GFAP in a Murine Model of Neonatal Hypoxic-ischemic Brain Injury
    AU  - Li Luo
    AU  - Xing Tu
    AU  - Xuexia Zhang
    AU  - Jing Liu
    AU  - Yilin Liu
    AU  - Wenyan Zhao
    AU  - Ke Niu
    AU  - Junhua Yang
    AU  - Guoying Li
    AU  - Mengxia Wang
    Y1  - 2019/05/10
    PY  - 2019
    N1  - https://doi.org/10.11648/j.ajp.20190502.13
    DO  - 10.11648/j.ajp.20190502.13
    T2  - American Journal of Pediatrics
    JF  - American Journal of Pediatrics
    JO  - American Journal of Pediatrics
    SP  - 51
    EP  - 55
    PB  - Science Publishing Group
    SN  - 2472-0909
    UR  - https://doi.org/10.11648/j.ajp.20190502.13
    AB  - Objective: To investigate the neuroprotective effects of grape seed proanthocyanidin extract(GSPE)on a model of neonatal hypoxic ischemic encephalopathy (HIE), we investigated the changes in neuronal cells and astrocytes after pre-treatment with GSPE. Methods: Seven-day-old pups were randomly divided into sham, HI, and GSPE+HI groups. The HIE model was established using a modified Rice-Vannucci method. GSPE was injected intraperitoneally 20 min before surgery. The change in markers of neuronal cells and astrocytes (NeuN/GFAP) were detected by immunofluorescence and Western blot. Results: Compared with the sham group, the expression of NeuN in the HI group was significantly reduced, and the expression of NeuN was significantly increased after GSPE pre-treatment. The expression of GFAP was opposite to NeuN. Conclusion: Our study showed that GSPE pre-treatment significantly protected neurons and inhibited astrocyte over-proliferation. Therefore, we believe that GSPE is a potential drug for the treatment of HIE and can prevent brain damage caused by hypoxia and ischemia.
    VL  - 5
    IS  - 2
    ER  - 

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Author Information
  • School of Biosciences & Biopharmaceutics, Guangdong Pharmaceutical University, Guangzhou, People's Republic of China

  • School of Biosciences & Biopharmaceutics, Guangdong Pharmaceutical University, Guangzhou, People's Republic of China

  • Department of Anesthesiology, The Fifth Affiliated Hospital, Sun Yat-Sen University, Zhuhai, People's Republic of China

  • School of Biosciences & Biopharmaceutics, Guangdong Pharmaceutical University, Guangzhou, People's Republic of China

  • School of Clinical Medicine, The First Affiliated Hospital of Guangdong Pharmaceutical University, Guangzhou, People's Republic of China

  • School of Clinical Medicine, The First Affiliated Hospital of Guangdong Pharmaceutical University, Guangzhou, People's Republic of China

  • School of Clinical Medicine, The First Affiliated Hospital of Guangdong Pharmaceutical University, Guangzhou, People's Republic of China

  • School of Biosciences & Biopharmaceutics, Guangdong Pharmaceutical University, Guangzhou, People's Republic of China

  • School of Biosciences & Biopharmaceutics, Guangdong Pharmaceutical University, Guangzhou, People's Republic of China

  • Intensive Care Unit, Guangdong No. 2 Provincial People's Hospital, Guangzhou, People's Republic of China

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