مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

video

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

sound

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Persian Version

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

View:

80
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Download:

86
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Cites:

Information Journal Paper

Title

Curcumin inhibits APOE4-induced injury by activating peroxisome proliferator-activated receptor-γ (PPARγ ) in SH-SY5Y cells

Pages

  1576-1583

Abstract

 Objective(s): The human Apolipoprotein E4 (APOE4) is associated with various brain injuries and neurodegenerative changes. Curcumin is an active ingredient isolated from the root of turmeric and is believed to have therapeutic effects on neurodegenerative diseases. The aim of this study was to investigate the effects of Curcumin on APOE4-induced neurological damage and explore its molecular mechanisms. Materials and Methods: SH-SY5Y cells were pretreated with Curcumin for 24 hr and transfected with human APOE4 gene using Lipofectamine 2000. Then, the effect of Curcumin on the transfected cells was detected by ELISA, immunofluorescence staining and Western blot. Results: The production or expression of proinflammatory cytokines and proteins, including tumor necrosis factor-α (TNF-α ), interleukin-1β (IL-1β ), nitric oxide (NO), inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) was significantly increased in SH-SY5Y cells transfected with APOE4, and Curcumin inhibited APOE4-induced cellular inflammatory damage. Western blot analysis showed that, after transfection with APOE4, the expression of total nuclear factor kappa B (NF-κ B) p65 and p-NF-κ B p65 in the nucleus was increased, and Curcumin inhibited the nuclear translocation of p65. The overexpression of APOE4 inhibited the expression of peroxisome proliferator-activated receptor-γ (PPARγ ), whereas Curcumin reversed and increased the expression of PPARγ protein. Down-regulating PPAR-γ with the inhibitor GW9662 and the shPPARγ gene confirmed that the NF-κ B signaling pathway was inhibited by PPARγ . Conclusion: This study suggests that APOE4 overexpression can induce cellular inflammatory damage, and pretreatment of Curcumin could exert an anti-inflammatory effect by upregulating the expression of PPARγ to inhibit the activation of NF-κ B signaling pathway.

Cites

  • No record.
  • References

  • No record.
  • Cite

    APA: Copy

    WANG, MINGHUI, Kou, Jiejian, Wang, Chunli, Yu, Xiuying, Xie, Xinmei, & Pang, Xiaobin. (2020). Curcumin inhibits APOE4-induced injury by activating peroxisome proliferator-activated receptor-γ (PPARγ ) in SH-SY5Y cells. IRANIAN JOURNAL OF BASIC MEDICAL SCIENCES, 23(12), 1576-1583. SID. https://sid.ir/paper/674841/en

    Vancouver: Copy

    WANG MINGHUI, Kou Jiejian, Wang Chunli, Yu Xiuying, Xie Xinmei, Pang Xiaobin. Curcumin inhibits APOE4-induced injury by activating peroxisome proliferator-activated receptor-γ (PPARγ ) in SH-SY5Y cells. IRANIAN JOURNAL OF BASIC MEDICAL SCIENCES[Internet]. 2020;23(12):1576-1583. Available from: https://sid.ir/paper/674841/en

    IEEE: Copy

    MINGHUI WANG, Jiejian Kou, Chunli Wang, Xiuying Yu, Xinmei Xie, and Xiaobin Pang, “Curcumin inhibits APOE4-induced injury by activating peroxisome proliferator-activated receptor-γ (PPARγ ) in SH-SY5Y cells,” IRANIAN JOURNAL OF BASIC MEDICAL SCIENCES, vol. 23, no. 12, pp. 1576–1583, 2020, [Online]. Available: https://sid.ir/paper/674841/en

    Related Journal Papers

  • No record.
  • Related Seminar Papers

  • No record.
  • Related Plans

  • No record.
  • Recommended Workshops






    Move to top
    telegram sharing button
    whatsapp sharing button
    linkedin sharing button
    twitter sharing button
    email sharing button
    email sharing button
    email sharing button
    sharethis sharing button