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CJAP ›› 2022, Vol. 38 ›› Issue (5): 480-484.doi: 10.12047/j.cjap.6269.2022.090

• ORIGINAL ARTICLES • Previous Articles     Next Articles

Effects of Butylphthalide on the expressions of HMGB1 and RAGE in frontal lobe of rats after chronic sleep deprivation

YANG Ying-xia1, GUO Yu-fen2, HUANG Hong-hong1, WANG Ling-xing1△   

  1. 1. Department of Neurology, Second Affiliated Hospital of Fujian Medical University, Quanzhou 362000;
    2. Department of Health Education, XiamenHuli District Maternity and Child Care Hospital, Xiamen 361000, China
  • Received:2022-02-14 Revised:2022-08-14 Online:2022-09-28 Published:2023-04-23

Abstract: Objective: To investigate the effects of Butylphthalide on the expressions of HMGB1 and RAGE in frontal lobe of rats after chronic sleep deprivation. Methods: Chronic sleep deprivation and butylphthalide treatment was performed in Sprague Dawley(SD)rats and the rats were divided into three groups (n=6): platform control group, chronic sleep deprivation group and chronic sleep deprivation + butylphthalide intervention group. Rats suffering chronic sleep deprivation were put in multiple platforms box for 18 h per day and sleep deprivation lasted for 28 days. Rats in butylphthalide intervention group were intraperitoneally injected with butylphthalide 100 mg/(kg·d) for 14 days after sleep deprivation. After collecting brains, high-mobility group box (HMGB1) and nuclear transcription factor kappB (NF-κB)p65 were detected by immunohistochemistry. The expression of HMGB1, silent information regulator of transcription 1 (SIRT1), receptor for advanced glycation end-products (RAGE) and NF-κB in frontal lobe were determinated by Western blot. Results: Compared with platform control group, the expression levels of HMGB1, RAGE and nuclear NF-κB p65 were increased significantly, while the expression of SIRT1 was decreased siginificantly in frontal lobe of chronic sleep deprivation group (all P<0.05). Compared with chronic sleep deprivation group, the expression levels of of HMGB1, RAGE and nuclear NF-κB p65 were decreased significantly, while the expression of SIRT1 was increased significantly in chronic sleep deprivation + butylphthalide intervention group (all P<0.05). Conclusion: Butylphthalide can inhibit HMGB1/RAGE/NF-κB pathway in frontal lobe of rats after chronic sleep deprivation by changing the expression of HMGB1 and RAGE, and reducing the nuclear translocation of NF-κBp65.

Key words: chronic sleep deprivation, butylphthalide, HMGB1, RAGE, rats

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