Upregulation of Pro-inflammatory Cytokine Expression Following Chronic Paracetamol Treatment in Astrocyte

Neurotox Res. 2018 Jul;34(1):137-146. doi: 10.1007/s12640-018-9875-5. Epub 2018 Feb 14.

Abstract

The present study aimed to investigate the effect of APAP treatment on the expression of pro-inflammatory cytokines in the astrocytes. The mouse astrocyte cells (C8-D1A) were treated with APAP at the concentration of 100 μM for 24 h, 16 and 28 days. The expressions of pro-inflammatory cytokines and NF-kB were determined using western blot analysis. Furthermore, the expression and localization of phosphorylation of NF-kB were detected by immunohistochemical and immunofluorescent analysis. The ultrastructure of C8-D1A cells was as well monitored. The results revealed that acute APAP treatment (24 h) had no effect on the expression of pro-inflammatory cytokines and pNF-kB. This treatment did not alter the ultrastructure of C8-D1A cells when compared with those in the control cells. However, the results obtained from the study on chronic APAP-treated cells (16 and 28 days) showed the different effect of APAP treatment. The results obtained from western blot analysis showed the increment of pro-inflammatory cytokine (IL-1β and TNF-α) expressions and the activation of NF-kB signaling pathway. Nuclear translocation of pNF-kB and alteration of several cell structures were well observed in the C8-D1A cells with chronic APAP treatment. The results obtained from this study suggest that chronic APAP treatment can induce an upregulation of pro-inflammatory cytokines (IL-1β and TNFα) in astrocytes. This alteration implies the involvement of the activation of NF-kB signaling pathway.

Keywords: Astrocyte; NF-kB signaling; Paracetamol; Pro-inflammatory cytokines; Ultrastructure.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetaminophen / pharmacology*
  • Analgesics, Non-Narcotic / pharmacology*
  • Animals
  • Astrocytes / drug effects*
  • Astrocytes / ultrastructure
  • Cell Line, Transformed
  • Dose-Response Relationship, Drug
  • Interleukin-1beta / metabolism*
  • Mice
  • NF-kappa B / metabolism
  • Time Factors
  • Tumor Necrosis Factor-alpha / metabolism*
  • Up-Regulation / drug effects*

Substances

  • Analgesics, Non-Narcotic
  • IL1B protein, mouse
  • Interleukin-1beta
  • NF-kappa B
  • Tumor Necrosis Factor-alpha
  • Acetaminophen