Skip to main content

Advertisement

Log in

Ketamine inhibits LPS-induced calcium elevation and NF-kappa B activation in monocytes

  • Original Paper
  • Published:
Inflammation Research Aims and scope Submit manuscript

Abstract

Objective:To investigate whether ketamine could inhibit lipopolysaccharide (LPS)-induced intracellular calcium elevation and NF-kappa B activation in monocytes.

Materials and methods:Isolated rat monocytes were challenged with 10 μg/ml LPS with or without the presence of various concentrations of ketamine (10, 100, 1000 μM). Intracellular calcium was monitored by laser confocal microscopy. NF-kappa B activity of the nuclear extracts of monocytes was analyzed by electrophoretic mobility shift assay (EMSA).

Results:LPS provoked a significant calcium elevation and enhanced NF-kappa B activity in monocytes. Ketamine above concentration of 100 μM inhibited endotoxin-induced intracellular calcium elevation and NF-kappa B activity. Ketamine itself had no effect on either of them.

Conclusions:These findings suggest that ketamine could suppress NF-kappa B in monocytes exposed to endotoxin, and this anti-inflammatory effect might act through attenuating intracellular calcium elevation.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to J. G. Xu.

Additional information

Received 31 October 2003; returned for revision 18 December 2003; accepted by I. Ahnfelt-Rønne 26 Januaryy 2004

Rights and permissions

Reprints and permissions

About this article

Cite this article

Sun, J., Zhou, Z.Q., Lv, R. et al. Ketamine inhibits LPS-induced calcium elevation and NF-kappa B activation in monocytes. Inflamm. res. 53, 304–308 (2004). https://doi.org/10.1007/s00011-004-1262-4

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00011-004-1262-4

Navigation