4.5 Article

Ifenprodil restores GDNF-evoked Ca2+ signalling and Na+/K+-ATPase expression in inflammation-pretreated astrocytes

Journal

JOURNAL OF NEUROCHEMISTRY
Volume 119, Issue 4, Pages 686-696

Publisher

WILEY-BLACKWELL
DOI: 10.1111/j.1471-4159.2011.07465.x

Keywords

astrocyte; calcium; GDNF; ifenprodil; IL-1 beta; NMDA

Funding

  1. Swedish Research Council [33X-06812]
  2. Edit Jacobson's Foundation
  3. Folksam's Forskningsstiftelse
  4. Arvid Carlsson's Foundation
  5. Sahlgrenska University Hospital, Gothenburg, Sweden [LUA/ALF GBG-11587]

Ask authors/readers for more resources

Glial cell line-derived neurotrophic factor (GDNF) plays an important role in neuroinflammatory and neuropathic pain conditions. Astrocytes produce and secrete GDNF, which interacts with its receptors to induce Ca2+ transients. This study aimed first to assess intracellular Ca2+ responses of astrocytes in primary culture when exposed to the neuroprotective and anti-inflammatory peptide GDNF. Furthermore, incubation with the inflammatory inducers lipopolysaccharide (LPS), NMDA, or interleukin 1-beta (IL-1 beta) attenuated the GDNF-induced Ca2+ transients. The next aim was to try to restore the suppressed GDNF responses induced by inflammatory changes in the astrocytes with an anti-inflammatory substance. Ifenprodil, an NMDA receptor antagonist at the NR2B subunit, was tested. It was shown to restore the GDNF-evoked Ca2+ transients and increased the Na+/K+-ATPase expression. Ifenprodil seems to be a potent anti-inflammatory substance for astrocytes which have been pre-activated by inflammatory stimuli.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available