Literature DB >> 25703023

Brain changes associated with thromboxane receptor antagonist SQ 29,548 treatment in a mouse model.

Andrew A Rebel1, Siri A Urquhart1, Kendra L Puig2, Atreyi Ghatak2, Stephen A Brose2, Mikhail Y Golovko2, Colin K Combs2.   

Abstract

The purpose of this study was to characterize behavioral and physiological effects of a selective thromboxane (TP) receptor antagonist, SQ 29,548, in the C57Bl/6 mouse model. At 6 months of age, male mice were given either sham or drug i.p. injections for 3 days at a dose of 2 mg/kg each day. On the day after the final injection, mice were subjected to behavioral testing before brain collection. Left hemisphere hippocampi were collected from all mice for protein analysis via Western blot. Right brain hemispheres were fixed and embedded in gelatin and then serially sectioned. The sections were immunostained with anti-c-Fos antibodies. Prostaglandin analysis was performed from remaining homogenized brain samples, minus the hippocampi. Injection of SQ 29,548 decreased selective brain prostaglandin levels compared with sham controls. This correlated with robust increases in limbic-region c-Fos immunoreactivity in the SQ 29,548-injected mice. However, drug-treated mice demonstrated no significant changes in relevant hippocampal protein levels compared with sham treatments, as determined from Western blots. Surprisingly, injection of SQ 29,548 caused mixed changes in parameters of depression and anxiety-like behavior in the mice. In conclusion, the results indicate that administration of peripheral TP receptor antagonists alters brain levels of prostanoids and influences neuronal activity, with only minimal alterations of behavior. Whether the drug affects neurons directly or through a secondary pathway involving endothelium or other tissues remains unclear.
© 2015 Wiley Periodicals, Inc.

Entities:  

Keywords:  anxiety; c-Fos; depression; thromboxane; thromboxane receptor

Mesh:

Substances:

Year:  2015        PMID: 25703023      PMCID: PMC4478107          DOI: 10.1002/jnr.23578

Source DB:  PubMed          Journal:  J Neurosci Res        ISSN: 0360-4012            Impact factor:   4.164


  81 in total

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