AI Article Synopsis

  • The study examines the molecular responses to spinal cord injury (SCI) in rats by focusing on the expression levels of liver X receptor α (LXRα) and Bcl-2-associated X protein (Bax).
  • The researchers induced SCI in male Wister rats and measured the expression of LXRα and Bax at various times post-injury, finding a complex pattern of changes in these genes.
  • Results indicated that Bax levels increased in the epicenter of the injury, while LXRα expression initially rose in the rostral area and gradually spread to other regions, suggesting inflammation occurs in a specific, time-dependent manner.

Article Abstract

Background: Study of molecular responses to central nervous system injury would be helpful for controlling the harmful pathways post-injury and triggering the useful pathways required for the treatment of injury.

Objective: To investigate the expression level of liver X receptor α (LXRα) which has anti-inflammatory effects and pro-apoptotic Bcl-2-associated X protein (Bax) upon spinal cord injury (SCI).

Design: To induce SCI, transection was carried out at T9 level of male Wister rats. Approximately 8 mm of rostral, caudal, and epicenter tissues of injured sites in treated rats were chosen for quantitative real-time polymerase chain reaction at the 6, 24, and 72 hours, and 7 and 10 days post-surgery.

Results: Our results showed a complicated temporal and spatial pattern of alteration in LXRα and Bax mRNA expression levels after SCI. LXRα expression level followed a homologues pattern (additive and subtractive wave) with a difference in time at three areas of studied. Rostral, caudal, and epicenter expression patterns of Bax were dissimilar in these areas. Gradual increase in the expression of Bax without any decrease at the rostral area was observed, presumably indicating the active transcription process of this gene, regardless of its protein situation.

Conclusion: A time lapse significant change in Bax expression level was observed only in the epicenter of injury, emphasizing that apoptotic responses are limited to this area. Furthermore, an increase in LXRα transcription level was observed first in rostral area and then extended to epicentral and caudal areas, implying that inflammation responses extended from rostral to caudal areas.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3555109PMC
http://dx.doi.org/10.1179/2045772312Y.0000000032DOI Listing

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