Progesterone treatment decreases traumatic brain injury induced anxiety and is correlated with increased serum IGF-1 levels; prefrontal cortex, amygdala, hippocampus neuron density; and reduced serum corticosterone levels in immature rats

Creative Commons License

Baykara B., Aksu İ., Buyuk E., Kiray M., Sisman A., Baykara B., ...More

BIOTECHNIC & HISTOCHEMISTRY, vol.88, no.5, pp.250-257, 2013 (SCI-Expanded) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 88 Issue: 5
  • Publication Date: 2013
  • Doi Number: 10.3109/10520295.2013.769630
  • Journal Name: BIOTECHNIC & HISTOCHEMISTRY
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.250-257
  • Keywords: amygdala, anxiety, brain injury, corticosterone, hippocampus, IGF-1, prefrontal cortex, DOPAMINERGIC ACTIVITY, MESSENGER-RNA, BEHAVIOR, MICE, FEAR, DYSFUNCTION, EXPRESSION, MECHANISM, EXERCISE, BDNF
  • Dokuz Eylül University Affiliated: Yes

Abstract

Traumatic brain injury (TBI) may cause neuropsychiatric problems, such as anxiety disorder, that have negative effects on cognitive functions and behavior. We investigated the effects of progesterone on traumatic brain injury induced anxiety in 7-day-old rat pups subjected to contusion injury. Progesterone treatment decreased TBI induced anxiety and serum corticosterone levels, and increased serum IGF-1 levels. Moreover, progesterone treatment increased amygdala, prefrontal cortex and hippocampal neuron density. We found a negative correlation between serum corticosterone levels and anxiety tests, and a positive correlation between serum IGF-1 levels and anxiety tests. In addition, progesterone treatment decreased serum corticosterone compared to the controls and sham. Our results indicate that single dose progesterone may be effective for treating anxiety caused by TBI.