کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
6280631 | 1615094 | 2015 | 5 صفحه PDF | دانلود رایگان |

- We evaluated the preventive effects of ginsenoside Rg1 on the post-traumatic stress disorder (PTSD) animal model.
- Administration ginsenoside Rg1 could prevent the model animal's PTSD-like behavior changes.
- Administration ginsenoside Rg1 could decrease the levels of CORT and CRH in model animals.
We investigated the preventive effects of Rg1 on a model of mouse post-traumatic stress disorder (PTSD) induced by electric shock combined with situation reminder and explored the underlying mechanism. In the experiment, before the PTSD animal model was developed, Rg1 (10, 5, and 2.5Â mg/kg) was orally administered for one week. After the animal model was established, PTSD-like behavior was observed using elevated plus maze, black and light box, and open field tests. One hour after the behavior test, all mice were sacrificed, and then serum corticosterone (CORT) and hypothalamus corticotrophin-releasing hormone (CRH) assays were performed. Results showed that Rg1 (5Â mg/kg) treatments relieved PTSD-like behavior by altering elevated serum corticosterone and hypothalamus CRH levels. By contrast, fluoxetine (3Â mg/kg) treatment reversed the behavior changes and had no effect on increased CORT and CRH levels. These findings confirmed the preventive effect of Rg1 in PTSD model. Decreasing CORT and CRH levels may be one of the underlying mechanisms.
Journal: Neuroscience Letters - Volume 605, 25 September 2015, Pages 24-28