4.4 Article

Inhibition of CB1 receptor ameliorates spatial learning and memory impairment in mice with traumatic brain injury

期刊

NEUROSCIENCE LETTERS
卷 696, 期 -, 页码 127-131

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.neulet.2018.12.024

关键词

Traumatic brain injury; Spatial memory; 2-Arachidonoyl glycerol; Hippocampus

资金

  1. Education Department [LQNK201736]
  2. innovation project of college students of Liaoning province, Liaoning, China [201610159003]

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Traumatic brain injury (TBI) is an increasingly prevalent condition affecting people of all ages and genders. The impairment of spatial learning and memory is one of the most common effects of TBI. Unfortunately, it currently lacks effective therapeutic interventions. The endocannabinoid (EC) system regulates a diverse array of physiological processes. Here, we found a 6.7-fold increase of 2-AG levels at 1 d post-TBI, declining thereafter. After 5 d, the levels were still 3.3-fold higher than in the controls. AM281, a CB1 receptor antagonist, reversed the TBI-reduced NMDA receptor subunits NR2B in the hippocampus and ameliorate the spatial learning and memory impairment at 7 d post-TBI, suggesting CB1 receptor is involved in the TBI-induced hippocampal-dependent spatial learning and memory impairment.

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