An enriched environment improves long-term functional outcomes in mice after intracerebral hemorrhage by mechanisms that involve the Nrf2/BDNF/glutaminase pathway. Issue 5 (May 2023)

• Record Type: Journal Article
• Authors: Jia, Peijun; Wang, Junmin; Ren, Xiuhua; He, Jinxin; Wang, Shaoshuai; Xing, Yinpei; Chen, Danyang; Zhang, Xinling; Zhou, Siqi; Liu, Xi; Yu, Shangchen; Li, Zefu; Jiang, Chao; Zang, Weidong; Chen, Xuemei; Wang, Jian
• Is Part Of: Journal of cerebral blood flow & metabolism. Volume 43:Issue 5(2023)
• Page Start: 694
• Page End: 711
• Publication Date: 2023-05
• Subjects: Anxiety behaviors -- enriched environment -- intracerebral hemorrhage -- nuclear regulatory factor 2 -- post-stroke depression; Cerebral circulation -- Periodicals; Brain -- Metabolism -- Periodicals; Brain -- Blood-vessels -- Periodicals; Cerebrovascular disease -- Periodicals; 612.824
• DOI: 10.1177/0271678X221135419
• Languages: English
• ISSNs: 0271-678X

Abstract

Post-stroke depression exacerbates neurologic deficits and quality of life. Depression after ischemic stroke is known to some extent. However, depression after intracerebral hemorrhage (ICH) is relatively unknown. Increasing evidence shows that exposure to an enriched environment (EE) after cerebral ischemia/reperfusion injury has neuroprotective effects in animal models, but its impact after ICH is unknown. In this study, we investigated the effect of EE on long-term functional outcomes in mice subjected to collagenase-induced striatal ICH. Mice were subjected to ICH with the standard environment (SE) or ICH with EE for 6 h/day (8:00 am–2:00 pm). Depressive, anxiety-like behaviors and cognitive tests were evaluated on day 28 with the sucrose preference test, tail suspension test, forced swim test, light-dark transition experiment, morris water maze, and novel object recognition test. Exposure to EE improved neurologic function, attenuated depressive and anxiety-like behaviors, and promoted spatial learning and memory. These changes were associated with increased expression of transcription factor Nrf2 and brain-derived neurotrophic factor (BDNF) and inhibited glutaminase activity in the perihematomal tissue. However, EE did not change the above behavioral outcomes in Nrf2 −/− mice on day 28. Furthermore, exposure to EE did not increase BDNF expression compared to exposure to SE in Nrf2 −/− mice on day 28 after ICH. These findings indicate that EE improves long-term outcomes in sensorimotor, emotional, and cognitive behavior after ICH and that the underlying mechanism involves the Nrf2/BDNF/glutaminase pathway.