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Multimodal Optical Imaging to Investigate Spatiotemporal Changes in Cerebrovascular Function in AUDA Treatment of Acute Ischemic Stroke.

Authors :
Wang, Han-Lin
Chen, Jia-Wei
Yang, Shih-Hung
Lo, Yu-Chun
Pan, Han-Chi
Liang, Yao-Wen
Wang, Ching-Fu
Yang, Yi
Kuo, Yun-Ting
Lin, Yi-Chen
Chou, Chin-Yu
Lin, Sheng-Huang
Chen, You-Yin
Source :
Frontiers in Cellular Neuroscience; 6/3/2021, Vol. 15, p1-18, 18p
Publication Year :
2021

Abstract

Administration of 12-(3-adamantan-1-yl-ureido)-dodecanoic acid (AUDA) has been demonstrated to alleviate infarction following ischemic stroke. Reportedly, the main effect of AUDA is exerting anti-inflammation and neovascularization via the inhibition of soluble epoxide hydrolase. However, the major contribution of this anti-inflammation and neovascularization effect in the acute phase of stroke is not completely elucidated. To investigate the neuroprotective effects of AUDA in acute ischemic stroke, we combined laser speckle contrast imaging and optical intrinsic signal imaging techniques with the implantation of a lab-designed cranial window. Forepaw stimulation was applied to assess the functional changes via measuring cerebral metabolic rate of oxygen (CMRO<subscript>2</subscript>) that accompany neural activity. The rats that received AUDA in the acute phase of photothrombotic ischemia stroke showed a 30.5 ± 8.1% reduction in the ischemic core, 42.3 ± 15.1% reduction in the ischemic penumbra (p < 0.05), and 42.1 ± 4.6% increase of CMRO<subscript>2</subscript> in response to forepaw stimulation at post-stroke day 1 (p < 0.05) compared with the control group (N = 10 for each group). Moreover, at post-stroke day 3, increased functional vascular density was observed in AUDA-treated rats (35.9 ± 1.9% higher than that in the control group, p < 0.05). At post-stroke day 7, a 105.4% ± 16.4% increase of astrocytes (p < 0.01), 30.0 ± 10.9% increase of neurons (p < 0.01), and 65.5 ± 15.0% decrease of microglia (p < 0.01) were observed in the penumbra region in AUDA-treated rats (N = 5 for each group). These results suggested that AUDA affects the anti-inflammation at the beginning of ischemic injury and restores neuronal metabolic rate of O<subscript>2</subscript> and tissue viability. The neovascularization triggered by AUDA restored CBF and may contribute to ischemic infarction reduction at post-stroke day 3. Moreover, for long-term neuroprotection, astrocytes in the penumbra region may play an important role in protecting neurons from apoptotic injury. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
16625102
Volume :
15
Database :
Complementary Index
Journal :
Frontiers in Cellular Neuroscience
Publication Type :
Academic Journal
Accession number :
150665085
Full Text :
https://doi.org/10.3389/fncel.2021.655305