| Autor: |
Wang L; Department of Neurology, The First Affiliated Hospital, Baotou Medical College, Baotou, China., Jia JX; Department of Human Anatomy, Baotou Medical College, Baotou, China.; Key Laboratory of Human Anatomy, Education Department of Inner Mongolia Autonomous Region, Baotou, China., Zhang SB; Department of Human Anatomy, Baotou Medical College, Baotou, China., Song W; Department of Human Anatomy, Baotou Medical College, Baotou, China.; Key Laboratory of Human Anatomy, Education Department of Inner Mongolia Autonomous Region, Baotou, China., Yan XS; Department of Human Anatomy, Baotou Medical College, Baotou, China.; Key Laboratory of Human Anatomy, Education Department of Inner Mongolia Autonomous Region, Baotou, China., Huo DS; Department of Human Anatomy, Baotou Medical College, Baotou, China.; Key Laboratory of Human Anatomy, Education Department of Inner Mongolia Autonomous Region, Baotou, China., Wang H; School of Health Sciences, University of Newcastle, Newcastle, Australia., Wu LE; Department of Neurology, The First Affiliated Hospital, Baotou Medical College, Baotou, China., Yang ZJ; Key Laboratory of Human Anatomy, Education Department of Inner Mongolia Autonomous Region, Baotou, China.; Department of Human Anatomy, Chifeng University, Chifeng, China. |
| Abstrakt: |
Cerebral ischemia-reperfusion injury (CIRI) occurs frequently clinically as a complication following cardiovascular resuscitation resulting in neuronal damage specifically to the hippocampal CA1 region with consequent cognitive impairment. Apoptosis and oxidative stress were proposed as major risk factors associated with CIRI development. Previously, glycosides obtained from Cistanche deserticola (CGs) were shown to play a key role in counteracting CIRI; however, the underlying mechanisms remain to be determined. This study aimed to investigate the neuroprotective effect of CGs on subsequent CIRI in rats. The model of CIRI was established for 2 hr and reperfusion for 24 hr by middle cerebral artery occlusion (MCAO) model. The MCAO rats were used to measure the antioxidant and anti-apoptotic effects of CGs on CIRI. Neurological function was evaluated by the Longa neurological function score test. 2,3,5-Triphenyltetrazolium chloride (TTC) staining was used to detect the area of cerebral infarction. Nissl staining was employed to observe neuronal morphology. TUNEL staining was used to detect neuronal apoptosis, while Western blot determined protein expression levels of factors for apoptosis-related and PI3K/AKT/Nrf2 signaling pathway. Data demonstrated that CGs treatment improved behavioral performance, brain injury, and enhanced antioxidant and anti-apoptosis in CIRI rats. In addition, CGs induced activation of PI3K/AKT/Nrf2 signaling pathway accompanied by inhibition of the expression of apoptosis-related factors. Evidence indicates that CGs amelioration of CIRI involves activation of the PI3K/AKT/Nrf2 signaling pathway associated with increased cellular viability suggesting these glycosides may be considered as an alternative compound for CIRI treatment. |
