Effect of sevoflurane on hippocampal CaMK Ⅱ/CREB signaling pathway in aged rats
10.3760/cma.j.issn.0254-1416.2017.02.010
- VernacularTitle:七氟醚对老龄大鼠海马CaMKⅡ/CREB信号通路的影响
- Author:
Ying WANG
;
Xiaodong WANG
;
Caixia WANG
;
Yi QIU
- Keywords:
Anesthetics,inhalation;
Aged;
Hippocampus;
Calcium-calmodulin-dependent protein kinase type 2;
Cyclic AMP response element-binding protein;
Cognitive
- From:
Chinese Journal of Anesthesiology
2017;37(2):163-166
- CountryChina
- Language:Chinese
-
Abstract:
Objective To evaluate the effect of sevoflurane on hippocampal calcium/calmodulindependent protein kinase Ⅱ (CaMK Ⅱ)/cyclic adenosine monophosphate response element-binding protein (CREB) signaling pathway in aged rats.Methods Sixty pathogen-free healthy male Sprague-Dawley rats,aged 18 months,weighing 600-750 g,were divided into 2 groups (n=30 each) using a random number table:control group (group C) and sevoflurane group (group Sev).Group Sev inhaled 2％ sevoflurane in the mixture of 50％ air and oxygen (2 L/min) for 4 h.Group C inhaled the mixture of 50％ air and oxygen (2 L/min) for 4 h.Morris water maze test was performed on 6 days before anesthesia and 1 day after anesthesia.The escape latency,swimming distance,frequency of crossing the original platform and time of staying at the platform quadrant Ⅱ were recorded.On 1,3 and 7 days after anesthesia,the rats were sacrificed,and the hippocampus was obtained for determination of the expression of CaMK Ⅱ,phosphorylated CaMK Ⅱ,CREB and phosphorylated CREB by Western blot.Results Compared with group C,the escape latency and swimming distance were significantly prolonged,the frequency of crossing the original platform was decreased,and the time of staying at the platform quadrant Ⅱ was reduced on 5th day of training and 1 day after anesthesia,and the expression of CaMK Ⅱ,phosphorylated CaMK Ⅱ,CREB and phosphorylated CREB was down-regulated after anesthesia in group Sev (P＜ 0.05).Conclusion Sevoflurane leads to cognitive decline through inhibiting hippocampal CaMK Ⅱ/CREB signaling pathway in aged rats.
