Effects of isoflurane anesthesia on expression of BDNF and phosphorylated ERK in neonatal rat hippocampus
10.3760/cma.j.issn.0254-1416.2012.06.015
- VernacularTitle:异氟醚麻醉对新生大鼠海马BDNF和磷酸化ERK表达的影响
- Author:
Ting LIU
;
Shouping WANG
;
Zhi WANG
;
Yingzhen CHEN
;
Shuling PENG
- Publication Type:Journal Article
- Keywords:
Isoflurane;
Brain-derived neurotrophic factor;
Extracellular signal-regulated MAP kinases;
Hippocampas
- From:
Chinese Journal of Anesthesiology
2012;32(6):702-704
- CountryChina
- Language:Chinese
-
Abstract:
ObjectiveTo investigate the effects of isoflurane anesthesia on the expression of brain-derived neurotrophic factor (BDNF) and phosphorylated extracellular signal-regulated kinase (p-ERK) in neonatal rat hippocampus.MethodsForty-eight SD rats of both sexes,aged 7 days,weighing 12-17 g,were randomly divided into 2 groups ( n =24 each):control group (group C) and isoflurane anesthesia group (group Ⅰ).In group Ⅰ,the rats were exposed to2.5％ isotlurane for 3 min and then 1.5％ isoflurane was inhaled for 4 h,while in group C the rats were exposed to air for4 h.Arterial blood samples were collected immediately after anesthesia for blood gas analysis and for determination of the blood glucose concentration.Five rats in each group were sacrificed at 0,6,24 and 48 h after anesthesia (T1-4) and hippocanpi were removed for determination of the expression of potassiumchloride cotransporter 2 (KCC2),potassium-chloride cotrmsporter 1 (NKCC1),BDNF and p-ERK by Western blot.NKCC1/KCC2 ratio was calculated.ResultsAcid-base imbalance,hypoxemia and glycopenia were not found immediately after anesthesia in both groups.Compared with group C,KCC2 expression was significantly down-regulated and NKCC1/KCC2 ratio was increased at T3 and T4,and the expression of BDNF and p-ERK was dewn-regnlated at T1 and T2 in group Ⅰ (P＜0.05).There was no significant difference in NKCCI expression at each time point between groups Ⅰ and C ( P ＞ 0.05 )、ConclusionIsoflurane anesthesia delays the neuronal development in neonatal rat hippocampus through down-regulating the expression of BDNF and p-ERK.
