Characterization of the Postconditioning Effect of Dexmedetomidine in Mouse Organotypic Hippocampal Slice Cultures Exposed to Oxygen and Glucose Deprivation

被引:110
作者
Dahmani, Souhayl
Rouelle, Danielle
Gressens, Pierre
Mantz, Jean
机构
[1] Hop Robert Debre, INSERM, U676, F-75019 Paris, France
[2] Hop Robert Debre, Robert Debre Univ Hosp, Dept Anesthesia & Pain Management, F-75019 Paris, France
[3] Beaujon Univ Hosp, AP HP, Dept Anesthesia & Intens Care, Clichy, France
关键词
CEREBRAL-ISCHEMIA; ALPHA(2)-AGONIST DEXMEDETOMIDINE; ALPHA(2A)-ADRENOCEPTOR SUBTYPE; INHALATIONAL ANESTHETICS; PRECONDITIONING AGENTS; BRAIN-INJURY; IN-VITRO; ISOFLURANE; RATS; NEURONS;
D O I
10.1097/ALN.0b013e3181ca6982
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Background: There is an increasing interest in the use of dexme-detomidine for anesthesia and sedation, Here, we used the mouse organotypic hippocampal slice culture to investigate whether dexmedetomidine exhibits postconditioning properties against oxygen and glucose deprivation (OGD). The role of the focal adhesion and extracellular-regulated kinases pathways in these effects were examined in both postconditioning and preconditioning. Materials and methods: Slices were obtained from P5 mouse. In postconditioning experiments, Dexmedetomidine (1 W) was incubated 60 min after the end of OGD. In preconditioning experiments, dexmedetomidine was applied 3 h before OGD. Pharmacologic modulation of the studied pathways was achieved by using selective inhibitors of these cascades. Cell death was assessed 72 h after OGD using propidium iodide labeling and protein expression of activated caspase 3. Results: Maximum cell death increased with the duration of OGD. Dexmedetomidine induced a postconditioning effect in the CA1 (but not dentate gyrus) subfield area, which was significantly reduced by modulators of the focal adhesion and the extracellular-regulated kinases pathways. The combination of the inhibitors of the two pathways completely abolished the postconditioning effect of dexmedetomidine. The preconditioning effect of dexmedetomidine against ischemia-induced injury was observed in all hippocampal subfield areas. Results obtained with the pharmacologic modulation used for postconditioning also applied to dexmedetomidine-induced preconditioning. Discussion: Dexmedetomidine exhibits significant, but moderate, postconditioning properties against oxygen and glucose deprivation-induced injury, Activation of focal adhesion and the imidazoline I receptors-extracellular-regulated kinases pathways is involved in dexmedetomidine-induced postconditioning and preconditioning as well.
引用
收藏
页码:373 / 383
页数:11
相关论文
共 39 条
[1]   Selective neuronal vulnerability and specific glial reactions in hippocampal and neocortical organotypic cultures submitted to ischemia [J].
Bernaudin, M ;
Nouvelot, A ;
MacKenzie, ET ;
Petit, E .
EXPERIMENTAL NEUROLOGY, 1998, 150 (01) :30-39
[2]   Isoflurane preconditions hippocampal neurons against oxygen-glucose deprivation -: Role of intracellular Ca2+ and mitogen-activated protein kinase signaling [J].
Bickler, PE ;
Zhan, XH ;
Fahlman, CS .
ANESTHESIOLOGY, 2005, 103 (03) :532-539
[3]   α2B-adrenergic receptor activates MAPK via a pathway involving arachidonic acid metabolism, matrix metalloproteinases, and epidermal growth factor receptor transactivation [J].
Cussac, D ;
Schaak, S ;
Denis, C ;
Paris, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (22) :19882-19888
[4]   Effects of dexmedetomidine on hippocampal focal adhesion kinase tyrosine phosphorylation in physiologic and ischemic conditions [J].
Dahmani, S ;
Rouelle, D ;
Gressens, P ;
Mantz, J .
ANESTHESIOLOGY, 2005, 103 (05) :969-977
[5]   Thiopental and isoflurane attenuate the decrease in hippocampal phosphorylated Focal Adhesion Kinase (pp125FAK) content induced by oxygen-glucose deprivation [J].
Dahmani, S ;
Tesnière, A ;
Rouelle, D ;
Desmonts, JM ;
Mantz, J .
BRITISH JOURNAL OF ANAESTHESIA, 2004, 93 (02) :270-274
[6]   Dexmedetomidine increases hippocampal phosphorylated extracellular signal-regulated protein kinase 1 and 2 content by an α2-adrenoceptor-independent mechanism:: Evidence for the involvement of imidazoline I1 receptors [J].
Dahmani, Souhayl ;
Paris, Andrea ;
Jannier, Virginie ;
Hein, Lutz ;
Rouelle, Danielle ;
Scholz, Jens ;
Gressens, Pierre ;
Mantz, Jean .
ANESTHESIOLOGY, 2008, 108 (03) :457-466
[7]   Ischemic tolerance and endogenous neuroprotection [J].
Dirnagl, U ;
Simon, RP ;
Hallenbeck, JM .
TRENDS IN NEUROSCIENCES, 2003, 26 (05) :248-254
[8]   ERK phosphorylation in intact, adult brain by α2-adrenergic transactivation of EGF receptors [J].
Du, Ting ;
Li, Baoman ;
Liu, Shufang ;
Zang, Peizhuo ;
Prevot, Vincent ;
Hertz, Leif ;
Peng, Liang .
NEUROCHEMISTRY INTERNATIONAL, 2009, 55 (07) :593-600
[9]   Effect of the α2-agonist dexmedetomidine on cerebral neurotransmitter concentrations during cerebral ischemia in rats [J].
Engelhard, K ;
Werner, C ;
Kaspar, S ;
Möllenberg, O ;
Blobner, M ;
Bachl, M ;
Kochs, E .
ANESTHESIOLOGY, 2002, 96 (02) :450-457
[10]   The effect of the α2-agonist dexmedetomidine and the N-methyl-D-aspartate antagonist S(+)-ketamine on the expression of apoptosis-regulating proteins after incomplete cerebral ischemia and reperfusion in rats [J].
Engelhard, K ;
Werner, C ;
Eberspächer, E ;
Bachl, M ;
Blobner, M ;
Hildt, E ;
Hutzler, P ;
Kochs, E .
ANESTHESIA AND ANALGESIA, 2003, 96 (02) :524-531