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DNA微阵列检测异氟醚麻醉的基因表达 被引量:1

CDNA microarray analysis of the differential gene expression by isoflurane anesthesia
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摘要 目的用DNA微阵列筛选异氟醚麻醉的表达基因。方法12只雄性Wister大鼠,分为2%异氟醚组(A组)和对照组(B组)。A组用2%异氟醚麻醉1h,B组直接处死后取脑组织。提取RNA,荧光标记,用有4096个位点的BiostarR40s基因芯片,检测差异表达的基因。结果发现了26个差异表达的基因,其中17个基因下调,9个基因上调。结论基因芯片检测出2%异氟醚麻醉1h有26个差异表达基因。 Objective To investigate the gene expression profiles from rats under isoflurane anesthesia with DNA microarrays. Methods Six-week-old male Wister rats (n= 12) were anesthetized with isoflurane (2% air mixture gas). At 1 h after anesthesia, rats were sacrificed to obtain the brain. RNA was extracted. CDNA probe labeled with fluorescence dye was made from poly A + RNA, hybridized with the BiostarR-40s rat microarray slide containing 4 096 genes. Results Preliminary analyses showed multiple genes were regulated in response to isoflurane treatment. There were 26 genes changed expression,of which, the expression levels of 17 genes decreased after isoflurane anesthesia and 9 genes upregulated. Conclusion By analyzing expression profiles obtained from rats under isoflurane anesthesia, we have shown that isoflurane anesthesia affected the expression of a small number of genes.
出处 《临床麻醉学杂志》 CAS CSCD 2006年第5期369-371,共3页 Journal of Clinical Anesthesiology
关键词 DNA 异氟醚 基因表达 DNA Isoflurane Gene expression
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  • 1Morgan PG,Sedensky MM.Mutations conferring new patterns of sensitivity to volatile anesthetics in caenorhabditis elegans.Anesthesiology,1994,81 :888-898.
  • 2Van Swinderen B,Ebert RH,Shook DR,et al. Quantitative trait loci controlling halothane sensitivity in caenorhabditis elegans.Proc Natl Acad Sci USA,1997,94:8232-8237.
  • 3Homanics GE,Ferguson C,Quinlan JJ,et al.Gene knockout of the alpha 6 subunit of the gamma-aminobutyric acid type A receptor:lack of effect on responses to ethanol,pentobarbital,and general anesthetics.Mol Pharm,1997,51:588-596.
  • 4Simpyon VJ,Rikke BA,Costello JM,et al.Identification of genetic region in mice that specifying sensitivity to propofol.Anesthesiology,1998,88:379-389.
  • 5Lander ES,Linton LM,Birren B,et al.Initial sequencing and analysis of the human genome.Nature,2001,409:860-921.

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  • 2Zhao ZQ, Morris CD, Budde JM, et al. Inhibition of myocardial apoptosis reduces infarct size and improves regional contractile dysfunction during reperfusion. Cardiovasc Res, 2003,59 : 132-142.
  • 3Qin F, Liang MC, Liang CS. Progressive left ventricular remodeling, myoeyte apoptosis, and protein signaling easeades after myocardial infarction in rabbits. Bioehim Biophys Aeta, 2005,1740: 499-513.
  • 4Zhao ZQ, Vinten-Johansen J. Myocardial apoptosis and ischemic preconditioning. Cardiovas Res, 2002, 55 : 438-455.
  • 5Khoynezhad A, Jalali Z, Tortolani AJ. Apoptosis: pathophysiology and herapeutic implications for the cardiac surgeon. Ann Thorac Surg, 2004, 78: 1109-1118.
  • 6Pchejetski D, Kunduzova O, Dayon A, et al. Oxidative stresS-dependent sphingosine kinase-1 inhibition mediates monoamine oxidase A-associated cardiac cell apoptosis. Circ Res, 2007, 100: 41-49.
  • 7Lu X, Hamilton JA, Shen J, et al. Role of tumor necrosis factor-alpha in myocardial dysfunction and apoptosis during hindlimb ischemia and reperfusion. Crit Care Med, 2006, 34: 484-491.
  • 8张野,顾尔伟,张健,李磊,陈志武.c—Jun氨基末端激酶在瑞芬太尼预处理减轻大鼠心肌缺血再灌注损伤中的作用[J].中华麻醉学杂志,2007,27(12):1093-1096. 被引量:7
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