Herpes virus-mediated preproenkephalin gene transfer to the amygdala is antinociceptive

被引:52
|
作者
Kang, W
Wilson, MA
Bender, MA
Glorioso, JC
Wilson, SP [1 ]
机构
[1] Univ S Carolina, Sch Med, Dept Pharmacol, Columbia, SC 29208 USA
[2] Univ Pittsburgh, Sch Med, Dept Mol Genet & Biochem, Pittsburgh, PA 15261 USA
关键词
analgesia; formalin test; naloxone; opioid peptide; rat;
D O I
10.1016/S0006-8993(98)00194-2
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
To evaluate the role of the amygdala in pain modulation and opioid-mediated antinociception, a recombinant, replication-defective herpes virus carrying the human preproenkephalin cDNA was injected bilaterally into the rat amygdala. Four days after gene delivery nociceptive behavior was assessed by the formalin test. Rats infected with the virus expressing preproenkephalin showed a selective, naloxone-reversible abolition of phase 2 flinching behavior compared to rats infected with a control virus. The results implicate the amygdala in the control of pain and in opioid analgesia and demonstrate the use of recombinant herpes viruses as tools for studying gene function in specific neural pathways of the central nervous system. (C) 1998 Elsevier Science B.V.
引用
收藏
页码:133 / 135
页数:3
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