Neuroanatomical and pharmacological assessment of Fos expression induced in the rat brain by the phosphodiesterase-4 inhibitor 6-(4-pyridylmethyl)-8-(3-nitrophenyl) quinoline.
第一作者:
Y,Bureau
第一单位:
Merck-Frosst Centre for Therapeutic Research, Merck Frosst Canada and Company, P.O. Box 1005, Pointe Claire-Dorval, QC H9R 4P8, Canada.
作者:
主题词
镇痛药(Analgesics);动物(Animals);脑(Brain);剂量效应关系, 药物(Dose-Response Relationship, Drug);基因表达(Gene Expression);吲哚类(Indoles);异吲哚类(Isoindoles);男(雄)性(Male);癌基因蛋白质v-fos(Oncogene Proteins v-fos);磷酸二酯酶抑制剂(Phosphodiesterase Inhibitors);吡啶类(Pyridines);喹啉类(Quinolines);大鼠(Rats);大鼠, Sprague-Dawley(Rats, Sprague-Dawley);时间因素(Time Factors)
DOI
10.1016/j.neuropharm.2006.06.018
PMID
16901513
发布时间
2013-06-05
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Neuropharmacology
974-85页
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