Zhu Y S, Jones S B, Burke R E, Franklin S O, Inturrisi C E
Department of Pharmacology, Cornell University Medical College, New York, NY 10021.
Life Sci. 1993;52(19):1577-84. doi: 10.1016/0024-3205(93)90058-b.
Expression of the striatal proenkephalin gene is modulated by dopaminergic input from the substantia nigra (SN). We have used rapid, specific and sensitive solution hybridization assays for the quantitation of tyrosine hydroxylase (TH) mRNA, preproenkephalin (PPenk) mRNA and total cellular RNA to compare ipsilateral and contralateral levels of these RNAs in tissue dissected from the origin and termination of the nigrostriatal pathway of individual rats following sham (vehicle) or 6-hydroxydopamine (6-OHDA) induced lesions of the SN. Three weeks after treatment the rats that had received 6-OHDA, but not sham treated controls, demonstrated a characteristic contralateral rotation in response to apomorphine. Four weeks after 6-OHDA treatment, TH mRNA levels were reduced below the limits of sensitivity of the assay (1 pg/ug RNA) in ipsilateral SN while the levels of TH mRNA in contralateral SN (4.8 pg/ug RNA) did not differ from that in sham treated animals. PPenk mRNA levels in striatum were increased 3 fold to 64.9 pg/ug RNA on the side of the 6-OHDA lesions while the contralateral PPenk mRNA levels (21.6 pg/ug RNA) did not differ from sham treatment. The 6-OHDA treatment did not alter the levels of total cellular RNA in either SN or striatum. These results provide quantitative evidence for the tonic inhibition of striatal proenkephalin gene expression by the dopaminergic nigrostriatal pathway.
纹状体前脑啡肽原基因的表达受黑质(SN)多巴胺能输入的调节。我们使用快速、特异且灵敏的溶液杂交分析法来定量酪氨酸羟化酶(TH)mRNA、前脑啡肽原(PPenk)mRNA和总细胞RNA,以比较在假手术(赋形剂)或6-羟基多巴胺(6-OHDA)诱导的SN损伤后,从个体大鼠黑质纹状体通路的起始端和终止端解剖的组织中这些RNA的同侧和对侧水平。治疗三周后,接受6-OHDA的大鼠,而非假手术对照组,对阿扑吗啡表现出特征性的对侧旋转。6-OHDA治疗四周后,同侧SN中TH mRNA水平降至检测灵敏度极限(1 pg/μg RNA)以下,而对侧SN中TH mRNA水平(4.8 pg/μg RNA)与假手术动物无差异。6-OHDA损伤侧纹状体中PPenk mRNA水平增加3倍至64.9 pg/μg RNA,而对侧PPenk mRNA水平(21.6 pg/μg RNA)与假手术处理无差异。6-OHDA治疗未改变SN或纹状体中总细胞RNA的水平。这些结果为多巴胺能黑质纹状体通路对纹状体前脑啡肽原基因表达的紧张性抑制提供了定量证据。