Wang J Q, McGinty J F
Department of Anatomy and Cell Biology, East Carolina University School of Medicine, Greenville, NC 27858-4354, USA.
Brain Res. 1997 Feb 14;748(1-2):62-70. doi: 10.1016/s0006-8993(96)01244-9.
Systemic administration of the muscarinic receptor antagonist, scopolamine, augments, whereas the muscarinic receptor agonist, oxotremorine, attenuates behaviors (locomotion and stereotypies) and preprodynorphin (PPD) and substance P (SP) gene expression in striatonigral neurons induced by the indirect dopamine receptor agonist, amphetamine (AMPH). In contrast, systemic scopolamine blocks, whereas oxotremorine augments, AMPH-stimulated preproenkephalin (PPE) gene expression in striatopallidal neurons. This study investigated the site of action of these effects by administering scopolamine and oxotremorine directly into the striatum and assessing the expression of neuropeptide mRNAs with quantitative in situ hybridization. Unilateral injection of scopolamine into the dorsal striatum augmented, and oxotremorine attenuated, AMPH (2.5 mg/kg, i.p.)-stimulated behaviors. Intrastriatal scopolamine at a concentration of 62 mM, but not 6.2 mM, increased basal levels of PPD and SP mRNAs in the dorsal striatum. In addition, both 6.2 and 62 mM scopolamine significantly augmented AMPH-stimulated PPD and SP mRNA levels. Intrastriatal infusion of 1.6 or 8.1 mM oxotremorine did not alter basal levels of striatal PPD and SP mRNAs. However, both concentrations of oxotremorine completely blocked AMPH-stimulated SP mRNA and oxotremorine at 8.1 mM blocked AMPH-stimulated PPD mRNA. In contrast, PPE induction by AMPH was blocked by 62, but not 6.2, mM scopolamine. Both concentrations of oxotremorine tended to augment basal and AMPH-stimulated PPE mRNA in the dorsal striatum but the trend was not significant. These data demonstrate an inhibition of striatonigral, and facilitation of striatopallidal, gene expression through activation of local striatal muscarinic receptors, which is consistent with the changes seen after systemic administration of muscarinic agents. Therefore, muscarinic cholinergic regulation of basal and stimulated expression of neuropeptide mRNA is processed within the striatum.
毒蕈碱受体拮抗剂东莨菪碱的全身给药增强了由间接多巴胺受体激动剂苯丙胺(AMPH)诱导的纹状体黑质神经元中的行为(运动和刻板行为)以及前强啡肽(PPD)和P物质(SP)基因表达,而毒蕈碱受体激动剂氧化震颤素则减弱了这些行为和基因表达。相反,全身给予东莨菪碱会阻断,而氧化震颤素会增强AMPH刺激的纹状体苍白球神经元中的前脑啡肽原(PPE)基因表达。本研究通过将东莨菪碱和氧化震颤素直接注射到纹状体中,并通过定量原位杂交评估神经肽mRNA的表达,来研究这些作用的作用位点。将东莨菪碱单侧注射到背侧纹状体中会增强,而氧化震颤素会减弱AMPH(2.5mg/kg,腹腔注射)刺激的行为。纹状体内注射浓度为62mM而非6.2mM的东莨菪碱会增加背侧纹状体中PPD和SP mRNA的基础水平。此外,6.2mM和62mM的东莨菪碱均显著增强了AMPH刺激的PPD和SP mRNA水平。纹状体内注入1.6或8.1mM的氧化震颤素不会改变纹状体中PPD和SP mRNA的基础水平。然而,两种浓度的氧化震颤素均完全阻断了AMPH刺激的SP mRNA,8.1mM的氧化震颤素阻断了AMPH刺激的PPD mRNA。相反,62mM而非6.2mM的东莨菪碱阻断了AMPH诱导的PPE。两种浓度的氧化震颤素都倾向于增强背侧纹状体中基础和AMPH刺激的PPE mRNA,但这种趋势并不显著。这些数据表明,通过激活局部纹状体毒蕈碱受体可抑制纹状体黑质的基因表达并促进纹状体苍白球的基因表达,这与全身给予毒蕈碱药物后观察到的变化一致。因此,毒蕈碱胆碱能对神经肽mRNA基础表达和刺激表达的调节在纹状体内进行。