Banegas Inmaculada, Prieto Isabel, Segarra Ana B, Vives Francisco, de Gasparo Marc, Duran Raquel, de Dios Luna Juan, Ramírez-Sánchez Manuel
Unit of Physiology,Department of Health Sciences, University of Jaén, 23071 Jaén, Spain.
Institute of Neurosciences, "Federico Olóriz" University of Granada, Granada, Spain.
Prog Neuropsychopharmacol Biol Psychiatry. 2017 Apr 3;75:213-218. doi: 10.1016/j.pnpbp.2017.02.015. Epub 2017 Feb 20.
Changes in the basal brain bilateral morphologic, neurochemical and/or functional patterns may be partly responsible for some brain disorders such as those involving mood. WKY and SHR strains as well as 6-hydroxydopamine (6-OHDA)-lesioned animals are validated models for the study of mood disorders. Because dopamine and enkephalins are involved in anxiety-related behaviors, the aim of our study was to analyze enkephalinase activity, assayed as aminopeptidase M activity, in the left and right medial prefrontal cortex (mPFC) of WKY and SHR treated with saline (sham group) or following left or right intrastriatal injections of the neurotoxic 6-OHDA. Sham left and sham right WKY exhibited a significant left predominance. Left 6-OHDA-lesioned rats inverted the left predominance of sham to right predominance. In right 6-OHDA-lesioned rats, the left predominance in sham right rats disappeared. Sham left as well as sham right SHR did not show any bilateral differences. In contrast, while the left lesion demonstrated a highly significant left predominance, the right lesion showed a slight but significant right predominance. A significant negative correlation between enkephalinase activity of the right mPFC and blood pressure and heart rate was observed only in left-lesioned SHR. Our results demonstrate that unilateral nigrostriatal injections of 6-OHDA influence the bilateral distribution of enkephalinase activity depending on both the side of the lesion and the strain analyzed. These results support the hypothesis that DA pathways may interact asymmetrically with enkephalins in the mPFC and that enkephalinase activity may play a role in the regulatory mechanisms underlying this interaction.
基底脑双侧形态学、神经化学和/或功能模式的变化可能部分导致了一些脑部疾病,如涉及情绪的疾病。WKY和SHR品系以及6-羟基多巴胺(6-OHDA)损伤的动物是研究情绪障碍的有效模型。由于多巴胺和脑啡肽参与与焦虑相关的行为,我们研究的目的是分析经生理盐水处理(假手术组)或在左侧或右侧纹状体内注射神经毒性6-OHDA后的WKY和SHR大鼠左右内侧前额叶皮质(mPFC)中脑啡肽酶活性(以氨肽酶M活性测定)。假手术左侧和假手术右侧的WKY大鼠表现出显著的左侧优势。左侧6-OHDA损伤的大鼠将假手术的左侧优势转变为右侧优势。右侧6-OHDA损伤的大鼠中,假手术右侧大鼠的左侧优势消失。假手术左侧以及假手术右侧的SHR大鼠未表现出任何双侧差异。相反,虽然左侧损伤显示出高度显著的左侧优势,但右侧损伤显示出轻微但显著的右侧优势。仅在左侧损伤的SHR大鼠中观察到右侧mPFC脑啡肽酶活性与血压和心率之间存在显著的负相关。我们的结果表明,单侧黑质纹状体注射6-OHDA会影响脑啡肽酶活性的双侧分布,这取决于损伤的侧别和所分析的品系。这些结果支持以下假设:多巴胺通路可能在mPFC中与脑啡肽不对称相互作用,并且脑啡肽酶活性可能在这种相互作用的调节机制中发挥作用。