Vles J S, de Louw A J, Steinbusch H, Markerink-van Ittersum M, Steinbusch H W, Blanco C E, Axer H, Troost J, de Vente J
Department of Neurology, University Hospital Maastricht, P.O. Box 5800, 6202 AZ, Maastricht, Netherlands.
Brain Res. 2000 Feb 28;857(1-2):219-34. doi: 10.1016/s0006-8993(99)02434-8.
An immunocytochemical technique was used to study the localization and developmental aspects of cyclic GMP (cGMP)-synthesizing structures in the cervical spinal cord of 2-week and 3-month-old Lewis rats in response to the nitric oxide (NO) donor sodium nitroprusside (SNP) and/or atrial natriuretic peptide (ANP). By using cell-specific markers, the cell structures involved were investigated. To visualize cGMP, a combined technique of low- and high-power magnification, using a confocal laser scanning microscope was used. NOS-mediated cGMP synthesis was observed in the cervical spinal cord in laminae I, II and III in 14-day-old rats, which activity was mainly absent at the age of 3 months. The involvement of NO in the NMDA-mediated increase in cGMP immunostaining (cGMP-IS) was demonstrated by the absence of cGMP-IS in slices incubated in the presence of NMDA together with the NOS inhibitor N(G)-nitro-L-arginine methyl ester (L-NAME). This NO-mediated effect of NMDA on cGMP-IS was completely absent in the 3-month-old rats. ANP-mediated cGMP synthesis resulted in an increase in cGMP in laminae I and II, which was generally similar at both ages. Astrocytes in both white and gray matter were found to be cGMP-IS in the basal, NO- and ANP-stimulated conditions. Using confocal laser microscopy, NO-mediated cGMP synthesis was observed in large cholinergic terminals nearby motor neurons in the ventral horn. An extensive colocalization between NO-stimulated cGMP synthesis and parvalbumin-positive (GABAergic) neurons and fibers was observed in all laminae. In the ANP-stimulated condition, a colocalization with parvalbumin structures was found in laminae II and III. No NO- or ANP-mediated cGMP synthesis was found in fibers immunopositive for the presynaptic glutamate transporter, serotonin, or tyrosine hydroxylase.
采用免疫细胞化学技术,研究2周龄和3月龄Lewis大鼠颈脊髓中,环磷酸鸟苷(cGMP)合成结构在一氧化氮(NO)供体硝普钠(SNP)和/或心房利钠肽(ANP)作用下的定位及发育情况。利用细胞特异性标志物,对相关细胞结构进行研究。为观察cGMP,采用共聚焦激光扫描显微镜的低倍和高倍放大组合技术。在14日龄大鼠的颈脊髓I、II和III层中观察到一氧化氮合酶(NOS)介导的cGMP合成,3月龄时该活性基本消失。在存在NMDA和NOS抑制剂N(G)-硝基-L-精氨酸甲酯(L-NAME)的情况下孵育的切片中,未观察到cGMP免疫染色(cGMP-IS)增加,这证明了NO参与NMDA介导的cGMP-IS增加。3月龄大鼠中完全不存在这种NMDA对cGMP-IS的NO介导效应。ANP介导的cGMP合成导致I层和II层中cGMP增加,两个年龄组的情况总体相似。在基础、NO和ANP刺激条件下,白质和灰质中的星形胶质细胞均为cGMP-IS。利用共聚焦激光显微镜,在腹角运动神经元附近的大型胆碱能终末中观察到NO介导的cGMP合成。在所有层中均观察到NO刺激的cGMP合成与小白蛋白阳性(γ-氨基丁酸能)神经元和纤维之间广泛共定位。在ANP刺激条件下,在II层和III层中发现与小白蛋白结构共定位。在对突触前谷氨酸转运体、5-羟色胺或酪氨酸羟化酶呈免疫阳性的纤维中,未发现NO或ANP介导的cGMP合成。