Nakamura F
Second Department of Surgery, Hokkaido University School of Medicine, Sapporo, Japan.
Hokkaido Igaku Zasshi. 1994 Jan;69(1):95-103.
Dynorphin, an opioid peptide, is thought to play an important role in the modulation of nociceptive neural networks at the level of the spinal cord. Fos protein is involved in the transcriptional regulation of the dynorphin gene. Although several studies have been carried out on dynorphin gene expression by noxious somatic stimuli, few have evaluated the effect of noxious visceral stimuli on the expression of dynorphin gene. In the present studies we analysed the expression of the dynorphin gene mediated by a noxious visceral stimulus in a rat model by exposure of abdominal tissue to carrageenan. Expression of preprodynorphin and c-fos mRNAs in the spinal cord neuron was examined using ribonuclease protection assays. After inflammation, a rapid increase in the levels of c-fos mRNA in the thoracic spinal cord was observed. c-fos mRNA levels rose within 30 minutes after injection, and remained elevated for 1 hour, subsequently falling to control levels. In contrast, preprodynorphin mRNA began to increase from 30 minutes after injection and remained elevated for at least 2 days. In situ hybridization with alpha 35S-labeled cRNA probe demonstrated that in the lower thoracic spinal cord preprodynorphin mRNA was expressed in dorsal horn neurons. In celiac ganglia, both preprodynorphin and c-fos mRNAs were not detected. In the peripancreatic abdominal tissue, there was acute severe inflammation consisting of necrosis and marked polymorphonuclear leucocytic infiltration. These data demonstrate that after abdominal tissue inflammation, activation of dynorphin biosynthesis occurred in thoracic spinal cord.(ABSTRACT TRUNCATED AT 250 WORDS)
强啡肽是一种阿片肽,被认为在脊髓水平对伤害性神经网络的调节中起重要作用。Fos蛋白参与强啡肽基因的转录调控。尽管已经有多项关于有害躯体刺激对强啡肽基因表达影响的研究,但很少有研究评估有害内脏刺激对强啡肽基因表达的作用。在本研究中,我们通过将腹部组织暴露于角叉菜胶,在大鼠模型中分析了有害内脏刺激介导的强啡肽基因表达。使用核糖核酸酶保护分析法检测脊髓神经元中前强啡肽原和c-fos mRNA的表达。炎症发生后,观察到胸段脊髓中c-fos mRNA水平迅速升高。注射后30分钟内c-fos mRNA水平上升,并持续升高1小时,随后降至对照水平。相比之下,前强啡肽原mRNA在注射后30分钟开始增加,并至少持续升高2天。用α 35S标记的cRNA探针进行原位杂交显示,在胸段脊髓下部,前强啡肽原mRNA在背角神经元中表达。在腹腔神经节中,未检测到前强啡肽原和c-fos mRNA。在胰腺周围腹部组织中,出现了由坏死和明显的多形核白细胞浸润组成的急性严重炎症。这些数据表明,腹部组织炎症后,胸段脊髓中强啡肽生物合成被激活。(摘要截短至250字)