Fan Fangcheng, Li Lei, Liu Wenkai, Yang Mengzhu, Ma Xiaoli, Sun Haiji
Key Laboratory of Animal Resistance Biology of Shandong Province, School of Life Science, Shandong Normal University, Jinan, 250014, China.
Qingdao No.31 Middle School, Qingdao, 266041, China.
Neurosci Lett. 2018 May 14;675:95-102. doi: 10.1016/j.neulet.2018.03.054. Epub 2018 Mar 23.
Restraint water-immersion stress (RWIS) is considered to be a compound stress model that includes psychological and physical stimulation and may cause gastric mucosal damage. Studies have shown that locus coeruleus (LC) is involved in the gastrointestinal function, but whether it is involved in RWIS-induced gastric mucosal damage has not yet been reported. Here, we investigated the expression of glial fibrillary acidic protein (GFAP), c-Fos, and phosphorylation extracellular signal regulated kinase 1/2 (p-ERK1/2) in the LC after RWIS using immunocytochemical staining and western blotting in order to explore whether the ERK1/2 signaling pathway interacts with the neuron-astrocyte network in the LC during RWIS and whether it is involved in causing RWIS-induced gastric mucosal damage. Expression of c-Fos, GFAP, and p-ERK1/2 increased significantly following RWIS and peaked at 3 h after RWIS. After intracerebroventricular injection of c-Fos antisense oligodeoxynucleotides (ASO) and astrocytic toxin L-a-aminoadipate (L-AA), the gastric mucosal damage and the activation of neurons and astrocytes in the LC significantly decreased. Intracerebroventricular injection of ERK1/2 signaling pathway inhibitor PD98059 suppressed gastric mucosal damage as well as the RWIS-induced activation of neurons and astrocytes in the LC. Activation of LC neurons and astrocytes induced by RWIS through the ERK1/2 signaling pathway may play a critical role in RWIS-induced gastric mucosa damage.
束缚水浸应激(RWIS)被认为是一种复合应激模型,包括心理和生理刺激,可能导致胃黏膜损伤。研究表明,蓝斑(LC)参与胃肠功能,但它是否参与RWIS诱导的胃黏膜损伤尚未见报道。在此,我们采用免疫细胞化学染色和蛋白质印迹法研究RWIS后LC中胶质纤维酸性蛋白(GFAP)、c-Fos和磷酸化细胞外信号调节激酶1/2(p-ERK1/2)的表达,以探讨ERK1/2信号通路在RWIS期间是否与LC中的神经元-星形胶质细胞网络相互作用,以及它是否参与导致RWIS诱导的胃黏膜损伤。RWIS后c-Fos、GFAP和p-ERK1/2的表达显著增加,并在RWIS后3小时达到峰值。脑室内注射c-Fos反义寡脱氧核苷酸(ASO)和星形胶质细胞毒素L-α-氨基己二酸(L-AA)后,胃黏膜损伤以及LC中神经元和星形胶质细胞的激活显著降低。脑室内注射ERK1/2信号通路抑制剂PD98059可抑制胃黏膜损伤以及RWIS诱导的LC中神经元和星形胶质细胞的激活。RWIS通过ERK1/2信号通路诱导的LC神经元和星形胶质细胞激活可能在RWIS诱导的胃黏膜损伤中起关键作用。