摘要
目的:观察盐酸氟西汀对抑郁模型大鼠胃窦黏膜肥大细胞胰蛋白酶-1(MCP-1)的影响。方法:将慢性、不可预见性、非同质性应激原作为抑郁模型,通过免疫荧光组织化学及RT-PCR技术研究盐酸氟西汀对抑郁模型大鼠胃窦黏膜MCP-1分泌的影响。结果:和正常对照组相比,抑郁模型组和生理盐水+抑郁模型组大鼠胃窦黏膜组织MCP-1平均免疫荧光强度值分别为(37.4±7.7)和(39.9±5.0),显著高于正常对照组(24.8±5.6)(P<0.01);盐酸氟西汀+正常对照组和盐酸氟西汀+抑郁模型组分别为(23.1±3.4)和(26.1±3.6),与正常对照组差异不明显(P>0.05)。抑郁模型组和生理盐水+抑郁模型组大鼠胃窦黏膜组织MCP-1mRNA表达分别为(0.759±0.357)和(0.781±0.451),显著高于正常对照组(0.476±0.029)(P<0.01);盐酸氟西汀+正常对照组和盐酸氟西汀+抑郁模型组分别为(0.460±0.027)和(0.488±0.030),与正常对照组差异不明显(P>0.05)。结论:盐酸氟西汀对抑郁模型大鼠具有下调胃窦部免疫反应的作用,对胃窦部具有保护作用。
Objective:To investigate the effect of fluoxetine hydrochloride on mast cell protease-1 (MCP-1)expression in depression model rats.Methods:The chronic stressed depression rat models were established by chronic unpredictable mild stress.Laser scanning confocal microscopy (LSCM)immunofluorecence and RT-PCR techniques were used to investigate MCP-1 expression in gastric antrum.Results:Fluoxetine was observed to play part inhibition effects on mast cells ultrastructure alterations.Compared to the normal control group,the average immunofluorescence intensity of gastric antrum MCP-1 significantly increased in chronic stress-induce depressed model group(37.4±7.7)or saline+depressed model group(39.9±5.0)(P0.01),while there was no significant difference between fluoxetine+normal control group(23.1±3.4) or fluoxetine+depressed model group(26.1±3.6)and normal control group(24.8±5.6).The average level of rMCP-1 mRNA in gastric antrum significantly increased in chronic stress-induce depressed model group(0.759±0.357)or saline+depressed model group(0.781±0.451)(P0.01),while there was no significant difference between fluoxetine+ normal control group (0.460±0.027)or fluoxetine+ depressed model group(0.488±0.030)and normal control group(0.476±0.029).Conclusion:Fluoxetine hydrochloride had negative immunoregulatory effects and might play aprotective role on gastric antrumin in depression model rats.
出处
《武汉大学学报(医学版)》
CAS
北大核心
2010年第5期596-599,共4页
Medical Journal of Wuhan University
关键词
抑郁模型
盐酸氟西汀
肥大细胞
胃窦
肥大细胞胰蛋白酶
Depression Model
Fluoxetine Hydrochloride
Mast Cells
Gastric Antrum
Mast Cell Protease-1