A histological study for the possible therapeutic effect of stem cells in methotrexate induced small intestinal injury in a male rat model

Sara Mohamed, S. Radwan, S. Atta, S. Hosny
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引用次数: 1

Abstract

Abstract: -Background and objectives: Methotrexate (MTX) is an antirheumatic and chemotherapeutic agent with highly adverse effect on gastrointestinal tract. Mesenchymal stem cell (MSCs) can exert a therapeutic action by regenerative capacity in intestinal damage. This study was done to demonstrate the possible therapeutic effect of MSCs in methotrexate induced intestinal injury in adult male albino rat.Methods and results: Male albino rats were used in this study. Group A (Control group), subgroup A-I rats received saline for 2 weeks and subgroup A-II received saline for 2 weeks then phosphate buffer saline once intraperitoneal (IP). Group B rats received MTX (14 mg/kg/week) intraperitoneal (IP) for 2 weeks. Group C, rats received MTX (14 mg/kg/week) intraperitoneal (IP) for 2 weeks. After 2 weeks, they were injected IP with MSCs (2 × 106 cells in 500 𝜇L PBS once). Groups AI&B were anaesthetized and sacrificed after 2 weeks while groups AII&C were sacrificed after 4 weeks. Blood samples were drawn from the tail vein to measure myeloperoxidase (MPO) and vascular endothelial growth factor (VEGF). Small intestinal specimens were obtained for evaluation by light microscopy. CD4+, and CD8+ immunohistochemistry and statistical analysis were applied. Significant increase in MPO and significant decrease in VEGF were reported in Group B. MTX induced pathological alterations in small intestinal tissues, mean number of mast cells and goblet cells associated with increased CD4+ and CD8+ immunoexpression. Nearly all changes were ameliorated following MSCs therapyConclusion: MSCs have significant effect in repairing the deleterious action of MTX in small intestinal tissues.
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干细胞对甲氨蝶呤诱导的雄性大鼠小肠损伤可能治疗作用的组织学研究
摘要:背景与目的:甲氨蝶呤(Methotrexate, MTX)是一种对胃肠道有高度不良反应的抗风湿病和化疗药物。间充质干细胞(MSCs)可通过其再生能力在肠损伤中发挥治疗作用。本研究旨在探讨骨髓间充质干细胞对甲氨蝶呤诱导的成年雄性白化大鼠肠道损伤的治疗作用。方法与结果:以雄性白化大鼠为研究对象。A组(对照组)、A- i亚组大鼠连续给予生理盐水2周,A- ii亚组大鼠连续给予生理盐水2周,然后腹腔注射磷酸缓冲盐水1次。B组大鼠腹腔注射MTX (14 mg/kg/周)2周。C组,大鼠腹腔注射MTX (14 mg/kg/周)2周。2周后,向其注射MSCs (2 × 106个细胞,500𝜇L PBS 1次)。AI&B组麻醉2周后处死,ai&c组4周后处死。取尾静脉血样测定髓过氧化物酶(MPO)和血管内皮生长因子(VEGF)。取小肠标本进行光镜检查。CD4+、CD8+免疫组化及统计学分析。b组MPO显著升高,VEGF显著降低,MTX诱导小肠组织病理改变,肥大细胞和杯状细胞平均数量增加,CD4+和CD8+免疫表达升高。结论:MSCs对修复MTX对小肠组织的有害作用有显著作用。
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