Yüncü Mehmet, Eralp Ayhan, Koruk Mehmet, Sari Ibrahim, Bağci Cahit, Inalöz Serap
Department of Histology and Embryology, Gaziantep University Medical School, Gaziantep, Turkey.
Med Princ Pract. 2004 Nov-Dec;13(6):346-52. doi: 10.1159/000080472.
The aim of the present study was to examine whether or not the administration of vitamin A (VA) protects against methotrexate (MTX)-induced damage to small intestinal epithelium.
Sixty-three male Wistar albino rats, 10-12 weeks old, weighing 240-280 g, were divided into three groups: (1) controls, (2) rats receiving MTX treatment alone, and (3) rats receiving MTX plus VA treatment. A single dose of MTX (20 mg/kg MTX in 20 ml vehicle) was administered to the rats intraperitoneally. For MTX plus VA treated groups, retinol palmitate (VA) 5,000 IU/kg dissolved in 0.5 ml sunflower oil was administered by intragastric tube 3 days prior to MTX treatment and continued till the rats were sacrificed. The control group was treated with vehicle. Both control and MTX-alone groups were also treated with sunflower oil as a placebo. The rats were sacrificed on the 2nd, 4th and 6th day after MTX treatment. Tissue samples from the jejunum were taken for histopathological analysis.
MTX treatment induced villus shortening and fusion, epithelial atrophy, crypt loss, inflammatory infiltrate in the lamina propria, and goblet cell depletion. The pre- and post-treatment administration of VA decreased the severity of jejunal damage caused by MTX treatment.
Our results confirmed that administration of VA decreased the MTX-induced damage to the small intestine. This protective effect of VA may have clinical applications in cancer chemotherapy.
本研究旨在探讨维生素A(VA)的给药是否能预防甲氨蝶呤(MTX)诱导的小肠上皮损伤。
将63只10 - 12周龄、体重240 - 280克的雄性Wistar白化大鼠分为三组:(1)对照组;(2)仅接受MTX治疗的大鼠组;(3)接受MTX加VA治疗的大鼠组。给大鼠腹腔注射单剂量MTX(20毫克/千克MTX溶于20毫升溶媒)。对于MTX加VA治疗组,在MTX治疗前3天通过胃管给予溶于0.5毫升葵花籽油的5000国际单位/千克视黄醇棕榈酸酯(VA),并持续至大鼠处死。对照组用溶媒治疗。对照组和仅MTX组也用葵花籽油作为安慰剂治疗。在MTX治疗后的第2、4和6天处死大鼠。取空肠组织样本进行组织病理学分析。
MTX治疗导致绒毛缩短和融合、上皮萎缩、隐窝消失、固有层炎性浸润以及杯状细胞减少。VA在治疗前和治疗后的给药减轻了MTX治疗引起的空肠损伤的严重程度。
我们的结果证实,VA给药减轻了MTX诱导的小肠损伤。VA的这种保护作用可能在癌症化疗中有临床应用。