Li Tiesong, Ito Kousei, Sumi Shin-Ichiro, Fuwa Toru, Horie Toshiharu
Laboratory of Biopharmaceutics, Graduate School of Pharmaceutical Sciences, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8675, Japan.
Cancer Chemother Pharmacol. 2009 Apr;63(5):873-80. doi: 10.1007/s00280-008-0809-4. Epub 2008 Aug 2.
Methotrexate (MTX) causes intestinal damage, resulting in diarrhea. The side effects often disturb the cancer chemotherapy. We previously reported that AGE protected the small intestine of rats from the MTX-induced damage. In the present paper, the mechanism of the protection of AGE against the MTX-induced damage of small intestine was investigated, using IEC-6 cells originating from rat jejunum crypt.
The viability and apoptosis of IEC-6 cells were examined in the presence of MTX and/or AGE.
The viability of IEC-6 cells exposed to MTX was decreased by the increase of MTX concentration. The MTX-induced loss of viable IEC-6 cells was almost completely prevented by the presence of more than 0.1% AGE. In IEC-6 cells exposed to MTX, the cromatin condensation, DNA fragmentation, caspase-3 activation and cytochrome c release were observed. These were preserved to the control levels by the presence of AGE. MTX markedly decreased intracellular GSH in IEC-6 cells, but the presence of AGE in IEC-6 cells with MTX preserved intracellular GSH to the control level. IEC-6 cells in G2/M stage markedly decreased 72 h after the MTX treatment, which was preserved to the control level by the presence of AGE. These results indicated that AGE protected IEC-6 cells from the MTX-induced damage.
The MTX-induced apoptosis of IEC-6 cells was shown to be depressed by AGE. AGE may be useful for the cancer chemotherapy with MTX, since AGE reduces the MTX-induced intestinal damage.
甲氨蝶呤(MTX)会导致肠道损伤,引发腹泻。这些副作用常常干扰癌症化疗。我们之前报道过晚期糖基化终末产物(AGE)可保护大鼠小肠免受MTX诱导的损伤。在本文中,利用源自大鼠空肠隐窝的IEC - 6细胞,研究了AGE对MTX诱导的小肠损伤的保护机制。
在MTX和/或AGE存在的情况下,检测IEC - 6细胞的活力和凋亡情况。
随着MTX浓度增加,暴露于MTX的IEC - 6细胞活力下降。当存在超过0.1%的AGE时,MTX诱导的IEC - 6活细胞损失几乎完全得到预防。在暴露于MTX的IEC - 6细胞中,观察到染色质凝聚、DNA片段化、半胱天冬酶 - 3激活和细胞色素c释放。而AGE的存在使这些情况维持在对照水平。MTX显著降低了IEC - 6细胞内的谷胱甘肽(GSH)水平,但在含有MTX的IEC - 6细胞中加入AGE可使细胞内GSH维持在对照水平。MTX处理72小时后,处于G2/M期的IEC - 6细胞显著减少,而AGE的存在使其维持在对照水平。这些结果表明AGE保护IEC - 6细胞免受MTX诱导的损伤。
结果显示AGE可抑制MTX诱导的IEC - 6细胞凋亡。由于AGE可减轻MTX诱导的肠道损伤,因此AGE可能对MTX癌症化疗有用。