Fujita Atsuyo, Sasaki Hideyuki, Doi Asako, Okamoto Kunihisa, Matsuno Shohei, Furuta Hiroto, Nishi Masahiro, Nakao Taisei, Tsuno Takuo, Taniguchi Hisaji, Nanjo Kishio
The First Department of Medicine, Wakayama Medical University, Kimiidera 811-1, Wakayama, PO 641-8509, Japan.
Diabetes Res Clin Pract. 2008 Jan;79(1):11-7. doi: 10.1016/j.diabres.2007.08.009. Epub 2007 Sep 25.
We investigated the preventive effects of ferulic acid (FA) and alpha-tocopherol (AT) on the progression of diabetic nephropathy. Otsuka Long-Evans Tokushima Fatty (OLETF) and Long-Evans Tokushima Otsuka (LETO) rats were used as type 2 diabetes and non-diabetes models, respectively. Two-thirds of the OLETF rats were fed 0.2% FA-containing or 0.5% AT-containing chow. Diabetic nephropathy was assessed based on urinary protein excretion and pathological changes which were scored based on the percentages of extracellular matrix area in the glomerular area. Furthermore, renal messenger RNA (mRNA) expression of intercellular adhesion molecule-1 (ICAM-1), cyclooxygenase-2 (COX-2) and transforming growth factor-beta1 (TGF-beta1) was quantified by real-time polymerase chain reaction. After 12 weeks of FA- or AT-supplementation, urinary protein in untreated-OLETF group was significantly higher than that in LETO group, thus FA-supplementation significantly decreased urinary protein excretion. Pathological scores in FA-supplemented group were significantly lower than those in untreated OLETF group. Supplementation with either FA or AT significantly prevented the elevation of TGF-beta1 mRNA expression caused by diabetes. Treatment with neither FA nor AT had a significant effect on COX-2 or ICAM-1 mRNA expressions. We have demonstrated the preventative effects of FA on diabetic nephropathy via suppression of TGF-beta1 upregulation, furthermore FA may be more potent than AT.
我们研究了阿魏酸(FA)和α-生育酚(AT)对糖尿病肾病进展的预防作用。大冢Long-Evans德岛肥胖(OLETF)大鼠和大冢Long-Evans德岛(LETO)大鼠分别用作2型糖尿病和非糖尿病模型。三分之二的OLETF大鼠喂食含0.2%FA或0.5%AT的饲料。基于尿蛋白排泄和病理变化评估糖尿病肾病,病理变化根据肾小球区域细胞外基质面积的百分比进行评分。此外,通过实时聚合酶链反应定量细胞间粘附分子-1(ICAM-1)、环氧合酶-2(COX-2)和转化生长因子-β1(TGF-β1)的肾信使核糖核酸(mRNA)表达。在补充FA或AT 12周后,未治疗的OLETF组尿蛋白显著高于LETO组,因此补充FA显著降低了尿蛋白排泄。补充FA组的病理评分显著低于未治疗的OLETF组。补充FA或AT均可显著预防糖尿病引起的TGF-β1 mRNA表达升高。单独使用FA或AT治疗对COX-2或ICAM-1 mRNA表达均无显著影响。我们已经证明FA通过抑制TGF-β1上调对糖尿病肾病具有预防作用,此外FA可能比AT更有效。