Rangan G K, Wang Y, Tay Y C, Harris D C
Department of Renal Medicine, University of Sydney at Westmead Hospital, Sydney, Australia.
Nephron. 2000 Dec;86(4):482-90. doi: 10.1159/000045838.
BACKGROUND/AIM: Inhibition of nuclear factor kappaB with the antioxidant pyrrolidine dithiocarbamate (PDTC) reduced tubulointerstitial injury in Adriamycin nephropathy (AN), whereas N-acetylcysteine (NAC) was ineffective. Here we hypothesize that PDTC reduces the renal cortical expression of nuclear factor kappaB dependent cytokines in AN.
Male Wistar rats received a single intravenous injection of doxorubicin hydrochloride (7.5 mg/kg). NAC (150 mg/kg twice daily i.p.), PDTC (50 mg/kg twice daily i.p.), or vehicle were commenced on day 14 and continued until day 30.
On day 30, mRNAs of selected cytokines were increased in AN (TNF-alpha 3.4-fold, MCP-1 5.1-fold, IL-10 2.7-fold, TGF-beta1 3.5-fold, all p < 0.05) as determined by RT-PCR. PDTC reduced IL-10 and TGF-beta1 mRNAs (p < 0.05), whereas the upregulation of MCP-1 and TNF-alpha mRNAs was not affected. In contrast, NAC increased TNF-alpha and IL-10 mRNAs (p < 0.05). Nuclear protein levels of activator protein-1 were increased in AN (4.4-fold, p < 0.01) and not significantly altered by PDTC (3.0-fold, p = 0.13) or NAC (5. 2-fold, p = 0.18).
The protective effects of PDTC in AN are not associated with a local reduction in TNF-alpha and MCP-1 gene expression. The latter may be due to continued transactivation by activator protein-1. These data also suggest that IL-10 and TGF-beta1 mRNA expressions are PDTC dependent and have a role in mediating tubulointerstitial injury.
背景/目的:抗氧化剂吡咯烷二硫代氨基甲酸盐(PDTC)抑制核因子κB可减轻阿霉素肾病(AN)中的肾小管间质损伤,而N-乙酰半胱氨酸(NAC)则无效。在此,我们假设PDTC可降低AN中肾皮质核因子κB依赖性细胞因子的表达。
雄性Wistar大鼠单次静脉注射盐酸阿霉素(7.5mg/kg)。在第14天开始给予NAC(150mg/kg,腹腔注射,每日两次)、PDTC(50mg/kg,腹腔注射,每日两次)或溶剂,并持续至第30天。
通过逆转录聚合酶链反应(RT-PCR)测定,在第30天,AN中所选细胞因子的mRNA水平升高(肿瘤坏死因子-α升高3.4倍,单核细胞趋化蛋白-1升高5.1倍,白细胞介素-10升高2.7倍,转化生长因子-β1升高3.5倍,所有p<0.05)。PDTC可降低白细胞介素-10和转化生长因子-β1的mRNA水平(p<0.05),而单核细胞趋化蛋白-1和肿瘤坏死因子-α的mRNA上调未受影响。相比之下,NAC可升高肿瘤坏死因子-α和白细胞介素-10的mRNA水平(p<0.05)。激活蛋白-1的核蛋白水平在AN中升高(4.4倍,p<0.01),PDTC(3.0倍,p=0.13)或NAC(5.2倍,p=0.18)对其无显著影响。
PDTC在AN中的保护作用与肿瘤坏死因子-α和单核细胞趋化蛋白-1基因表达的局部降低无关。后者可能是由于激活蛋白-1的持续反式激活。这些数据还表明,白细胞介素-10和转化生长因子-β1的mRNA表达依赖于PDTC,并在介导肾小管间质损伤中起作用。