Haddad Yara, Vallerand Diane, Brault Antoine, Spénard Jean, Haddad Pierre S
Natural Health Products and Metabolic Diseases Laboratory, Department of Pharmacology Université de Montréal and Montreal Diabetes Research Center, Montreal, QC, Canada H3C 3J7.
Int J Hepatol. 2011;2011:136816. doi: 10.4061/2011/136816. Epub 2011 Oct 16.
We explored the therapeutic effect of NCX 1000, a derivative of ursodeoxycholic acid (UDCA) with nitric oxide (NO) donating properties, alone or in combination with vitamin E, in an experimental model of NASH in the rat. Methods. A control group was fed a standard liquid diet (Control), and the NASH groups were fed a high-fat liquid diet for 12 weeks without (NASH) or with simultaneous daily gavage with either NCX 1000 at 15 or 30 mg/kg (N15 and N30, resp.), or N15 plus vitamin E 100 mg/kg (N15 + VitE) for the last 6 weeks; UDCA 17.2 mg/kg was used as a reference. Results. NASH rats developed all key features of the disease. Treatments with N30 improved liver histology, decreased lipid peroxidation, and completely suppressed increases in LDH release, plasma insulin, and TNF-α. It also decreased O(2) (∙-) release and returned liver weight and glutathione back to normal. All effects were similar to the reference treatment, UDCA. The N15 treatment was less efficient than the N30 group, but became comparable to the latter when combined to vitamin E. Conclusion. Our study demonstrates that NCX 1000 has potent cytoprotective, antioxidant, and hypoinsulinemic properties that can be enhanced by combination with vitamin E.
我们在大鼠非酒精性脂肪性肝炎(NASH)实验模型中,探究了熊去氧胆酸(UDCA)的衍生物NCX 1000(具有释放一氧化氮(NO)特性)单独使用或与维生素E联合使用的治疗效果。方法。对照组喂食标准液体饮食(对照组),NASH组喂食高脂液体饮食12周,其中一组在最后6周不进行处理(NASH组),另外几组在最后6周每天同时灌胃给予15或30mg/kg的NCX 1000(分别为N15和N30组),或N15加100mg/kg维生素E(N15 + VitE组);以17.2mg/kg的UDCA作为对照。结果。NASH大鼠出现了该疾病的所有关键特征。N30处理改善了肝脏组织学,降低了脂质过氧化,并完全抑制了乳酸脱氢酶释放、血浆胰岛素和肿瘤坏死因子-α的升高。它还减少了超氧阴离子(O(2) (∙-))的释放,并使肝脏重量和谷胱甘肽恢复正常。所有效果与对照处理UDCA相似。N15处理的效果不如N30组,但与维生素E联合使用时与后者相当。结论。我们的研究表明,NCX 1000具有强大的细胞保护、抗氧化和降胰岛素特性,与维生素E联合使用可增强这些特性。