Muriel Pablo, Deheza Rogelio
Sección Externa de Farmacología, Cinvestav-IPN Apdo, DF México.
Liver Int. 2003 Aug;23(4):262-8. doi: 10.1034/j.1600-0676.2003.00837.x.
BACKGROUND/AIMS: To evaluate liver-beneficial properties of metadoxine, not related with alcohol metabolism, bioactivation of external toxins or antioxidant mechanisms, the chronic bile duct ligation (BDL) model was used and results were compared with colchicine.
Seven groups (n=6) of male Wistar rats were used. Four groups were BDL and received metadoxine (60 mg/kg/12 h i.p.), colchicine (10 microg/rat/day/p.o.), both or vehicles; three groups were sham-appropriate controls. Collagen content was determined by measuring hydroxyproline in liver samples; malondialdehyde (MDA) was used to estimate lipid peroxidation levels; glycogen was determined utilizing the anthrone reagent; gomory's trichromic stains of liver sections were performed.
Collagen increased four-fold by BDL, metadoxine, colchicine or both prevented fibrosis partially; MDA levels increased three-fold by BDL and no treatment had any significant effect; glycogen was almost depleted in the cirrhotic group, metadoxine preserved glycogen; bilirubins, and alanine aminotransferase and gamma-glutamyltranspeptidase activities increased several-fold in the BDL group, and both drugs prevented these effects partially. The histopathological analysis correlated with biochemical data.
Both compounds showed similar antifibrotic properties; metadoxine was more effective in preserving glycogen. Besides its antioxidant effects and its ability to induce alcohol metabolism, metadoxine possesses important antifibrotic and antinecrotic properties, and maintains energy stores efficiently.
背景/目的:为评估美他多辛对肝脏的有益作用,该作用与酒精代谢、外源性毒素的生物活化或抗氧化机制无关,采用慢性胆管结扎(BDL)模型,并将结果与秋水仙碱进行比较。
使用七组(n = 6)雄性Wistar大鼠。四组为BDL组,分别接受美他多辛(60 mg/kg/12 h腹腔注射)、秋水仙碱(10 μg/大鼠/天/口服)、两者联合或赋形剂;三组为假手术对照组。通过测量肝脏样本中的羟脯氨酸来测定胶原蛋白含量;使用丙二醛(MDA)评估脂质过氧化水平;利用蒽酮试剂测定糖原;对肝脏切片进行戈莫里三色染色。
BDL使胶原蛋白增加了四倍,美他多辛、秋水仙碱或两者联合可部分预防纤维化;BDL使MDA水平增加了三倍,且无治疗有任何显著效果;肝硬化组糖原几乎耗尽,美他多辛可保留糖原;BDL组胆红素、丙氨酸转氨酶和γ-谷氨酰转肽酶活性增加了数倍,两种药物均可部分预防这些作用。组织病理学分析与生化数据相关。
两种化合物均显示出相似的抗纤维化特性;美他多辛在保留糖原方面更有效。除了其抗氧化作用和诱导酒精代谢的能力外,美他多辛还具有重要的抗纤维化和抗坏死特性,并能有效维持能量储备。