Suzuki Takehito, Fukuoka Hideo, Ushikoshi Setsuo, Sato Reiichiro, Morita Hidetoshi, Takizawa Tatsuya
School of Veterinary Medicine, Azabu University, Sagamihara, Japan.
Anim Sci J. 2015 May;86(5):532-40. doi: 10.1111/asj.12328. Epub 2014 Dec 11.
Hepatoprotective effects of Rhizopus oryzae/ U-1 aqueous extract (RU) were demonstrated in carbon tetrachloride (CCl4 )-induced liver-injured rats. In order to investigate the RU effects, the rats were administered RU at a dose of 10 or 100 mg/kg of body weight for 10 days before induction of the liver injury by oral administration of CCl4 (125 mg/kg body weight). (i) Pretreatment with RU caused a significant decrease in serum lactate dehydrogenase (LDH), alanine aminotransferase (ALT) and aspartate aminotransferase (AST) activities that were increased by the administration of CCl4 . (ii) RU pretreatment (100 mg/kg) increased 5-bromo-2'-deoxyuridine incorporation at 48 h after CCl4 treatment in hepatocytes. (iii) Histological hematoxylin and eosin staining of the liver showed that RU pretreatment reduced the damage induced by CCl4 administration. (iv) Reverse transcriptase PCR analysis showed RU retreatment caused a transient but significant increase in hepatocyte growth factor (HGF) and a sustained and significant increase in insulin-like growth factor-I (IGF-I) gene expression in hepatocytes injured by CCl4 treatment. From these results, we conclude that oral pre-administration of RU was effective to suppress liver injury induced by the subsequent oral CCl4 administration, and RU-induced increase in IGF-I and HGF gene expression may be, even in part, involved in biological actions of RU in rats.
米根霉/U-1水提取物(RU)对四氯化碳(CCl4)诱导的肝损伤大鼠具有肝脏保护作用。为了研究RU的作用,在通过口服给予CCl4(125mg/kg体重)诱导肝损伤前10天,以10或100mg/kg体重的剂量给大鼠施用RU。(i)用RU预处理可使因施用CCl4而升高的血清乳酸脱氢酶(LDH)、丙氨酸氨基转移酶(ALT)和天冬氨酸氨基转移酶(AST)活性显著降低。(ii)RU预处理(100mg/kg)可增加CCl4处理后48小时肝细胞中5-溴-2'-脱氧尿苷的掺入。(iii)肝脏组织学苏木精和伊红染色显示,RU预处理减轻了CCl4给药所致的损伤。(iv)逆转录酶PCR分析表明,RU再处理可使CCl4处理损伤的肝细胞中肝细胞生长因子(HGF)短暂但显著增加,胰岛素样生长因子-I(IGF-I)基因表达持续且显著增加。从这些结果来看,我们得出结论,口服预先施用RU可有效抑制随后口服CCl4给药诱导的肝损伤,并且RU诱导的IGF-I和HGF基因表达增加可能至少部分参与了RU在大鼠中的生物学作用。