Department of Infectious Diseases, Affiliated Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu 610072, Sichuan, China.
Department of Infectious Diseases, Affiliated Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu 610072, Sichuan, China.
J Ethnopharmacol. 2015 Feb 23;161:53-9. doi: 10.1016/j.jep.2014.12.003. Epub 2014 Dec 9.
Modified sini decoction (MSND) is a well-known traditional Chinese medical formula that has been used to treat cardiovascular and liver diseases for many years. We investigated the effects of MSND on acute liver failure and identified the possible mechanisms of these effects.
Acute liver failure was induced by intraperitoneal injection of d-galactosamine (d-GalN) into specific pathogen-free male Wistar rats. Next, the rats were treated with Stronger Neo-Minophagen C and MSND via gavage. Biochemical parameters, histological changes in the liver, the survival of rats and the mRNA levels of toll-like receptor 4 (TLR4), nuclear factor kappa B (NF-κB), high mobility group box 1 (HMGB1) caspase-3 and proliferating cell nuclear antigen (PCNA) were analyzed.
MSND prolonged the survival times of the acute liver failure rats. The biochemical parameters were improved, and necrosis in the liver tissues was reduced by both Stronger Neo-Minophagen C (SNMC) and MSND, but MSND induced greater effects. The mRNA expressions of HMGB1, TLR4, NF-κB, and Caspase-3 were remarkably decreased, and the expression of PCNA was remarkably increased by SNMC and MSND, and the effects of MSND were greater.
MSND protected the liver and increased the survival rate of acute liver failure rats. These effects were likely mediated by the inhibitions of the inflammatory reaction and apoptosis and the promotion of liver tissue regeneration.
改良四逆汤(MSND)是一种著名的中药方剂,多年来一直用于治疗心血管和肝脏疾病。我们研究了 MSND 对急性肝衰竭的影响,并确定了这些影响的可能机制。
通过腹腔注射半乳糖胺(d-GalN)在无菌雄性 Wistar 大鼠中诱导急性肝衰竭。然后,通过灌胃给予大鼠强力新肝宁和 MSND。分析生化参数、肝组织学变化、大鼠存活率以及 Toll 样受体 4(TLR4)、核因子 kappa B(NF-κB)、高迁移率族蛋白 1(HMGB1)、半胱氨酸天冬氨酸蛋白酶-3(Caspase-3)和增殖细胞核抗原(PCNA)的 mRNA 水平。
MSND 延长了急性肝衰竭大鼠的存活时间。两种药物(强力新肝宁和 MSND)均改善了生化参数,减轻了肝组织坏死,但 MSND 的作用更为明显。HMGB1、TLR4、NF-κB 和 Caspase-3 的 mRNA 表达明显降低,PCNA 的表达明显增加,而 MSND 的作用更为显著。
MSND 保护肝脏并提高急性肝衰竭大鼠的存活率。这些作用可能是通过抑制炎症反应和细胞凋亡以及促进肝组织再生来介导的。