Duggina Pragathi, Kalla Chandra Mouli, Varikasuvu Seshadri Reddy, Bukke Suman, Tartte Vijaya
Department of Biotechnology, Sri Venkateswara University, Tirupati, Andhra Pradesh, India.
J Physiol Biochem. 2015 Sep;71(3):435-54. doi: 10.1007/s13105-015-0423-y. Epub 2015 Jul 14.
This study was designed to investigate the protective effects of the centella triterpene saponins (EXT) on cyclophosphamide (CYP)-induced hepatotoxicity and immunosuppression in rats. The phytochemical profile of EXT was analyzed for centella saponins by using high-performance liquid chromatographic (HPLC). Therapeutic efficacy of EXT (250 mg/kg/day p.o) on hematological profile of blood, liver function markers, and cytokine profiles in CYP (10 mg/kg/day p.o)-treated rats. In addition, weights of immune organs (spleen and thymus) and histopathological changes in the liver, intestine, and spleen were also evaluated. The active principles in EXT were identified as madecassoside, asiaticoside, and asiatic acid by HPLC analysis. Upon administration of EXT, enhanced levels of glutamate pyruvate transaminase, alkaline phosphatase, and lipid peroxidation were found reduced while the levels of reduced glutathione and hematological parameters and relative weights of immune organs were restored to normal in CYP-treated rats. The hepatic mRNA level of TNF-α, which was increased during CYP administration, was significantly decreased by the EXT treatment. The decreased levels of mRNA expression of other cytokines like IFN-γ, IL-2, GM-CSF, after CYP treatment, were also found elevated upon administration of the EXT. Histopathological examination of the intestine, liver, and spleen indicated that the extract could attenuate the CYP-induced hepatic and immune organ damage. These results indicated that EXT modulated the immune and hepatic system function of rats against CYP-induced immunosuppression and hepatotoxicity by restoring the cytokine production, antioxidant system, and multiorgan injury. Thus, triterpene saponins may provide protective and/or therapeutic alternative against the immune-mediated liver diseases.
本研究旨在探讨积雪草三萜皂苷(EXT)对环磷酰胺(CYP)诱导的大鼠肝毒性和免疫抑制的保护作用。采用高效液相色谱(HPLC)法分析EXT中积雪草皂苷的植物化学特征。研究EXT(250mg/kg/天,口服)对CYP(10mg/kg/天,口服)处理的大鼠血液学指标、肝功能标志物和细胞因子谱的治疗效果。此外,还评估了免疫器官(脾脏和胸腺)的重量以及肝脏、肠道和脾脏的组织病理学变化。通过HPLC分析确定EXT中的活性成分是羟基积雪草苷、积雪草苷和积雪草酸。给予EXT后,发现CYP处理的大鼠中谷氨酸丙酮酸转氨酶、碱性磷酸酶水平和脂质过氧化增强程度降低,而还原型谷胱甘肽水平、血液学参数和免疫器官相对重量恢复正常。CYP给药期间升高的肝肿瘤坏死因子-α(TNF-α)mRNA水平经EXT处理后显著降低。CYP处理后其他细胞因子如干扰素-γ(IFN-γ)、白细胞介素-2(IL-2)、粒细胞-巨噬细胞集落刺激因子(GM-CSF)的mRNA表达水平降低,给予EXT后也升高。肠道、肝脏和脾脏的组织病理学检查表明,该提取物可减轻CYP诱导的肝脏和免疫器官损伤。这些结果表明,EXT通过恢复细胞因子产生、抗氧化系统和多器官损伤来调节大鼠的免疫和肝脏系统功能,对抗CYP诱导的免疫抑制和肝毒性。因此,三萜皂苷可能为免疫介导的肝脏疾病提供保护和/或治疗选择。