Andrographis paniculata Leaves Extract Inhibit TNF-α and Caspase-3 Expression of Septic Rats’ Intestinal Tissues

Ryco Giftyan Ardika, B. Budiono, Nyoman Suci Widiastiti, Nani Maharani, N. Susilaningsih, Ferry Sandra
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Abstract

BACKGROUND: Microcirculation and cellular disturbances caused by sepsis might trigger significant intestinal damage. Andrographis paniculata extract decreases inflammatory intestinal epithelial cells with its role as an antiparasitic and anti-inflammatory agent. However, A. paniculata extract’s effect on sepsis have not been commonly studied, especially in the intestinal tissues. Therefore, this study was conducted to determine A. paniculata leaves extract (APLE) effect in sepsis-induced intestinal tissues of rats by examining the expression of inflammatory cytokines involved in sepsis, namely tumor necrosis factor (TNF)-α and Caspase-3.METHODS: Rats were divided into five groups; two groups received no pretreatment and the other three groups received 200, 400, and 500 mg/kg BW/day APLE, respectively. Three pretreated groups and one group with no pretreatment were then injected with 1 mg/200 g BW lipopolysaccharides (LPS) intraperitoneally to create septic rat models. Three days after the LPS-induction, rats were euthanized and the expression of TNF-α and Caspase-3 were assessed based on the immunohistochemical staining of rats’ intestinal tissues.RESULTS: Compared with NaCl (sham), LPS significantly (p<0.001) induced TNF-α expression from 6.60±1.36 to 25.37±1.74. Pretreatment of 200, 400, and 500 mg/kg BW/day APLE could significantly (p<0.001) inhibit the LPS-induced TNF-α expression (18.82±1.36, 11.45±1.18, and 6.89±1.90, respectively). Similar with TNF-α, compared with NaCl (sham), LPS significantly (p<0.001) induced Caspase-3 expression from 6.92±1.66 to 23.59±2.25. Pretreatment of 200, 400, and 500 mg/kg BW/day APLE could significantly (p<0.001) inhibit the LPS-induced Caspase-3 expression (17.47±1.68, 12.99±1.51, and 5.59±1.51, respectively).CONCLUSION: The pretreatment of APLE could inhibit the LPS-induced TNF-α and Caspase-3 expression, therefore APLE could be suggested as a potential sepsis-preventing agent.KEYWORDS: Andrographis paniculata, sepsis, TNF-α, Caspase-3, lipopolysaccharide 
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穿心莲叶提取物抑制败血症大鼠肠组织中 TNF-α 和 Caspase-3 的表达
背景:败血症导致的微循环和细胞紊乱可能会引发严重的肠道损伤。穿心莲提取物具有抗寄生虫和抗炎作用,可减少炎性肠上皮细胞。然而,穿心莲提取物对败血症的影响尚未得到广泛研究,尤其是对肠道组织的影响。因此,本研究通过检测参与败血症的炎性细胞因子(即肿瘤坏死因子(TNF)-α和Caspase-3)的表达,来确定A. paniculata叶提取物(APLE)对败血症诱导的大鼠肠道组织的影响。然后向三组预处理组和一组未预处理组腹腔注射 1 毫克/200 克体重的脂多糖(LPS),建立败血症大鼠模型。结果:与氯化钠(假)相比,LPS能显著(p<0.001)诱导TNF-α的表达,从6.60±1.36升至25.37±1.74。预处理 200、400 和 500 毫克/千克体重/天的 APLE 可显著(p<0.001)抑制 LPS 诱导的 TNF-α 表达(分别为 18.82±1.36、11.45±1.18 和 6.89±1.90)。与 TNF-α 相似,与氯化钠(假)相比,LPS 显著(p<0.001)诱导 Caspase-3 的表达,从 6.92±1.66 升至 23.59±2.25。200、400和500毫克/千克体重/天的APLE预处理可明显(p<0.001)抑制LPS诱导的Caspase-3表达(分别为17.47±1.68、12.99±1.51和5.59±1.51)。结论:APLE预处理可抑制LPS诱导的TNF-α和Caspase-3的表达,因此APLE可作为一种潜在的败血症预防剂。 关键词:穿心莲 败血症 TNF-α Caspase-3 脂多糖
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