Department of Biology, Faculty of Science, Al-Baha University, Al-Baha, Saudi Arabia.
Faculty of Medicine, Al-Baha University, Al-Baha, KSA.
J Med Life. 2024 Jul;17(7):728-738. doi: 10.25122/jml-2024-0050.
The liver is a critical organ in the human body and is frequently exposed to numerous exogenous toxic substances, including silver nanoparticles (AgNPs). This study aimed to examine the anti-inflammatory, anti-angiogenic, and hepatoprotective effects of () extract on AgNP-induced liver toxicity in Swiss mice. Fifty mice were divided into five groups. Group I (negative control) consisted of ten mice. Group II received oral extracts (80 mg/kg/bw) for 14 days. Group III was injected intraperitoneally (i.p.) with AgNPs at a daily dose of 35 mg/kg/bw for 3 days. Group IV received i.p. AgNPs for 3 days, followed by saline for 14 days. Group V received i.p. AgNPs for 3 days, followed by oral (80 mg/kg/bw) for 14 days. Liver function tests, pro and anti-inflammatory cytokines, antioxidant activities, protein carbonyl (PC) levels, liver histopathological analysis, immunohistochemical expressions of transcription factor (NF-κB), and vascular endothelial growth factor (VEGF) were examined. Group III had elevated levels of liver function, a significant increase of pro and anti-inflammatory cytokines, antioxidant activity, and PC levels. Histological observations revealed congested sinusoids filled with red blood cells (RBCs) and hepatocyte necrosis. Also, positive expressions of NF-κB and VEGF were detected compared with Group I. However, the administration of to Group V revealed significant changes with evident improvements in liver function biomarkers, pro and anti-inflammatory cytokines, antioxidant activities, oxidative stress markers (PC), and histopathological and immunohistochemical parameters compared to Group III. The results revealed that has promising and potential hepatoprotective, anti-inflammatory, and anti-angiogenic effects against liver toxicity. Further detailed studies are recommended to explore the potential of as a treatment for human liver ailments.
肝脏是人体的重要器官,经常会接触到许多外源性的有毒物质,包括银纳米粒子(AgNPs)。本研究旨在探讨()提取物对 AgNP 诱导的瑞士小鼠肝毒性的抗炎、抗血管生成和肝保护作用。将 50 只小鼠分为五组。第 I 组(阴性对照组)由 10 只小鼠组成。第 II 组连续 14 天口服()提取物(80mg/kg/bw)。第 III 组连续 3 天每天腹腔注射(i.p.)AgNPs 剂量为 35mg/kg/bw。第 IV 组连续 3 天腹腔注射 AgNPs 后,再给予生理盐水 14 天。第 V 组连续 3 天腹腔注射 AgNPs 后,再给予()提取物(80mg/kg/bw)口服 14 天。检测肝功能、促炎和抗炎细胞因子、抗氧化活性、蛋白羰基(PC)水平、肝组织病理学分析、转录因子(NF-κB)和血管内皮生长因子(VEGF)的免疫组织化学表达。第 III 组肝功能升高,促炎和抗炎细胞因子、抗氧化活性和 PC 水平显著增加。组织学观察显示充血的窦状隙充满红细胞(RBCs)和肝细胞坏死。与第 I 组相比,还检测到 NF-κB 和 VEGF 的阳性表达。然而,与第 III 组相比,给予()提取物到第 V 组显示出显著的变化,肝功能生物标志物、促炎和抗炎细胞因子、抗氧化活性、氧化应激标志物(PC)以及组织病理学和免疫组织化学参数均有明显改善。结果表明,()提取物具有潜在的肝保护、抗炎和抗血管生成作用,可减轻肝毒性。建议进一步进行详细研究,以探索()提取物作为人类肝脏疾病治疗方法的潜力。