Department of Cell Biology and Genetics, Guangxi Medical University, Nanning, Guangxi, China; Key Laboratory of Longevity and Aging-Related Diseases of Chinese Ministry of Education, Guangxi Medical University, Nanning, Guangxi, China; Key Laboratory of Basic Research on Regional Diseases (Guangxi Medical University), Education Department of Guangxi Zhuang Autonomous Region, Nanning, Guangxi, China.
Department of Parasitology, Guangxi Medical University, Nanning, Guangxi, China.
Biomed Pharmacother. 2024 Sep;178:117240. doi: 10.1016/j.biopha.2024.117240. Epub 2024 Aug 1.
Infection with Schistosoma japonicum (S. japonicum) is an important zoonotic parasitic disease that causes liver fibrosis in both human and domestic animals. The activation of hepatic stellate cells (HSCs) is a crucial phase in the development of liver fibrosis, and inhibiting their activation can alleviate this progression. Total flavonoids of litchi seed (TFL) is a naturally extracted drug, and modern pharmacological studies have shown its anti-fibrotic and liver-protective effects. However, the role of TFL in schistosomiasis liver fibrosis is still unclear. This study investigated the therapeutic effects of TFL on liver fibrosis in S. japonicum infected mice and explored its potential mechanisms. Animal study results showed that TFL significantly reduced the levels of Interleukin-1β (IL-1β), Tumor Necrosis Factor-α (TNF-α), Interleukin-4 (IL-4), and Interleukin-6 (IL-6) in the serum of S. japonicum infected mice. TFL reduced the spleen index of mice and markedly improved the pathological changes in liver tissues induced by S. japonicum infection, decreasing the expression of alpha-smooth muscle actin (α-SMA), Collagen I and Collagen III protein in liver tissues. In vitro studies indicated that TFL also inhibited the activation of HCSs induced by Transforming Growth Factor-β1 (TGF-β1) and reduced the levels of α-SMA. Gut microbes metagenomics study revealed that the composition, abundance, and functions of the mice gut microbiomes changed significantly after S. japonicum infection, and TLF treatment reversed these changes. Therefore, our study indicated that TFL alleviated granulomatous lesions and improved S. japonicum induced liver fibrosis in mice by inhibiting the activation of HSCs and by improving the gut microbiomes.
日本血吸虫(S. japonicum)感染是一种重要的人畜共患寄生虫病,可导致人和家畜肝纤维化。肝星状细胞(HSCs)的激活是肝纤维化发展的关键阶段,抑制其激活可以缓解这一进程。荔枝核总黄酮(TFL)是一种天然提取药物,现代药理学研究表明其具有抗纤维化和保肝作用。然而,TFL 在日本血吸虫病肝纤维化中的作用尚不清楚。本研究探讨了 TFL 对日本血吸虫感染小鼠肝纤维化的治疗作用,并探讨了其潜在机制。动物研究结果表明,TFL 可显著降低日本血吸虫感染小鼠血清中白细胞介素 1β(IL-1β)、肿瘤坏死因子-α(TNF-α)、白细胞介素 4(IL-4)和白细胞介素 6(IL-6)水平。TFL 降低了感染日本血吸虫小鼠的脾指数,并显著改善了肝组织的病理变化,降低了肝组织中α-平滑肌肌动蛋白(α-SMA)、I 型胶原和 III 型胶原蛋白的表达。体外研究表明,TFL 还可抑制转化生长因子-β1(TGF-β1)诱导的 HCS 激活,并降低α-SMA 水平。肠道微生物宏基因组学研究表明,日本血吸虫感染后小鼠肠道微生物的组成、丰度和功能发生了显著变化,而 TLF 治疗可逆转这些变化。因此,我们的研究表明,TFL 通过抑制 HSCs 的激活和改善肠道微生物群来缓解日本血吸虫引起的肉芽肿病变和改善肝纤维化。