Leng Yue, Wang Fang, Chen Changbao, Wan Xilin, Li Xinyang, Wang Huan, Wang Shumin
Department of Ginseng Scientific Research Institute, Changchun University of Chinese Medicine, 130117 Changchun, Jilin, China.
Front Biosci (Landmark Ed). 2023 Feb 2;28(2):23. doi: 10.31083/j.fbl2802023.
spore powder (GLSP) has abundant pharmacological activities. However, the difference in the hepatoprotective function of sporoderm-broken and sporoderm-unbroken Ganoderma spore powder has not been studied. This study is the first to investigate the effects of both sporoderm-damaged and sporoderm-intact GLSP on the improvement of acute alcoholic liver injury in mice and gut microbiota of mice.
Serum aspartate aminotransferase (AST) and alanine aminotransferase (ALT) levels and interleukin 1β (IL-1β), interleukin 18 (IL-18), and tumor necrosis factor-α (TNF-α) levels in liver tissues from mice in each group were detected by enzyme-linked immunosorbent assay (ELISA) kits, and histological analysis of liver tissue sections was performed to evaluate the liver-protecting effects of both sporoderm-broken and sporoderm-unbroken GLSP. Additionally, 16S rDNA sequencing of feces from the bowels of mice was performed to compare the regulatory effects of both sporoderm-broken and sporoderm-unbroken GLSP on the gut microbiota of mice.
Compared with those in the 50% ethanol model group (MG), sporoderm-broken GLSP significantly reduced serum AST and ALT levels ( 0.0001) and the release of the inflammatory factors, including IL-1β, IL-18, and TNF-α ( 0.0001), and effectively improved the pathological state of liver cells; sporoderm-unbroken GLSP significantly reduced the ALT content ( = 0.0002) and the release of the inflammatory factors, including IL-1β ( 0.0001), IL-18 ( = 0.0018), and TNF-α ( = 0.0005), and reduced the serum AST content, but the reduction was not significant; compared with the gut microbiota of the MG, sporoderm-broken GLSP reduced the levels of and , increased the relative abundance of beneficial bacteria such as , and decreased the abundance levels of harmful bacteria, such as and _; sporoderm-unbroken GLSP could reduce the abundance levels of harmful bacteria, such as and ; and GLSP treatment alleviates the downregulation of the levels of translation, ribosome structure and biogenesis, and lipid transport and metabolism in liver-injured mice; Conclusions: GLSP can alleviate the imbalance of gut microbiota and improve liver injury, and the effect of sporoderm-broken GLSP is better.
孢子粉(GLSP)具有丰富的药理活性。然而,破壁灵芝孢子粉和未破壁灵芝孢子粉在肝脏保护功能上的差异尚未得到研究。本研究首次探讨了破壁和未破壁GLSP对小鼠急性酒精性肝损伤改善作用及小鼠肠道微生物群的影响。
采用酶联免疫吸附测定(ELISA)试剂盒检测各组小鼠血清天冬氨酸转氨酶(AST)和丙氨酸转氨酶(ALT)水平以及肝组织中白细胞介素1β(IL-1β)、白细胞介素18(IL-18)和肿瘤坏死因子-α(TNF-α)水平,并对肝组织切片进行组织学分析,以评估破壁和未破壁GLSP的肝脏保护作用。此外,对小鼠肠道粪便进行16S rDNA测序,比较破壁和未破壁GLSP对小鼠肠道微生物群的调节作用。
与50%乙醇模型组(MG)相比,破壁GLSP显著降低血清AST和ALT水平(P<0.0001)以及包括IL-1β、IL-18和TNF-α在内的炎症因子释放(P<0.0001),并有效改善肝细胞病理状态;未破壁GLSP显著降低ALT含量(P = 0.0002)以及包括IL-1β(P<0.0001)、IL-18(P = 0.0018)和TNF-α(P = 0.0005)在内的炎症因子释放,并降低血清AST含量,但降低不显著;与MG的肠道微生物群相比,破壁GLSP降低了[具体细菌名称1]和[具体细菌名称2]的水平,增加了有益菌如[具体有益菌名称]的相对丰度,并降低了有害菌如[具体有害菌名称1]和[具体有害菌名称2]的丰度水平;未破壁GLSP可降低有害菌如[具体有害菌名称1]和[具体有害菌名称2]的丰度水平;GLSP治疗可缓解肝损伤小鼠中翻译、核糖体结构与生物发生以及脂质转运与代谢水平的下调;结论:GLSP可缓解肠道微生物群失衡并改善肝损伤,且破壁GLSP的效果更佳。