Regulation and mechanism of Bletilla striata polysaccharide on delaying aging in Drosophila melanogaster

被引:2
作者
Hafeez, Eqra [1 ]
Du, Dongsheng [2 ]
Ni, Hang [1 ]
Zhu, Kai [1 ]
Hu, Fan [1 ]
Zhou, Jihai [2 ]
Chen, Dongsheng [1 ]
机构
[1] Anhui Normal Univ, Coll Life Sci, Anhui Prov Key Lab Mol Enzymol & Mech Major Dis, Wuhu 241000, Peoples R China
[2] Anhui Normal Univ, Coll Life Sci, Anhui Prov Key Lab Biodivers Conservat & Ecol Secu, Wuhu 241000, Peoples R China
基金
美国国家科学基金会;
关键词
Bletilla striata polysaccharide; Anti-aging; Antioxidant; Intestinal homeostasis; Alzheimer's disease; Oxidative stress; Drosophila melanogaster; LIFE-SPAN; OXIDATIVE STRESS; WATER CRISIS; LEAD; NEURODEGENERATION; HOMEOSTASIS; DYSBIOSIS; EXPOSURE; FLINT;
D O I
10.1016/j.ijbiomac.2025.143382
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Bletilla striata polysaccharide (BSP) is a natural bioactive compound known for its promising health benefits, including antioxidant, immunomodulatory, and anti-inflammatory effects. However, its potential in combating aging remains largely unexplored. This study aims to investigate the anti-aging effects of BSP in the Drosophila melanogaster model. The results show that BSP supplementation significantly extends the lifespan of flies in a concentration-dependent manner, with the most pronounced effects observed at a concentration of 3 mg/mL. Lifespan extension is associated with enhanced antioxidative capacities, as evidenced by increased SOD and CAT activities, and decreased MDA content. Additionally, BSP ameliorates age-related symptoms, including improved climbing ability and enhanced intestinal barrier function. Furthermore, BSP supplementation enhances resistance to H2O2-induced oxidative and starvation stresses, attenuates the lead (Pb)-induced toxicity, and delays the onset of Alzheimer's phenotypes in flies. RNA-Seq analysis reveals that BSP supplementation leads to the differential expression of 992 genes. KEGG pathway analysis highlights significant changes in metabolic pathways, including galactose metabolism, starch and sucrose metabolism, and carbon metabolism. Key genes such as Mal-A1, Amy-d, Men-b, Pgm-1, Mdh1, and Hex-C are downregulated, while CG32026, CG11291, and Ald2 are upregulated. These findings suggest BSP exhibits significant anti-aging and protective properties, making it a potential therapeutic agent.
引用
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页数:13
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