Le My Phuong Thi, Marasinghe Chathuri Kaushalya, Je Jae-Young
Department of Food and Nutrition, Pukyong National University, Busan 48513, Republic of Korea.
Major of Human Bioconvergence, Division of Smart Healthcare, Pukyong National University, Busan 48513, Republic of Korea.
Int J Biol Macromol. 2024 Dec;282(Pt 4):137186. doi: 10.1016/j.ijbiomac.2024.137186. Epub 2024 Nov 2.
Foam cell formation is a key hallmark in atherosclerosis and associated cardiovascular diseases (CVDs). The potential anti-atherosclerotic potential of chitosan oligosaccharides (COS) was investigated using oxLDL-treated RAW264.7 murine cells. COS treatment led to a significant inhibition of lipid accumulation, as demonstrated by Oil Red O staining, and reduced levels of total cholesterol, free cholesterol, cholesterol esters, and triglycerides in.oxLDL-treated RAW264.7 cells. COS blocked cholesterol influx through down-regulating class A1 scavenger receptors (SR-A1) and cluster of differentiation 36 (CD36) expression and stimulated cholesterol efflux through up-regulating ABC transporters ABCA-1 and ABCG-1 expressions. Additionally, COS treatment stimulated nuclear signaling pathways involving peroxisome proliferator-activated receptor-γ (PPAR-γ) and liver X receptor α (LXR-α), and also led to the phosphorylation of AMP-activated protein kinase (AMPK). COS further demonstrated anti-inflammatory effects by inhibiting the production of pro-inflammatory cytokines and the expression of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) in oxLDL-treated RAW264.7 cells, through suppression of NF-κB signaling. Furthermore, COS alleviated oxidative stress induced by oxLDL by activating Nrf2 signaling and enhancing the expression of antioxidant genes, including heme oxygenase-1 (HO-1), superoxide dismutase (SOD), glutathione peroxidase (Gpx), and catalase (CAT). In conclusion, COS can be beneficial in preventing atherosclerosis and related diseases.
泡沫细胞形成是动脉粥样硬化及相关心血管疾病(CVD)的关键标志。使用氧化型低密度脂蛋白(oxLDL)处理的RAW264.7小鼠细胞研究了壳寡糖(COS)潜在的抗动脉粥样硬化潜力。油红O染色显示,COS处理导致脂质积累显著受到抑制,且oxLDL处理的RAW264.7细胞中的总胆固醇、游离胆固醇、胆固醇酯和甘油三酯水平降低。COS通过下调A类1型清道夫受体(SR-A1)和分化簇36(CD36)的表达来阻断胆固醇内流,并通过上调ABC转运蛋白ABCA-1和ABCG-1的表达来刺激胆固醇外流。此外,COS处理激活了涉及过氧化物酶体增殖物激活受体-γ(PPAR-γ)和肝X受体α(LXR-α)的核信号通路,还导致了AMP激活的蛋白激酶(AMPK)的磷酸化。COS通过抑制促炎细胞因子的产生以及oxLDL处理的RAW264.7细胞中诱导型一氧化氮合酶(iNOS)和环氧化酶-2(COX-2)的表达,通过抑制NF-κB信号传导,进一步显示出抗炎作用。此外,COS通过激活Nrf2信号并增强抗氧化基因的表达,包括血红素加氧酶-1(HO-1)、超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(Gpx)和过氧化氢酶(CAT),减轻了oxLDL诱导的氧化应激。总之,COS可能对预防动脉粥样硬化及相关疾病有益。