Carboxymethyl chitosan oligosaccharide prevents the progression of chronic kidney disease as a Nrf2-dependent apoptosis inhibitor

Xiaozheng Yuan , Huan He , Youtao Xu, Xinru Chen, Jiawen Wu, Xianpeng Zhong, Xiyu Li, Jing Qiao
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Abstract

Chronic Kidney Disease (CKD) has become a global public health problem, for which satisfactory treatments remain an urgent need. Carboxymethyl chitosan oligosaccharide (CMCOS) is a small molecule derivative of the natural product chitin, which is easy to absorb with variety of biological activities. Our previous research has demonstrated the renal protective effects of CMCOS, while the underlying mechanism is poorly understood. This study reports that the renal protective effects of CMCOS are associated with anti-apoptosis in glomerular podocytes and renal tubular epithelial cells, which maintains the integrity of renal structure and function. Furthermore, CMCOS suppresses tissue oxidative stress and intracellular accumulation of reactive oxygen species both in vitro and in vivo, demonstrating positive correlations with its apoptosis inhibition. Mechanistically, CMCOS enhances endogenous antioxidant defense and relieves oxidative stress in the renal microenvironment through activation of the nuclear factor-erythroid 2-related factor 2 (Nrf2)/heme oxygenase-1 (HO-1) signaling pathway. Specific inhibition of Nrf2 abolishes the apoptosis-inhibitory effect of CMCOS, indicating a dependence on this pathway. In conclusion, CMCOS activates Nrf2/HO-1 signaling pathway to inhibited oxidative stress-related apoptosis in renal parenchymal cells, thereby alleviating the progression of CKD. Our findings provide a new basis for the medicinal development of carbohydrates.

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羧甲基壳聚糖低聚糖作为nrf2依赖性细胞凋亡抑制剂可预防慢性肾脏疾病的进展
慢性肾脏疾病(CKD)已成为一个全球性的公共卫生问题,令人满意的治疗仍然是迫切需要的。羧甲基壳聚糖(Carboxymethyl chitosan oligosaccharides, CMCOS)是天然产物甲壳素的小分子衍生物,易于吸收,具有多种生物活性。我们之前的研究已经证实了CMCOS的肾脏保护作用,但其潜在机制尚不清楚。本研究报道CMCOS的肾保护作用与抗肾小球足细胞和肾小管上皮细胞凋亡有关,维持肾脏结构和功能的完整性。此外,CMCOS在体外和体内均能抑制组织氧化应激和细胞内活性氧的积累,显示出其抑制细胞凋亡的正相关。机制上,CMCOS通过激活核因子-红细胞2相关因子2 (Nrf2)/血红素加氧酶-1 (HO-1)信号通路,增强内源性抗氧化防御,缓解肾微环境中的氧化应激。特异性抑制Nrf2可消除CMCOS的细胞凋亡抑制作用,表明其依赖于该途径。综上所述,CMCOS激活Nrf2/HO-1信号通路,抑制肾实质细胞氧化应激相关的凋亡,从而缓解CKD的进展。我们的发现为碳水化合物的药用开发提供了新的基础。
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