Structure characterization of polysaccharides from Cistanche deserticola and their neuroprotective effects against oxidative stress in slow transit constipation mice

氧化应激 丙二醛 肌间神经丛 谷胱甘肽 医学 超氧化物歧化酶 生物化学 生物 病理 内科学 免疫组织化学
作者
Hongyu Jiang,Rong Ma,Fulong Ji,Yong Liu,Bo Wang,Siqi Fu,Lushun Ma,Song Wang,Chunxiang Liu,Zheng Guo,Rui Li,Yuchao Wang,Weiwei Sun,Dong Li,Caixia Dong,Daqing Sun
出处
期刊:International Journal of Biological Macromolecules [Elsevier]
卷期号:260: 129527-129527
标识
DOI:10.1016/j.ijbiomac.2024.129527
摘要

Oxidative stress-induced enteric neuropathy is an important factor in slow transit constipation (STC). Cistanche deserticola crude polysaccharides (CDCP) are natural antioxidants with various biological activities. We prepared CDCP through water-extract and alcohol-precipitation methods. The structural characteristics of CDCP were analyzed by infrared spectroscopy and methylation analysis. The results showed that CDCP was primarily composed of (1 → 4)-linked glucans with minor amounts of pectic polysaccharides. Different doses of CDCP (100, 200, and 400 mg/kg) were administered to loperamide-induced STC mice to explore the therapeutic effects of CDCP. Compared with the untreated group, CDCP treatment significantly improved constipation symptoms, relevant gut-regulating peptides levels, colonic pathological damage, and colonic myenteric nerons injury. CDCP enhanced the antioxidant capacity by decreasing Malondialdehyde (MDA) content, increasing Superoxide Dismutase (SOD) activity and Reduced Glutathione (GSH) content. CDCP significantly reduced oxidative stress-induced injury by preserving mitochondrial function in the colonic myenteric plexus. Furthermore, the neuroprotective effects of CDCP might be associated with the Nrf2/Keap1 pathway. Thus, our findings first revealed the potential of CDCP to protect the colonic myenteric plexus against oxidative stress-induced damage in STC, establishing CDCP as promising candidates for natural medicine in the clinical management of STC.
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