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

被引:11
作者
Jiang, Hong-yu [1 ,2 ]
Ma, Rui-an [3 ,4 ]
Ji, Fu -long [1 ]
Liu, Yong [1 ]
Wang, Bo [1 ]
Fu, Si-qi [1 ]
Ma, Lu-shun [1 ]
Wang, Song [1 ]
Liu, Chun-xiang [1 ]
Guo, Zheng [1 ]
Li, Rui [1 ]
Wang, Yu-chao [1 ]
Sun, Wei [1 ]
Dong, Liang [2 ]
Dong, Cai-xia [4 ]
Sun, Da-qing [1 ]
机构
[1] Tianjin Med Univ, Gen Hosp, Dept Pediat Surg, Tianjin 300052, Peoples R China
[2] Tianjin Univ, Tianjin Childrens Hosp, Childrens Hosp, Dept Gen Surg, Tianjin 300074, Peoples R China
[3] Jiamusi Univ, Coll Pharm, Dept Pharmacognosy, Jiamusi 154007, Peoples R China
[4] Tianjin Med Univ, Sch Pharm, Tianjin Key Lab Technol Enabling Dev Clin Therapeu, Tianjin 300070, Peoples R China
关键词
Slow transit constipation (STC); Cistanche deserticola crude polysaccharides (CDCP); Neuroprotective effects; ENTERIC NERVOUS-SYSTEM; Y; C; MA; NITRIC-OXIDE; FUNCTIONAL CONSTIPATION; NEURONS; CELLS; ANTIOXIDANT;
D O I
10.1016/j.ijbiomac.2024.129527
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
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 stressinduced 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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页数:16
相关论文
共 89 条
[1]   Mitochondria in Health and Disease [J].
Annesley, Sarah J. ;
Fisher, Paul R. .
CELLS, 2019, 8 (07)
[2]   The Molecular Mechanisms Regulating the KEAP1-NRF2 Pathway [J].
Baird, Liam ;
Yamamoto, Masayuki .
MOLECULAR AND CELLULAR BIOLOGY, 2020, 40 (13)
[3]   SIRT3 activation promotes enteric neurons survival and differentiation [J].
Balasubramaniam, Arun ;
Li, Ge ;
Ramanathan, Anita ;
Mwangi, Simon Musyoka ;
Hart, C. Michael ;
Arbiser, Jack L. ;
Srinivasan, Shanthi .
SCIENTIFIC REPORTS, 2022, 12 (01)
[4]   Global prevalence of functional constipation according to the Rome criteria: a systematic review and meta-analysis [J].
Barberio, Brigida ;
Judge, Ciaran ;
Savarino, Edoardo V. ;
Ford, Alexander C. .
LANCET GASTROENTEROLOGY & HEPATOLOGY, 2021, 6 (08) :638-648
[5]   The role of glial cells and apoptosis of enteric neurones in the neuropathology of intractable slow transit constipation [J].
Bassotti, G ;
Villanacci, V ;
Maurer, CA ;
Fisogni, S ;
Di Fabio, F ;
Cadei, M ;
Morelli, A ;
Panagiotis, T ;
Cathomas, G ;
Salemi, B .
GUT, 2006, 55 (01) :41-46
[6]   Slow transit constipation: A functional disorder becomes an enteric neuropathy [J].
Bassotti, Gabrio ;
Villanacci, Vincenzo .
WORLD JOURNAL OF GASTROENTEROLOGY, 2006, 12 (29) :4609-4613
[7]   Mechanisms, Evaluation, and Management of Chronic Constipation [J].
Bharucha, Adil E. ;
Lacy, Brian E. .
GASTROENTEROLOGY, 2020, 158 (05) :1232-+
[8]   Chronic Constipation [J].
Bharucha, Adil E. ;
Wald, Arnold .
MAYO CLINIC PROCEEDINGS, 2019, 94 (11) :2340-2357
[9]   Chronic idiopathic constipation in adults: epidemiology, pathophysiology, diagnosis and clinical management [J].
Black, Christopher J. ;
Ford, Alexander C. .
MEDICAL JOURNAL OF AUSTRALIA, 2018, 209 (02) :86-91
[10]   NEW METHOD FOR QUANTITATIVE-DETERMINATION OF URONIC ACIDS [J].
BLUMENKR.N ;
ASBOEHAN.G .
ANALYTICAL BIOCHEMISTRY, 1973, 54 (02) :484-489