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Chaenomeles sinensis polysaccharide and its carboxymethylated derivative alleviate dextran sulfate sodium-induced ulcerative colitis via suppression of inflammation and oxidative stress
被引:18
|作者:
Li, Chong
[3
]
Jiao, Yukun
[4
]
Shen, Shumin
[2
]
Zhao, Wenchang
[1
]
Zhang, Qian
[2
]
Zhang, Shaojie
[1
]
机构:
[1] Guangdong Prov Key Lab Res & Dev Nat Drugs, Dongguan Key Lab TCM Prevent & Treatment Digest Di, Dongguan Key Lab Screening & Res Antiinflammatory, Guangdong Med Univ, Dongguan 523808, Peoples R China
[2] Guangdong Pharmaceut Univ, Guangdong Prov Engn Ctr Top Precise Drug Delivery, Sch Pharm, Guangdong Prov Key Lab Adv Drug Delivery, Guangzhou 510006, Peoples R China
[3] Chinese Acad Sci, Guangzhou Inst Biomed & Hlth, Joint Sch Life Sci, CAS Key Lab Regenerat Biol, Guangzhou 510530, Guangdong, Peoples R China
[4] Chinese Acad Sci, Shanghai Inst Mat Med, Carbohydrate Based Drug Res Ctr, State Key Lab Drug Res, Shanghai 201203, Peoples R China
关键词:
Chaenomeles sinensis Thouin Koeh;
Polysaccharide;
Carboxymethylation;
Ulcerative colitis;
Inflammation;
Oxidative stress;
ANTIOXIDANT ACTIVITIES;
BOWEL-DISEASE;
EXTRACT;
MICE;
D O I:
10.1016/j.biopha.2023.115941
中图分类号:
R-3 [医学研究方法];
R3 [基础医学];
学科分类号:
1001 ;
摘要:
Chaenomeles sinensis fruit polysaccharide (CSP) and carboxymethylated CSP (CSP-M) were prepared using ultrasound extraction and the sodium hydroxide-chloroacetic acid method. Structural analysis revealed that both CSP and CSP-M mainly consisted of glucose, arabinose, rhamnose, glucuronic acid, galactose, and xylose, and the introduction of carboxymethyl did not damage the polymer chain of CSP. In vivo studies verified that both CSP and CSP-M could remarkably alleviate the symptoms of ulcerative colitis (UC) mice and reduce intestinal epithelial cell depletion, along with the infiltration of inflammatory cells in colon tissue, by mediating the expression of myeloperoxidase (MPO), inflammatory factors [tumour necrosis factor-alpha (TNF-alpha), interleukin-1 beta (IL-1 beta), and IL-6], and oxidative stress factors [malondialdehyde (MDA), superoxide dismutase (SOD), glutathione (GSH), and nitric oxide (NO)]. Most importantly, the introduction of carboxymethyl significantly enhanced the anti-UC activity of CSP, confirming the efficacy of carboxymethylation as a method to enhance the biological activities of CSP, thereby suggesting the potential of CSP-M as a therapeutic option for UC.
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