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Effects of Chitosan Oligosaccharides on Human Blood Components
Chitosan oligosaccharide (COS) is known for its unique biological activities such as anti-tumor, anti-inflammatory, anti-oxidant, anti-bacterial activity, biological recognition, and immune enhancing effects, and thus continuous attracting many research interests in drug, food, cosmetics, biomateria...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6286974/ https://www.ncbi.nlm.nih.gov/pubmed/30559672 http://dx.doi.org/10.3389/fphar.2018.01412 |
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author | Guo, Xi Sun, Tong Zhong, Rui Ma, Lu You, Chao Tian, Meng Li, Hao Wang, Chengwei |
author_facet | Guo, Xi Sun, Tong Zhong, Rui Ma, Lu You, Chao Tian, Meng Li, Hao Wang, Chengwei |
author_sort | Guo, Xi |
collection | PubMed |
description | Chitosan oligosaccharide (COS) is known for its unique biological activities such as anti-tumor, anti-inflammatory, anti-oxidant, anti-bacterial activity, biological recognition, and immune enhancing effects, and thus continuous attracting many research interests in drug, food, cosmetics, biomaterials and tissue engineering fields. In comparison to its corresponding polymer, COS has much higher absorption profiles at the intestinal level, which results in permitting its quick access to the blood flow and potential contacting with blood components. However, the effects of COS on blood components remain unclear to date. Herein, two COS with different molecular weight (MW) were characterized by FTIR and (1)H NMR, and then their effects on human blood components, including red blood cells (RBCs) (hemolysis, deformability, and aggregation), coagulation system [activated partial thromboplastin time (APTT), prothrombin time (PT), thrombin time (TT), and the concentration of fibrinogen (Fib)], complement (C3a and C5a activation), and platelet (activation and aggregation), were comprehensively studied. In the case of RBCs, COS exhibited a low risk of hemolysis in a dose and molecular weight dependent manner and the irreversible aggregation was observed in their high concentration. For coagulation system, COS has a mild anticoagulation activity through blocking the intrinsic coagulation pathway. In addition, COS showed no effect on complement activation in C3a and C5a and on platelet activation while inhibition of platelet aggregation was evident. Finally, the mechanism that effects of COS on blood components was discussed and proposed. |
format | Online Article Text |
id | pubmed-6286974 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-62869742018-12-17 Effects of Chitosan Oligosaccharides on Human Blood Components Guo, Xi Sun, Tong Zhong, Rui Ma, Lu You, Chao Tian, Meng Li, Hao Wang, Chengwei Front Pharmacol Pharmacology Chitosan oligosaccharide (COS) is known for its unique biological activities such as anti-tumor, anti-inflammatory, anti-oxidant, anti-bacterial activity, biological recognition, and immune enhancing effects, and thus continuous attracting many research interests in drug, food, cosmetics, biomaterials and tissue engineering fields. In comparison to its corresponding polymer, COS has much higher absorption profiles at the intestinal level, which results in permitting its quick access to the blood flow and potential contacting with blood components. However, the effects of COS on blood components remain unclear to date. Herein, two COS with different molecular weight (MW) were characterized by FTIR and (1)H NMR, and then their effects on human blood components, including red blood cells (RBCs) (hemolysis, deformability, and aggregation), coagulation system [activated partial thromboplastin time (APTT), prothrombin time (PT), thrombin time (TT), and the concentration of fibrinogen (Fib)], complement (C3a and C5a activation), and platelet (activation and aggregation), were comprehensively studied. In the case of RBCs, COS exhibited a low risk of hemolysis in a dose and molecular weight dependent manner and the irreversible aggregation was observed in their high concentration. For coagulation system, COS has a mild anticoagulation activity through blocking the intrinsic coagulation pathway. In addition, COS showed no effect on complement activation in C3a and C5a and on platelet activation while inhibition of platelet aggregation was evident. Finally, the mechanism that effects of COS on blood components was discussed and proposed. Frontiers Media S.A. 2018-12-03 /pmc/articles/PMC6286974/ /pubmed/30559672 http://dx.doi.org/10.3389/fphar.2018.01412 Text en Copyright © 2018 Guo, Sun, Zhong, Ma, You, Tian, Li and Wang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology Guo, Xi Sun, Tong Zhong, Rui Ma, Lu You, Chao Tian, Meng Li, Hao Wang, Chengwei Effects of Chitosan Oligosaccharides on Human Blood Components |
title | Effects of Chitosan Oligosaccharides on Human Blood Components |
title_full | Effects of Chitosan Oligosaccharides on Human Blood Components |
title_fullStr | Effects of Chitosan Oligosaccharides on Human Blood Components |
title_full_unstemmed | Effects of Chitosan Oligosaccharides on Human Blood Components |
title_short | Effects of Chitosan Oligosaccharides on Human Blood Components |
title_sort | effects of chitosan oligosaccharides on human blood components |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6286974/ https://www.ncbi.nlm.nih.gov/pubmed/30559672 http://dx.doi.org/10.3389/fphar.2018.01412 |
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