Academic literature on the topic 'POLYSACCHARIDES MUSHROOM'
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Journal articles on the topic "POLYSACCHARIDES MUSHROOM"
Chun, Sechul, Judy Gopal, and Manikandan Muthu. "Antioxidant Activity of Mushroom Extracts/Polysaccharides—Their Antiviral Properties and Plausible AntiCOVID-19 Properties." Antioxidants 10, no. 12 (November 26, 2021): 1899. http://dx.doi.org/10.3390/antiox10121899.
Full textZhao, Jiahui, Yixin Hu, Chao Qian, Muhammad Hussain, Shizhu Liu, Anqiang Zhang, Rongjun He, and Peilong Sun. "The Interaction between Mushroom Polysaccharides and Gut Microbiota and Their Effect on Human Health: A Review." Biology 12, no. 1 (January 12, 2023): 122. http://dx.doi.org/10.3390/biology12010122.
Full textBadshah, Syed Lal, Anila Riaz, Akhtar Muhammad, Gülsen Tel Çayan, Fatih Çayan, Mehmet Emin Duru, Nasir Ahmad, Abdul-Hamid Emwas, and Mariusz Jaremko. "Isolation, Characterization, and Medicinal Potential of Polysaccharides of Morchella esculenta." Molecules 26, no. 5 (March 8, 2021): 1459. http://dx.doi.org/10.3390/molecules26051459.
Full textSivanesan, Iyyakkannu, Manikandan Muthu, Judy Gopal, and Jae-Wook Oh. "Mushroom Polysaccharide-Assisted Anticarcinogenic Mycotherapy: Reviewing Its Clinical Trials." Molecules 27, no. 13 (June 25, 2022): 4090. http://dx.doi.org/10.3390/molecules27134090.
Full textBaeva, Ekaterina, Roman Bleha, Ekaterina Lavrova, Leonid Sushytskyi, Jana Čopíková, Ivan Jablonsky, Pavel Klouček, and Andriy Synytsya. "Polysaccharides from Basidiocarps of Cultivating Mushroom Pleurotus ostreatus: Isolation and Structural Characterization." Molecules 24, no. 15 (July 28, 2019): 2740. http://dx.doi.org/10.3390/molecules24152740.
Full textTung, Yu-Tang, Chun-Hsu Pan, Yi-Wen Chien, and Hui-Yu Huang. "Edible Mushrooms: Novel Medicinal Agents to Combat Metabolic Syndrome and Associated Diseases." Current Pharmaceutical Design 26, no. 39 (November 10, 2020): 4970–81. http://dx.doi.org/10.2174/1381612826666200831151316.
Full textAzizur Rahman, Mohammad, Tawhidur Rahman, Moshiur Rahman, and Mirza Arif. "Usage of Mushrooms in Culinary and Medicinal Purposes." Biomedical Research and Clinical Reviews 6, no. 1 (January 12, 2022): 01–07. http://dx.doi.org/10.31579/2692-9406/087.
Full textPatel, Dinesh K., Sayan Deb Dutta, Keya Ganguly, Seong-Jun Cho, and Ki-Taek Lim. "Mushroom-Derived Bioactive Molecules as Immunotherapeutic Agents: A Review." Molecules 26, no. 5 (March 4, 2021): 1359. http://dx.doi.org/10.3390/molecules26051359.
Full textStavsky, Е. А., T. V. Teplyakova, А. P. Nadeev, М. А. Ermachenko, А. А. Stavskaya, А. D. Sсhmidt, А. М. Borzenko, Yu D. Zarubina, А. N. Zhayvoron, and А. S. Shestak. "COMPARATIVE EVALUATION OF THE WOUND-HEALING ACTIVITY OF OINTMENTS OBTAINED ON THE BASIS OF SOME BIOLOGICALLY ACTIVE COMPLEXES FROM HIGHER BASIDIOMYCETES." Sibirskij medicinskij vestnik 6, no. 3 (2022): 62–73. http://dx.doi.org/10.31549/2541-8289-2022-6-3-62-73.
Full textAramabašić Jovanović, Jelena, Mirjana Mihailović, Aleksandra Uskoković, Nevena Grdović, Svetlana Dinić, and Melita Vidaković. "The Effects of Major Mushroom Bioactive Compounds on Mechanisms That Control Blood Glucose Level." Journal of Fungi 7, no. 1 (January 16, 2021): 58. http://dx.doi.org/10.3390/jof7010058.
Full textDissertations / Theses on the topic "POLYSACCHARIDES MUSHROOM"
Bitencourt, Evandro Leite. "Prospecção química de carboidratos isolados dos basidiomas das linhagens branca e cinza do cogumelo medicinal Grifola frondosa (“Maitake”)." Universidade Federal de Goiás, 2015. http://repositorio.bc.ufg.br/tede/handle/tede/4757.
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Fundação de Amparo à Pesquisa do Estado de Goiás - FAPEG
Mushrooms have been valued as a functional food and dietary supplement for humanity, due to the presence of substances with high nutritional value and/or therapeutic. Among the mushrooms recognized for its therapeutic properties we have is the leafy Grifola, popularly known as “Maitake”, which has important pharmacological actions such as anti-tumor, immunomodulatory, antiinflammatory, antioxidant, and others, which have been mainly related to its carbohydrates. Nevertheless, this study aimed to review the chemistry of the polysaccharides from mushroom of the two lines ("white" and "gray", represented as Gfb and Gfc, respectively) of G. frondosa leafy that have been cultivated in Brazil. From these type it was obtained branched -glucans containing links of type (13) (16) and heteropolysaccharides formed mainly by galactose (heterogalactan) or mannose (heteromannan). The heterogalactan composed mainly of fucose (15.7%), mannose (20.5%) and galactose (63.8%) was denominated fucomannogalactan (FMG-Gfb). It contains a main chain consisting of units of α-D-Galp and 3-Me-O-α-D-Galp connected (16), which are present partially substituted by O-2 disaccharide 3-O- α-D-Manp-α-L-Fucp to a lesser extent with terminal non-reducing α-L-Fucp and α-D-Manp. The heteromannan composed of fucose (6.9%), xylose (33.1%) and mannose (60.0%), a fucoxylomannan (FXM-Gfc) was found to be composed of a backbone of units α-D-Manp (13) connected, and a part of them substituted by O-3 side chains made of fucose and xylose. The results of this study suggest that there are no significant differences between the carbohydrate of both strains, showing that white strain it provide the therapeutic effects attributed to carbohydrates of another strain.
Os cogumelos têm sido valorizados como alimento funcional e suplemento alimentar para a humanidade, devido à presença de substâncias com alto valor nutricional e/ou medicinal. Dentre os cogumelos reconhecidos pelas suas propriedades terapêuticas encontra-se o Grifola frondosa, popularmente conhecido como Maitake, o qual possui importantes ações farmacológicas como antitumoral, imunomoduladora, anti-inflamatória, antioxidante, entre outras, as quais têm sido relacionadas, principalmente, aos seus carboidratos. Diante do exposto, o presente trabalho teve como objetivo a avaliação química dos polissacarídeos dos basidiomas das duas linhagens (branca e cinza, representadas como Gfb e Gfc, respectivamente) de G. frondosa que vem sendo cultivadas no Brasil. A partir destes foram obtidas as -glucanas ramificadas contendo ligações do tipo (13) (16) e os heteropolissacarídeos formados principalmente por galactose (heterogalactana) ou manose (heteromanana). A heterogalactana constituída, principalmente, por fucose (15,7%), manose (20,5%) e galactose (63,8%), foi denominada de fucomanogalactana (FMG-Gfb). Esta contém uma cadeia principal formada por unidades de α-D-Galp e de 3-O-Me-α-D-Galp ligadas (16), as quais se apresentam parcialmente substituídas em O-2 pelo dissacarídeo 3-O-α-DManp- α-L-Fucp e em menor proporção com terminais não redutores de α-LFucp e α-D-Manp. A heteromanana, composta por fucose (6,9%), xilose (33,1%) e manose (60,0%), ou seja, uma fucoxilomanana (FXM-Gfc) mostrou ser constituída por uma cadeia principal composta por unidades de α-D-Manp (13) ligadas, sendo uma parte destas substituídas em O-3 por cadeias laterais formadas por fucose e xilose. Os resultados obtidos neste estudo sugerem que não há diferenças significativas entre os carboidratos de ambas as linhagens, evidenciando que a linhagem branca deve apresentar os efeitos terapêuticos atribuídos aos carboidratos da outra linhagem.
Lima, Adriane Trindade Medeiros. "Avalia??o do potencial antioxidante e antiinflamat?rio de galactomanana do fungo Tyllopiillus ballllouiii." Universidade Federal do Rio Grande do Norte, 2009. http://repositorio.ufrn.br:8080/jspui/handle/123456789/12552.
Full textCoordena??o de Aperfei?oamento de Pessoal de N?vel Superior
Polymers of mushroom cellular wall are recognized for presenting a lot of biological activities such as anti-inflammatory, antioxidant and anti-tumoral action. Polysaccharides from mushrooms of different molecular mass obtained mushrooms can activate leucocytes, stimulate fagocitic, citotoxic and antimicrobial activity including oxygen reactive species production. In this study were investigated chemical characteristics, in vitro antioxidant activity and anti-inflammatory action in an acute inflammation model of the polysaccharides extracted from Tylopilus ballouii. Results showed that were mainly extracted polysaccharides and that it primarily consisted of mannose and galactose with variable amounts of xylose and fucose. Infrared analysis showed a possible interation between this polysaccharides and proteins. In addition, molecular mass was about 140KDa. Antioxidant activity was tested by superoxide and hydroxyl radical scavenging assay, total antioxidant activity and lipid peroxidation assay. For superoxide and hydroxyl radical generation inhibition, polysaccharides have an IC50 of 2.36 and 0.36 mg/mL, respectively. Lipid peroxidation assay results showed that polysaccharides from Tylopilus ballouii present an IC50 of 3.42 mg/mL. Futhermore, anti-inflammatory assay showed that polysaccharides cause an paw edema decreasing in 32.8, 42 and 56% in 30, 50 and 70 mg/Kg dose, respectively. Thus, these results can indicate a possible use for these polysaccharides from Tylopilus ballouii as an anti-inflammatory and antioxidant.
Pol?meros da parede celular de fungos s?o conhecidos por possu?rem muitas atividades biol?gicas como suas a??es antiinflamat?rias, antioxidante e antitumoral. Polissacar?deos de diferentes pesos moleculares obtidos de cogumelos podem ativar os leuc?citos, estimular a atividade fagoc?tica, citot?xica e antimicrobiana, incluindo a produ??o de esp?cies reativas de oxig?nio. No presente estudo, foi investigada a caracter?stica qu?mica dos polissacar?deos extra?dos de Tylopilus ballouii sua atividade antioxidante in vitro e a sua atividade antiinflamat?ria no modelo de inflama??o aguda. Os resultados mostraram que foram extra?dos predominantemente polissacar?deos e esses consistiram primariamente de manose e galactose e possui quantidades vari?veis de xilose e fucose. As an?lises de infravermelho mostraram a poss?vel intera??o entre estes polissacar?deos e prote?nas. Al?m disso, seu peso molecular ? de cerca de 140 kDa. A atividade antioxidante foi testada com rela??o ao seq?estro sobre os radicais super?xido e hidroxila, atividade antioxidante total e peroxida??o lip?dica. Com rela??o ? inibi??o da forma??o dos radicais super?xido e hidroxila, os polissacar?deos atingiram um IC50 de 1,64 e 1,25 mg/ml, respectivamente. Os resultados do ensaio de peroxida??o lip?dica mostraram que os polissacar?deos de Tylopilus ballouii apresentam um IC50 de 1,65 mg/ml. Al?m disso, a atividade antiinflamat?ria mostrou que eles agem reduzindo o edema em 32,8, 42 e 56% nas doses de 30, 50 e 70 mg/kg, respectivamente. Assim, estes resultados podem indicar o poss?vel uso dos polissacar?deos de Tylopilus ballouii como antiinflamat?rio e antioxidante.
Du, Bin. "Effect of molecular weight and structure on anti-inflammatory properties of polysaccharide from submerged mycelial fermentation of schizophyllum commune /Du Bin." HKBU Institutional Repository, 2016. https://repository.hkbu.edu.hk/etd_oa/363.
Full textSalvador, Cátia Sofia Clemente. "Caracterização de cogumelos silvestres da espécie Amanita ponderosa: produção de metabolitos com atividade biológica." Doctoral thesis, Universidade de Évora, 2014. http://hdl.handle.net/10174/13391.
Full textWang, Wan-Jhen, and 王婉媜. "The Effect of Mushroom Polysaccharides on Primary Tumor Microenvironment." Thesis, 2013. http://ndltd.ncl.edu.tw/handle/06903542228437615798.
Full text國立臺灣大學
漁業科學研究所
101
Cytokine and growth factor secreted by tumor cells can actively recruit blood monocytes at the tumor microenvironment, where the recruiting monocytes differentiated into tumor-associated macrophages which promote tumor progression, thereby resulting a favorable tumor microenvironment for tumor growth. The tumor microenvironment subverted the immune system and enhanced tumor growth through strong immune suppressive mechanisms within the tumor microenvironment. The current study is to investigate whether oral mushroom polysaccharides have any effect on molecular profiles within the serum, lung and tumor microenvironment and tumor-associated macrophage phenotypes. The current study showed that oral Schizophyllan treatment significantly increased IFN-γ mRNA expression, but significantly reduced COX-2 mRNA expression within the lung. For LLC1 tumor model, oral Schizophyllan or oral Ganoderma lucidum polysaccharides treatments significantly reduced TGF-β production in serum. In addition, IL-12 and IFN-γ mRNA expression were significantly increased, but IL-6, IL-10, COX-2 and TGF-β mRNA expression were substantially declined within the tumor microenvironment after oral Schizophyllan or oral Ganoderma lucidum polysaccharides treatments. Moreover, oral Ganoderma lucidum polysaccharides treatment significantly increased M1 phenotype of tumor-associated macrophages, but significantly reduced M2 phenotype of tumor-associated macrophages. Taken together, our study highlights the efficacious effect of mushroom polysaccharides for ameliorating the immune suppression in the tumor microenvironment. Increased M1 phenotype of tumor-associated macrophages and attenuated M2 phenotype of tumor-associated macrophages could be achieved by ingesting mushroom polysaccharides through altering the tumor microenvironment.
"In vivo and in vitro study of immunomodulatory activities of mushroom sclerotial polysaccharides." Thesis, 2008. http://library.cuhk.edu.hk/record=b6074643.
Full textIn the future, further investigation of the detailed structure of mushroom sclerotial polysaccharides is required to explain the immunomodulatory mechanism so that the effective dosage for immunomodulation as well as antitumor effects can be determined. Furthermore, phage display can be applied to find out any novel glucan receptors specific to the mushroom sclerotial polysaccharides.
In vitro antitumor study indicated that PTRW had a significant (p<0.05) inhibitory effect (>40%) on the human monocytic leukemic cells (THP-1) in addition to HL-60 and K562 cells. In vitro immunomodulatory study showed that both PRW and PRSon had significant proliferative effects (p<0.05) on human normal spleen monocyte/macrophage cell, MD. Moreover, PRSon was shown to have a significant increase (p<0.05) in the growth of human natural killer cells, NK-92M1; however, PTRW showed a significant inhibition (p<0.05) on this cell line.
Mushroom sclerotia have a rich source of polysaccharides when compared with fruit bodies. It was previously reported that the polysaccharides from novel mushroom sclerotia, namely, Pleurotus tuber-regium and Polyporus rhinocerus, had potent in vitro and in vivo antitumor effects. In this project, hot water-soluble sclerotial polysaccharides of Pleurotus tuber-regium (PTRW), hot water-soluble and sonication-assisted cold alkali-soluble sclerotial polysaccharides of Polyporus rhinocerus (PRW and PRSon, respectively) were chosen for investigation of their in vivo and in vitro immunomodulatory effects.
Polysaccharides have long been proposed to exert their antitumor and thus immunomodulating functions through glucan receptors and among the four being discovered, Dectin-1 has drawn most attention recently. In the in vivo study, PRSon showed an increase in the expression of Dectin-1 on mice spleen MNCs while PTRW showed an increase in the expression of the previously widely-reported complement receptor (CR3). There was also an increase of Dectin-1 expression on PEC in the mice injected with PRSon. In the in vitro study, the three mushroom sclerotial polysaccharides were incubated with NK-92M1, MD and THP-1 cells. There was a significant increase (p<0.05) of Dectin-1 expression on NK-92MI cells incubated with PTRW. On the other hand, PTRW caused a significant decrease ( p<0.05) of Dectin-1 expression while PRSon showed a significant increase (p<0.05) on THP-1 cells. The cytokine profile of extra-cellular media indicated that the inhibition of THP-1 cells by PTRW should be related to the innate immunity. In the in vitro study, human primary immune cells, CD56+ NK cells were used to incubate with sclerotial polysaccharides and there was a significant stimulation (p<0.05) of their growth when compared with the control.
The in vivo immunomodulatory study was carried out by injecting the abovementioned sclerotial polysaccharides intraperitoneal to 7-8 weeks old healthy male BALB/c mice. The spleens excised from groups injected with PTRW and PRW were found to have significant increase of weight ( p<0.001). Flow cytometric analysis revealed that the NK cell population in spleen mononuclear cells (MNCs) of mice injected with PRW and PRSon was increased when compared with the control. In addition, ail three sclerotial polysaccharides showed a large increase of T helper cell population as well as CD4+/CD8+ ratio in spleen MNCs. On the other hand, the macrophage population in peritoneal exudates cells (PEC) was found to be increased in the groups of mice injected with PTRW and PRW.
Lai, Kin Ming Connie.
Adviser: Cheung Chi Keung.
Source: Dissertation Abstracts International, Volume: 70-06, Section: B, page: 3412.
Thesis (Ph.D.)--Chinese University of Hong Kong, 2008.
Includes bibliographical references (leaves 120-137).
Electronic reproduction. Hong Kong : Chinese University of Hong Kong, [2012] System requirements: Adobe Acrobat Reader. Available via World Wide Web.
Electronic reproduction. [Ann Arbor, MI] : ProQuest Information and Learning, [200-] System requirements: Adobe Acrobat Reader. Available via World Wide Web.
Abstracts in English and Chinese.
School code: 1307.
Ho, Shu-Ying, and 何淑螢. "The Effect of Mushroom Polysaccharides on Intestinal Mucosal Immune System." Thesis, 2013. http://ndltd.ncl.edu.tw/handle/17428955621835487187.
Full text國立臺灣大學
漁業科學研究所
101
Mushroom polysaccharides are distinguished as important immunostimulant in animal body. Administrate glucan to animal inducing different isotype immunoglobulin secretion. Immunoglobulin A is the major antibody in the intestinal mucus, and transcytosis of IgA across epithelia is mediated by the poly-Ig receptor. Neutralization is important protection mechanism against antigen by IgA in gut. In the present study simulate acting intestinal mucosal immune system. Further to study the effects of mushroom polysaccharide on immunoglobulin A (IgA), immunoglobulin G (IgG), immunoglobulin M (IgM) concentration in serum and small intestine washing fluid (SIWF) and intestine tissue poly-immunoglobulin receptor (poly-Ig receptor) mRNA expression. Feeding mice polysaccharide IgA and IgG in SIWF are increase significantly, and IgG and IgM in serum are also increase significantly. The results suggest that the effect of polysaccharides was induced at intestinal mucosa firstly, and induced body circulation immune response further. Poly-Ig receptor mRNA expression increase significantly, too. Our study highlights the efficacious effect of mushroom polysaccharides increasing immunoglobulin concentration in intestinal tract and serum immunoglobulin concentration, and increase poly-Ig receptor mRNA expression in intestine tissue. Mushroom polysaccharide may stimulate intestinal mucosal immune system to protect the intestinal tract from being damaged by the bacterial over-population.
Junghsun, Hsu, and 許榮郇. "The Immune Function Analysis Of Unilateral and Compound Mushroom Polysaccharides." Thesis, 2015. http://ndltd.ncl.edu.tw/handle/28900225597454377720.
Full text中州科技大學
保健食品系
104
The mushroom or related health care products were variety on the market, including of the extract was from the single mushroom such as Ganoderma lucidum, Antrodia camphorata or others or, the compound productions were made from various mushrooms extract. By this productions, we mainly investigate to compare the effect of one type extract from Ganoderma lucidum or Agaricus blazei Murill and the compound extracts mixture from Ganoderma lucidum and Agaricus blazei Murill (1:1 mixture) on the immunomodulation function, so as to assess the proliferation of T cells and B cells in the spleen, Nature killer cell (NK cell) activity and the phagocytic cells capacity. Experimental results shown that the proliferation of T cell and B cell were significantly enhanced in the concentration of the 160 mg / kg / day by the oral feeding unilateral mushroom polysaccharides for six weeks but, the significantly enhancement activity was presented from the compound mushrooms polysaccharides for six weeks in the concentration of 120 mg / kg / day. This presented data indicated that oral feeding with compound mushrooms extract was higher effective promotion in the T cell and B cell proliferation than the oral with unilateral mushroom polysaccharides. In the nature killer cell activity experiment and the phagocytic cell activity assay, the experimental results shown that since the spleen nature killer cell was exhibited significantly activity than the control group and, the similar experimental situation was also presented in the spleen phagocytic capacity assay. Experimental results shown that the cytotoxic activity in the nature killer cell and the phagocytotic capacity in the phagocytic cells, it was significantly enhanced in the concentration of the 40 mg / kg / day by the oral feeding unilateral mushroom polysaccharides for six weeks but, the significantly enhancement activity was presented from the compound mushrooms polysaccharides for six weeks in the concentration of 20 mg / kg / day. This presented data indicated that oral feeding with compound mushrooms extract was higher effective promotion in cytotoxic and phagocytotic capacity than the oral with unilateral mushroom polysaccharides. Therefore, oral with compound mushrooms extracts was better than the unilateral mushroom polysaccharides n the proliferation of T cells and B cells, cytotoxic activity from NK cell and the phagocytotic capacity of phagocytic cells which were observed in the various dose concentration experiment.
"Antitumor effects of polysaccharides extracted from mushroom sclerotia: an in vitro and in vivo study." 2005. http://library.cuhk.edu.hk/record=b5892540.
Full textThesis (M.Phil.)--Chinese University of Hong Kong, 2005.
Includes bibliographical references (leaves 121-141).
Abstracts in English and Chinese.
Chapter Chapter 1. --- Introduction --- p.1
Chapter 1.1 --- Introduction on growth cycle of mushroom --- p.1
Chapter 1.2 --- Literature review of mushroom biological activities --- p.3
Chapter 1.2.1 --- Various bioactivities of mushroom --- p.3
Chapter 1.2.2 --- Components responsible for various bioactivities of mushrooms --- p.3
Chapter 1.3 --- Mushroom polysaccharides and polysaccharide-protein complexes --- p.5
Chapter 1.3.1 --- Polysaccharides important for antitumor effects --- p.5
Chapter 1.3.2 --- Polysaccharide-protein complexes important for antitumor effects --- p.7
Chapter 1.4 --- Structure-function relationship of antitumor activities of polysaccharides --- p.8
Chapter 1.4.1 --- Effect of molecular mass --- p.8
Chapter 1.4.2 --- Effect of linkages --- p.9
Chapter 1.4.3 --- Effect of degree of branching --- p.9
Chapter 1.4.4 --- Effect of conformation --- p.10
Chapter 1.5 --- Immunomodulatory effects of mushroom polysaccharides and polysaccharide-protein complexes --- p.11
Chapter 1.5.1 --- Immunomodulatory effects of polysaccharides --- p.11
Chapter 1.5.1.1 --- Bioactive polysaccharides in Lentinus edodes --- p.11
Chapter 1.5.1.2 --- Bioactive polysaccharides in Ganoderma lucidum --- p.12
Chapter 1.5.2 --- Immunomodulatory effects of polysaccharide-protein complexes --- p.12
Chapter 1.5.2.1 --- Bioactive polysaccharide-protein complexes in Trametes versicolor --- p.13
Chapter 1.5.3 --- Immunotherapeutic effects of mushroom polysaccharides --- p.14
Chapter 1.6 --- Cell cycle and apoptosis --- p.14
Chapter 1.6.1 --- Introduction of cell cycle --- p.14
Chapter 1.6.2 --- Cell cycle regulation --- p.15
Chapter 1.6.3 --- Antitumor effects through apoptotic gene regulation --- p.17
Chapter 1.7 --- Mushroom sclerotium with antitumor activity --- p.20
Chapter 1.7.1 --- Literature review on Pleurotus tuber-regium --- p.20
Chapter 1.7.2 --- Literature review on Poria cocos --- p.22
Chapter 1.7.3 --- Literature review on Polyporus rhinocerus --- p.23
Chapter 1.8 --- Objectives --- p.23
Chapter Chapter 2. --- Materials and Methods --- p.25
Chapter 2.1 --- Materials --- p.25
Chapter 2.1.1 --- Mushroom sclerotia --- p.25
Chapter 2.1.2 --- Animal Model --- p.25
Chapter 2.1.3 --- Cell lines --- p.27
Chapter 2.2 --- Methods --- p.28
Chapter 2.2.1 --- Extraction Scheme for mushroom sclerotia --- p.28
Chapter 2.2.1.1 --- Hot water extraction only --- p.28
Chapter 2.2.1.2 --- Sequential extraction scheme --- p.28
Chapter 2.2.2 --- Measurement of monosaccharide profile --- p.31
Chapter 2.2.2.1 --- Acid Depolymerisation --- p.31
Chapter 2.2.2.2 --- Neutral Sugar Derivatization --- p.31
Chapter 2.2.2.3 --- Gas Chromatography (GC) --- p.32
Chapter 2.2.3 --- High Pressure Liquid Chromatography (HPLC) --- p.33
Chapter 2.2.3.1 --- Size exclusion chromatography --- p.33
Chapter 2.2.3.2 --- Anion exchange chromatography --- p.34
Chapter 2.2.4 --- Linkage analysis by methylation --- p.34
Chapter 2.2.4.1 --- Preparation of partially methylated polysaccharides --- p.34
Chapter 2.2.4.2 --- Preparation of partially methylated alditol acetates (PMAAs) --- p.37
Chapter 2.2.4.3 --- Gas chromatography-Mass spectrometry (GC-MS) analysis --- p.37
Chapter 2.2.5 --- Determination of total sugar by phenol-sulphuric acid Method --- p.38
Chapter 2.2.6 --- Determination of acidic sugars by measurement of uronic acid content --- p.39
Chapter 2.2.7 --- Determination of protein content by Lowry-Folin method --- p.40
Chapter 2.2.8 --- Chemical modification by carboxymethylation --- p.41
Chapter 2.2.9 --- In vitro antitumor assay --- p.41
Chapter 2.2.9.1 --- Trypan blue exclusion assay --- p.42
Chapter 2.2.9.2 --- MTT Assay --- p.42
Chapter 2.2.10 --- Cell cycle analysis by Flow Cytometry --- p.43
Chapter 2.2.11 --- In vivo antitumor and immunomodulatory assay --- p.44
Chapter 2.2.11.1 --- Measurement on tumor growth --- p.44
Chapter 2.2.11.2 --- Blood sampling for immunostimulatory effects --- p.45
Chapter 2.2.12 --- Mouse Cytokine Array --- p.45
Chapter 2.2.13 --- Quantification of Mouse IL-13 by ELISA --- p.46
Chapter 2.2.14 --- Enumeration of peritoneal cells --- p.47
Chapter 2.2.15 --- Enumeration of splenocytes --- p.49
Chapter 2.2.16 --- Statistical methods --- p.50
Chapter Chapter 3. --- Results and Discussion --- p.51
Chapter 3.1 --- Yield of crude mushroom sclerotial extracts --- p.51
Chapter 3.2 --- Chemical composition of crude mushroom sclerotial extracts --- p.57
Chapter 3.2.1 --- Total carbohydrate content --- p.57
Chapter 3.2.2 --- Uronic acid content --- p.58
Chapter 3.2.3 --- Soluble protein content --- p.58
Chapter 3.3 --- Monosaccharide profiles of mushroom sclerotial extracts by GC --- p.60
Chapter 3.4 --- Chromatographic analyses of mushroom sclerotial extracts --- p.65
Chapter 3.4.1 --- Molecular weight profile by size exclusion chromatography (SEC) --- p.65
Chapter 3.4.2 --- Charge distribution by ion exchange chromatography (IEC) --- p.73
Chapter 3.5 --- Antitumor effects of mushroom sclerotial extracts from hot water extraction alone --- p.73
Chapter 3.5.1 --- In vitro antiproliferative study by HL-60 --- p.73
Chapter 3.5.2 --- In vitro antiproliferative study by MCF-7 --- p.74
Chapter 3.5.3 --- In vivo antitumor study by BALB/c mice --- p.75
Chapter 3.6 --- Antitumor effects of extracts from sequential extraction scheme --- p.76
Chapter 3.6.1 --- In vitro antiproliferative study by HL-60 --- p.76
Chapter 3.6.2 --- In vitro antiproliferative study by MCF-7 --- p.78
Chapter 3.6.3 --- In vivo antitumor study by BALB/c mice --- p.80
Chapter 3.7 --- Comparison of in vitro and in vivo activities of mushroom sclerotial extracts --- p.82
Chapter 3.8 --- Dose-response relationship of hot water extract from PR on cancer cell lines --- p.85
Chapter 3.8.1 --- In vitro dose-response antiproliferation of PR-W and PR-HWE on HL-60 --- p.85
Chapter 3.8.2 --- In vitro dose-response antiproliferation of PR-W on K562 and S180 --- p.88
Chapter 3.8.3 --- In vivo dose-response relationship of PR-W on S180 --- p.91
Chapter 3.9 --- Flow cytometric analysis of PR-W on cancer cell lines --- p.92
Chapter 3.9.1 --- Antiproliferative effect of PR-W on HL-60 --- p.92
Chapter 3.9.2 --- Antiproliferative effect of PR-W on K562 --- p.95
Chapter 3.9.3 --- Proposed mechanisms of cell cycle arrest by PR-W --- p.98
Chapter 3.10 --- Host-mediated antitumor mechanism of PR-W --- p.100
Chapter 3.10.1 --- Mouse cytokine array --- p.100
Chapter 3.10.2 --- Quantification of IL-13 by ELISA --- p.105
Chapter 3.10.3 --- Immunostimulatory effects of PR-W on mice --- p.109
Chapter 3.11 --- Correlation between antitumor activity and structure of mushroom sclerotial extract from hot water extraction alone --- p.114
Chapter Chapter 4. --- Conclusions and Future works --- p.118
List of References --- p.121
Related Publications --- p.142
"Antitumor activities of polysaccharides from the long-veiled lady mushroom Dictyophora indusiata." 2002. http://library.cuhk.edu.hk/record=b5891173.
Full textThesis (M.Phil.)--Chinese University of Hong Kong, 2002.
Includes bibliographical references (leaves 113-125).
Abstracts in English and Chinese.
Acknowledgements --- p.i
Abstract --- p.ii
Abstract (Chinese Version) --- p.iv
Table of Contents --- p.vi
List of Tables --- p.x
List of Figures --- p.xi
List of Abbreviations --- p.xiii
Chapter Chapterl 1 --- ntroduction --- p.1
Chapter Chapter 2 --- Literature Review --- p.5
Chapter 2.1 --- Mushroom Polysaccharides From Basidiomycetes --- p.5
Chapter 2.1.1 --- Antitumor and Immunomodulatory Activity --- p.6
Chapter 2.1.2 --- Antiviral Activity --- p.9
Chapter 2.1.3 --- Hypoglycermic Activity --- p.11
Chapter 2.1.4 --- Free Radical Scavenging Activity --- p.11
Chapter 2.2 --- Mushroom Dictyophora indusiata --- p.13
Chapter 2.2.1 --- Nutritional Value --- p.13
Chapter 2.2.2 --- Structural Characteristic of Dictyophora indusiata Polysaccharides --- p.14
Chapter 2.2.3 --- Biological Activity --- p.16
Chapter 2.3 --- In vivo Antitumor Study --- p.19
Chapter 2.4 --- Induction of Cytokines Production in Immune System --- p.21
Chapter 2.5 --- In vitro Antitumor Study --- p.25
Chapter 2.6 --- Cell Cycle Regulation --- p.28
Chapter Chapter 3 --- Materials & Methods --- p.34
Chapter 3.1 --- Extraction --- p.34
Chapter 3.1.1 --- Extraction of Dictyophora indusiata Polysaccharides --- p.34
Chapter 3.1.2 --- Purification of Dictyophora indusiata Polysaccharides --- p.35
Chapter 3.1.2.1 --- Preparation of DEAE-cellulose Ion Exchanger --- p.35
Chapter 3.1.2.2 --- Fractionation --- p.35
Chapter 3.2. --- Characterization of Dictyophora indusiata Polysaccharides --- p.39
Chapter 3.2.1 --- Polysaccharide Content Determination --- p.39
Chapter 3.2.2 --- Protein Content Determination --- p.39
Chapter 3.2.3 --- Gas Chromatography (GC) --- p.40
Chapter 3.2.4 --- Uronic Acid Content Determination --- p.42
Chapter 3.2.5 --- High Performance Liquid Chromatography (HPLC) --- p.43
Chapter 3.3 --- In vivo Studies --- p.44
Chapter 3.3.1 --- Animals --- p.44
Chapter 3.3.2 --- Maintenance of Sarcoma 180 Cell Line --- p.44
Chapter 3.3.3 --- Effect of DI3 Fraction on Sarcoma 180 Solid Tumor --- p.45
Chapter 3.3.4 --- Effect of DI3c Fraction on Tumor Necrosis Factor-Alpha (TNF-α) and Interleukin 2 (IL-2) Production --- p.47
Chapter 3.3.4.1 --- Treatment of Mice --- p.47
Chapter 3.3.4.2 --- Preparation of Mouse Serum --- p.47
Chapter 3.3.4.3 --- Enzyme-linked Immunosorbent Assay (ELISA) for TNF-α Production --- p.48
Chapter 3.3.4.4 --- Enzyme-linked Immunosorbent Assay (ELISA) for IL-2 Production --- p.49
Chapter 3.4 --- In vitro Studies --- p.51
Chapter 3.4.1 --- Maintenance of Cell Lines --- p.51
Chapter 3.4.2 --- Effect on Cancer Cell Lines --- p.52
Chapter 3.4.3 --- Cytotoxicity on Normal Cell Line --- p.52
Chapter 3.4.4 --- Trypan Blue Exclusion Method --- p.53
Chapter 3.4.5 --- MTT Assay --- p.54
Chapter 3.4.6 --- BrdU Incorporation --- p.55
Chapter 3.5 --- Statistical Analysis --- p.56
Chapter Chapter 4 --- Results --- p.57
Chapter 4.1 --- Extraction and Fractionation of Polysaccharides from Dictyophora indusiata --- p.57
Chapter 4.1.1 --- Percentage Yield of Crude DI Polysaccharides --- p.57
Chapter 4.1.2 --- Percentage Yield of DI3 Fractions --- p.57
Chapter 4.2 --- Characterization of DI3 Fractions --- p.62
Chapter 4.2.1 --- Polysaccharide and Protein Contents of DI3 Fractions --- p.62
Chapter 4.2.2 --- Relative Monosaccharide and Uronic Acid Content in Different DI3 Fractions --- p.62
Chapter 4.2.3 --- Estimated Molecular Weight of DI3 Fractions --- p.65
Chapter 4.3 --- Antitumor Effect of Dictyophora indusiata Polysaccharides In vivo --- p.70
Chapter 4.3.1 --- In vivo Antitumor Effect of Crude DI Polysaccharides --- p.70
Chapter 4.3.2 --- In vivo Antitumor Effect of Various Fractions of DI3 --- p.70
Chapter 4.3.3 --- Effect of DI3c on TNP-α and IL-2 Production in Mice --- p.78
Chapter 4.4 --- In vitro Effects of DI3 Fractions on Cell Density and Viability on Normal and Cancer Cell Lines --- p.86
Chapter 4.4.1 --- Effects of DI3 Fractions on Cell Density and Viability of Human Leukemic HL-60 and K-562 and Mouse Sarcoma 180 Cells --- p.86
Chapter 4.4.2 --- Effects of DI3 Fractions on the Growth of Human Liver Cancer HepG2 and Normal Monkey Kidney Vero Cells --- p.86
Chapter 4.4.3 --- Effect of DI3b Fraction on Proliferation of HL-60 Cells Determined by BrdU Incorporation --- p.94
Chapter Chapter 5 --- Discussions --- p.96
Chapter 5.1 --- Extraction and Characterization of DI3 Fractions --- p.96
Chapter 5.2 --- Antitumor Effects of Dictyophora indusiata Polysaccharides --- p.101
Chapter 5.3 --- Further Studies --- p.109
Chapter Chapter 6 --- Conclusion --- p.111
References --- p.113
Books on the topic "POLYSACCHARIDES MUSHROOM"
AHCC: Japan's medical breakthrough in natural immunotherapy. Laguna Beach, CA: Basic Health Publications, 2010.
Find full textThe constituents of medicinal plants. 3rd ed. Wallingford: CABI, 2021. http://dx.doi.org/10.1079/9781789243079.0000.
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Wang, Yuxiao, Xiaojun Huang, and Shaoping Nie. "Novel Prospective of Wild Mushroom Polysaccharides as Potential Prebiotics." In Fungal Biology, 211–26. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-030-02622-6_10.
Full textPengelly, Andrew. "Polysaccharides." In The constituents of medicinal plants, 147–67. 3rd ed. Wallingford: CABI, 2021. http://dx.doi.org/10.1079/9781789243079.0009.
Full textZhu, Fengmei, Bin Du, and Baojun Xu. "Preparation and Characterization of Polysaccharides from Mushrooms." In Polysaccharides, 1–16. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-03751-6_10-1.
Full textZhu, Fengmei, Bin Du, and Baojun Xu. "Preparation and Characterization of Polysaccharides from Mushrooms." In Polysaccharides, 1009–27. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-16298-0_10.
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Full textSmiderle, Fhernanda Ribeiro, Andrea Caroline Ruthes, and Marcello Iacomini. "Natural Polysaccharides from Mushrooms: Antinociceptive and Anti-inflammatory Properties." In Polysaccharides, 2151–78. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-16298-0_77.
Full textSchwartz, Betty, Yitzhak Hadar, and Daniel Sliva. "The Use of Edible Mushroom Water Soluble Polysaccharides in the Treatment and Prevention of Chronic Diseases: A Mechanistic Approach." In Antitumor Potential and other Emerging Medicinal Properties of Natural Compounds, 263–83. Dordrecht: Springer Netherlands, 2013. http://dx.doi.org/10.1007/978-94-007-6214-5_18.
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Full textYurchak, V., and N. Sharkova. "Development of Dietary Additive of Shiitake Mushrooms Enhanced with Active Polysaccharides for Pasta Production." In Bioenhancement and Fortification of Foods for a Healthy Diet, 221–36. Boca Raton: CRC Press, 2022. http://dx.doi.org/10.1201/9781003225287-15.
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Dahmen, Joseph, and Amber Frid-Jimenez. "They Grow Without Us." In 2017 ACSA Annual Conference. ACSA Press, 2017. http://dx.doi.org/10.35483/acsa.amp.105.22.
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