Aloe arborescens polysaccharides: In vitro immunomodulation and potential cytotoxic activity

Nazeam, Jilan A.; Gad, Haidy A.; Ahmed Esmat; El-Hefnawy, Hala M.; Singab, Abdel Naser B.;

Abstract


Different polysaccharides were isolated from the leaves of Aloe arborescens using the gradient power of hydrogen followed by antitumor and immunomodulatory assay. The total polysaccharide content of different fractions, watersoluble polysaccharide (WAP), acid-soluble polysaccharide (ACP), and alkaline-soluble polysaccharide (ALP), was estimated using a phenol-sulfuric acid spectrophotometric method. WAP possessed a higher content of mannose and glucose than either ACP or ALP. In vitro antitumor activity was investigated in three different cancer cell lines, and in vitro immunomodulatory potential was assessed through phagocytosis and lymphocyte transformation assay. The results showed that WAP and ALP exhibited the most significant cytotoxicity against HepG2 human liver cancer cells, with IC50 values of 26.14 and 21.46 lg/ mL, respectively. In contrast, ALP was able to enhance lymphocyte transformation, whereas WAP had the most potent phagocytic activity. Molecular weight, total sugar and uronic acid content, Fourier transform-infrared analysis, and linkage type of bioactive polysaccharides were investigated. These findings revealed that the potential antitumor activity of the natural agents WAP and ALP was through an immunomodulation mechanism, which verifies the use of the plant as adjuvant supplement for cancer patients suffering immunosuppression during chemotherapy.


Other data

Title Aloe arborescens polysaccharides: In vitro immunomodulation and potential cytotoxic activity
Authors Nazeam, Jilan A.; Gad, Haidy A.; Ahmed Esmat ; El-Hefnawy, Hala M.; Singab, Abdel Naser B.
Keywords Aloe arborescens;Cytokines;Cytotoxic activity;Immunomodulator;Phagocytosis;Polysaccharides
Issue Date 1-May-2017
Publisher MARY ANN LIEBERT, INC
Journal Journal of Medicinal Food 
Volume 20
Issue 5
ISSN 1096620X
DOI 10.1089/jmf.2016.0148
PubMed ID 28414560
Scopus ID 2-s2.0-85027960563
Web of science ID WOS:000401245300008

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Citations 12 in pubmed
Citations 31 in scopus


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