Please use this identifier to cite or link to this item: http://localhost:80/xmlui/handle/123456789/15231
Title: Effects of Cordyceps sinensis on macrophage function in high-fat diet fed rats and its anti-proliferative effects on IMR-32 human neuroblastoma cells
Authors: Dos Santos, Leandro Freire
Rubel, Rosalia
Bonatto, Sandro Jose Ribeiro
Yamaguchi, Adriana Aya
Torres, Maria Fernanda
Soccol, Vanete Thomaz
Da Silva, Andre Luís Lopes
Soccol, Carlos Ricardo
Keywords: Anti-tumoral
Cordyceps sinensis
high-fat diet
macrophage funcion.
Issue Date: 20-Jan-2018
Publisher: Karachi:Pakistan Journal of Pharmaceutical Sciences, university of Karachi.
Citation: Dos Santos, L. F., Rubel, R., Ribeiro Bonatto, S. J., Yamaguchi, A. A., Torres, M. F., Soccol, V. T., ... & Soccol, C. R. (2018). Effects of Cordyceps sinensis on macrophage function in high-fat diet fed rats and its anti-proliferative effects on IMR-32 human neuroblastoma cells. Pakistan Journal of Pharmaceutical Sciences, 31(1).
Abstract: Macrophages have been considered an elusive yet emerging therapeutic target in tumor development since they are an important component in tumor microenvironment. The purpose of the present study was to evaluate the effect of C. sinensis on macrophage function (a component of tumor microenvironment which can alter the virulence of cancer) in high-fat diet fed rats. IMR-32 human neuroblastoma cell cytotoxicity was also investigated. The following parameters were observed to evaluate macrophage function: superoxide anion, hydrogen peroxide, nitric oxide, lysosomal volume and phagocytic capacity. High fat diet (HFD) plus C. sinensis supplementation promoted a decreased superoxide anion and hydrogen peroxide levels as well as lysosomal volume and phagocytic capacity. Nitric oxide was increased in the same group. In summary, C. sinensis offered an important anti-tumoral perspective from the standpoint of the tumor microenvironment and in vitro IMR-32 cytotoxicity
URI: http://142.54.178.187:9060/xmlui/handle/123456789/15231
ISSN: 1011-601X
Appears in Collections:Issue 01

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