In Vitro and In Vivo Antitumoral Activity of Exobiopolymers from the Royal Sun Culinary-Medicinal Mushroom Agaricus brasiliensis (Agaricomycetes).

We studied antitumor activity in vitro and in vivo and partial chemical characterization of exobiopolymers (EBPs) of Agaricus brasiliensis produced by submerged cultivation. The EBPs comprised 61.2% total sugar and 22.3% total protein, and the chromatographic profile mainly identified mannose (65.5%), galactose (17.5%), and glucose (13.1%). In vitro analysis revealed a dose with antitumor effectiveness, time-dependent treatment, and 46% inhibition of solid Walker 256 tumors in rats. Metabolic changes were significant in the spleens of the animals; this is possibly related to higher immune activity triggered by the presence of EBPs in the treated group. The increase of nitric oxide production by peritoneal macrophages from animals may be related to the tumor reduction observed, because nitric oxide acts as an important effector pathway in the defense of the organism.

Análise do potencial antioxidante do consumo oral da farinha produzida com micélio de Agaricus brasiliensis em hamsters hipercolesterolêmicos / The antioxidant potential of oral intake of flour produced from Agaricus brasiliensis mycelium in hamsters with hypercholesterolemia

O sistema de defesa antioxidante inibe ou reduz os danos causados às células pelas espécies reativas de oxigênio. Alguns compostos antioxidantes presentes na dieta auxiliam na defesa antioxidante do plasma. O potencial antioxidante do consumo oral de farinha produzida com micélio de Agaricus brasiliensis fermentado sobre grãos de trigo foi analisado nos plasmas de hamsters Golden Syrian machos hipercolesterolêmicos, que foram divididos em quatro grupos: P(dieta padrão), H (dieta hipercolesterolêmica padrão), C (dieta padrão + 10 % de farinha de trigo contendo micélio de A. brasiliensis), e HC (dieta hipercolesterolêmica padrão + 10 % de farinha de trigo contendo micélio deA. brasiliensis). Os animais foram alimentados durante 40 dias e depois sacrificados para coletar materiais biológicos.A análise da capacidade antioxidante mostrou que a dieta do grupo C induziu maior aumento significativo da concentração de antioxidantes no plasma (0,39 mg.mL-1, expresso em ácido ascórbico). O grupo HC apresentou maiorcapacidade antioxidante do que grupo H (p < 0,05), pois inibiu 20,2 % do branqueamento da crocina. O grupo H inibiu10,4 %, porém o grupo HC demonstrou capacidade antioxidante semelhante ao do grupo P (16,64 %). O consumo da farinha de trigo contendo micélio de A. brasiliensis estimulou a proteção antioxidante no plasma dos animais...

Production of cachexia mediators by Walker 256 cells from ascitic tumors.

In neoplasic cachexia, chemical mediators seem to act as initiators or perpetuators of this process. Walker 256 cells, whose metabolic properties have so far been little studied with respect to cancer cachexia, are used as a model for the study of this syndrome. The main objective of this research was to pinpoint the substances secreted by these cells that may contribute to the progression of the cachectic state. Since inflammatory mediators seem to be involved in the manifestation of this syndrome, the in vitro production of nitric oxide (NO), cytokines (tumor necrosis factor alpha (TNF-alpha) and interleukin-6 (IL-6)), and prostaglandin E2 (PGE2) was evaluated in Walker 256 cells isolated from ascitic tumors. After 4 or 5 h, a significant increase in NO production was observed (2.55 +/- 1.56 and 4.05 +/- 1.99 nmol NO per 10(7) cells, respectively). When isolated from a 6-day-old tumor, a significantly lower production of IL-6 and higher production of TNF-alpha than in cells from a 4-day-old tumor were observed, indicating a relationship between the production of cytokines and the time of tumor development after implantation. Considerable production of PGE(2) by Walker 256 cells isolated from the 6-day-old tumor was also observed. Polyamines were also determined in Walker 256 cells. Levels of putrescine, spermidine, and spermine did not show significant differences in tumors developed during 4 or 6 days. Direct evidence of the release of proinflammatory cytokines and PGE2 by Walker 256 cells suggests that these mediators can drive the cachectic syndrome in the host, the effect being dependent on tumor development time.