Effect of shark liver oil on peritoneal murine macrophages in responses to killed-Candida albicans

Shark Liver Oil [SLO] is an immunomodulator. Macrophages play a key role in host defense against pathogens like fungi. Candida albicans have mechanisms to escape immune system. We determined the effect of killed-Candida on the in vitro viability of macrophages and the effect of SLO on augmentation of this potency. Peritoneal macrophages were separated and cultured [3-105/well]. At first, the effect of killed-Candida [200 cells/well] on macrophage viability was evaluated, using MTT test. Then, MTT was performed on macrophages stimulated with killed-Candida in the presence of SLO. Killed-Candida suppressed the ability of MTT reduction and hence macrophages viability [P=0.026], but addition of SLO [100 mg/ml] significantly enhanced cell viability [P=0.00]. So, SLO could neutralize the inhibitory effect of Candida. Simultaneous with cytotoxic effect of killed-Candida cells on macrophages viability, SLO augment macrophages viability. So, it can be applied in candidiasis as a complement

Effect of cell wall, cytoplasmic fraction and killed-Candida albicans on nitric oxide production by peritoneal macrophages from BALB/c mice

The fractions of Candida albicans have been used as an immunomodulator. The present work assessed the effect of different fractions of C. albicans on nitric oxide [NO] production by mice peritoneal macrophages. Cell wall and cytoplasmic fractions of C. albicans ATCC 10321 strain were extracted. Mice peritoneal macrophages were purified and cultured. Different concentrations of both fractions and also killed C. albicans cells were used for macrophages stimulation and evaluation of NO production. NO amount was detected in culture supernatants of macrophages by Griess reagent. Also, MTT assay was performed to assess the viability of macrophages. The results elucidated that suppressive effect of cell wall proteins on NO release was significant at the dose of 100 micro g/ml [P=0.01], while cytoplasmic fraction increased NO amount at the dose of 1 micro g/ml compared to the control group [P=0.003]. Augmentation of NO production was statistically significant at 200 killed C. albicans per well [P=0.006]. According to our findings, cytoplasmic fractions and killed C. albicans have a positive effect on NO production by peritoneal macrophages, while cell wall fractions did not. Therefore, it is proposed that C. albicans fractions can be studied more as inflammation modulators