2003
DOI: 10.1016/s0006-291x(03)00579-5
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Chitosan induces different l-arginine metabolic pathways in resting and inflammatory macrophages

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Cited by 96 publications
(57 citation statements)
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“…Peluso et al (1994) also demonstrated that chitosan could stimulate the macrophages in the rats and increase NO secretion. Porporatto et al (2003) have shown the similar result that 0.05 % ~ 0.1 % chitosan significantly enhanced the content of NO and the expression of iNOS mRNA in rat macrophages. Shi (2004) also showed that chitosan supplementation had better effects on the splenocyte of broilers iNOS and NO production in dose-dependent manner, but its effect on iNOS gene expression had not been studied.…”
Section: Discussionsupporting
confidence: 62%
See 1 more Smart Citation
“…Peluso et al (1994) also demonstrated that chitosan could stimulate the macrophages in the rats and increase NO secretion. Porporatto et al (2003) have shown the similar result that 0.05 % ~ 0.1 % chitosan significantly enhanced the content of NO and the expression of iNOS mRNA in rat macrophages. Shi (2004) also showed that chitosan supplementation had better effects on the splenocyte of broilers iNOS and NO production in dose-dependent manner, but its effect on iNOS gene expression had not been studied.…”
Section: Discussionsupporting
confidence: 62%
“…iNOS is responsible for generating high levels of NO in activated macrophages, and its expression is essential for the functions of NO in the regulation of immune responses (Xing and Schat 2000). Porporatto et al (2003) found that chitosan significantly enhanced the NO content and iNOS expression in rat macrophages. This implied that enhanced immune functions by chitosan are associated with the activation and strengthening of secretory functions of macrophages and increased expression of iNOS.…”
Section: Introductionmentioning
confidence: 99%
“…The findings of the current research were consistent with those of previous studies. It was reported that the strong stimulatory activity of chitosan has been mainly attributed to the N-acetyl-d-glucosamine residues and its effect could be mediated by combined action with a macrophage mannose specific receptor (Porporatto et al 2003;Feng et al 2004). Zhao (2004) indicated that macrophages activated by oligochitosan in- Porporatto et al (2005) found that chitosan could be absorbed by the antigen-presenting cells and profoundly affected immunity by activating the T cell in the intestinal mucosa of rats.…”
Section: Discussionmentioning
confidence: 99%
“…Results of the in vitro trial showed that chitosan significantly enhanced the NO content and iNOS expression in rat macrophages (Porporatto et al 2003). However, Yang et al (2010) indicated that chitosan markedly inhibited the LPS-induced NO production of RAW 264.7 cells.…”
Section: Introductionmentioning
confidence: 97%
“…A quitosana e respetivos oligômeros inibem a ativação e a expressão da metaloproteinase-2 da matriz em fibroblastos humanos (Kim e Kim, 2006), estimulando a cicatrização dos tecidos. O efeito imunoestimulador de derivados de quitosana tem sido atribuído à presença dos grupos N-acetil-D-glucosamina (Porporatto et al, 2003), que atuam estimulando as células inflamatórias como os neutrófilos PMN, macrófagos e fibroblastos. A quitosana promove a produção do fator de transformação do crescimento β (TGF-β) e do fator de crescimento derivado de plaquetas por monócitos humanos derivados de macrófagos (Ueno et al, 2001a) envolvidos na resposta inflamatória.…”
Section: Anti-inflamatóriaunclassified