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      Evaluation of aloin and aloe-emodin as anti-inflammatory agents in aloe by using murine macrophages.

      Bioscience, biotechnology, and biochemistry
      Aloe, chemistry, Animals, Anthraquinones, pharmacology, Anti-Inflammatory Agents, Cell Line, Cell Survival, drug effects, Cyclooxygenase 2, genetics, Dinoprostone, biosynthesis, secretion, Emodin, analogs & derivatives, Flavonols, Gene Expression Regulation, Enzymologic, Isoflavones, Lipopolysaccharides, Macrophages, cytology, metabolism, Mice, Nitric Oxide, Nitric Oxide Synthase Type II, RNA, Messenger

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          Abstract

          The aloe ingredients responsible for physiological effects and the concentrations required to exert their biological activities are not fully understood. This study compares the anti-inflammatory effects of aloin and aloe-emodin with other polyphenols. Our results demonstrated that aloe-emodin dose-dependently inhibited inducible nitric oxide synthase (iNOS) mRNA expression and nitric oxide (NO) production at 5-40 microM. In addition, the levels of cyclooxygenase-2 (COX-2) mRNA and prostaglandin E2 (PGE2) production were suppressed by 40 microM aloe-emodin. Aloin also suppressed the production of NO at 5-40 microM, although it did not suppress PGE2 production. The present results indicate that aloin and aloe-emodin possibly suppress the inflammatory responses by blocking iNOS and COX-2 mRNA expression. The anti-inflammatory effect of aloe-emodin was comparable to that of kaempferol and quercetin, indicating aloe-emodin as a possible key constituent responsible for the anti-inflammatory activity of aloe.

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