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Antiinflammatory and Antihyperalgesic Activity of C-Phycocyanin

医学 药理学 痛觉过敏 一氧化氮合酶 促炎细胞因子 肿瘤坏死因子α 一氧化氮 髓过氧化物酶 伤害 卡拉胶 前列腺素E2 前列腺素E 细胞因子 体内 炎症 免疫学 内分泌学 内科学 生物 受体 生物技术
作者
Chao-Ming Shih,Shin‐Nan Cheng,Chih‐Shung Wong,Yu-Ling Kuo,Tz‐Chong Chou
出处
期刊:Anesthesia & Analgesia [Lippincott Williams & Wilkins]
卷期号:108 (4): 1303-1310 被引量:127
标识
DOI:10.1213/ane.0b013e318193e919
摘要

In Brief BACKGROUND: C-phycocyanin (C-PC), a biliprotein found in blue green algae, such as Spirulina platensis, is often used as a dietary nutritional supplement due to its various therapeutic values. In addition, the antiinflammatory activity of C-PC partly through inhibition of proinflammatory cytokine formation, inducible nitric oxide synthase (iNOS) and cyclooxygeanase-2 (COX-2) expression has been demonstrated in many in vitro and in vivo studies. However, whether C-PC also has antihyperalgesic activity in inflammatory nociception has not been investigated. METHODS: Using a carrageenan-induced thermal hyperalgesia model, we evaluated the effect of C-PC on nociception by measuring paw withdrawal latency. To clarify the mechanisms involved, the expression of iNOS and COX-2 and the formation of nitrate and tumor necrosis factor-α (TNF-α) in the rat paw were determined. RESULTS: Pre- or posttreatment with C-PC (30 or 50 mg/kg, IP) significantly attenuated carrageenan-induced inflammatory nociception and the induction of iNOS and COX-2 at the late phase, (4 h) accompanied by an inhibition of the formation of TNF-α, prostaglandin E2, nitrate and myeloperoxidase activity. CONCLUSIONS: Based on these results, it is suggested that the inhibition of NO and prostaglandin E2 over-production through suppressing iNOS and COX-2 induction and attenuation of TNF-α formation and neutrophil infiltration into inflammatory sites by C-PC may contribute, at least in part, to its antihyperalgesic activity. IMPLICATIONS: We first demonstrated that c-phycocyanin attenuates carrageenan-induced inflammatory nociception, which may be associated with the inhibition of nitric oxide and prostaglandin E2 over-production (through suppressing inducible nitric oxide synthase), cyclooxygeanase-2 induction, attenuation of tumor necrosis factor-α formation and neutrophil infiltration into inflammatory sites. These findings suggest that c-phycocyanin may be a potential therapeutic drug for reducing inflammatory nociception.

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