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藻蓝蛋白的抗炎和抗痛觉过敏活性。

Antiinflammatory and antihyperalgesic activity of C-phycocyanin.

作者信息

Shih Chao-Ming, Cheng Shin-Nan, Wong Chih-Shung, Kuo Yu-Ling, Chou Tz-Chong

机构信息

Chia-Yi Christian Hospital, Taipei, Taiwan, Republic of China.

出版信息

Anesth Analg. 2009 Apr;108(4):1303-10. doi: 10.1213/ane.0b013e318193e919.

Abstract

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-alpha (TNF-alpha) 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-alpha, prostaglandin E(2), nitrate and myeloperoxidase activity.

CONCLUSIONS

Based on these results, it is suggested that the inhibition of NO and prostaglandin E(2) over-production through suppressing iNOS and COX-2 induction and attenuation of TNF-alpha formation and neutrophil infiltration into inflammatory sites by C-PC may contribute, at least in part, to its antihyperalgesic activity.

摘要

背景

C-藻蓝蛋白(C-PC)是一种存在于蓝绿藻(如钝顶螺旋藻)中的双蛋白,因其具有多种治疗价值,常被用作膳食营养补充剂。此外,许多体外和体内研究已证明,C-PC的抗炎活性部分是通过抑制促炎细胞因子的形成、诱导型一氧化氮合酶(iNOS)和环氧合酶-2(COX-2)的表达来实现的。然而,C-PC在炎性痛觉过敏中是否也具有抗痛觉过敏活性尚未得到研究。

方法

使用角叉菜胶诱导的热痛觉过敏模型,通过测量爪部缩足潜伏期来评估C-PC对痛觉的影响。为阐明其中涉及的机制,测定了大鼠爪部iNOS和COX-2的表达以及硝酸盐和肿瘤坏死因子-α(TNF-α)的形成。

结果

C-PC(30或50mg/kg,腹腔注射)预处理或后处理均显著减轻了角叉菜胶诱导的炎性痛觉过敏以及后期(4小时)iNOS和COX-2的诱导,同时抑制了TNF-α、前列腺素E2、硝酸盐的形成和髓过氧化物酶活性。

结论

基于这些结果,提示C-PC通过抑制iNOS和COX-2的诱导来抑制NO和前列腺素E2的过度产生,并减轻TNF-α的形成以及中性粒细胞向炎症部位的浸润,这可能至少部分地促成了其抗痛觉过敏活性。

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