Romay C, Ledón N, González R
Depto. Farmacologia, Centro Nac. Invest. Científicas, CNIC, Habana, Cuba.
Inflamm Res. 1998 Aug;47(8):334-8. doi: 10.1007/s000110050338.
To examine the effects of C-phycocyanin, a pigment found in blue-green algae which acts as an antioxidant in vitro and in vivo, in different animal models of inflammation.
Male Sprague Dawley rats and OF1 mice were used.
Oedema was induced by: a) AA (0.5 mg/ear) or TPA (4 microg/ear) in the mouse ear b) carrageenan injection (0.1 mL of 1% suspension) in the rat paw (+/-adrenalectomy) and c) cotton pellet implantation in the rat axilla. Phycocyanin (50-300mg/kg, p.o.) or indomethacin (1 mg/ear or 3-10mg/kg, p.o.) as control were tested in the four animal models.
Measurement of the increase in the weight (mg) of 6 mm ear punch biopsies from treated ears were made in comparison to control ears, together with myeloperoxidase (MPO) activity as an index of neutrophil infiltration. The increase in the paw thickness (mm) was measured with a dial caliper. Cotton pellet was implanted and seven days afterwards the granuloma was removed and the dry weight was determined. Acute toxicity was studied in mice and rats. Statistics were performed using one-way analysis of variance with the Duncan Multirange test.
Phycocyanin reduced significantly (p < 0.05) and in a dose-dependent manner ear oedema induced by AA and TPA in mice as well as carrageenan-induced rat paw oedema (both in intact and adrenalectomized animals). In the TPA test, phycocyanin also reduced MPO content. Phycocyanin also exerted an inhibitory effect in the cotton pellet granuloma test. In the acute toxicity test in rats and mice, even at the highest dose tested (3000 mg/kg, p.o.), no toxicity was found.
Phycocyanin shows anti-inflammatory activity in four experimental models of inflammation. Its antioxidative and oxygen free radical scavenging properties may contribute, at least in part, to its anti-inflammatory activity.
研究蓝藻中发现的一种色素C-藻蓝蛋白在不同炎症动物模型中的作用,该色素在体内外均具有抗氧化作用。
使用雄性Sprague Dawley大鼠和OF1小鼠。
通过以下方式诱导水肿:a)在小鼠耳部注射AA(0.5mg/耳)或TPA(4μg/耳);b)在大鼠爪部注射角叉菜胶(0.1mL 1%悬浮液)(±肾上腺切除术);c)在大鼠腋窝植入棉球。在四种动物模型中测试了藻蓝蛋白(50 - 300mg/kg,口服)或吲哚美辛(1mg/耳或3 - 10mg/kg,口服)作为对照。
测量处理耳部6mm打孔活检组织重量(mg)的增加,并与对照耳部进行比较,同时测量髓过氧化物酶(MPO)活性作为中性粒细胞浸润的指标。用游标卡尺测量爪部厚度(mm)的增加。植入棉球,7天后取出肉芽肿并测定干重。在小鼠和大鼠中研究急性毒性。使用单因素方差分析和邓肯多重极差检验进行统计学分析。
藻蓝蛋白显著降低(p < 0.05)并呈剂量依赖性地减轻小鼠中由AA和TPA诱导的耳部水肿以及角叉菜胶诱导的大鼠爪部水肿(完整动物和肾上腺切除动物均如此)。在TPA试验中,藻蓝蛋白还降低了MPO含量。藻蓝蛋白在棉球肉芽肿试验中也发挥了抑制作用。在大鼠和小鼠的急性毒性试验中,即使在测试的最高剂量(3000mg/kg,口服)下,也未发现毒性。
藻蓝蛋白在四种炎症实验模型中显示出抗炎活性。其抗氧化和清除氧自由基的特性可能至少部分地促成了其抗炎活性。