Romay C, Ledón N, González R
Departamento de Farmacología, Centro Nacional de Investigaciones Científícas, CNIC, Habana, Cuba.
Arzneimittelforschung. 2000 Dec;50(12):1106-9. doi: 10.1055/s-0031-1300340.
Recently it was demonstrated that phycocyanin, a biliprotein isolated from microalgae Spirulina, exerts anti-inflammatory activity in several animal models of inflammation. In this report, the effects of phycocyamin on prostaglandin E2 (PGE2) concentrations and phospholipase A2 (PLA2) activity were determined in arachidonic acid (AA) and 12-O-tetradecanoyl phorbol 13-acetate (TPA)-induced mouse ear oedema, respectively. Phycocyanin (50-200 mg/kg p.o.) inhibited in a dose-dependent manner PGE2 levels in mouse ear treated with AA. Also, phycocyanin (100-400 mg/kg p.o.) moderately reduced PLA2 activity in TPA-induced mouse ear inflammation test. In this model triamcinolone (10 mg/kg p.o.) used as reference drug exerted a remarkable inhibitory effect on PLA2 activity. These results provide the first evidence that the anti-inflammatory effects of phycocyanin may result, at least partially, from inhibition of PGE2 production and a moderate inhibition of PLA2 activity.
最近有研究表明,从微藻螺旋藻中分离出的一种双蛋白——藻蓝蛋白,在多种炎症动物模型中具有抗炎活性。在本报告中,分别在花生四烯酸(AA)和12-O-十四酰佛波醇-13-乙酸酯(TPA)诱导的小鼠耳肿胀模型中,测定了藻蓝蛋白对前列腺素E2(PGE2)浓度和磷脂酶A2(PLA2)活性的影响。藻蓝蛋白(50-200毫克/千克,口服)以剂量依赖性方式抑制了用AA处理的小鼠耳中PGE2的水平。此外,在TPA诱导的小鼠耳炎症试验中,藻蓝蛋白(100-400毫克/千克,口服)适度降低了PLA2的活性。在该模型中,用作参考药物的曲安奈德(10毫克/千克,口服)对PLA2活性有显著的抑制作用。这些结果首次证明,藻蓝蛋白的抗炎作用可能至少部分源于对PGE2产生的抑制以及对PLA2活性的适度抑制。