Deiters Barthold, Prehm Peter
Muenster University Hospital, Institute of Physiological Chemistry and Pathobiochemistry, Waldeyerstr, 15, D-48129 Münster, Germany.
Arthritis Res Ther. 2008;10(1):R8. doi: 10.1186/ar2357. Epub 2008 Jan 18.
Osteoarthrosis is characterized by cartilage erosion, proteolysis of aggrecan and collagen, and disturbed rates of synthesis of aggrecan and hyaluronan by chondrocytes, with hyaluronan over-production being an early reaction. We considered that inhibition of hyaluronan export might prevent subsequent proteoglycan loss and collagen degradation.
To test this hypothesis, we studied a tissue culture model using bovine cartilages explants activated with IL-1alpha to induce osteoarthritic reactions using the phosphodiesterase-5 inhibitors tadalafil, zaprinast and vardenafil.
These drugs inhibited hyaluronan export, but they did not inhibit hyaluronan synthase activity. Simultaneously, they inhibited proteoglycan loss and collagen degradation, but not their synthesis. They also reduced the release of gelatinases into the culture media and diffusion of the indicator protein horseradish peroxidase through the cartilage explants. The mechanism of action of these compounds may be through inhibition of hyaluronan exporter multidrug resistance-associated protein 5 (MRP5), because the effective drug concentrations were much higher than required for phosphodiesterase-5 inhibition and intracellular cGMP accumulation.
Inhibition of hyaluronan over-production may be an appropriate target to attenuate IL-1-induced reactions in osteoarthritic cartilage.
骨关节炎的特征是软骨侵蚀、聚集蛋白聚糖和胶原蛋白的蛋白水解,以及软骨细胞中聚集蛋白聚糖和透明质酸合成速率紊乱,透明质酸过度产生是早期反应。我们认为抑制透明质酸输出可能会阻止随后的蛋白聚糖丢失和胶原蛋白降解。
为了验证这一假设,我们研究了一种组织培养模型,该模型使用用白细胞介素-1α激活的牛软骨外植体,以使用磷酸二酯酶-5抑制剂他达拉非、扎普司特和伐地那非诱导骨关节炎反应。
这些药物抑制了透明质酸输出,但没有抑制透明质酸合酶活性。同时,它们抑制了蛋白聚糖丢失和胶原蛋白降解,但没有抑制它们的合成。它们还减少了明胶酶释放到培养基中以及指示蛋白辣根过氧化物酶通过软骨外植体的扩散。这些化合物的作用机制可能是通过抑制透明质酸输出转运体多药耐药相关蛋白5(MRP5),因为有效药物浓度远高于磷酸二酯酶-5抑制和细胞内cGMP积累所需的浓度。
抑制透明质酸过度产生可能是减轻骨关节炎软骨中白细胞介素-1诱导反应的合适靶点。