外用R-85355,一种有效的选择性5-脂氧合酶抑制剂,不能改善牛皮癣。

P C van de Kerkhof, H van Pelt, G P Lucker, P M Steijlen, A Heremans
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引用次数: 8

摘要

已经研究了5-脂氧合酶抑制剂的抗银屑病疗效。在这些化合物中,R-68151特别令人感兴趣,因为它被证明能抑制5-脂氧合酶,而不抑制12-脂氧合酶、环氧合酶和血栓素- a2合成酶。R-68151已被证明对牛皮癣有轻度至中度的治疗效果。在本研究中,研究了一种新的5-脂氧合酶R-85355对牛皮癣的疗效。与R-68151相比,R-85355在体外抑制a -23187刺激的白三烯- b4产生方面的效力是R-68151的3倍。在一项左右双盲比较研究中,研究了该化合物在饱和状态下对11例慢性稳定斑块型银屑病患者的抗银屑病疗效。此外,还评估了表皮增生、角化和炎症的各种标志物。在单个患者中,与安慰剂相比,在临床严重程度评分或细胞生物学标志物方面,没有观察到R-85355的左右差异。目前的研究表明,选择性和高效的5-脂氧合酶抑制剂对慢性斑块型银屑病的局部治疗无效。
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Topical R-85355, a potent and selective 5-lipoxygenase inhibitor, fails to improve psoriasis.

Inhibitors of 5-lipoxygenase have been studied with respect to antipsoriatic efficacy. Of these compounds, R-68151 is of particular interest as it proved to inhibit 5-lipoxygenase without inhibiting 12-lipoxygenase, cyclooxygenase and thromboxane-A2 synthetase. R-68151 has been shown to have a mild-to-moderate therapeutic effect in psoriasis. In the present study a new 5-lipoxygenase, R-85355, was investigated with respect to its efficacy in psoriasis. R-85355 is 3 times more potent compared to R-68151 with respect to inhibition of in vitro A-23187-stimulated leukotriene-B4 production by polymorphonuclear leukocytes. In a left-right double-blind comparative study, the compound was studied at saturation with respect to its antipsoriatic efficacy in 11 patients with chronic stable plaque psoriasis. In addition, various markers for epidermal proliferation, keratinization and inflammation were assessed. In no single patient was a left-right difference observed in favour of R-85355 compared to placebo with respect to clinical severity scores or the cell-biological markers. The present study indicates that a selective and highly potent 5-lipoxygenase inhibitor was not effective in the topical treatment of chronic plaque psoriasis.

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