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首页> 外文期刊>Journal of pharmacological sciences. >The Combined Effect of Topical CX-659S, a Novel Diaminouracil Derivative, With Topical Corticosteroid on the Three Types of Allergic Responses in Mice or Guinea Pigs
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The Combined Effect of Topical CX-659S, a Novel Diaminouracil Derivative, With Topical Corticosteroid on the Three Types of Allergic Responses in Mice or Guinea Pigs

机译:新型二氨基尿嘧啶衍生物外用CX-659S与外用皮质类固醇对小鼠或豚鼠三种类型的过敏反应的联合作用

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References(44) Cited-By(5) CX-659S ((S)-6-amino-5-(6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxamido)-3-methyl-1-phenyl-2,4(1H,3H)-pyrimidinedione), a newly discovered anti-inflammatory compound, exerts inhibitory effects against picryl chloride-, oxazolone-, and dinitrochlorobenzene-induced acute contact hypersensitivity responses (CHRs) characterized by Th1-type reactions. Furthermore, this compound suppressed chronic CHRs characterized by Th2-type reactions, which is well known to mimic many, if not all, events occurring within the lesional skin of patients with atopic dermatitis (AD). The present study was conducted to determine the combined effect of topical CX-659S with topical corticosteroid on immediate type (ITR), late type (LTR), and delayed type hypersensitivity (DTHR) allergic reactions that are involved in AD. An ineffective dose of CX-659S (0.03 mg/ear) combined with betamethasone valerate (BV) significantly potentiated inhibitory activity of BV alone (0.1 μg/ear and 0.3 μg/ear) on both the ITR and the LTR in mice with the ovalbumin (OVA)-induced biphasic cutaneous reaction. Furthermore, the combined effect of CX-659S with BV was also observed on dinitrochlorobenzene (DNCB)-induced DTHR in guinea pigs. These results indicate that CX-659S has a combined effect with corticosteroids on every ITR, LTR, and DTHR. Proper treatment with corticosteroids for a safe and effective treatment of AD is needed. Thus, the combination therapy of topical CX-659S with topical corticosteroid would be one of the potential approaches for devising a proper treatment with corticosteroids.
机译:参考文献(44)Cited-By(5)CX-659S((S)-6-amino-5-(6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxamido)-3-methyl-1-苯基-2,4(1H,3H)-嘧啶二酮)是一种新发现的消炎化合物,对以氯化吡啶草酰,恶唑酮和二硝基氯苯引起的急性接触超敏反应(CHR)具有抑制作用,其特征是Th1型反应。此外,该化合物抑制了以Th2型反应为特征的慢性CHRs,众所周知,CHRs可模仿特应性皮炎(AD)患者病变皮肤内发生的许多(如果不是全部)事件。进行本研究是为了确定局部CX-659S与局部皮质类固醇对AD涉及的速发型(ITR),迟发型(LTR)和迟发型超敏反应(DTHR)过敏反应的联合作用。无效剂量的CX-659S(0.03 mg / ear)与戊酸倍他米松(BV)组合可显着增强单独的BV(0.1μg/ ear和0.3μg/ ear)对卵白蛋白小鼠的ITR和LTR的抑制活性。 (OVA)诱导的双相皮肤反应。此外,还观察到CX-659S与BV联合作用对豚鼠二硝基氯苯(DNCB)诱导的DTHR。这些结果表明,CX-659S与皮质类固醇对每种ITR,LTR和DTHR具有联合作用。需要用皮质类固醇适当治疗,以安全有效地治疗AD。因此,局部CX-659S与局部皮质类固醇的联合治疗将是设计适当治疗皮质类固醇的潜在方法之一。

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