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首页> 外文期刊>The American Journal of Pathology >Hair growth modulation by topical immunophilin ligands: Induction of anagen, inhibition of massive catagen development, and relative protection from chemotherapy-induced alopecia
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Hair growth modulation by topical immunophilin ligands: Induction of anagen, inhibition of massive catagen development, and relative protection from chemotherapy-induced alopecia

机译:局部免疫亲和素配体对毛发生长的调节:毛发生长素的诱导,抑制大量的致癌物的形成以及对化学疗法引起的脱发的相对保护

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摘要

Selected immunophilin ligands (IPLs) are not only potent immunosuppressants but also modulate hair growth. Their considerable side effects, however, justify at best topical applications of these drugs for the management of clinical hair growth disorders. Therefore, we have explored hair growth manipulation by topical cyclosporin A (CsA) and FK 506 in previously established murine models that mimic premature hair follicle regression (catagen) or chemotherapy-induced alopecia, two major pathomechanisms underlying human hair loss. We confirm that topical CsA and FK 506 induce active hair growth (anagen) in the back skin of C57BL/6 mice with all follicles in the resting stage (telogen) and show that both IPLs also inhibit massive, dexamethasone-induced, premature catagen development in these mice. Furthermore, we demonstrate that CsA and FK 506 provide relative protection from alopecia and follicle dystrophy induced by cyclophosphamide, possibly by favoring the dystrophic anagen pathway of follicle response to chemical damage. Although it remains to be established whether these IPLs exert the same effects on human hair follicles, our study provides proof of the principle that topical IPLs can act as potent manipulators of clinically relevant hair-cycling pathomechanisms. This strongly encourages one to explore the use of topical IPLs in the management of human hair growth disorders.
机译:所选的亲免蛋白配体(IPL)不仅是有效的免疫抑制剂,而且还调节头发的生长。然而,它们的相当大的副作用证明这些药物最好地局部用于临床毛发生长疾病的治疗。因此,我们已经探索了局部环孢菌素A(CsA)和FK 506在先前建立的模仿早发毛囊消退(催化)或化学疗法引起的脱发的小鼠模型中的毛发生长控制,这是人类脱发的两种主要致病机理。我们确认,局部CsA和FK 506会在C57BL / 6小鼠的所有毛囊处于静止期(telogen)的C57BL / 6小鼠的背部皮肤中诱导活跃的毛发生长(毛发生长),并显示这两个IPL也会抑制地塞米松诱导的过早的过早的毛发生长在这些小鼠中。此外,我们证明CsA和FK 506提供相对保护免受环磷酰胺诱导的脱发和毛囊营养不良,可能是通过促进对化学损伤的卵泡营养不良性途径。尽管这些IPL对人的毛囊是否具有相同的作用尚待确定,但我们的研究提供了局部IPL可以作为临床上相关的毛发循环机制有效操纵者的原理的证据。这强烈鼓励人们探索局部IPL在人类毛发生长疾病管理中的使用。

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