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外用组胺通过受体依赖性机制刺激非节段性白癜风的色素再生。

Topical Histamine Stimulates Repigmentation of Nonsegmental Vitiligo by a Receptor-Dependent Mechanism.

作者信息

Liu Jun, Xu Yan, Lin Tzu-Kai, Lv Chengzhi, Elias Peter M, Man Mao-Qiang

机构信息

Dalian Skin Disease Hospital, Dalian, People's Republic of China.

出版信息

Skin Pharmacol Physiol. 2017;30(3):139-145. doi: 10.1159/000464335. Epub 2017 Apr 19.

Abstract

BACKGROUND

Though vitiligo is a common depigmentary disorder, it still represents a substantial therapeutic challenge. Therapeutic options are limited in part due to its uncertain etiology.

OBJECTIVE

Because recent studies suggest that histamine stimulates melanogenesis in vitro, we determined here whether topical histamine stimulates repigmentation in patients with stable, nonsegmental vitiligo.

METHODS

A total of 23 otherwise normal volunteers with vitiligo, including 14 males and 9 females aged 6-59 years (mean age 29.2 ± 2.8), were enrolled in this study. 1% histamine in distilled water was applied to the lesions twice daily for 5 weeks, while comparable lesions, treated with distilled water alone, served as the controls. The melanin index was measured on the uninvolved and lesional skin sites before and after 5 weeks of treatments using the melanin/erythema probe connected to a Courage-Khazaka MPA5 (Cologne, Germany). Changes in epidermal permeability barrier were also assessed at the same time point. To determine whether histamine-induced repigmentation is receptor-dependent, both ears of C57BL/6J mice were treated topically with 5% cimetidine, a histamine type 2 receptor (H2r) antagonist, twice daily for 10 days. One hour after each cimetidine application, the right ear was treated topically with 10% histamine, while vehicle alone was applied to the left ear. Changes in melanin index were measured 24 h after the last application of histamine and vehicle as described in the human study.

RESULTS

In patients with vitiligo treated with vehicle alone for 5 weeks, the melanin index remained unchanged, while topical histamine treatment increased the melanin index by 38% (p < 0.001 vs. both vehicle and pretreatment), which was paralleled by a >60% reduction in lesion surface area. Moreover, topical histamine accelerated permeability barrier recovery. No adverse events were observed following histamine applications. In mice, topical histamine significantly increased the melanin index, while topical co-applications of the H2r antagonist (cimetidine) prevented the expected histamine-induced increase in melanin index.

CONCLUSIONS

These studies indicate that topical histamine or an H2r agonist could be useful for treating nonsegmental vitiligo, but further clinical studies in large populations will be required to validate the efficacy and safety of this approach.

摘要

背景

尽管白癜风是一种常见的色素脱失性疾病,但它仍然是一个重大的治疗挑战。由于其病因不明,治疗选择有限。

目的

鉴于最近的研究表明组胺在体外可刺激黑素生成,我们在此确定局部应用组胺是否能刺激稳定型非节段性白癜风患者的色素再生。

方法

本研究共纳入23名其他方面正常的白癜风志愿者,包括14名男性和9名女性,年龄在6至59岁之间(平均年龄29.2±2.8岁)。将1%的组胺溶于蒸馏水中,每天两次涂抹于皮损处,持续5周,而仅用蒸馏水治疗的类似皮损作为对照。使用连接到德国科隆Courage-Khazaka MPA5的黑素/红斑探头,在治疗5周前后测量非皮损和皮损皮肤部位的黑素指数。同时在同一时间点评估表皮通透性屏障的变化。为了确定组胺诱导的色素再生是否依赖受体,对C57BL/6J小鼠的双耳每天两次局部应用5%西咪替丁(一种组胺2型受体(H2r)拮抗剂),持续10天。每次应用西咪替丁1小时后,右耳局部应用10%组胺,而左耳仅应用赋形剂。如人体研究中所述,在最后一次应用组胺和赋形剂24小时后测量黑素指数的变化。

结果

在仅用赋形剂治疗5周的白癜风患者中,黑素指数保持不变,而局部应用组胺治疗使黑素指数增加了38%(与赋形剂和治疗前相比,p<0.001),同时皮损表面积减少了>60%。此外,局部应用组胺加速了通透性屏障的恢复。应用组胺后未观察到不良事件。在小鼠中,局部应用组胺显著增加了黑素指数,而局部联合应用H2r拮抗剂(西咪替丁)可阻止预期的组胺诱导的黑素指数增加。

结论

这些研究表明,局部应用组胺或H2r激动剂可能对治疗非节段性白癜风有用,但需要在大量人群中进行进一步的临床研究来验证这种方法的有效性和安全性。

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