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黄褐斑的新机制见解

New Mechanistic Insights of Melasma.

作者信息

Liu Wei, Chen Qin, Xia Yumin

机构信息

Department of Dermatology, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, 710004, People's Republic of China.

出版信息

Clin Cosmet Investig Dermatol. 2023 Feb 13;16:429-442. doi: 10.2147/CCID.S396272. eCollection 2023.

Abstract

Melasma is a common acquired disorder of pigmentation that negatively impacts quality of life. Present treatments show poor therapeutic effect with frequent recurrence. This in large part is due to the currently limited understanding of the disease's etiology. It is urgent to elucidate the pathogenesis of melasma to further the discovery of new therapeutic strategies. Recent studies show that melasma is triggered or aggravated by a variety of factors, including genetic susceptibility, ultraviolet radiation, and sex hormone dysregulation. Ultraviolet B radiation upregulates the expression of several melanocyte-specific genes and stimulates the release of key factors that participate in the synthesis of melanin. There is a significant increase in melanin in both the epidermal and dermal layers of affected skin, possibly due to abnormalities in crosstalk between the melanocytes and other cells. Melanogenesis is regulated through various signaling networks including the Wnt/β-catenin, PI3K/Akt, cAMP/PKA, and SCF/c-kit-mediated signaling pathways. In addition, inflammatory mediators, oxidative stress, neuroactive molecules, sebocytes, etc, have also been proved to be related to the pathogenesis of melasma. This review provides a comprehensive update on the current understanding of the pathogenesis of melasma.

摘要

黄褐斑是一种常见的获得性色素沉着紊乱疾病,对生活质量有负面影响。目前的治疗方法疗效不佳且频繁复发。这在很大程度上是由于目前对该疾病病因的了解有限。阐明黄褐斑的发病机制以进一步发现新的治疗策略迫在眉睫。最近的研究表明,黄褐斑由多种因素引发或加重,包括遗传易感性、紫外线辐射和性激素失调。紫外线B辐射上调几种黑素细胞特异性基因的表达,并刺激参与黑色素合成的关键因子的释放。受影响皮肤的表皮和真皮层中的黑色素显著增加,这可能是由于黑素细胞与其他细胞之间的相互作用异常所致。黑色素生成通过各种信号网络进行调节,包括Wnt/β-连环蛋白、PI3K/Akt、cAMP/PKA和SCF/c-kit介导的信号通路。此外,炎症介质、氧化应激、神经活性分子、皮脂腺细胞等也已被证明与黄褐斑的发病机制有关。本综述全面更新了目前对黄褐斑发病机制的认识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d4f/9936885/f6c88cdd2de2/CCID-16-429-g0001.jpg

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