Grupo Boticário, Research & Development, São José dos Pinhais, Brazil.
Laboratório de Espectroscopia Vibracional Biomédica, Universidade do Vale do Paraíba, São José dos Campos, Brazil.
J Cosmet Dermatol. 2020 Jan;19(1):190-198. doi: 10.1111/jocd.12974. Epub 2019 May 27.
BACKGROUND: Striae distensae, commonly known as stretch marks, are cutaneous lesions that accompany the hormonal upheavals of the major stages of life: puberty and pregnancy. Stretch marks occur in 90% of women, and they appear as red or purple lines that slowly fade to pale lines on the skin. There have been few studies regarding stretch mark origins, and new preventive and corrective treatments are needed. AIMS: The aim of this work was to understand the primary genes and proteins involved in the regulation of striae compared to normal skin and to identify the differentially expressed genes and biochemical aspects of SA and SR Importantly, this is the first published study to use a molecular high-throughput approach combined with in vivo evaluation. METHODS: In this study, we analyzed the molecular differences between skin with and without stretch marks (rubra [SR] and alba [SA]) of female volunteers using DNA microarray (Whole Human Genome Microarray Kit, 4×44 K, Agilent Technologies) analyses of cutaneous biopsies (2 mm) and in vivo confocal Raman spectroscopy of selected buttock regions, a technique recently introduced as a noninvasive skin evaluation method. RESULTS: We identified gene expression alterations related to ECM, cellular homeostasis, and hormones such as secretoglobulins. Spectral analyses of collagen, fibrillin, and glycosaminoglycans were conducted by Raman spectroscopy at different skin depths. The main differences observed when comparing skin with and without stretch marks were at depths between 75 and 95 μm, corresponding to the dermal-epidermal junction and dermis regions and showing differences between normal skin and stretched skin regarding collagen, collagen hydration, and elastin fibers. CONCLUSION: The results obtained by RNA and protein analyses are complementary and show that significant changes occur in the skin affected by stretch marks. These results suggest new strategies and opportunities to treat this skin disorder and for the development of new and eficiente cosmetic products.
背景:妊娠纹,通常称为伸展纹,是伴随生命重大阶段激素变化而出现的皮肤损伤:青春期和怀孕期。90%的女性都会出现妊娠纹,它们最初表现为红色或紫色的线条,然后慢慢褪色为皮肤上的白色线条。关于妊娠纹的起源,研究甚少,需要新的预防和治疗方法。
目的:本研究旨在了解与正常皮肤相比,妊娠纹调节中涉及的主要基因和蛋白质,并确定 SA 和 SR 中的差异表达基因和生化方面。重要的是,这是首次使用分子高通量方法结合体内评估发表的研究。
方法:在这项研究中,我们使用 DNA 微阵列(Whole Human Genome Microarray Kit,4×44 K,Agilent Technologies)分析了女性志愿者有和无妊娠纹(rubra [SR] 和 alba [SA])皮肤之间的分子差异,对 2mm 皮肤活检进行分析,并对选定的臀部区域进行体内共焦拉曼光谱分析,这是一种最近引入的非侵入性皮肤评估方法。
结果:我们确定了与细胞外基质、细胞内稳态和激素(如分泌球蛋白)相关的基因表达改变。通过拉曼光谱对胶原蛋白、原纤维蛋白和糖胺聚糖进行光谱分析,在不同的皮肤深度进行。在比较有和无妊娠纹的皮肤时,观察到的主要差异出现在 75 到 95μm 的皮肤深度之间,对应于表皮-真皮交界处和真皮区域,显示出正常皮肤和伸展皮肤之间在胶原蛋白、胶原蛋白水合作用和弹性纤维方面的差异。
结论:RNA 和蛋白质分析的结果是互补的,表明伸展纹影响的皮肤发生了显著变化。这些结果为治疗这种皮肤疾病和开发新的有效美容产品提供了新的策略和机会。
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