Natural multi-target inhibitors from Adhatoda vasica and Calotropis procera for dermal regeneration

IF 1.7 3区 生物学 Q2 MULTIDISCIPLINARY SCIENCES
Waseem Ahmed, Rafia Azmat, Abdul Qayyum, Hadi Abbas, Mohamed Fawzy Ramadan
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引用次数: 0

Abstract

Natural plant-derived compounds are increasingly explored as alternatives for managing skin disorders associated with oxidative stress, enzymatic degradation, and fibroblast dysfunction. In this study, bioactive constituents from Adhatoda vasica and Calotropis procera were isolated and characterized using UF-HPLC-DAD and Fourier-transform infrared (FTIR) spectroscopy. Identified compounds included viscic acid, pasakbumin C, 8′Z-enyl congeners, 5-(8′Z,11′Z-heptadecadienyl)-1,3-benzenediol, 9′-(o-methyl) protocetraric acid, and calophynic acid. The biological activities of leaf and seed extracts were evaluated through in vitro enzymatic assays targeting tyrosinase (monophenolase and diphenolase), collagenase, elastase, and hyaluronidase. A. vasica leaf extracts exhibited notable tyrosinase inhibition, with IC₅₀ values of 22.16 µg/mL for monophenolase and 15.5 µg/mL for diphenolase, while C. procera also demonstrated significant inhibitory activity. Both extracts showed appreciable anti-collagenase, anti-elastase, anti-hyaluronidase, and antioxidant activities, suggesting protective potential against extracellular matrix degradation and oxidative damage. Cytotoxicity assessment using LDH release assays confirmed concentration-dependent effects, and ultrastructural analyses using scanning and transmission electron microscopy revealed extract-induced morphological changes in dermal fibroblasts, including alterations in cell wall integrity, cytoplasmic organization, and intercellular structure. The results suggest that A. vasica and C. procera are promising sources of bioactive compounds with potential applications in dermatological formulations, including topical preparations to manage skin disorders and prevent enzymatic skin degradation.

Graphical Abstract

用于皮肤再生的天然多靶点抑制剂。
天然植物源性化合物被越来越多地用于治疗与氧化应激、酶降解和成纤维细胞功能障碍相关的皮肤疾病。本研究采用uv - hplc - dad和傅里叶变换红外(FTIR)光谱技术,对水仙花(Adhatoda vasica)和原花椒(Calotropis procera)的活性成分进行了分离和表征。鉴定的化合物包括粘酸、pasakumin C、8'Z-烯基同系物、5-(8'Z,11' z -庚二烯基)-1,3-苯二醇、9'-(o-甲基)原癸酸和钙绿酸。通过体外酪氨酸酶(单酚酶和二酚酶)、胶原酶、弹性酶和透明质酸酶的酶活性评价叶片和种子提取物的生物活性。瓦西卡叶提取物对酪氨酸酶有明显的抑制作用,单酚酶的IC₅0值为22.16µg/mL,二酚酶的IC₅0值为15.5µg/mL,而C. procera也表现出显著的抑制活性。两种提取物均具有明显的抗胶原酶、抗弹性酶、抗透明质酸酶和抗氧化活性,提示对细胞外基质降解和氧化损伤具有保护作用。使用LDH释放试验进行的细胞毒性评估证实了浓度依赖性效应,使用扫描和透射电镜进行的超微结构分析显示,提取物诱导的真皮成纤维细胞形态学改变,包括细胞壁完整性、细胞质组织和细胞间结构的改变。结果表明,白曲霉和黑曲霉是有前景的生物活性化合物来源,在皮肤病制剂中具有潜在的应用前景,包括治疗皮肤疾病和防止酶促皮肤降解的外用制剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
The Science of Nature
The Science of Nature 综合性期刊-综合性期刊
CiteScore
3.40
自引率
0.00%
发文量
47
审稿时长
4-8 weeks
期刊介绍: The Science of Nature - Naturwissenschaften - is Springer''s flagship multidisciplinary science journal. The journal is dedicated to the fast publication and global dissemination of high-quality research and invites papers, which are of interest to the broader community in the biological sciences. Contributions from the chemical, geological, and physical sciences are welcome if contributing to questions of general biological significance. Particularly welcomed are contributions that bridge between traditionally isolated areas and attempt to increase the conceptual understanding of systems and processes that demand an interdisciplinary approach.
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