Ojha Madhavi, Manocha Nilanshu, Kumar Vinod, Karthikeyan Ganeshan, Toor Devinder
Amity Institute of Virology and Immunology, Amity University Uttar Pradesh, Sector-125, Noida 201313, Uttar Pradesh, India.
Magan Centre for Applied Mycology, Faculty of Engineering and Applied Sciences, Cranfield University, Cranfield MK43 0AL, UK.
Pharmaceuticals (Basel). 2025 Feb 22;18(3):304. doi: 10.3390/ph18030304.
Psoriasis, a prevalent dermatological disorder, poses therapeutic challenges due to limited effective treatments or adverse side-effects. Traditional medicinal plants like and , historically used in Ayurvedic and Siddha practices, show potential in treating inflammatory skin diseases. This study aims to explore their in vitro and in vivo anti-psoriatic properties to develop safer and more effective therapies. : Chloroform:methanol fractions from ethanol extracts of and were evaluated for anti-psoriatic activity. In vitro assays using HaCaT cells assessed cell viability, apoptosis, and inflammatory markers. In vivo studies utilized an IMQ-induced psoriasis mouse model, evaluating skin lesions, histopathology, and cytokine profiles. : Chloroform fractions significantly reduced HaCaT cell viability and induced apoptosis. They also dose-dependently downregulated IL-8 and RANTES levels. In vivo, these fractions reduced skin inflammation, edema, and psoriasis scores. Histopathological analysis showed decreased epidermal thickness and dermal inflammation. Key psoriasis biomarkers IL-17 and IL-23 were significantly reduced. : Chloroform:methanol fractions from and demonstrated potent anti-psoriatic effects in vitro and in vivo. These findings support their potential as novel phytotherapeutic agents for managing psoriasis, offering promise for further development and clinical application.
银屑病是一种常见的皮肤病,由于有效治疗方法有限或存在不良副作用,给治疗带来了挑战。传统药用植物如[植物名称1]和[植物名称2],在阿育吠陀和悉达医学实践中历史悠久,在治疗炎症性皮肤病方面显示出潜力。本研究旨在探索它们的体外和体内抗银屑病特性,以开发更安全、更有效的疗法。方法:对[植物名称1]和[植物名称2]乙醇提取物的氯仿:甲醇馏分进行抗银屑病活性评估。使用HaCaT细胞进行的体外试验评估细胞活力、凋亡和炎症标志物。体内研究利用咪喹莫特诱导的银屑病小鼠模型,评估皮肤病变、组织病理学和细胞因子谱。结果:氯仿馏分显著降低HaCaT细胞活力并诱导凋亡。它们还剂量依赖性地下调IL-8和RANTES水平。在体内,这些馏分减轻了皮肤炎症、水肿和银屑病评分。组织病理学分析显示表皮厚度和真皮炎症减少。关键的银屑病生物标志物IL-17和IL-23显著降低。结论:[植物名称1]和[植物名称2]的氯仿:甲醇馏分在体外和体内均显示出强大的抗银屑病作用。这些发现支持它们作为治疗银屑病的新型植物治疗剂的潜力,为进一步开发和临床应用带来了希望。