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通过综合策略用于脱发治疗的载白藜芦醇多功能纳米囊泡

Resveratrol-Loaded Versatile Nanovesicle for Alopecia Therapy via Comprehensive Strategies.

作者信息

Zhang Xuefei, Hao Jiabao, Lu Tianli, Dong Yating, Sun Yingying, Yu Yingjun, Li Shuxuan, Yu Shihui, Hu Haiyan

机构信息

School of Pharmaceutical Sciences, Sun Yat-Sen University, Guangzhou, Guangdong Province, People's Republic of China.

School of Traditional Dai-Thai Medicine, West Yunnan University of Applied Sciences, Jinghong, Yunnan Province, People's Republic of China.

出版信息

Int J Nanomedicine. 2024 Dec 24;19:13875-13900. doi: 10.2147/IJN.S477820. eCollection 2024.

DOI:10.2147/IJN.S477820
PMID:39735326
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11681813/
Abstract

INTRODUCTION

Alopecia is a systemic disease with multiple contributing factors. Effective treatment is challenging when only hair growth mechanisms are targeted while ignoring the role of maintaining hair follicle microenvironment homeostasis, which is crucial for cell growth and angiogenesis. Oxidative stress and inflammation are major disruptors of this microenvironment, leading to inhibited cell proliferation and compromised hair follicle circulation. Drugs with antioxidant and anti-inflammatory effects could potentially restore microenvironment homeostasis, offering a promising strategy for alopecia treatment.

METHODS

Resveratrol (RES), a potent antioxidant and anti-inflammatory agent, was selected as the model drug and encapsulated into an active carrier-PPD-Lip to create PPD-Lip@RES. The efficacy of PPD-Lip@RES was comprehensively evaluated in both in vitro and in vivo aspects, and its underlying mechanism was also primarily explored.

RESULTS

PPD-Lip@RES promoted the proliferation and migration of dermal papilla cells, up-regulated the expression of positive hair growth regulators, and facilitated angiogenesis. It also activated hair follicle stem cells by increasing the expression of Ki67, K5, β-catenin, CD31, and CK19. In the telogen effluvium model, PPD-Lip@RES resulted in more robust hair regeneration, with less hair shedding compared to the minoxidil group. Furthermore, it showed significant therapeutic effects in severe androgenetic alopecia, outperforming finasteride and even the healthy control group.

CONCLUSION

The results suggested that PPD-Lip@RES, as a systemic intervention strategy, could effectively facilitate hair growth by targeting both the pathological and physiological processes involved in hair loss. Its superior performance in both telogen effluvium and androgenetic alopecia models indicates its potential as an advanced treatment option for alopecia.

摘要

引言

脱发是一种由多种因素导致的全身性疾病。仅针对头发生长机制进行治疗而忽视维持毛囊微环境稳态的作用,这对细胞生长和血管生成至关重要,因此有效治疗具有挑战性。氧化应激和炎症是这种微环境的主要破坏因素,导致细胞增殖受抑制和毛囊血液循环受损。具有抗氧化和抗炎作用的药物可能恢复微环境稳态,为脱发治疗提供了一种有前景的策略。

方法

白藜芦醇(RES)是一种有效的抗氧化和抗炎剂,被选为模型药物并封装到活性载体PPD-Lip中制成PPD-Lip@RES。对PPD-Lip@RES的疗效进行了体外和体内的综合评估,并初步探索了其潜在机制。

结果

PPD-Lip@RES促进了真皮乳头细胞的增殖和迁移,上调了头发生长正向调节因子的表达,并促进了血管生成。它还通过增加Ki67、K5、β-连环蛋白、CD31和CK19的表达来激活毛囊干细胞。在休止期脱发模型中,与米诺地尔组相比,PPD-Lip@RES导致更强劲的头发生长,脱发更少。此外,它在重度雄激素性脱发中显示出显著的治疗效果,优于非那雄胺,甚至优于健康对照组。

结论

结果表明,PPD-Lip@RES作为一种全身性干预策略,通过针对脱发所涉及的病理和生理过程,可有效促进头发生长。其在休止期脱发和雄激素性脱发模型中的卓越表现表明其作为脱发先进治疗选择的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ac/11681813/1ef7eded15de/IJN-19-13875-g0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ac/11681813/d09808e9adcc/IJN-19-13875-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ac/11681813/b4c32f908f99/IJN-19-13875-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ac/11681813/197fdbf35e31/IJN-19-13875-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ac/11681813/b8c753a092d7/IJN-19-13875-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ac/11681813/0b386ea2ed89/IJN-19-13875-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ac/11681813/062d230211d4/IJN-19-13875-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ac/11681813/c1967b7f2472/IJN-19-13875-g0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ac/11681813/1ef7eded15de/IJN-19-13875-g0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ac/11681813/d09808e9adcc/IJN-19-13875-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ac/11681813/b4c32f908f99/IJN-19-13875-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ac/11681813/197fdbf35e31/IJN-19-13875-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ac/11681813/b8c753a092d7/IJN-19-13875-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ac/11681813/0b386ea2ed89/IJN-19-13875-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ac/11681813/062d230211d4/IJN-19-13875-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ac/11681813/c1967b7f2472/IJN-19-13875-g0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ac/11681813/1ef7eded15de/IJN-19-13875-g0009.jpg

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