A Senomorphlytic Three‐Drug Combination Discovered in Salsola collina for Delaying Aging Phenotypes and Extending Healthspan

Author:

Wang Jiqun1ORCID,Liu Wenwen2ORCID,Huang Yunyuan3ORCID,Wang Guangwei4ORCID,Guo Xiaobo1,Shi Donglei2,Sun Tianyue1,Xiao Chaojiang5,Zhang Chao1,Jiang Bei5ORCID,Guo Yuan4ORCID,Li Jian126ORCID

Affiliation:

1. State Key Laboratory of Bioreactor Engineering Shanghai Frontiers Science Center of Optogenetic Techniques for Cell Metabolism Frontiers Science Center for Materiobiology and Dynamic Chemistry Shanghai Key Laboratory of New Drug Design School of Pharmacy East China University of Science and Technology Shanghai 200237 China

2. Key Laboratory of Tropical Biological Resources of Ministry of Education School of Pharmaceutical Sciences Hainan University Haikou 570228 China

3. Hubei Key Laboratory of Genetic Regulation and Integrative Biology School of Life Sciences Central China Normal University Wuhan Hubei 430079 China

4. School of Chemical Engineering Key Laboratory of Synthetic and Natural Functional Molecule of the Ministry of Education Northwest University Xi'an 710127 China

5. Yunnan Key Laboratory of Screening and Research on Anti‐pathogenic Plant Resources from Western Yunnan, Institute of Materia Medica & College of Pharmacy Dali University Dali Yunnan 671000 China

6. Key Laboratory of Xinjiang Phytomedicine Resource and Utilization Ministry of Education School of Pharmacy Shihezi University Shihezi 832003 China

Abstract

AbstractThe pursuit of pharmacological interventions in aging aims focuses on maximizing safety and efficacy, prompting an exploration of natural products endowed with inherent medicinal properties. Subsequently, this work establishes a unique library of plant extracts sourced from Yunnan Province, China. Screening of this herbal library herein revealed that Salsola collina (JM10001) notably enhances both lifespan and healthspan in C. elegans. Further analysis via network pharmacology indicates that the p53 signaling pathway plays a crucial role in mediating the anti‐aging effects of JM10001. Additionally, this work identifies that a composition, designated as JM10101 and comprising three chemical constituents of JM10001, preserves the original lifespan‐extending activity in C. elegans. Both JM10001 and JM10101 mitigate aging symptoms in senescence‐accelerated mice treated with doxorubicin and in naturally aged mice. Notably, JM10101 exhibits a more sophisticated senomorphlytic role encompassing both senomorphic and senolytic functions than JM10001 in the modulation of senescent cells, offering a promising strategy for the discovery of combination drugs in the rational development of anti‐aging therapies.

Funder

National Natural Science Foundation of China

Innovative Research Team of High-level Local University in Shanghai

State Key Laboratory of Bioreactor Engineering

Publisher

Wiley

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