Evidence map›Paper›PMID 42092960›Full record

ArticleChinese medicine2026

A stabilized enrichment method for rosemary diterpenoids and their therapeutic potential in diabetic kidney disease.

Jiali Wei, Qian Xiao, Hua Yang, Fei Li, Ping Li

Abstract read
In one paragraph

Article in Chinese medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Jiali WeiState Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, 211198, China.
Qian XiaoState Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, 211198, China.
Hua YangState Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, 211198, China.
Fei LiState Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, 211198, China. lifeicpu@163.com.
Ping LiState Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, 211198, China. liping2004@126.com.

Funding

the National Key Research and Development Program of China No. 2023YFC3504404
6 · The paper itself

Abstract

backgroundAs a traditional medicinal herb, rosemary leaves have shown potential for the treatment for diabetic kidney disease (DKD). However, the bioactive compounds responsible for its anti-DKD effects remain unidentified, and the instability of its primary phytochemicals limits its practical application.

methodsThis study investigated the active components of rosemary leaves and characterized their degradation pathways using UPLC-Q/TOF-MS/MS. Four solvent-extracted fractions were evaluated using an in vitro DKD model to identify the major anti-DKD constituents. A targeted enrichment method was then developed to isolate these bioactive compounds. Finally, a DKD model was established in C57BL/6J mice using high-fat diet combined with streptozotocin injection to evaluate the therapeutic effects of the enriched extracts. The pharmacokinetic profiles of the major components of TD were further investigated.

results38 chemical constituents were characterized with diterpenoids were identified as the primary anti-DKD constituents by in vitro DKD model. Considering their pronounced susceptibility to oxidative degradation, a novel enrichment strategy for total diterpenoids (TD) was developed based on water and ethanol. Vitamin C served as a stabilizer to improve TD stability, leading to a TD extraction yield of 40.12% and the diterpenoid content of 81.80%. In vivo studies revealed that TD attenuated renal injury, improved glucose and lipid dysmetabolism, and reduced renal oxidative stress in DKD mice. The in vivo absorption profiles showed that TD also exhibited good bioavailability.

conclusionThis study provides an effective method for TD enrichment and demonstrates the renoprotective effects of TD. These findings offer new insights on the broader use of rosemary leaves and the development of natural product-based therapies for DKD.

Indexed as

Anti-diabetic kidney disease effectChemical profilingDiterpenoidsEnrichmentRosmarinus officinalis L.

Identifiers

PMID42092960
PMCPMC13147855

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