Evidence map›Paper›PMID 42884180›Full record

ReviewInternational journal of molecular sciences2026

Multi-Target Regulation of Diabetic Nephropathy by Alkaloids: Molecular Targets, Signaling Pathways and Therapeutic Potential.

Jiying Wang, Qing Li, Wentao Chen, Lingli Zhou, Rongyu Li, Na Zhou, Shifang Luo, Linao Zhang, Xue Wu, Yuhuan Xie and 1 more

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Jiying WangYunnan Key Laboratory of Dai and Yi Medicine, Yunnan University of Chinese Medicine, Kunming 650500, China.
Qing LiYunnan Key Laboratory of Dai and Yi Medicine, Yunnan University of Chinese Medicine, Kunming 650500, China.
Wentao ChenYunnan Key Laboratory of Dai and Yi Medicine, Yunnan University of Chinese Medicine, Kunming 650500, China.
Lingli ZhouYunnan Key Laboratory of Dai and Yi Medicine, Yunnan University of Chinese Medicine, Kunming 650500, China.
Rongyu LiYunnan Key Laboratory of Dai and Yi Medicine, Yunnan University of Chinese Medicine, Kunming 650500, China.
Na ZhouYunnan Key Laboratory of Dai and Yi Medicine, Yunnan University of Chinese Medicine, Kunming 650500, China.
Shifang LuoYunnan Key Laboratory of Dai and Yi Medicine, Yunnan University of Chinese Medicine, Kunming 650500, China.
Linao ZhangYunnan Key Laboratory of Dai and Yi Medicine, Yunnan University of Chinese Medicine, Kunming 650500, China.
Xue WuYunnan Key Laboratory of Dai and Yi Medicine, Yunnan University of Chinese Medicine, Kunming 650500, China.
Yuhuan XieCollege of Basic Medical Sciences, Yunnan University of Chinese Medicine, Kunming 650500, China.
Peixin GuoYunnan Key Laboratory of Dai and Yi Medicine, Yunnan University of Chinese Medicine, Kunming 650500, China.

Funding

High-level Discipline Construction Project of Dai Medicine, National Administration of Traditional Chinese Medicine zyzdxk-2023192Open Research Fund Program of Yunnan Key Laboratory for Dai and Yi Medicines 2024SS24018
6 · The paper itself

Abstract

In the context of the global diabetes epidemic, diabetic nephropathy (DN)-a condition directly associated with diabetes-has become the primary cause of end-stage renal disease, significantly impacting patients' quality of life and placing substantial demands on public healthcare resources. The pathogenesis of DN is characterized by metabolic disturbances induced by high glucose levels, hemodynamic abnormalities, and the synergistic amplification of various stress signals. These factors collectively contribute to the progressive loss of nephrons and irreversible renal dysfunction. Although current standard treatments can partially slow disease progression, they significantly fail to meet clinical needs. Therefore, there is an urgent necessity to identify multi-target intervention strategies that utilize novel mechanisms of action. Alkaloids, a class of natural nitrogen-containing compounds known for their significant structural diversity, have recently demonstrated multiple renoprotective effects in experimental models of DN. This review is based on a search of the PubMed, Web of Science and CNKI databases. The keywords alkaloids, diabetic nephropathy, diabetic nephropathies, diabetic kidney disease, inflammation, oxidative stress, fibrosis, autophagy and apoptosis were used to search for original research articles in both Chinese and English, published between 2010 and 2026, which investigated the mechanisms by which alkaloid compounds exert their anti-DN effects. Focusing on anti-inflammatory effects, anti-oxidative stress, anti-renal fibrosis, autophagy modulation, apoptosis regulation and ferroptosis inhibition, the review then summarized the relevant literature by systematizing the experimental models, intervention protocols, dosages and key results. This provided a new theoretical perspective and experimental basis for the clinical translation and new drug development of alkaloid compounds for the treatment of DN. The review provides a new theoretical perspective and an experimental basis for the clinical translation of, and new drug development based on, alkaloid compounds for the treatment of DN.

Indexed as

AlkaloidsDiabetic NephropathiesSignal TransductionAnimalsApoptosisAutophagyHumansMolecular Targeted TherapyOxidative StressAlkaloidsalkaloidsdiabetic nephropathymolecular mechanismstherapeutic prospects

Identifiers

PMID42884180
PMCPMC13665509

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.