Evidence map›Paper›PMID 39995132›Full record

ArticleCurrent medicinal chemistry2026

Therapeutic Effect of Rosolic Acid against Endothelial Dysfunction in Diabetic Wistar Rats.

Karan Naresh Amin, Kunka Mohanram Ramkumar

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Article in Current medicinal chemistry, 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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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

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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

2 authors.

Karan Naresh AminDepartment of Biotechnology, School of Bioengineering, SRM Institute of Science and Technology, Kattankulathur, 603203, Chennai, Tamilnadu, India.
Kunka Mohanram RamkumarDepartment of Biotechnology, School of Bioengineering, SRM Institute of Science and Technology, Kattankulathur, 603203, Chennai, Tamilnadu, India.

Funding

Science and Engineering Research Board (SERB), Government of India EMR/2016/006196
6 · The paper itself

Abstract

introductionEndothelial dysfunction (ED) results from impaired vascular endothelial cell function, disrupting key processes such as hemostasis, vascular tone regulation, vasculogenesis, angiogenesis, and inflammation. These processes are mediated by a complex signaling network involving hormones, cytokines, and chemokines. ED is recognized as a major contributor to the onset and progression of several micro- and macrovascular diseases, including diabetes. Our previous study demonstrated that the polyphenol Rosolic acid (RA) protects against endoplasmic reticulum (ER) stress-induced ED

methodsIn this study, we investigated RA's protective effects against diabetes-induced ED using high-fat diet (HFD)-fed and streptozotocin-induced type-2 diabetic rat models. We evaluated RA's impact on vascular function and metabolic parameters in these models.

resultsRA significantly mitigated diabetes-induced ED in the aortic tissues of HFDfed diabetic Wistar rats. RA treatment improved glucose tolerance and reduced hyperlipidemia, showing efficacy comparable to the anti-diabetic drug Gliclazide. Moreover, RA elevated Nrf2 levels and its downstream target genes in aortic tissues while reducing ED markers such as Intercellular Adhesion Molecule 1 (ICAM1), vascular cell adhesion molecule 1 (VCAM1), and endothelin-1.

conclusionThese findings highlight RA as a promising therapeutic agent for diabetes and its associated vascular complications, with potential for broader clinical applications.

Indexed as

Diabetes Mellitus, ExperimentalEndothelium, VascularHypoglycemic AgentsSalicylatesAnimalsDiet, High-FatMaleNF-E2-Related Factor 2RatsRats, WistarStreptozocinHypoglycemic AgentsNF-E2-Related Factor 2SalicylatesStreptozocindiabetesEndothelial dysfunctionNrf2rosolic acidsmall moleculesvascular complications.

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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.