Evidence map›Paper›PMID 42453573›Full record

ArticleFrontiers in pharmacology2026

Multi-target antidiabetic and organ-protective effects of a polyherbal ethanol extract in STZ-induced diabetic rats.

Mohd Adnan Kausar, Kehkashan Parveen, Sadaf Anwar, Yusuf Saleem Khan, Ayman A Saleh, Mai Ali Abdelfattah Ahmed, Ehab Adel Awad Abdel Razek, Suhel Parvez, Waseem Ahmad Siddiqui

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Article in Frontiers in pharmacology, 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

9 authors.

Mohd Adnan KausarDepartment of Biochemistry, College of Medicine, University of Ha'il, Hail, Saudi Arabia.
Kehkashan ParveenDepartment of Medical Elementology and Toxicology, School of chemical and Life Sciences, Jamia Hamdard, New Delhi, India.
Sadaf AnwarDepartment of Biochemistry, College of Medicine, University of Ha'il, Hail, Saudi Arabia.
Yusuf Saleem KhanDepartment of Anatomy, College of Medicine, University of Ha'il, Hail, Saudi Arabia.
Ayman A SalehDepartment of Pathology, College of Medicine, University of Ha'il, Hail, Saudi Arabia.
Mai Ali Abdelfattah AhmedDepartment of Pediatrics, College of Medicine, University of Ha'il, Hail, Saudi Arabia.
Ehab Adel Awad Abdel RazekDepartment of Sports Science and Physical Activity, College of Education, University of Ha'il, Hail, Saudi Arabia.
Suhel ParvezDepartment of Medical Elementology and Toxicology, School of chemical and Life Sciences, Jamia Hamdard, New Delhi, India.
Waseem Ahmad SiddiquiInterdisciplinary Biotechnology Unit, Aligarh Muslim University, Aligarh, Uttar Pradesh, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: In diabetes mellitus conditions, hyperglycemia leads to oxidative stress, inflammation, and β-cell dysfunction, and traditional pharmacotherapy targets only a single pathway, which gives suboptimal outcomes and drug-related problems. A novel, polyherbal ethanol extract (PHE) formulation from Methods: Male Wistar rats were made diabetic using intraperitoneal administration of streptozotocin (55 mg/kg) and randomly segregated into five groups: Normal, STZ-induced diabetic, STZ + PHE (200 mg/kg/day), Normal + PHE, and STZ + metformin (Met; 300 mg/kg/day). After 8 weeks of treatment, FBG, HbA1c, insulin, lipid profile, proinflammatory cytokines (TNF-α, IL-1β), oxidative stress biomarkers, and liver function markers were determined. Histological examination was performed on liver and pancreatic tissues with H&E staining, along with assessment of pancreatic insulin immunoreactivity. GC-MS analysis was conducted to characterize the phytochemical constituents of PHE. Results: PHE treatment significantly reduced FBG by 33%, HbA1c by 15%, and restored serum insulin levels (+34%) versus untreated diabetics (p < 0.05). Dyslipidemia was corrected, with LDL-C reduced by 30% and HDL-C increased by 46%. Hepatic ALT and AST levels were also attenuated after PHE treatment. Oxidative stress was alleviated, and TNF-α and IL-1β levels in the liver and pancreas were markedly suppressed. Histology showed preserved hepatocyte integrity and islet morphology, and immunohistochemistry confirmed improved β-cell integrity and enhanced insulin immunoreactivity. Conclusion: The polyherbal preparation produced impressive control over glycemia, strong antioxidant and anti-inflammatory effects, and protection of liver and pancreatic architecture. These effects translate into its potential as a phytotherapeutic candidate for safely managing diabetes and its complications, warranting further molecular and clinical research.

Indexed as

diabetes mellitushepatic injuryoxidative stresspancreaspolyherbal extract

Identifiers

PMID42453573
PMCPMC13364602

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