# Crude Extract and Phenol-Rich Fractions from Vernonia amygdalina Leaves Ameliorates Streptozotocin-Induced Type 1 Diabetes in Rats by Mitigating Hepatic Injury, Dyslipidemia, and Production of Oxido-Inflammatory Markers

**Authors:** Olawale Razaq Ajuwon, Damilola Rebecca Oladejo, Akinwunmi Oluwaseun Adeoye, John Adeolu Falode, Basiru Olaitan Ajiboye, Foluso Oluwagbemiga Osunsanmi, Babatunji Emmanuel Oyinloye

PMC · DOI: 10.3390/jox16020053 · 2026-03-20

## TL;DR

This study shows that extracts from Vernonia amygdalina leaves can help reduce diabetes-related liver damage and inflammation in rats.

## Contribution

The study demonstrates the therapeutic potential of Vernonia amygdalina leaf extracts in mitigating type 1 diabetes complications.

## Key findings

- Vernonia amygdalina leaf extracts reduced hyperglycaemia and hepatic injury in diabetic rats.
- Crude extract showed better antidiabetic effects than metformin and other fractions.
- Phytochemicals in the extracts improved antioxidant and anti-inflammatory responses.

## Abstract

Diabetes mellitus (DM) is a major disorder contributing to human mortality and morbidity globally. The use of medicinal plants in the management of diabetes is gaining global popularity due to their accessibility and cost-effectiveness. In this study, we evaluated the ameliorative potential of Vernonia amygdalina leaves crude extract (CE), free phenol (FP), and bound phenol (BP) fractions (50 mg/kg body weight) in a rat model of streptozotocin (STZ)-induced type 1 diabetes (T1DM). The effects of these treatments for 28 days on glucose, insulin, glycated hemoglobin, hepatic injury indices, and lipid profile were assessed in the serum. Furthermore, redox biomarkers (liver) and inflammatory mediators (serum and liver) were analyzed. Our results indicated that CE, FP, and BP fractions of Vernonia amygdalina inhibited the deleterious effects of T1DM by attenuating hyperglycaemia, insulin deficiency, hepatic injury, and dyslipidemia. Also, CE, FP, and BP fractions differentially improved antioxidant enzymes activity and reduced oxidative and inflammatory markers production. Specifically, CE showed superior effects compared with FP, BP, and metformin across multiple biomarkers, including glycated hemoglobin, α-amylase, α-glucosidase, hepatic glycogen, total cholesterol, LDL-cholesterol, protein carbonyl, SOD, IL-1β, and IL-10. The antidiabetic effects produced by CE, FP, and BP fractions of Vernonia amygdalina may be ascribed to the presence of different bioactive phytochemicals as revealed by HPLC analysis. Overall, our data would suggest a potential therapeutic role for Vernonia amygdalina leaves extracts in addressing hepatic complications due to T1DM.

## Linked entities

- **Chemicals:** streptozotocin (PubChem CID 29327), metformin (PubChem CID 4091), alpha-amylase (PubChem CID 17396988), IL-10 (PubChem CID 146070)
- **Diseases:** type 1 diabetes (MONDO:0005147), diabetes mellitus (MONDO:0005015)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Genes:** Crp (C-reactive protein) [NCBI Gene 25419] {aka Aa1249, Ab1-341, Ab2-196, Ac1-114, Ac1262, Ac2-069}, Ggt1 (gamma-glutamyltransferase 1) [NCBI Gene 116568] {aka GGLUT, Ggt, Ggtp}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, Met (MET proto-oncogene, receptor tyrosine kinase) [NCBI Gene 24553] {aka Hgfr}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, Lpl (lipoprotein lipase) [NCBI Gene 24539], Cat (catalase) [NCBI Gene 24248] {aka CS1, Cas1, Cat01, Catl, Cs-1}, SI (sucrase-isomaltase) [NCBI Gene 6476], Got2 (glutamic-oxaloacetic transaminase 2) [NCBI Gene 25721] {aka ASPATA, mAAT}, Tnf (tumor necrosis factor) [NCBI Gene 24835] {aka RATTNF, TNF-alpha, Tnfa}, SOD1 (superoxide dismutase 1) [NCBI Gene 6647] {aka ALS, ALS1, HEL-S-44, IPOA, SOD, STAHP}, Lipg (lipase G, endothelial type) [NCBI Gene 291437] {aka lipase}, Pdlim3 (PDZ and LIM domain 3) [NCBI Gene 114108] {aka Actn2lp, Alp}, Lipc (lipase C, hepatic type) [NCBI Gene 24538], IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, Il10 (interleukin 10) [NCBI Gene 25325] {aka IL10X, If2a}, Il1b (interleukin 1 beta) [NCBI Gene 24494] {aka IL-1F2}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}
- **Diseases:** necrotic (MESH:D009336), degeneration of liver cells (MESH:D006528), Hypercholesterolemia (MESH:D006937), metabolic syndromes (MESH:D024821), Liver Dysfunction (MESH:D017093), lipid dysfunction (MESH:D052439), CVD (MESH:D002318), glucose intolerance (MESH:D018149), toxicity (MESH:D064420), hepatic complications (MESH:D008107), congestive heart failure (MESH:D006333), lipid (MESH:D011017), Hyperglycemia (MESH:D006943), hypertension (MESH:D006973), Type 1 Diabetes (MESH:D003922), or resistance (MESH:D060467), Hepatic Inflammation (MESH:D007249), Diabetes (MESH:D003920), Atherogenic (MESH:D050197), vacuolar (MESH:C536522), hyperglycemic (MESH:D006944), injury to (MESH:D014947), Hepatic Injury (MESH:D056486), metabolic disorders (MESH:D008659), Insulin Resistance (MESH:D007333), autoimmune (MESH:D001327), stroke (MESH:D020521), Dyslipidemia (MESH:D050171), hepatopathy (MESH:D020754), Hyperlipidemia (MESH:D006949), I (MESH:D006969), coronary heart disease (MESH:D003327), death (MESH:D003643), obesity (MESH:D009765), hypertriglyceridemia (MESH:D015228), type 1 and type 2 DM (MESH:D003924), Oxido (MESH:D020167), hyperinsulinemia (MESH:D006946), tissue-wasting disorder (MESH:D019282)
- **Chemicals:** polyphenol (MESH:D059808), myrtenol (MESH:C534317), NO (MESH:D009614), metformin (MESH:D008687), haematoxylin (MESH:D006416), Carbohydrate (MESH:D002241), vernodalol (MESH:C000602211), potassium hydroxide (MESH:C029943), 8-hydroxy-2-deoxyguanosine (MESH:D000080242), TC (MESH:D013667), alcohol (MESH:D000438), eosin (MESH:D004801), tannins (MESH:D013634), S (MESH:D013455), benzophenone (MESH:C047723), sesquiterpenes (MESH:D012717), alkaloids (MESH:D000470), flavonoids (MESH:D005419), HCl (MESH:D006851), sodium sulfate (MESH:C012036), Lipid (MESH:D008055), Glucose (MESH:D005947), sulfuric acid (MESH:C033158), NaOH (MESH:D012972), formic acid (MESH:C030544), vernodalin (MESH:C465365), TG (MESH:D014280), anthrone (MESH:C004522), water (MESH:D014867), potassium phosphate (MESH:C013216), paraffin (MESH:D010232), BP (-), ROS (MESH:D017382), cholesterol (MESH:D002784), phenolic acids (MESH:C017616), 5,5'-dithiobis-2-nitrobenzoic acid (MESH:D004228), acetonitrile (MESH:C032159), Formaldehyde (MESH:D005557), STZ (MESH:D013311), saponins (MESH:D012503), nitric acid (MESH:D017942), stilbenes (MESH:D013267), citrate (MESH:D019343), nitrotyrosine (MESH:C002744), hepatic glycogen (MESH:D008112), ethyl acetate (MESH:C007650), phospholipids (MESH:D010743), blood glucose (MESH:D001786), GSH (MESH:D005978), glycogen (MESH:D006003), Phenol (MESH:D019800), Luteolin (MESH:D047311), acetone (MESH:D000096), sodium pentobarbital (MESH:D010424), methanol (MESH:D000432), fatty acid (MESH:D005227), lignans (MESH:D017705), H2O2 (MESH:D006861), H&amp;E (MESH:D006371), phenols (MESH:D010636)
- **Species:** Homo sapiens (human, species) [taxon 9606], Gymnanthemum amygdalinum (species) [taxon 82755], Mus musculus (house mouse, species) [taxon 10090], Rodentia (rodent, order) [taxon 9989], Rattus norvegicus (brown rat, species) [taxon 10116]
- **Mutations:** M30A
- **Cell lines:** -EL — Anguilla anguilla (European freshwater eel), Spontaneously immortalized cell line (CVCL_YP04)

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13010673/full.md

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Source: https://tomesphere.com/paper/PMC13010673