Evidence map›Paper›PMID 42613896›Full record

ArticleMolecular nutrition & food research2026

Bee Bread Protects Small Intestinal Mucosa and Modulates Local Redox Responses in Streptozotocin-Induced Diabetic Rats.

Ebru Karadag Sari, Buket Bakιr, Sükran Yediel Aras, Sevda Elis Yιldιz, Arzu Gezer

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Article in Molecular nutrition & food research, 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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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

5 authors.

Ebru Karadag SariFaculty of Veterinary Medicine, Department of Histology and Embryology, Kafkas University, Kars, Türkiye.
Buket BakιrFaculty of Veterinary Medicine, Department of Histology and Embryology, Tekirdağ Namık Kemal University, Tekirdağ, Türkiye.
Sükran Yediel ArasFaculty of Health Sciences, Department of Midwifery, Kafkas University, Kars, Türkiye.
Sevda Elis YιldιzFaculty of Health Sciences, Department of Midwifery, Kafkas University, Kars, Türkiye.
Arzu GezerVocational School of Health Services, Atatürk University, Erzurum, Türkiye.

Funding

Department of Pathology, Faculty of Veterinary Medicine, Cumhuriyet UniversityScientific Research Projects Commission of Kafkas University 2021-TS-33
6 · The paper itself

Abstract

Bee Bread (BB), a fermented bee product rich in antioxidant compounds, exerts protective effects against diabetes-associated small intestinal damage. This study investigated the effects of BB on small intestinal morphology, mucosal integrity, and antioxidant enzyme activity in streptozotocin (STZ)-induced diabetic rats. Forty Wistar albino rats were randomly divided into five groups: control, sham (50 mg/kg sodium citrate), diabetes (DM; 50 mg/kg STZ), BB (100 mg/kg), and Diabetes + Bee Bread (DM+BB). After 15 days, intestinal tissues were examined using histopathological, immunohistochemical (IHC), and scanning electron microscopy (SEM) analyses. Diabetic rats exhibited hyperglycemia (363.63 ± 14.64 mg/dL vs. 97.25 ± 2.71 mg/dL in controls at day 15; p < 0.001), weight loss, villus elongation, epithelial desquamation, and mucosal disorganization. BB supplementation reduced blood glucose levels (approximately 15%-16% in the DM+BB group), attenuated weight loss, and preserved small intestinal architecture, with significant differences in villus length among groups (p < 0.05). Mn-SOD immunoreactivity showed no significant differences among groups (p > 0.05), although redistribution was observed in diabetic tissues. CAT immunoreactivity remained weak and unchanged across groups. SEM analysis confirmed improved villus architecture and preserved goblet cell morphology following BB treatment. BB attenuated diabetes-induced small intestinal injury and preserved intestinal mucosal architecture, findings that may be associated with localized adaptive redox responses.

Indexed as

Diabetes Mellitus, ExperimentalHoneyIntestinal MucosaIntestine, SmallAnimalsAntioxidantsBlood GlucoseCatalaseMaleOxidation-ReductionRatsRats, WistarStreptozocinSuperoxide DismutaseAntioxidantsBlood GlucoseCatalaseStreptozocinSuperoxide DismutaseapitherapyBee BreaddiabetesintestineMn‐SOD

Identifiers

PMID42613896
PMCPMC13487359

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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.