Royal jelly attenuates DMBA induced preneoplastic lesions in rat mammary gland and skin.

Royal jelly attenuates DMBA induced preneoplastic lesions in rat mammary gland and Skin.

Alireza Salehi, Faeze Bani Yaghoobi, S Hosseini, Saeid Hashemi

Sci Rep

Apr 5, 2026

Sources

0:00 / 0:00

Sign in to access this feature

Create a free account or sign in to use AI summaries, listen to articles, download PDFs, and save to your library.

150 views

Abstract

UNLABELLED: 7,12-Dimethylbenz[a]anthracene (DMBA) induces reactive oxygen species (ROS) formation, oxidative stress, and apoptosis in target tissues. Royal jelly (RJ) is rich in flavonoids, phenolic acids, and peptides. This study evaluated whether RJ can mitigate DMBA-induced oxidative, apoptotic, and histopathological changes in the rat mammary gland and skin. Female Wistar rats were divided into four groups, including the Control (no treatment), RJ (300 mg/kg/week, orally), DMBA (single dose 80 mg/kg, IP), and DMBA + RJ (same doses). After 8 weeks, mammary gland and skin specimens were collected. Oxidative stress markers were quantified in tissue homogenates. Apoptotic gene and protein expression were measured by qRT-PCR and Western blot, respectively. Ki67 expression was assessed by immunohistochemistry. Additionally, histopathological evaluation (H&E stain) was conducted. DMBA significantly increased MDA, reduced GPx, SOD, and TAC. Pro-apoptotic markers were upregulated, while Bcl2 was downregulated. Histopathology revealed vacuolar degeneration, necrosis, mitotic figures, and corpora amylacea in the mammary gland, and epidermal hyperplasia, mitotic figures, follicular hyperplasia, and focal necrosis in skin. RJ co-treatment restored GPx and SOD levels to almost those of the control group, reduced MDA, decreased p53 andto near-control levels, and increased Bcl2 to the approximate level of the control group. Moreover, RJ treatment normalized the mammary gland histologically, while skin showed attenuated necrosis and decreased epidermal hyperplasia and mitotic index. RJ effectively countered DMBA-induced oxidative stress and apoptosis in the rat mammary gland while preserving tissue integrity. In skin, RJ mitigated oxidative damage and reduced proliferation. These outcomes suggest RJ’s potential as an adjuvant antioxidant in glandular disorders, while showing the anticarcinogenic potential. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1038/s41598-026-44968-6.