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Dahdouh, Faouzi, Chainez Djeffal, Hanane, Bourouba, Amira, Bousba, Rania, Bourouba, Amina, Djebar - Berrebbah, Houria. (1404). Apis meliffera intermissa venom attenuated colitis-associated cancer progression in azoxymethane treated mice. سامانه مدیریت نشریات علمی, 80(3), 711-718. doi: 10.32592/ARI.2025.80.3.711
Faouzi Dahdouh; Hanane Chainez Djeffal; Amira Bourouba; Rania Bousba; Amina Bourouba; Houria Djebar - Berrebbah. "Apis meliffera intermissa venom attenuated colitis-associated cancer progression in azoxymethane treated mice". سامانه مدیریت نشریات علمی, 80, 3, 1404, 711-718. doi: 10.32592/ARI.2025.80.3.711
Dahdouh, Faouzi, Chainez Djeffal, Hanane, Bourouba, Amira, Bousba, Rania, Bourouba, Amina, Djebar - Berrebbah, Houria. (1404). 'Apis meliffera intermissa venom attenuated colitis-associated cancer progression in azoxymethane treated mice', سامانه مدیریت نشریات علمی, 80(3), pp. 711-718. doi: 10.32592/ARI.2025.80.3.711
Dahdouh, Faouzi, Chainez Djeffal, Hanane, Bourouba, Amira, Bousba, Rania, Bourouba, Amina, Djebar - Berrebbah, Houria. Apis meliffera intermissa venom attenuated colitis-associated cancer progression in azoxymethane treated mice. سامانه مدیریت نشریات علمی, 1404; 80(3): 711-718. doi: 10.32592/ARI.2025.80.3.711

Apis meliffera intermissa venom attenuated colitis-associated cancer progression in azoxymethane treated mice

Archives of Razi Institute
مقاله 20، دوره 80، شماره 3، مرداد و شهریور 2025، صفحه 711-718    اصل مقاله (615.16 K)
نوع مقاله: Original Articles
شناسه دیجیتال (DOI): 10.32592/ARI.2025.80.3.711
نویسندگان
Faouzi Dahdouh* 1، 2؛ Hanane Chainez Djeffal1؛ Amira Bourouba3؛ Rania Bousba3؛ Amina Bourouba3؛ Houria Djebar - Berrebbah1
1Department of Biology, Faculty of Sciences, Badji-Mokhtar, Annaba University, Annaba, BP 23000, Algeria.
2Department of Natural Sciences, Higher School of Technological Education, Skikda 21000, Algeria.
3Department of Biology, Faculty of Sciences, Badji-Mokhtar, Annaba University, Annaba, BP 23000, Algeria
چکیده
Colitis-associated colorectal cancer (CAC) is a serious condition driven by chronic inflammation in the colon, representing a significant challenge in both preventative and therapeutic contexts. Apis mellifera intermissa venom has shown promising therapeutic potential in various disease models, particularly those involving inflammation and tumorigenesis. This study evaluates the therapeutic effects of venom derived from honeybees native to Algeria on the progression of CAC in azoxymethane (AOM)-treated mice. A total of 28 male mice were randomly allocated into four groups (n=7 per group): a control group received a tap drinking water, an AOM group (10 mg AOM /kg body weight), a bee venom group (0.76 mg/kg body weight), and a combined bee venom + AOM group. CAC was induced in mice by a single intraperitoneal injection (i.p) of AOM, and a high-fat diet (45% fat by diet weight) for two weeks. The potential therapeutic effect was evaluated by administering bee venom intraperitoneally on a daily basis for two weeks. AOM significantly reduced body weight, food and water intake while increasing colon weight. Hematological analysis revealed significant reductions in red blood cells (RBC), hemoglobin (HGB), and hematocrit (HCT), coupled with increased white blood cell counts, mean corpuscular volume (MCV), and mean corpuscular hemoglobin (MCH). Elevated serum C-reactive protein (CRP) levels further confirmed systemic inflammation. Macroscopic examination and histopathological analyses of the colon revealed extensive pathological changes in the AOM group, including severe mucosal inflammation, necrotic epithelial damage, and substantial immune cell infiltration. Noteworthy, co-treatment with bee venom effectively mitigated these pathological alterations. Bee venom significantly restored hematological profiles by improving RBC count, HGB, and HCT levels while reducing the elevated WBC count, MCV, and MCH values. CRP levels were significantly reduced, reflecting the anti-inflammatory effects of the venom. Also, macroscopic evaluations demonstrated the preservation of colon morphology, while histopathological assessments revealed an improved epithelial integrity with fewer signs of necrosis and cellular atypia. These findings suggest that Apis mellifera intermissa venom holds potential as an adjunct therapeutic agent for suppressing CAC progression, warranting further investigation into its underlying mechanisms and clinical applicability.
کلیدواژه‌ها
Colitis-associated cancer؛ Azoxymethane؛ Hematological parameters؛ Apis mellifera intermissa venom؛ mice
مراجع
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