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Modeling Colitis-Associated Cancer with Azoxymethane AOM and Dextran Sulfate Sodium DSS
Published on: September 11, 2012
Apis meliffera intermissa venom attenuated colitis-associated cancer progression in azoxymethane treated mice
Dahdouh Faouzi1,2, Djeffal Hanane Chainez1, Bourouba Amira1
1Department of Biology, Laboratory of Cell Toxicology, Faculty of Sciences, Badji-Mokhtar, Annaba University, Annaba, BP 23000, Algeria.
Abstract:
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.
Insights
Algerian bee venom shows promise in treating colitis-associated colorectal cancer (CAC). This study found bee venom mitigated inflammation and pathological changes in mice, suggesting its potential as an adjunct therapy for CAC.
Area of Science:
- Immunology and Cancer Research
- Pharmacology and Toxicology
- Gastroenterology
Background:
- Colitis-associated colorectal cancer (CAC) arises from chronic colon inflammation, posing therapeutic challenges.
- Apis mellifera intermissa venom exhibits anti-inflammatory and anti-tumorigenic properties in preclinical models.
- Investigating novel therapeutic strategies for CAC is crucial due to its significant morbidity and mortality.
Purpose of the Study:
- To evaluate the therapeutic potential of Algerian Apis mellifera intermissa venom against azoxymethane (AOM)-induced CAC in mice.
- To assess the impact of bee venom on hematological parameters, systemic inflammation, and colon histopathology in a CAC model.
Main Methods:
- Male mice were divided into four groups: control, AOM-induced CAC, bee venom treatment, and combined AOM + bee venom treatment.
- Colitis-associated colorectal cancer was induced using azoxymethane (AOM) and a high-fat diet.
- Bee venom was administered intraperitoneally daily for two weeks, with subsequent analysis of body weight, food/water intake, hematology, serum C-reactive protein (CRP), and colon histopathology.
Main Results:
- AOM induction led to reduced body weight, food/water intake, altered hematological profiles (decreased RBC, HGB, HCT; increased WBC, MCV, MCH), elevated CRP, and severe colon pathology.
- Co-treatment with bee venom significantly ameliorated these effects, restoring normal hematological values, reducing CRP levels, and improving colon morphology and epithelial integrity.
- Bee venom treatment alone did not show adverse effects and maintained normal physiological parameters.
Conclusions:
- Apis mellifera intermissa venom demonstrates significant therapeutic potential in mitigating the progression of colitis-associated colorectal cancer in a mouse model.
- The venom's anti-inflammatory and protective effects on colon tissue suggest it could be a valuable adjunct therapy for CAC.
- Further research is warranted to elucidate the specific mechanisms of action and explore clinical applications of bee venom in CAC management.
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