口服联合天然免疫刺激剂抑制7,12- dmba /巴豆油诱导的瑞士白化小鼠两步皮肤癌

Q3 Medicine The gulf journal of oncology Pub Date : 2023-01-01
Mohammed Abdellaoui, Assia Kadi, Yamina Abrazi, Yacine Kadi, Adnane Gary, Hind Kherfi, Zinelaabidine Cheraiet, Mahfoud Messarah
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引用次数: 0

摘要

背景:免疫系统在对抗癌症中起着至关重要的作用,那么对免疫系统的自然刺激是否有可能减缓或阻止癌症的发展呢?我们的体内研究旨在评估五种免疫刺激剂(β -葡聚糖和阿拉伯半乳聚糖作为多糖)和三种蘑菇提取物(灵芝、舞茸和香菇)联合使用对7,12-二甲基苯并[a]蒽(DMBA)/巴豆油诱导的瑞士白化小鼠乳头状瘤的保护作用。方法:我们使用血细胞计数分析来广泛估计免疫反应和生化技术来确定氧化应激下超氧化物歧化酶(SOD),过氧化氢酶(CAT)和谷胱甘肽过氧化物酶(GPx)酶活性的变化,这些酶活性可能具有预防癌症发展的功能。结果:DMBA/巴豆油皮肤应用引起小鼠背部鳞状细胞(乳头状瘤)癌前增生。肿瘤的发生伴随着SOD和GPx活性的降低。免疫刺激剂治疗后,皮肤乳头瘤的发生率完全消失,SOD活性几乎恢复正常,但CAT和GPx活性未恢复正常。免疫细胞(淋巴细胞、单核细胞和白细胞)水平的增加反映了免疫系统活性的明显增强。讨论:对同时接受癌变方案治疗的小鼠的健康表皮观察表明,抑制棘细胞增殖导致增生的完全抑制。此外,这批免疫细胞水平的增加反映了炎症反应。事实上,先前的研究报告称,包括倍他卢坎在内的免疫刺激剂涉及一些炎症介质的释放,这些炎症介质可能是其抗癌活性的起源。癌症的发生显然破坏了抗氧化酶的活性,但这两个过程之间的关系往往是复杂的。参考文献数据表明,在同时接受癌变方案的处理小鼠中观察到的CAT和GPx的低催化活性可能会诱导H2O2的积累,而H2O2通常被描述为癌细胞凋亡的诱导剂。结论:本研究使用的免疫刺激剂可能通过增强免疫系统整体功能和调节抗氧化防御,对皮肤癌变具有有效的保护作用。关键词:免疫刺激剂,β -葡聚糖,阿拉伯半乳聚糖,灵芝,舞茸,香菇,DMBA,巴豆油,氧化应激,致癌作用缩写:C, control group;Dc:药物对照组;Pc,阳性对照组;DMBA, 7,12二甲基苯并[a]蒽;NK,自然杀手;猫,过氧化氢酶;超氧化物歧化酶,GPx,谷胱甘肽过氧化物酶;是,免疫增强药;白细胞;LY,淋巴细胞;密苏里州,单核细胞;ROS,活性氧;美国国家统计局(Office national des aliments de bassia)。
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Oral Intake of Combined Natural Immunostimulants Suppresses the 7,12-DMBA/ Croton Oil Induced Two-step Skin Carcinogenesis in Swiss Albino Mice.

Background: The immune system is critical in fighting cancer, so is it possible that the natural stimulation of this system can slow down or stop the evolution of cancer? Our in vivo study aimed to evaluate the protective effect of the combination of five types of immunostimulants, which are Beta-glucan and Arabinogalactan as polysaccharides and three mushroom extracts (Reishi, Maitake, and Shiitake), on 7,12-Dimethyl Benz[a]anthracene (DMBA)/ Croton oil-induced papilloma in Swiss albino mice.

Methodology: We used blood count analyses to estimate broadly the immunological reaction and biochemical techniques to determine the oxidative stress variations in the enzymatic activity of Superoxide dismutase (SOD), Catalase (CAT), and Glutathion peroxidase (GPx), which could have a preventive function against cancer development.

Results: The cutaneous application of the DMBA/Croton oil caused precancerous hyperplasia in squamous cells (papilloma) on the back of the mice. Tumor development was accompanied by a decrease in SOD and GPx activities. The treatment with the immunostimulants led to the total disappearance of the incidence of skin papillomas and also showed a nearly back to normal SOD activity but not CAT and GPx activities. The increase in the level of immune cells (lymphocytes, monocytes, and white blood cells) reflected a clear enhancement of the immune system activity.

Discussion: The healthy epidermis observed with treated mice simultaneously subjected to the cancerogenosis protocol suggests the inhibition of spinous cell proliferation leading to the total suppression of the hyperplasia. Moreover, the increase in the level of immune cells in this batch reflects an inflammatory reaction. Indeed, previous studies reported that immunostimulants, including Betaglucan involve a release of some inflammatory mediators who would be at the origin of its anticancer activity. Cancerogenesis has clearly disrupted the activities of the antioxidant enzymes, but the relationship between the two process is often complex. Bibliographic data led us to suggest that low catalytic activities of CAT and GPx observed in treated mice simultaneously subjected to the cancerogenesis protocol, would have induce an accumulation of H2O2 which has often been described as an inducer of cancer cells apoptosis.

Conclusion: Immunostimulants used in our study could have an effective protective effect against skin carcinogenesis via the enhancement of the global function of the immune system and modulation of the antioxidant defense.

Keywords: Immunostimulants, Beta-glucan, Arabinogalactan, Reishi, Maitake, Shiitake, DMBA, Croton oil, Oxidative stress, Carcinogenesis.

Abbreviations: C, control group; Dc, drug control group; Pc, positive control group; St, sick treated group;DMBA, 7,12 Dimethyl Benz[a]anthracene; NK, natural killer; CAT, catalase; SOD, superoxide dismutase, GPx, glutathione peroxidase; IS, immunostimulants; WBC, White blood cells; LY, Lymphocytes; MO, Monocytes; ROS, Reactive oxygen species; ONAB, Office national des aliments de bétail.

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来源期刊
The gulf journal of oncology
The gulf journal of oncology Medicine-Medicine (all)
CiteScore
0.90
自引率
0.00%
发文量
37
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