Estimating Anticancer Effects of Yohimbine in DMBA-Induced Oral Carcinogenesis Hamster Model: Utilizing Biochemical and Immunohistochemical Techniques

IF 2.8 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Cell Biochemistry and Function Pub Date : 2024-10-16 DOI:10.1002/cbf.4132
Nasimudeen R. Jabir, Shams Tabrez, Nojood Altwaijry, Mohd Shahnawaz Khan, Arun Kumar Ramu, Bakrudeen Ali Ahmed
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Abstract

Yohimbine is a potent bioactive indole alkaloid, isolated from a variety of biological sources and has long been used as a natural stimulant and aphrodisiac, particularly to treat erectile dysfunction. However, some literature also points toward its anticancer effect in different experimental models. The current study aimed to address a clinical concern on the therapeutic utilization of yohimbine as a repurposed drug. We employed 7,12-dimethylbenz[a]anthracene (DMBA)-induced hamster buccal pouch carcinogenesis model juxtaposed with biochemical investigation of several detoxification and antioxidant markers, such as Cyt p450, Cyt b5, thiobarbituric acid reactive substance (TBARS), glutathione (GSH), glutathione reductase (GR), glutathione S transferase (GST), DT-diaphorase, vitamin C, vitamin E, superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GPx). The immunohistochemical assessment of cyclooxygenase-2 (COX-2), interleukin-6 (IL-6), proliferating cell nuclear antigen (PCNA), and cyclin D1 expression were also performed to observe the effect of yohimbine on these markers. The hamsters treated with DMBA presented the growth of tumors in the buccal pouches, accompanied by significant changes in the liver and buccal mucosa levels of Phase I & II detoxification enzymes and lipid peroxidation (LPO). A significant rise in the range of 2- to 3.5-fold was observed in Cyt p450, Cyt b5, and LPO in DMBA-treated animals. However, oral administration of yohimbine significantly restored the LPO, antioxidant, and detoxifying enzyme activities. Additionally, the levels of COX-2, IL-6, PCNA, and cyclin D1 were also found to be downregulated by yohimbine treatment. In conclusion, yohimbine improved the biochemical and immunohistochemical markers of DMBA-induced oral cancer and reverted to near normal values via ameliorating the underlying inflammation and oxidative stress conditions. Our study highlighted the potential of yohimbine as anticancer agent, especially against oral cancer and suggested its possible use as repurposed drug.

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估计育亨宾在 DMBA 诱导的仓鼠口腔癌模型中的抗癌作用:利用生化和免疫组化技术
育亨宾是从多种生物资源中分离出来的一种强效生物活性吲哚生物碱,长期以来一直被用作天然兴奋剂和壮阳药,尤其是用于治疗勃起功能障碍。然而,一些文献也指出它在不同的实验模型中具有抗癌作用。本研究旨在解决临床上对育亨宾作为再利用药物的治疗用途的关注。我们采用了 7,12-二甲基苯并[a]蒽(DMBA)诱导的仓鼠颊囊癌变模型,并对几种解毒和抗氧化标志物(如 Cyt p450、Cyt b5、硫代巴比妥酸还原酶)进行了生化研究、硫代巴比妥酸活性物质 (TBARS)、谷胱甘肽 (GSH)、谷胱甘肽还原酶 (GR)、谷胱甘肽 S 转移酶 (GST)、DT-二磷酸酶、维生素 C、维生素 E、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)。此外,还对环氧化酶-2(COX-2)、白细胞介素-6(IL-6)、增殖细胞核抗原(PCNA)和细胞周期蛋白 D1 的表达进行了免疫组化评估,以观察育亨宾对这些标志物的影响。经 DMBA 处理的仓鼠的颊囊中出现肿瘤生长,同时肝脏和颊粘膜中的 I& II 期解毒酶和脂质过氧化物(LPO)水平也发生了显著变化。在经 DMBA 处理的动物体内,观察到 Cyt p450、Cyt b5 和 LPO 的含量明显升高,升幅在 2 至 3.5 倍之间。然而,口服育亨宾可明显恢复 LPO、抗氧化和解毒酶活性。此外,育亨宾还能降低 COX-2、IL-6、PCNA 和细胞周期蛋白 D1 的水平。总之,育亨宾通过改善潜在的炎症和氧化应激条件,改善了 DMBA 诱导的口腔癌的生化和免疫组化指标,并使其恢复到接近正常值。我们的研究突显了育亨宾作为抗癌剂的潜力,尤其是针对口腔癌的抗癌剂,并建议将其用作再用途药物。
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来源期刊
Cell Biochemistry and Function
Cell Biochemistry and Function 生物-生化与分子生物学
CiteScore
6.20
自引率
0.00%
发文量
93
审稿时长
6-12 weeks
期刊介绍: Cell Biochemistry and Function publishes original research articles and reviews on the mechanisms whereby molecular and biochemical processes control cellular activity with a particular emphasis on the integration of molecular and cell biology, biochemistry and physiology in the regulation of tissue function in health and disease. The primary remit of the journal is on mammalian biology both in vivo and in vitro but studies of cells in situ are especially encouraged. Observational and pathological studies will be considered providing they include a rational discussion of the possible molecular and biochemical mechanisms behind them and the immediate impact of these observations to our understanding of mammalian biology.
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