探索芦丁对高蔗糖饮食诱导的黑腹果蝇氧化应激和生殖毒性的改善潜力

IF 3.3 4区 医学 Q2 REPRODUCTIVE BIOLOGY Reproductive toxicology Pub Date : 2024-11-05 DOI:10.1016/j.reprotox.2024.108742
Abhratanu Ganguly , Sayantani Nanda , Moutushi Mandi , Kanchana Das , Prem Rajak
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引用次数: 0

摘要

蔗糖是许多经常食用的食品中的重要成分。然而,长期接触过量的蔗糖会引发健康问题。生殖系统具有微妙的生理机能,可能会受到包括蔗糖在内的各种化学压力的影响。因此,本体内研究旨在揭示高蔗糖饮食(HSD)对黑腹果蝇生殖健康的影响。此外,本研究还评估了一种生物活性化合物芦丁对高蔗糖饮食的保护潜力。在本研究中,1龄幼虫单独或与芦丁(100-300µM)一起暴露于 HSD(30%),直至成虫阶段。HSD干扰了雄性成虫的性梳形态,同时也影响了雌性成虫的受精率和卵的孵化率。此外,HSD 还会引发生殖腺产生 ROS 和氧化应激,并调节雌雄雌鸟的内源性抗氧化剂,如 SOD、过氧化氢酶和谷胱甘肽。核破碎和组织损伤以及蛋白质和脂质氧化也很明显。细胞铁水平的升高表明成人的芬顿反应活跃。此外,HSD 还调节了生殖和代谢介质的活性,包括卵黄素、苹果酸脱氢酶、葡萄糖-6-磷酸脱氢酶和血管紧张素转换酶,这些介质对整体生殖健康至关重要。有趣的是,与芦丁(主要是 200µM 的芦丁)联合处理可减轻这些不利影响并恢复生殖能力。芦丁的保护潜力可能归因于它能使氧化还原平衡正常化、减少氧化应激和优化参与生殖生理的关键酶。这些研究结果表明,芦丁具有潜在的治疗意义,可对抗 HSD 诱导的生殖危害。
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Exploring the ameliorative potential of rutin against High-Sucrose Diet-induced oxidative stress and reproductive toxicity in Drosophila melanogaster
Sucrose is a vital ingredient in numerous food items consumed regularly. However, exposure to excessive sucrose for a prolonged period can promote health issues. The reproductive system has a delicate physiology that can be targeted by various chemical stressors, including sucrose. Hence, the present in vivo study aims to unveil the impacts of High-Sucrose Diet (HSD) on the reproductive fitness of Drosophila melanogaster. In addition, the present work has also assessed the protective potential of a bioactive compound, rutin, against it. Here, first instar larvae were exposed to HSD (30 %) alone and in combination with rutin (100–300 µM) till their adult stage. HSD disturbed sex comb morphology in adult males, while fecundity and hatchability of eggs in females. Moreover, HSD triggered gonadal ROS production, oxidative stress, and modulated endogenous antioxidants such as SOD, catalase, and glutathione in both sexes. Nuclear fragmentation and tissue injuries, along with protein and lipid oxidation, were also apparent. Elevated levels of cytosolic Iron suggested an active Fenton reaction in adults. Further, HSD modulated the activities of reproductive and metabolic mediators, including vitellogenin, malate dehydrogenase, glucose-6-phosphate dehydrogenase, and angiotensin-converting enzymes that are critical to maintain the overall reproductive fitness. Interestingly, co-treatment with rutin, mainly at 200 µM, mitigated these adverse effects and restored reproductive fitness. The protective potential of rutin might be attributed to its ability to normalize redox homeostasis, reduce oxidative stress, and optimize critical enzymes involved in reproductive physiology. These findings suggest that rutin has potential therapeutic implications for counteracting the reproductive hazards induced by HSD.
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来源期刊
Reproductive toxicology
Reproductive toxicology 生物-毒理学
CiteScore
6.50
自引率
3.00%
发文量
131
审稿时长
45 days
期刊介绍: Drawing from a large number of disciplines, Reproductive Toxicology publishes timely, original research on the influence of chemical and physical agents on reproduction. Written by and for obstetricians, pediatricians, embryologists, teratologists, geneticists, toxicologists, andrologists, and others interested in detecting potential reproductive hazards, the journal is a forum for communication among researchers and practitioners. Articles focus on the application of in vitro, animal and clinical research to the practice of clinical medicine. All aspects of reproduction are within the scope of Reproductive Toxicology, including the formation and maturation of male and female gametes, sexual function, the events surrounding the fusion of gametes and the development of the fertilized ovum, nourishment and transport of the conceptus within the genital tract, implantation, embryogenesis, intrauterine growth, placentation and placental function, parturition, lactation and neonatal survival. Adverse reproductive effects in males will be considered as significant as adverse effects occurring in females. To provide a balanced presentation of approaches, equal emphasis will be given to clinical and animal or in vitro work. Typical end points that will be studied by contributors include infertility, sexual dysfunction, spontaneous abortion, malformations, abnormal histogenesis, stillbirth, intrauterine growth retardation, prematurity, behavioral abnormalities, and perinatal mortality.
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