评估含咖啡因能量饮料对成年雄性白化大鼠甲状腺的毒性作用:评估细胞凋亡和再生

N. Elrewieny, R. Eltokhy, H. Aboubakr, Passant Essam Eldin Shibel, S. Alsaeed
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引用次数: 0

摘要

背景:青壮年很少意识到含咖啡因能量饮料的负面影响。工作目的:通过生化、组织学和免疫组化检查,以及细胞凋亡/再生率的迹象,研究含咖啡因的能量饮料对白化大鼠甲状腺的危害。材料和方法:将 24 只成年白化大鼠分为 3 组:第 1 组以基础饮食和蒸馏水饲养,第 2 组和第 3 组给予 2 种不同剂量的能量饮料,为期 14 天。第 2 组大鼠每天摄入低剂量的咖啡因能量饮料(10 毫克/千克),而第 3 组大鼠每天摄入高剂量的咖啡因能量饮料(20 毫克/千克)。最后,对大鼠的T3、T4和促甲状腺激素进行测定,并使用ki-67和caspase-3进行组织病理学和免疫组化研究。结果:第 1、第 2 和第 3 组的平均游离 T3 和 T4 值明显高于第 1、第 2 和第 3 组。3 个研究组的 ki-67 存在明显差异;第 3 组的 ki-67 平均值最高,其次分别是对照组和第 2 组,而 3 个研究组的 caspase 3 则无明显差异。结论:口服能量饮料与甲状腺中Ki-67的显著过度表达有关,这表明甲状腺损伤后会出现增殖反应,而在第2组中,游离t3和t4会显著增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of Toxic Effects of Caffeinated Energy Drinks on Thyroid Gland of Adult Male Albino Rats: Assessment of Apoptosis and Regeneration
Background: Young adults and adolescents are rarely aware of the negative effects of caffeinated energy beverages. Aim of the work: to investigate the hazards of caffeinated energy drinks on the thyroid gland in albino rats by biochemical, histological, and immunohistochemical examinations, and examining the signs of the apoptosis/regeneration rate. Material and methods: 24 adult albino rats were classified into 3 groups; Group 1 were kept on basal diet and distilled water, Group 2 and Group 3 were given energy drinks in 2 different doses for 14 days. Rats in Group 2 were given a daily low dose of caffeinated energy drinks daily (10 mg/kg), while the Group 3 of rats were given a daily high dose of caffeinated energy drinks (20 mg/kg). Finally, T3, T4 and TSH were measured, histopathology and immunohistochemical study using ki-67 and caspase-3 were performed. Results: the mean free T3 and T4 in (groups 1, 2 and 3) showed statistically significant higher values. There was a significant difference regarding ki-67 in the 3 studied groups; the mean ki-67 score showed the highest value in group 3 followed by the control group and group 2 respectively, while there was a non-significant difference regarding caspase 3 in the 3 studied groups. Conclusion: oral consumption of energy drinks was associated with significantly overexpression of Ki-67 in thyroid gland suggesting a proliferative response to thyroid gland injury and significant increase in free t3 and t4 in group 2.
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