被动吸烟和味精给药实验中生物能量学过程的性别和年龄因素

A. Rutska, I. Krynytska
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引用次数: 0

摘要

背景主动吸烟和被动吸烟每年造成500多万人死亡。同时,目前食品技术的一个特点是使用对人类健康并不总是安全的食品添加剂,如味精。客观的本研究的目的是确定被动吸烟和长期服用味精的大鼠在性别和年龄方面线粒体酶活性的变化。方法。利用琥珀酸脱氢酶(SDG)和细胞色素氧化酶(CO)活性评价循环中性粒细胞线粒体的生物能量过程。结果。在成年雄性大鼠中,被动吸烟与MSG给药相结合伴随着对生物能量学过程的显著抑制,与完整动物相比,琥珀酸脱氢酶活性降低了47.1%(p<0.001),与对照组相比,在烟草烟雾的隔离作用和细胞色素氧化酶活性降低27.5%(p<0.001)的情况下。结论。因此,研究结果表明,低剂量摄入味精通过影响呼吸链功能和ATP的产生,增强了烟草烟雾破坏细胞生物能量过程的能力。因此,建议研究E621的既定毒性剂量,并研究MSG对活体“安全”(允许)剂量影响的分子机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
GENDER AND AGE ASPECTS OF BIOENERGETICS PROCESSES IN EXPERIMENTAL PASSIVE TOBACCO SMOKING AND MONOSODIUM GLUTAMATE ADMINISTRATION
Background. Active smoking and exposure to passive smoke are responsible for more than 5 million deaths each year. At the same time, a characteristic feature of present food technologies is the use of food additives that are not always safe for human health, such as monosodium glutamate (MSG). Objective. The aim of the research was to determine the changes in mitochondrial enzymes activity in rats in case of passive tobacco smoke combined with prolonged administration of MSG in the sex and age aspects. Methods. The evaluation of bioenergetics processes in the mitochondria of circulating neutrophils was carried out using succinate dehydrogenase (SDG) and cytochrome oxidase (CO) activity.  Results. Passive tobacco smoke combined with the MSG administration in mature male-rats is accompanied by a significant inhibition of bioenergetics processes, as evidenced by a decrease in succinate dehydrogenase activity by 47.1% (p<0.001) compared to the intact animals, which is by 27.9% (p<0.001) below this index in case of the isolated effect of tobacco smoke and reduction of cytochrome oxidase activity by 27.5% (p<0.001) compared to the control group. Conclusions. Thus, the findings suggest that low dose intake of monosodium glutamate enhances the ability of tobacco smoke to disrupt the cell's bioenergetics processes by affecting the respiratory chain function and generation of ATP. Therefore, it is advisable to investigate the established toxic doses of E621, as well as to study the molecular mechanisms of the ‘safe’ (allowed) doses of MSG effect on a living organism.
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