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ENA-A一种活性矿物质资源A可延长与SMP30基因敲除小鼠抗氧化机制相关的寿命。

ENA-A actimineral resource A extends lifespan associated with antioxidant mechanism in SMP30 knockout mice.

作者信息

Han Jung-Youn, Hwang Meeyul, Hwa Sung-Yong, Park Jin-Kyu, Ki Mi-Ran, Hong Il-Hwa, Kim Ah-Young, Lee Eun-Mi, Lee Eun-Joo, Min Chang-Woo, Kang Kyung-Ku, Lee Myeong-Mi, Sung Soo-Eun, Jeong Kyu-Shik

机构信息

Department of Pathology, College of Veterinary Medicine, Kyungpook National University, Daegu, 702-701, Republic of Korea.

出版信息

Mol Cell Biochem. 2014 Jun;391(1-2):175-82. doi: 10.1007/s11010-014-2000-z. Epub 2014 Mar 7.

Abstract

ENA-actimineral resource A (ENA-A) is an alkaline mineral water and has a few biological activities such as antioxidant activity. The aim of this study was to examine the effects of ENA-A on lifespan in mice using senescence marker protein-30 knockout mice. The present study had groups of 18-week-old mice (n = 24), 26-week-old mice (n = 12), and 46-week-old mice (n = 20). Each differently aged mice group was divided into three subgroups: a control group, a 5 % ENA-A-treated group, and a 10 % ENA-A-treated group. Mice in the 18-week-old group were treated with vitamin C drinking water 1.5 g/L. However, the mice in the 26-week-old and 46-week-old groups were not treated with vitamin C. The experiments were done for 18 weeks. All vitamin C-treated mice were alive at week 18 (100% survival rate). In the non-vitamin C group, the 10% ENA-A-treated mice were alive at week 18. The control and 5% ENA-A-treated mice died by week 15. As expected, vitamin C was not detected in the non-vitamin C-treated group. However, vitamin C levels were increased in an ENA-A dose-dependent manner in the vitamin C-treated group. In the TUNEL assay, a number of positive hepatocytes significantly decreased in an ENA-A dose-dependent manner. Periodic acid Schiff positive hepatocytes were significantly increased in an ENA-A dose-dependent manner. In addition, the expression level of CuZnSOD was increased by the ENA-A treatment. These data suggest that the intake of ENA-A has a critical role in the anti-aging mechanism and could be applied toward the lifespans of humans.

摘要

能源与活性矿物质资源A(ENA-A)是一种碱性矿泉水,具有一些生物活性,如抗氧化活性。本研究的目的是使用衰老标记蛋白-30基因敲除小鼠来研究ENA-A对小鼠寿命的影响。本研究有18周龄小鼠组(n = 24)、26周龄小鼠组(n = 12)和46周龄小鼠组(n = 20)。每个不同年龄的小鼠组又分为三个亚组:对照组、5% ENA-A处理组和10% ENA-A处理组。18周龄组的小鼠饮用含1.5 g/L维生素C的饮用水。然而,26周龄和46周龄组的小鼠未接受维生素C处理。实验进行了18周。所有接受维生素C处理的小鼠在第18周时均存活(存活率100%)。在非维生素C组中,10% ENA-A处理的小鼠在第18周时存活。对照组和5% ENA-A处理的小鼠在第15周时死亡。正如预期的那样,在未接受维生素C处理的组中未检测到维生素C。然而,在接受维生素C处理的组中,维生素C水平以ENA-A剂量依赖性方式升高。在TUNEL检测中,阳性肝细胞数量以ENA-A剂量依赖性方式显著减少。过碘酸希夫阳性肝细胞以ENA-A剂量依赖性方式显著增加。此外,ENA-A处理可提高CuZnSOD的表达水平。这些数据表明,ENA-A的摄入在抗衰老机制中起关键作用,并且可能适用于人类寿命。

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