Hormetic effect of 3-Bromopyruvate on age-induced alterations in erythrocyte membrane transporters and oxidative biomarkers in rats.

IF 2.2 4区 医学 Q3 GERIATRICS & GERONTOLOGY
J. Arya, Raushan Kumar, Shambhoo Sharan Tripathi, S. Rizvi
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引用次数: 1

Abstract

3-bromopyruvate (3-BP) is a glycolytic inhibitor and a potential calorie restriction mimic that shows a variety of beneficial effects in several aging model systems. A chronic low dose of 3-BP was given to male Wistar rats for four weeks. The effect of 3-BP on age-dependent alteration on the activities of various transporters/exchangers and redox biomarkers (protein carbonyl (PC), sialic acid (SA), sulfhydryl group (-SH), intracellular calcium ion [Ca2+]i, and osmotic fragility) was studied. In aged rats, 3-BP treatment increases the membrane-bound activities of Na+/K+-ATPase (NKA) and Ca2+-ATPase (PMCA), along with levels of -SH and SA. It also exerts a concomitant decrease in Na+/H+ exchanger (NHE) activity and the levels of [Ca2+]i, PC, and osmotic fragility in aged groups. 3-BP can be considered as a potential anti-aging agent that induces a hormetic effect leading to amelioration of age-dependent impairment of membrane-bound ATPases and alterations in the redox biomarker level.
3-溴吡喃酸酯对大鼠红细胞膜转运蛋白和氧化生物标志物年龄诱导变化的激素作用。
3-溴丙酮酸盐(3-BP)是一种糖酵解抑制剂,也是一种潜在的热量限制模拟物,在几种衰老模型系统中显示出多种有益效果。雄性Wistar大鼠给予3-BP的慢性低剂量,持续四周。研究了3-BP对各种转运蛋白/交换蛋白和氧化还原生物标志物(蛋白质羰基(PC)、唾液酸(SA)、巯基(-SH)、细胞内钙离子[Ca2+]i和渗透脆性)活性的年龄依赖性改变的影响。在老年大鼠中,3-BP治疗增加了Na+/K+-ATP酶(NKA)和Ca2+-ATP酶的膜结合活性,以及-SH和SA的水平。它还降低了老年组的Na+/H+交换剂(NHE)活性和[Ca2+]i、PC和渗透脆性的水平。3-BP可被认为是一种潜在的抗衰老剂,其诱导激素效应,从而改善膜结合ATP酶的年龄依赖性损伤和氧化还原生物标志物水平的改变。
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来源期刊
Rejuvenation research
Rejuvenation research 医学-老年医学
CiteScore
4.50
自引率
0.00%
发文量
41
审稿时长
3 months
期刊介绍: Rejuvenation Research publishes cutting-edge, peer-reviewed research on rejuvenation therapies in the laboratory and the clinic. The Journal focuses on key explorations and advances that may ultimately contribute to slowing or reversing the aging process, and covers topics such as cardiovascular aging, DNA damage and repair, cloning, and cell immortalization and senescence. Rejuvenation Research coverage includes: Cell immortalization and senescence Pluripotent stem cells DNA damage/repair Gene targeting, gene therapy, and genomics Growth factors and nutrient supply/sensing Immunosenescence Comparative biology of aging Tissue engineering Late-life pathologies (cardiovascular, neurodegenerative and others) Public policy and social context.
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