Tomczewski Michelle Victoria, Fernandes Maria Fernanda, Grewal Rajan Singh, Duncan Robin Elaine
Department of Kinesiology and Health Sciences, Faculty of Health, University of Waterloo, 200 University Ave W., BMH1044, Waterloo, ON N2L 3G1, Canada.
Life (Basel). 2022 Oct 27;12(11):1717. doi: 10.3390/life12111717.
Lysophosphatidic acid acyltransferases/acylglycerophosphate acyltransferases (LPAATs/AGPATs) are a group of homologous enzymes that catalyze the formation of phosphatidic acid (PA) from lysophosphatidic acid. We have previously reported that LPAATδ/AGPAT4 localizes to mitochondria, suggesting a potential role in energy metabolism. However, in prior studies of young -deficient mice (age 9-12 weeks old), we found no differences in body weights, food intakes, activity levels, respiratory gas exchange, or energy expenditure compared to their wildtype () littermates. To test whether mice may develop differences in metabolic measures with advancing age, we recorded body weights and food intakes, and used metabolic chambers to assess ambulatory and locomotor activity levels, oxygen consumption (VO), carbon dioxide production (VCO), respiratory exchange ratio (RER), and total energy expenditure (heat). Fourteen-month-old mice had significantly lower mean body weights compared to littermate controls (44.6 ± 1.08 g vs. 53.5 ± 0.42 g, respectively), but no significant differences in food intake or activity levels. This phenotypic difference was accompanied by significantly elevated 24 h daily, and 12 h light and dark photoperiod average VO (20% higher) and VCO (30% higher) measures, as well as higher RER and total energy expenditure (heat) values compared to control littermates. Thus, an age-related metabolic phenotype is evident in mice. Future studies should examine the role of the lipid-modifying enzyme LPAATδ across the lifespan for greater insight into its role in normal and pathophysiology.
溶血磷脂酸酰基转移酶/酰基甘油磷酸酰基转移酶(LPAATs/AGPATs)是一组同源酶,可催化溶血磷脂酸形成磷脂酸(PA)。我们之前报道过LPAATδ/AGPAT4定位于线粒体,提示其在能量代谢中可能发挥作用。然而,在之前对年轻缺陷小鼠(9至12周龄)的研究中,我们发现与野生型同窝小鼠相比,它们在体重、食物摄入量、活动水平、呼吸气体交换或能量消耗方面没有差异。为了测试小鼠是否会随着年龄增长在代谢指标上出现差异,我们记录了体重和食物摄入量,并使用代谢室评估动态和运动活动水平、氧气消耗(VO)、二氧化碳产生(VCO)、呼吸交换率(RER)和总能量消耗(热量)。与同窝对照小鼠相比,14月龄的小鼠平均体重显著更低(分别为44.6±1.08克和53.5±0.42克),但在食物摄入量或活动水平上没有显著差异。这种表型差异伴随着每日24小时以及12小时光照和黑暗光周期平均VO(约高20%)和VCO(约高30%)测量值显著升高,以及与对照同窝小鼠相比更高的RER和总能量消耗(热量)值。因此,小鼠中与年龄相关的代谢表型是明显的。未来的研究应该研究脂质修饰酶LPAATδ在整个生命周期中的作用,以更深入了解其在正常生理和病理生理中的作用。