Lomas-Soria Consuelo, Rodríguez-González Guadalupe L, Ibáñez Carlos A, Reyes-Castro Luis A, Nathanielsz Peter W, Zambrano Elena
Departamento de Biología de la Reproducción, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City 14080, Mexico.
CONAHCyT-Cátedras, Investigador por México, Departamento de Biología de la Reproducción, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City 14080, Mexico.
Biology (Basel). 2023 Aug 24;12(9):1166. doi: 10.3390/biology12091166.
We investigated whether maternal obesity affects the hepatic mitochondrial electron transport chain (ETC), sirtuins, and antioxidant enzymes in young (110 postnatal days (PND)) and old (650PND) male and female offspring in a sex- and age-related manner. Female Wistar rats ate a control (C) or high-fat (MO) diet from weaning, through pregnancy and lactation. After weaning, the offspring ate the C diet and were euthanized at 110 and 650PND. The livers were collected for RNA-seq and immunohistochemistry. Male offspring livers had more differentially expressed genes (DEGs) down-regulated by both MO and natural aging than females. C-650PND vs. C-110PND and MO-110PND vs. C-110PND comparisons revealed 1477 DEGs in common for males (premature aging by MO) and 35 DEGs for females. Analysis to identify KEGG pathways enriched from genes in common showed changes in 511 and 3 KEGG pathways in the male and female livers, respectively. Mitochondrial function pathways showed ETC-related gene down-regulation. All ETC complexes, , , , and , exhibited gene down-regulation and decreased protein expression at young and old ages in MO males vs. C males; meanwhile, MO females down-regulated only at 650PND. Conclusions: MO accelerates the age-associated down-regulation of ETC pathway gene expression in male offspring livers, thereby causing sex-dependent oxidative stress, premature aging, and metabolic dysfunction.
我们研究了母体肥胖是否会以性别和年龄相关的方式影响幼年(出生后110天(PND))和老年(650 PND)雄性和雌性后代的肝脏线粒体电子传递链(ETC)、沉默调节蛋白和抗氧化酶。雌性Wistar大鼠从断奶开始,经过怀孕和哺乳期,食用对照(C)或高脂(MO)饮食。断奶后,后代食用C饮食,并在110和650 PND时安乐死。收集肝脏进行RNA测序和免疫组织化学分析。与雌性相比,雄性后代肝脏中受MO和自然衰老下调的差异表达基因(DEG)更多。C-650 PND与C-110 PND以及MO-110 PND与C-110 PND的比较显示,雄性有1477个共同的DEG(MO导致早衰),雌性有35个DEG。对共同基因富集的KEGG通路进行分析表明,雄性和雌性肝脏中分别有511条和3条KEGG通路发生了变化。线粒体功能通路显示与ETC相关的基因下调。与C组雄性相比,MO组雄性在幼年和老年时,所有ETC复合物I、II、III、IV和V均表现出基因下调和蛋白表达降低;同时,MO组雌性仅在650 PND时下调。结论:MO加速了雄性后代肝脏中与年龄相关的ETC通路基因表达下调,从而导致性别依赖性氧化应激、早衰和代谢功能障碍。