Effect of Maternal High Fructose and Offspring High Fat Intake on Programmed Hypertension in Young Adult: the Role of Nutrient Sensing Signaling in the Brain

There is now substantial epidemiological evidence suggesting the origin of susceptibility for metabolic syndromes (MetS) and associated cardiovascular dysfunctions in adulthood can be traced back to the early life. We have previously demonstrated that maternal high fructose diet (HFD) induces programmed hypertension in adult offspring; however, the cellular and molecular signaling contributing to the developmental programming of adult hypertension is not fully understood. There are a number of nutrient sensing pathways, including silent information regulator transcript (SIRT), AMP‐activated protein kinase (AMPK), and phosphatidylinositol 3‐kinase/Akt/mammalian target of rapamycin (PI3K/Akt/mTOR) located in the central nervous system and are responsible for the detection of sugars, amino acids, lipids and the surrogate metabolite level for the maintenance of metabolic homeostasis. Perturbation of these signaling pathways could lead to MetS and the associated cardiovascular complications. This study was designed to investigate the role of these nutrient sensing pathways in the brain on developmental programming of hypertension in offspring to maternal HFD, and the influence of high fat diet (HFatD) in offspring to these nutrient sensing pathways. Female Sprague‐Dawley rats were fed with 60% HFD or normal diet (ND) during gestation and lactation periods. After weaning both HFD and ND offspring were subjected to HFatD or ND from the age of 3 to 12 weeks. Blood pressure was monitored under conscious condition via tail‐cuff method from week 6 to 12. Expression of nutrient sensing signals in the forebrain hypothalamus was examined by Western blot analysis. Tissue oxidative stress was quantified by electron spin resonance spectroscopy. Maternal HFD induced programmed MetS and hypertension that became significant at age of 9 weeks and maintained in young adult at age of 12 weeks. Changes in both metabolic and blood pressure phenotypes were appreciably enhanced in HFD offspring with additional HFatD intake after weaning. Protein expressions of SIRT1, phosphorylated AMPK (p‐AMPK), and p‐Akt in the hypothalamus were downregulated in the HFD offspring, which were further suppressed in offspring fed with HFatD. These molecular changes were associated with tissue oxidative stress in the hypothalamus.This abstract is from the Experimental Biology 2019 Meeting. There is no full text article associated with this abstract published in The FASEB Journal.