Intrauterine Growth Restriction Increases TNFα and Activates the Unfolded Protein Response in Male Rat Pups

• Published in: Journal of obesity Vol. 2014; no. 2014; pp. 1 - 9
• Main Authors: Joss-Moore, Lisa A., Wang, Yan, Bierer, Ryann, Lang, Brook Y., Campbell, Michael S., Riddle, Emily S., Bagley, Heidi N.
• Format: Journal Article
• Language: English
• Published: Cairo, Egypt Hindawi Publishing Corporation 01.01.2014; Wiley
• Subjects: Adipocytes - metabolism; Adipose Tissue - metabolism; Animals; Fetal Growth Retardation - metabolism; Glucose Intolerance - etiology; Glucose Intolerance - metabolism; Inflammation - etiology; Inflammation - metabolism; Insulin - metabolism; Insulin Resistance; Male; Obesity - etiology; Obesity - genetics; Obesity - metabolism; Rats, Sprague-Dawley; RNA, Messenger - metabolism; Signal Transduction; Tumor Necrosis Factor-alpha - blood; Tumor Necrosis Factor-alpha - metabolism; Unfolded Protein Response - genetics
• ISSN: 2090-0708; 2090-0716
• DOI: 10.1155/2014/829862

Intrauterine growth restriction (IUGR) programs adult disease, including obesity and insulin resistance. Our group previously demonstrated that IUGR dysregulates adipose deposition in male, but not female, weanling rats. Dysregulated adipose deposition is often accompanied by the release of proinflammatory signaling molecules, such as tumor necrosis factor alpha (TNFα). TNFα contributes to adipocyte inflammation and impaired insulin signaling. TNFα has also been implicated in the activation of the unfolded protein response (UPR), which impairs insulin signaling. We hypothesized that, in male rat pups, IUGR would increase TNFα, TNFR1, and components of the UPR (Hspa5, ATF6, p-eIF2α, and Ddit3) prior to the onset of obesity. We further hypothesized that impaired glucose tolerance would occur after the onset of adipose dysfunction in male IUGR rats. To test this hypothesis, we used a well-characterized rat model of uteroplacental insufficiency-induced IUGR. Our primary findings are that, in male rats, IUGR (1) increased circulating and adipose TNFα, (2) increased mRNA levels of UPR components as well as p-eIF2a, and (3) impaired glucose tolerance after observed TNFα increased and after UPR activation. We speculate that programmed dysregulation of TNFα and UPR contributed to the development of glucose intolerance in male IUGR rats.