Obesity impairs glucose and lipid metabolism, and increases the risk of coronary heart disease (CHD). Obese pre-menopausal females have ~1/2 the CHD risk of obese males; this protection is reduced when ovarian function is lost with menopause. There is an important therapeutic opportunity in understanding the mechanisms of this protection. The goal of this project is to define mechanisms by which female sex protects against obesity-induced glucose and lipid abnormalities, and see if we can augment this pathway in males. In the liver, the presence of impaired glucose and lipid biology in obesity has been attributed to a defect in insulin-induced AKT signaling to regulate glucose, but intact SREBP1c signaling to promote lipogenesis. This model is not sufficient to explain dyslipidemia with obesity. We've developed in-vivo approaches to understand the integrated relationships of adipose, muscle and liver, which allow us to provide a unifying model of both lipid and glucose abnormalities of obesity: Excess delivery of fatty acids (FA) to the liver arises due to impaired suppression of lipolysis by insulin. In response to this FA flux, the liver re-esterifies FA into triglyceride (TG) resulting in fatty liver and export of VLDL-TG. Fatty liver results in impaired insulin-regulation of glucose metabolism. While each of these steps is supported in the literature, the integrated control that determines the balance between health and disease has been elusive. Additionally, females are protected from FA-induced insulin resistance, which we propose is mediated by estrogen-regulated FA metabolism in muscle and liver. We've discovered that estrogen corrects both the glucose and lipid defects in obesity -promoting insulin- regulation of glucose metabolism, while blocking dyslipidemia. Using an innovative in vivo approach with dual tracers for glucose and lipid flux, we discovered that this protective effect requires estrogen signaling through estrogen receptor alpha (ER?). We coupled mRNA sequencing and mice lacking ER? in the liver and found that ER? influences numerous liver genes involved in glucose and lipid metabolism, and also indirectly regulates these pathways by induction of the negative transcriptional regulator Small Heterodimer Partner (SHP). This liver estrogen pathway is also important in males -and can likely be augmented to prevent CHD. We hypothesize three critical actions of estrogen mediated through ER?: 1) it limits FA delivery to the liver by promoting muscle FA oxidation (AIM1), 2) it activates via SHP a transcriptional network in the liver that promotes insulin suppression of gluconeogenesis, promotes FA oxidation, and prevents FA-driven VLDL production (AIM2). Males have low ER? signaling, but this protection and can be augmented (AIM3). Our studies are significant because they are expected to: 1) identify the physiological basis by which female sex reduces CHD risk and provide a foundation for translating this protection into healthcare, 2) define the extent that beneficial testosterone effects in males are mediated through its conversion to estrogen, and if augmenting the liver ER? pathway in males can prevent FA-mediated dyslipidemia and glucose intolerance.

Public Health Relevance

Obesity has dramatically increased the burden of cardiovascular disease, and a major goal of the NIH/NHLBI is to reduce this burden. The goal of this application is to discover hepatic pathways that improve glucose and lipid abnormalities in obesity, which is expected to help reverse the impact of obesity on cardiovascular risk. Our project also identifies pathways that mediate sex-differences in cardiovascular disease, which is also an NIH priority area.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK109102-04
Application #
9432504
Study Section
Integrative Physiology of Obesity and Diabetes Study Section (IPOD)
Program Officer
Teff, Karen L
Project Start
2016-03-01
Project End
2021-02-28
Budget Start
2018-03-01
Budget End
2019-02-28
Support Year
4
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Vanderbilt University Medical Center
Department
Type
DUNS #
079917897
City
Nashville
State
TN
Country
United States
Zip Code
37232
Palmisano, Brian T; Stafford, John M; Pendergast, Julie S (2017) High-Fat Feeding Does Not Disrupt Daily Rhythms in Female Mice because of Protection by Ovarian Hormones. Front Endocrinol (Lausanne) 8:44
Palmisano, Brian T; Zhu, Lin; Stafford, John M (2017) Role of Estrogens in the Regulation of Liver Lipid Metabolism. Adv Exp Med Biol 1043:227-256
Zhu, Lin; Shi, Jeanne; Luu, Thao N et al. (2017) Hepatocyte estrogen receptor alpha mediates estrogen action to promote reverse cholesterol transport during Western-type diet feeding. Mol Metab :
Palmisano, Brian T; Le, Thao D; Zhu, Lin et al. (2016) Cholesteryl ester transfer protein alters liver and plasma triglyceride metabolism through two liver networks in female mice. J Lipid Res 57:1541-51