Nonalcoholic fatty liver disease (NAFLD) is a chronic, progressive liver disease that affects 30% of all US adults. NAFLD is strongly linked to type 2 diabetes, with an estimated 80% of type 2 diabetics having NAFLD. Unfortunately, the Veteran population has a significantly higher prevalence of diabetes than the general population (20-25% vs. 6-8%), and, therefore, it would be expected to have a similarly higher prevalence of NAFLD. Because NAFLD leads to a significant number of patients with cirrhosis and need for liver transplantation, this condition is an important issue for the VA healthcare system. Despite the strong association between NAFLD and type 2 diabetes, a unifying pathophysiology remains poorly understood. The overall hypothesis of this proposal is that hepatic lipid intermediate/metabolite accumulation and hepatic insulin resistance develops due to hepatic mitochondrial dysfunction, which leads to dysregulated hepatic glucose output and ultimately development of type 2 diabetes. In addition, targeting hepatic mitochondrial dysfunction and hepatic insulin resistance with lifestyle modifications and/or pharmacological interventions will effectively treat NAFLD and type 2 diabetes. We will conduct studies in the Otsuka Long-Evans Tokushima Fatty (OLETF) rat, a well characterized rodent model of hyperphagia-induced obesity, NAFLD, and type 2 diabetes to examine the following specific aims. 1) Determine whether hepatic insulin resistance associated with NAFLD develops secondary to mitochondrial dysfunction and is a significant contributing factor in the development of type 2 diabetes. 2) Determine the effectiveness of daily exercise vs. caloric restriction (with and without metformin) in the treatment of NAFLD and type 2 diabetes.
For Aim 1, OLETF rats will be studied at different ages throughout the spectrum of pre-insulin resistance, insulin resistance, and development of frank type 2 diabetes.
For Aim 2, OLETF rats will be treated with exercise, caloric restriction, metformin, or combination therapies. The studies will employ in-vivo hyperinsulinemic-euglycemic clamps to assess systemic and hepatic insulin sensitivity and thorough examinations of hepatic mitochondrial function/content and lipid intermediate/metabolites accumulation. This project is extremely novel as it will examine the role of hepatic mitochondrial dysfunction and hepatic insulin resistance throughout the initiation, development, and progression of systemic insulin resistance and type 2 diabetes. In addition, it will comprehensively examine the effectiveness of lifestyle modifications and pharmacological interventions in the treatment of NAFLD and type 2 diabetes. These studies will provide future insight into reducing the incidence of type 2 diabetes and NAFLD in our Veteran population.
Prevalence rates for type 2 diabetes and nonalcoholic fatty liver disease (NAFLD), a chronic, progressive liver disease that can lead to cirrhosis and liver transplantation, are extremely high in the Veteran population. Although 80% of patients with type 2 diabetes also have NAFLD, we do not fully understand why the two conditions commonly occur in tandem. Thus, the overall goals of the current proposal are to examine the mechanisms contributing to NAFLD and type 2 diabetes, particularly the role of insulin resistance and mitochondrial dysfunction in the liver. In addition, we will determine the effectiveness of exercise vs. diet, with and without the oral hypoglycemic medication metformin, in the treatment of NAFLD and type 2 diabetes. This application will help to identify therapeutic targets and better treatment options with future application in reducing the incidence of type 2 diabetes and NAFLD in Veterans.
|Fletcher, Justin A; Linden, Melissa A; Sheldon, Ryan D et al. (2018) Fibroblast growth factor 21 increases hepatic oxidative capacity but not physical activity or energy expenditure in hepatic peroxisome proliferator-activated receptor ? coactivator-1?-deficient mice. Exp Physiol 103:408-418|
|Jeong, Youngjae; Daghlas, Salah A; Kahveci, Alp S et al. (2018) Soluble activin receptor type IIB decoy receptor differentially impacts murine osteogenesis imperfecta muscle function. Muscle Nerve 57:294-304|
|Panasevich, Matthew R; Schuster, Colin M; Phillips, Kathryn E et al. (2017) Soy compared with milk protein in a Western diet changes fecal microbiota and decreases hepatic steatosis in obese OLETF rats. J Nutr Biochem 46:125-136|
|Habibi, Javad; Aroor, Annayya R; Sowers, James R et al. (2017) Sodium glucose transporter 2 (SGLT2) inhibition with empagliflozin improves cardiac diastolic function in a female rodent model of diabetes. Cardiovasc Diabetol 16:9|
|Dirkes, Rebecca K; Ortinau, Laura C; Rector, R Scott et al. (2017) Insulin-Stimulated Bone Blood Flow and Bone Biomechanical Properties Are Compromised in Obese, Type 2 Diabetic OLETF Rats. JBMR Plus 1:116-126|
|Sheldon, Ryan D; Nicole Blaize, A; Fletcher, Justin A et al. (2016) Gestational exercise protects adult male offspring from high-fat diet-induced hepatic steatosis. J Hepatol 64:171-8|
|Szary, Nicholas; Rector, R Scott; Uptergrove, Grace M et al. (2015) High Intrinsic Aerobic Capacity Protects against Ethanol-Induced Hepatic Injury and Metabolic Dysfunction: Study Using High Capacity Runner Rat Model. Biomolecules 5:3295-308|
|Linden, Melissa A; Lopez, Kristi T; Fletcher, Justin A et al. (2015) Combining metformin therapy with caloric restriction for the management of type 2 diabetes and nonalcoholic fatty liver disease in obese rats. Appl Physiol Nutr Metab 40:1038-47|
|Roberts, Michael D; Mobley, C Brooks; Toedebush, Ryan G et al. (2015) Western diet-induced hepatic steatosis and alterations in the liver transcriptome in adult Brown-Norway rats. BMC Gastroenterol 15:151|
|Oberlin, Douglas J; Mikus, Catherine R; Kearney, Monica L et al. (2014) One bout of exercise alters free-living postprandial glycemia in type 2 diabetes. Med Sci Sports Exerc 46:232-8|
Showing the most recent 10 out of 17 publications