Obesity is a global public health problem. An increased understanding of the basic physiology and neurobiology of body weight homeostasis is critical in the prevention and treatment of obesity and related co-morbidities such as diabetes mellitus and coronary artery disease. Over the last decade, several critical metabolic signals and candidate central neuronal pathways that mediate their effects have been identified. Ghrelin, the endogenous ligand for the growth hormone secretagogue receptor (GHSR, ghrelin receptor) has emerged as one of these potentially key metabolic signals. Ghrelin is a hormone that stimulates food intake, promotes the accumulation of body fat, and decreases energy expenditure. Previous work has also indicated that ghrelin signaling is required for development of the full phenotype of diet-induced obesity. Ghrelin also affects blood glucose levels, the release of insulin and possibly the sensitivity to insulin. The primary purpose of this current proposal is to gain a better understanding of ghrelin's role in the regulation of body weight homeostasis. The proposed experiments include neuroanatomical approaches to determine the projections of ghrelin-responsive neurons. In addition, a novel mouse model will be used to investigate the role of ghrelin receptor expression in two specific central nervous system sites -- the arcuate nucleus and the dorsal vagal complex -- in ghrelin's effects on food intake, the development of diet-induced obesity, glucose homeostasis, and locomotor activity. The proposed research will be performed under the mentorship of an internationally recognized expert in functional neuroanatomy, and is part of a training and career development plan designed to facilitate the applicant's transition to successful independent clinical scientist. Other elements of the development plan will include laboratory technique training, data presentations and various laboratory, mentor and scientific meetings. The proposed research will take place in the Division of Endocrinology, Diabetes and Metabolism at Beth Israel Deaconess Medical Center, where all the resources (equipment, technical expertise) to carry out the proposed research are readily available.
Frazão, Renata; Cravo, Roberta M; Donato Jr, Jose et al. (2013) Shift in Kiss1 cell activity requires estrogen receptor ?. J Neurosci 33:2807-20 |
Perello, Mario; Scott, Michael M; Sakata, Ichiro et al. (2012) Functional implications of limited leptin receptor and ghrelin receptor coexpression in the brain. J Comp Neurol 520:281-94 |
Sakata, Ichiro; Park, Won-Mee; Walker, Angela K et al. (2012) Glucose-mediated control of ghrelin release from primary cultures of gastric mucosal cells. Am J Physiol Endocrinol Metab 302:E1300-10 |
Scott, Michael M; Perello, Mario; Chuang, Jen-Chieh et al. (2012) Hindbrain ghrelin receptor signaling is sufficient to maintain fasting glucose. PLoS One 7:e44089 |
Davis, J F; Perello, M; Choi, D L et al. (2012) GOAT induced ghrelin acylation regulates hedonic feeding. Horm Behav 62:598-604 |
Cabral, Agustina; Suescun, Olga; Zigman, Jeffrey M et al. (2012) Ghrelin indirectly activates hypophysiotropic CRF neurons in rodents. PLoS One 7:e31462 |
Chuang, Jen-Chieh; Sakata, Ichiro; Kohno, Daisuke et al. (2011) Ghrelin directly stimulates glucagon secretion from pancreatic alpha-cells. Mol Endocrinol 25:1600-11 |
Klöckener, Tim; Hess, Simon; Belgardt, Bengt F et al. (2011) High-fat feeding promotes obesity via insulin receptor/PI3K-dependent inhibition of SF-1 VMH neurons. Nat Neurosci 14:911-8 |
Cravo, R M; Margatho, L O; Osborne-Lawrence, S et al. (2011) Characterization of Kiss1 neurons using transgenic mouse models. Neuroscience 173:37-56 |
Donato Jr, Jose; Cravo, Roberta M; Frazão, Renata et al. (2011) Leptin's effect on puberty in mice is relayed by the ventral premammillary nucleus and does not require signaling in Kiss1 neurons. J Clin Invest 121:355-68 |
Showing the most recent 10 out of 25 publications