(Behavioral and Cognitive Core) Metabolic disorders, including diabetes, are characterized by abnormalities in circulating substrates (glucose, lipids) as well as their causes and consequences vis--vis peripheral tissues including the endocrine pancreas, liver, adipose tissue, and others. While this peripheral focus has been vital for developing current therapeutic approaches, recent years have seen a steady progression in understanding the importance of the central nervous system (CNS) in terms of receiving signals from these peripheral organs, integrating them with circulating nutrients and diverse non-homeostatic factors, and then coordinating activity among diverse systems to optimally control glycemia and other parameters. An important component of this activity is the CNS control of behavior. Recognizing the importance of the interplay between the CNS and peripheral metabolism, NIDDK modified the RFP for the current round of MMPC applications by explicitly naming behavioral assays as key phenotypic endpoints to be offered. This innovation is timely and nicely fits with a successful internal behavioral core that has historically served UC's MDI and Obesity Research Center. Although this internal core wasn't explicitly advertised, investigators in other institutions and industry learned of it and utilized it on a limited basis; however, we have been unable to make these services widely available to non-UC investigators due to funding limitations. We are proposing that this already-existing core become an official Behavior and Cognitive Core of the UC-MMPC, thereby making its services and considerable behavioral expertise broadly available to non-UC investigators. By doing so, we are also taking advantage of the extremely well-established MMPC core structure and its mechanism for the retrieval of service fees. There are four broad, long-range aims of this Core:
Specific Aim 1 : To provide sophisticated state-of-the-art behavioral assays that allow investigators to better characterize mouse models of metabolic disorders.
Specific Aim 2 : To advise investigators on the most appropriate behavioral tests, as well as the optimal sequence to be used when performing different assays.
Specific Aim 3 : To train investigators in the execution and analysis of specialized behavioral procedures established and routinely practiced in the Core.
Specific Aim 4 : To continuously improve current paradigms and develop new ones, including methods to enhance the efficiency and accuracy of behavioral assessments in mice.

Project Start
2001-07-01
Project End
Budget Start
2017-07-01
Budget End
2018-06-30
Support Year
17
Fiscal Year
2017
Total Cost
Indirect Cost
Name
University of Cincinnati
Department
Type
DUNS #
041064767
City
Cincinnati
State
OH
Country
United States
Zip Code
45221
Rebholz, Sandra L; Melchior, John T; Davidson, W Sean et al. (2018) Studies in genetically modified mice implicate maternal HDL as a mediator of fetal growth. FASEB J 32:717-727
Shen, Ling; Liu, Yin; Tso, Patrick et al. (2018) Silencing steroid receptor coactivator-1 in the nucleus of the solitary tract reduces estrogenic effects on feeding and apolipoprotein A-IV expression. J Biol Chem 293:2091-2101
Tso, Patrick; Vurma, Mustafa; Ko, Chih-Wei et al. (2018) Effect of mono- and diglycerides on the digestion and absorption of lutein in lymph fistula rats. Am J Physiol Gastrointest Liver Physiol 315:G95-G103
Wang, Tony Y; Portincasa, Piero; Liu, Min et al. (2018) Mouse models of gallstone disease. Curr Opin Gastroenterol 34:59-70
Zhang, Ming; Sun, Kaiji; Wu, Yujun et al. (2017) Interactions between Intestinal Microbiota and Host Immune Response in Inflammatory Bowel Disease. Front Immunol 8:942
Woods, Stephen C; May, Aaron A; Liu, Min et al. (2017) Using the cerebrospinal fluid to understand ingestive behavior. Physiol Behav 178:172-178
Rao, Raghavendra; Roche, Alexander; Febres, Gerardo et al. (2017) Circulating Apolipoprotein A-IV presurgical levels are associated with improvement in insulin sensitivity after Roux-en-Y gastric bypass surgery. Surg Obes Relat Dis 13:468-473
Li, Xiaoming; Wang, Fei; Xu, Min et al. (2017) ApoA-IV improves insulin sensitivity and glucose uptake in mouse adipocytes via PI3K-Akt Signaling. Sci Rep 7:41289
Zhang, Yupeng; He, Jing; Zhao, Jing et al. (2017) Effect of ApoA4 on SERPINA3 mediated by nuclear receptors NR4A1 and NR1D1 in hepatocytes. Biochem Biophys Res Commun 487:327-332
Ma, Xiaoshi; Dai, Zhaolai; Sun, Kaiji et al. (2017) Intestinal Epithelial Cell Endoplasmic Reticulum Stress and Inflammatory Bowel Disease Pathogenesis: An Update Review. Front Immunol 8:1271

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