? LEADERSHIP and ADMINISTRATIVE CORE (LAC) Taking advantage of the University of Texas Health Science Center at San Antonio?s exceptional basic research programs in aging biology and its numerous educational resources in gerontology, we propose an Older Americans Independence Center (OAIC) with the overarching goal of establishing an interdisciplinary research program to promote healthy aging. We will achieve this goal by (i) advancing aging research from model systems (C. elegans, Drosophila) and rodents to studies in non-human primates (common marmoset); (ii) translating pre-clinical animal research to human interventions; and (iii) training the next generation of gerontology-oriented translational scientists. The Leadership and Administrative Core (LAC) will provide leadership and develop an infrastructure that fosters integration of aging-related basic and clinical sciences, catalyzes scientific discoveries, promotes education and mentorship, and partners with other scientists and the community at large, with the overarching goal of developing novel interventions to improve the health, quality of life, and independence of older Americans. The LAC will monitor, stimulate, sustain, evaluate, and report progress toward our goal through the following Specific Aims: 1) Provide logistical support and promote operational cohesiveness to the OAIC; 2) Promote research protocol adherence and maintain regulatory compliance with university and governmental policies for the responsible conduct of research supported by the OAIC; 3) Disseminate the scientific innovation accomplished by OAIC investigators, inside and outside our institution, regarding novel aging- modulating interventions to enhance and extend human health; 4) Stimulate and facilitate interdisciplinary collaboration among OAIC investigators, cores, committees, and projects, to advance basic science in aging biology from the bench to the bedside; 5) Select and monitor pilot and exploratory studies and Scholars aligned with the OAIC theme; 6) Monitor and evaluate OAIC progress, foster institutional collaborations, and leverage resources; 7) Provide programmatic and scientific guidance to training programs, pilot studies, and resource cores; and 8) Be an active member of the national OAIC program to help advance the mission of promoting independence of older Americans.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Center Core Grants (P30)
Project #
1P30AG044271-01A1
Application #
8878946
Study Section
Special Emphasis Panel (ZAG1-ZIJ-8 (J1))
Project Start
Project End
Budget Start
2015-06-15
Budget End
2016-04-30
Support Year
1
Fiscal Year
2015
Total Cost
$131,505
Indirect Cost
$42,598
Name
University of Texas Health Science Center
Department
Type
DUNS #
800772162
City
San Antonio
State
TX
Country
United States
Zip Code
78229
Sills, Aubrey M; Artavia, Joselyn M; DeRosa, Brian D et al. (2018) Long-term treatment with the mTOR inhibitor rapamycin has minor effect on clinical laboratory markers in middle-aged marmosets. Am J Primatol :e22927
Noël, Polly Hitchcock; Wang, Chen-Pin; Finley, Erin P et al. (2018) Provider-Related Linkages Between Primary Care Clinics and Community-Based Senior Centers Associated With Diabetes-Related Outcomes. J Appl Gerontol :733464818782853
Reveles, Kelly R; Mortensen, Eric M; Koeller, Jim M et al. (2018) Derivation and Validation of a Clostridium difficile Infection Recurrence Prediction Rule in a National Cohort of Veterans. Pharmacotherapy 38:349-356
Lee, Hak Joo; Feliers, Denis; Barnes, Jeffrey L et al. (2018) Hydrogen sulfide ameliorates aging-associated changes in the kidney. Geroscience 40:163-176
Arora, Sukeshi Patel; Mahalingam, Devalingam (2018) Immunotherapy in colorectal cancer: for the select few or all? J Gastrointest Oncol 9:170-179
Kraig, Ellen; Linehan, Leslie A; Liang, Hanyu et al. (2018) A randomized control trial to establish the feasibility and safety of rapamycin treatment in an older human cohort: Immunological, physical performance, and cognitive effects. Exp Gerontol 105:53-69
Ipson, B R; Fletcher, M B; Espinoza, S E et al. (2018) Identifying Exosome-Derived MicroRNAs as Candidate Biomarkers of Frailty. J Frailty Aging 7:100-103
Weiss, Roxanne; Fernandez, Elizabeth; Liu, Yuhong et al. (2018) Metformin reduces glucose intolerance caused by rapamycin treatment in genetically heterogeneous female mice. Aging (Albany NY) :
Qin, Kunhua; Zhang, Ning; Zhang, Zhao et al. (2018) SIRT6-mediated transcriptional suppression of Txnip is critical for pancreatic beta cell function and survival in mice. Diabetologia 61:906-918
Salmon, Adam B; Dorigatti, Jonathan; Huber, Hillary F et al. (2018) Maternal nutrient restriction in baboon programs later-life cellular growth and respiration of cultured skin fibroblasts: a potential model for the study of aging-programming interactions. Geroscience 40:269-278

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