Grant Abstract: Muscle Regrowth during Physical Rehabilitation and Amino Acid Supplementation

Grant Number: 5K01HD057332-04
PI Name: Dreyer
Project Title: Muscle Regrowth during Physical Rehabilitation and Amino Acid Supplementation

Abstract: DESCRIPTION (provided by applicant): The purpose of this proposal is to further the candidate?s scientific development in translational and clinical research and to make possible his transition to become an independent translational scientist in rehabilitation. The University of Oregon provides an outstanding academic and research environment and infrastructure to facilitate the candidate?s education and training in the conduct of translational research. Career Goals: This award will support the candidate?s successful transition from a junior researcher into a mid level independent investigator by providing an array of formal and informal career development activities, and a research project for hands-on learning and acquisition of essential preliminary data under the supervision of an exceptional mentoring team. The specific short-term career goals will include training in muscle metabolism, stable isotope techniques and rehabilitation research; training in the responsible conduct of research and other standard scientific skills; performance of a research study for the acquirement of practical clinical research skills and of preliminary data for future research applications in rehabilitation science. The long-term scientific goal is for the candidate to become an expert in skeletal muscle metabolism and rehabilitation with continuous funding for medical research. Research Plan: The general hypothesis is that in older adults muscle regrowth after an acute musculoskeletal stress will be positively influenced by traditional physical rehabilitation, and further enhanced by nutritional supplementation. Using state-of-the-art stable isotope methodologies for the study of muscle metabolism and methodologies for the measurement of cell signaling, we will test the following specific hypotheses: 1a) To determine the effects of ischemia-reperfusion injury on cell signaling and gene expression in skeletal muscle during TKR surgery; 1b) To determine if acute changes in muscle cell signaling and gene expression correlate with muscle atrophy measured 2 weeks later by MRI; 2) To determine if muscle protein synthesis is acutely increased with the ingestion of EAA following TKA; 3) To determine the effects of EAA Supplementation during PT rehabilitation on muscle mass, strength, and function before and after TKA. Public Benefit: This research will focus rehabilitation efforts on specific and currently unresolved mechanisms responsible for muscle loss following total knee replacement in older adults. While knee pain due to bone arthritis is often alleviated after knee replacement, complete return of physical function and independence is difficult to achieve. This research will help to restore physical function and independence in the rapidly growing population of older adults with knee arthritis.

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