This is a proposal to investigate the roles of lactate as an oxidizable substrate and gluconeogenic precursor during exercise. Our operating hypothesis is termed """"""""THE LACTATE SHUTTLE."""""""" We hypothesize that during exercise, lactate is formed at sites of high glycogenolysis and glycolysis and reaches sites of high cellular respiration and gluconeogenesis via the interstitium and plasma. Sites of production include fast glycolytic muscle fibers, fibers undergoing epinephrine stimulation,k and possibly, liver (glucagon stimulation). Removal sites include red skeletal muscle fibers, heart, and liver. Moreover, we hypothesize that lactate is a major gluconeogenic precursor essentially important for the maintenance of blood glucose homeostasis. Moreover we hypothesize that the lactate shuttle provides a mechanism through which metabolism within and between tissues is organized and regulated. In particular, we plan to study how acute and chronic exercise (training) affects the lactate shuttle. For these purposes, we propose a series of kinetic isotope tracer studies, as well as studies using infusion of unlabeled materials and blockers and inhibitors in laboratory rats. By this means we hope to elucidate the hormonal and other signals coordinating the shuttle mechanism. These studies will be complemented by studies using the techniques and approaches of exercise physiology and biochemistry. We plan to isolate sarcolemmal vesicles and to describe tissue differences and training effects on the lactate transporter. We plan also to determine if mitochondrial LDH differs between muscle fiber types and responds to training in ways to explain functioning of the lactate shuttle. Moreover, the activities of glycolytic, TCA cycle and electron transport chain enzyme and components in skeletal muscle, heart and liver will be studied in vitro to provide a mechanistic explanation of metabolite kinetics in vivo.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
2R01DK019577-09A4
Application #
3226455
Study Section
Respiratory and Applied Physiology Study Section (RAP)
Project Start
1990-04-01
Project End
1993-03-31
Budget Start
1990-04-01
Budget End
1991-03-31
Support Year
9
Fiscal Year
1990
Total Cost
Indirect Cost
Name
University of California Berkeley
Department
Type
Schools of Arts and Sciences
DUNS #
094878337
City
Berkeley
State
CA
Country
United States
Zip Code
94704
McClelland, Grant B; Khanna, Savita; Gonzalez, Gilda F et al. (2003) Peroxisomal membrane monocarboxylate transporters: evidence for a redox shuttle system? Biochem Biophys Res Commun 304:130-5
Brooks, G A (2002) Lactate shuttles in nature. Biochem Soc Trans 30:258-64
McClelland, Grant B; Brooks, George A (2002) Changes in MCT 1, MCT 4, and LDH expression are tissue specific in rats after long-term hypobaric hypoxia. J Appl Physiol 92:1573-84
Trimmer, J K; Casazza, G A; Horning, M A et al. (2001) Autoregulation of glucose production in men with a glycerol load during rest and exercise. Am J Physiol Endocrinol Metab 280:E657-68
Trimmer, J K; Casazza, G A; Horning, M A et al. (2001) Recovery of (13)CO2 during rest and exercise after [1-(13)C]acetate, [2-(13)C]acetate, and NaH(13)CO3 infusions. Am J Physiol Endocrinol Metab 281:E683-92
Bergman, B C; Horning, M A; Casazza, G A et al. (2000) Endurance training increases gluconeogenesis during rest and exercise in men. Am J Physiol Endocrinol Metab 278:E244-51
Brooks, G A (2000) Intra- and extra-cellular lactate shuttles. Med Sci Sports Exerc 32:790-9
Dubouchaud, H; Butterfield, G E; Wolfel, E E et al. (2000) Endurance training, expression, and physiology of LDH, MCT1, and MCT4 in human skeletal muscle. Am J Physiol Endocrinol Metab 278:E571-9
Liu, J; Yeo, H C; Overvik-Douki, E et al. (2000) Chronically and acutely exercised rats: biomarkers of oxidative stress and endogenous antioxidants. J Appl Physiol 89:21-8
Brooks, G A; Dubouchaud, H; Brown, M et al. (1999) Role of mitochondrial lactate dehydrogenase and lactate oxidation in the intracellular lactate shuttle. Proc Natl Acad Sci U S A 96:1129-34

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