Analyze Diet

Topic:Glycogen

Glycogen is a polysaccharide that serves as a primary form of energy storage in horses, predominantly found in the liver and muscle tissues. It acts as a readily available energy source that can be mobilized during periods of increased metabolic demand, such as exercise or stress. The synthesis and breakdown of glycogen are regulated by hormonal and enzymatic pathways, which are influenced by factors like diet, exercise, and overall health status. Understanding glycogen metabolism is important for optimizing performance, managing dietary needs, and preventing metabolic disorders in equine populations. This page compiles peer-reviewed research studies and scholarly articles that explore the role, regulation, and physiological implications of glycogen in equine health and performance.
A review of equine muscle disorders.
Neuromuscular disorders : NMD    April 9, 2008   Volume 18, Issue 4 277-287 doi: 10.1016/j.nmd.2008.01.001
Aleman M.Muscle disorders are a common cause of disability in horses. For many years, clinical manifestations such as muscle pain, exercise intolerance, weakness, and stiffness were believed to be caused by a single syndrome. However, in the past years a broad spectrum of muscle disorders have been recognized including glycogen and polysaccharide storage myopathies, malignant hyperthermia, mitochondrial myopathy, hyperkalemic periodic paralysis and others. For some, a specific mutation has been identified. Recognition of the myopathic clinical phenotype and thorough clinical, electrodiagnostic, and his...
Glycogen synthase (GYS1) mutation causes a novel skeletal muscle glycogenosis.
Genomics    March 20, 2008   Volume 91, Issue 5 458-466 doi: 10.1016/j.ygeno.2008.01.011
McCue ME, Valberg SJ, Miller MB, Wade C, DiMauro S, Akman HO, Mickelson JR.Polysaccharide storage myopathy (PSSM) is a novel glycogenosis in horses characterized by abnormal glycogen accumulation in skeletal muscle and muscle damage with exertion. It is unlike glycogen storage diseases resulting from known defects in glycogenolysis, glycolysis, and glycogen synthesis that have been described in humans and domestic animals. A genome-wide association identified GYS1, encoding skeletal muscle glycogen synthase (GS), as a candidate gene for PSSM. DNA sequence analysis revealed a mutation resulting in an arginine-to-histidine substitution in a highly conserved region of G...
Effects of dexamethasone administration on insulin resistance and components of insulin signaling and glucose metabolism in equine skeletal muscle.
American journal of veterinary research    January 3, 2008   Volume 69, Issue 1 51-58 doi: 10.2460/ajvr.69.1.51
Tiley HA, Geor RJ, McCutcheon LJ.To determine the effects of dexamethasone treatment on selected components of insulin signaling and glucose metabolism in skeletal muscle obtained from horses before and after administration of a euglycemic-hyperinsulinemic clamp (EHC). Methods: 6 adult Standardbreds. Methods: In a balanced crossover study, horses received either dexamethasone (0.08 mg/kg, IV, q 48 h) or an equivalent volume of saline (0.9% NaCl) solution, IV, for 21 days. A 2-hour EHC was administered for measurement of insulin sensitivity 1 day after treatment. Muscle biopsy specimens obtained before and after the EHC were a...
Estimated prevalence of polysaccharide storage myopathy among overtly healthy Quarter Horses in the United States.
Journal of the American Veterinary Medical Association    September 4, 2007   Volume 231, Issue 5 746-750 doi: 10.2460/javma.231.5.746
McCue ME, Valberg SJ.To estimate the prevalence of polysaccharide storage myopathy (PSSM) among Quarter Horses in the United States and evaluate possible relationships between muscle glycogen concentration, turnout time, and exercise level. Methods: Cross-sectional study. Methods: 164 overtly healthy Quarter Horses > 2 years old from 5 states. Methods: Horses with a history of exertional rhabdomyolysis or any other muscular disease were excluded. Muscle biopsy specimens were examined histologically for evidence of PSSM and were submitted for determination of muscle glycogen concentration. A diagnosis of PSSM wa...
Characterization of the equine glycogen debranching enzyme gene (AGL): Genomic and cDNA structure, localization, polymorphism and expression.
Gene    August 23, 2007   Volume 404, Issue 1-2 1-9 doi: 10.1016/j.gene.2007.07.034
Herszberg B, Mata X, Giulotto E, Decaunes P, Piras FM, Chowdhary BP, Chaffaux S, Guérin G.Glycogen debranching enzyme (AGL) is a multifunctional enzyme acting in the glycogen degradation pathway. In humans, the AGL activity deficiency causes a type III glycogen storage disease (Cori-Forbes disease). One particularity of AGL gene expression lies in the multiple alternative splicing in its 5' region. The AGL gene was localized on ECA5q14-q15. The sequence of the equine cDNA was determined to be 7.5 kb in length with an open reading frame of 4602 bp. The gene is 69 kb long and contains 35 exons. The equine AGL gene has an ubiquitous expression and presents five tissue-dependent cDNA v...
Time course of insulin sensitivity and skeletal muscle glycogen synthase activity after a single bout of exercise in horses.
Journal of applied physiology (Bethesda, Md. : 1985)    June 21, 2007   Volume 103, Issue 3 1063-1069 doi: 10.1152/japplphysiol.01349.2006
Pratt SE, Geor RJ, Spriet LL, McCutcheon LJ.The time course of insulin sensitivity, skeletal muscle glycogen and GLUT4 content, and glycogen synthase (GS) activity after a single bout of intense exercise was examined in eight horses. On separate days, a euglycemic-hyperinsulinemic clamp (EHC) was undertaken at 0.5, 4, or 24 h after exercise or after 48 h of rest [control (Con)]. There was no increase in mean glucose infusion rate (GIR) with exercise (0.5-, 4-, and 24-h trials), and GIR was significantly decreased at 0.5 h postexercise (GIR: 8.6 +/- 2.7, 6.7 +/- 2.0, 9.0 +/- 2.0, and 10.6 +/- 2.2 mg.kg(-1).min(-1) for Con and at 0.5, 4, ...
Effects of dietary glycaemic response after exercise on blood concentrations of substrates used indirectly for muscle glycogenesis.
Equine veterinary journal. Supplement    April 4, 2007   Issue 36 585-589 doi: 10.1111/j.2042-3306.2006.tb05609.x
Lacombe VA, Hinchcliff KW, Kohn CW, Reed SM, Taylor LE.Exercise depletes muscle glycogen stores, which could subsequently impair performance. Muscle glycogen replenishment is determined by substrate availability. Objective: To study the effects of feeding meals of varying glycaemic responses on blood concentrations of substrates used for glycogenesis in horses with exercise-induced glycogen depletion. Methods: In a 3-way crossover study, 7 horses received each of 3 isocaloric diets for 72 h after undergoing glycogen-depleting exercise: 1) a high soluble-carbohydrate diet, which induced a high-glycaemic (HGI) response; 2 and 3) a low soluble-carboh...
Synthesis of proglycogen and macroglycogen in skeletal muscle of standardbred trotters after intermittent exercise.
Equine veterinary journal. Supplement    April 4, 2007   Issue 36 335-339 doi: 10.1111/j.2042-3306.2006.tb05564.x
Bröjer J, Holm S, Jonasson R, Hedenström U, Essén-Gustavsson B.The degradation of glycogen and its two forms, proglycogen (PG) and macroglycogen (MG) has been studied in horses performing different types of exercise, but no information is available about the resynthesis of PG and MG after exercise. Objective: To determine the resynthesis of PG and MG in skeletal muscle after intermittent uphill exercise. Methods: At a training camp 9 well-trained Standardbred trotters performed a training session comprising a warm-up period, 7 repeated 500 m bouts of exercise on an uphill slope and a recovery period. Muscle biopsies (m. gluteus medius) for analysis of PG,...
Route of carbohydrate administration affects early post exercise muscle glycogen storage in horses.
Equine veterinary journal. Supplement    April 4, 2007   Issue 36 590-595 doi: 10.1111/j.2042-3306.2006.tb05610.x
Geor RJ, Larsen L, Waterfall HL, Stewart-Hunt L, McCutcheon LJ.No studies in horses have examined the effect of route of carbohydrate (glucose) administration on the rate of muscle glycogen storage following glycogen-depleting exercise. Objective: Glucose delivery from the gastrointestinal tract limits the rate of muscle glycogen storage following glycogen-depleting exercise. Methods: In a crossover design, 7 fit horses completed treadmill exercise (EX) on 3 occasions to deplete muscle glycogen by approximately 50%. After EX horses received: 1) i.v. glucose infusion (IV; 0.5 g/kg bwt/h for 6 h), 2) oral glucose boluses (OR; 1 g/kg bwt at 0, 2 and 4 h post...
Prevalence of polysaccharide storage myopathy in horses with neuromuscular disorders.
Equine veterinary journal. Supplement    April 4, 2007   Issue 36 340-344 doi: 10.1111/j.2042-3306.2006.tb05565.x
McCue ME, Ribeiro WP, Valberg SJ.Controversy exists as to the prevalence of polysaccharide storage myopathy (PSSM) in breeds of horses and its impact on performance. Objective: To determine 1) the prevalence of PSSM in horses that presented with a neuromuscular disorder, as well as breed, sex and age distributions and clinical signs 2) effect of diagnostic criteria on prevalence, breed distribution and age of horses diagnosed with PSSM. Methods: Fresh frozen biopsies (n = 1426) submitted to the Neuromuscular Diagnostic Laboratory at the University of Minnesota were searched to identify horses diagnosed with PSSM. Horses with ...
Recruitment pattern of muscle fibre type during flat and sloped treadmill running in thoroughbred horses.
Equine veterinary journal. Supplement    April 4, 2007   Issue 36 349-353 doi: 10.1111/j.2042-3306.2006.tb05567.x
Eto D, Yamano S, Hiraga A, Miyata H.There is little information about the muscle fibre recruitment pattern during sloped and flat track running in Thoroughbred horses. Objective: To examine the glycogen depletion pattern of each muscle fibre type during running on a flat and sloped treadmill. Methods: Thirteen Thoroughbred horses (3-9 years old) were used. They were initially subjected to incremental exercise tests on a treadmill at 10 and 0% inclines in each horse to determine running speed at 90 and 60% VO2max. Needle biopsy samples were obtained from the middle gluteal muscle immediately after the running at 90% VO2max for 4 ...
Glycaemic and insulinaemic response of quarter horses to concentrates high in fat and low in soluble carbohydrates.
Equine veterinary journal. Supplement    April 4, 2007   Issue 36 643-647 doi: 10.1111/j.2042-3306.2006.tb05619.x
Zeyner A, Hoffmeister C, Einspanier A, Gottschalk J, Lengwenat O, Illies M.Quarter Horses are particularly susceptible to polysaccharide storage myopathy (PSSM). Nutritional therapy and possibly prophylaxis includes fat-supplemented diets whilst starch supply should be kept to a minimum. Objective: To investigate the glycaemic and insulinaemic response of clinically normal Quarter Horses to concentrates high in fat and low in starch. Methods: Twelve Quarter Horses were studied. The precondition for inclusion in the study population was that the horses had not shown clinical signs of myopathy. The Quarter Horses were fed according to a 4 x 4 Latin square design haylag...
Effects of short-term training on insulin sensitivity and skeletal muscle glucose metabolism in standardbred horses.
Equine veterinary journal. Supplement    April 4, 2007   Issue 36 226-232 doi: 10.1111/j.2042-3306.2006.tb05544.x
Stewart-Hunt L, Geor RJ, McCutcheon LJ.Increased insulin sensitivity occurs after a period of exercise training, but the mechanisms underlying this training-associated increase in insulin action have not been investigated. Objective: To examine the effects of short-term endurance training (7 consecutive days) and a subsequent period of inactivity (5 days) on whole body insulin sensitivity and GLUT-4 protein and the activities of glycogen synthase (GS) and hexokinase (HK) in skeletal muscle. It was hypothesised that training would increase insulin sensitivity in association with increased GLUT-4 protein and activities of GS and HK, ...
Allele frequency and likely impact of the glycogen branching enzyme deficiency gene in Quarter Horse and Paint Horse populations.
Journal of veterinary internal medicine    October 27, 2006   Volume 20, Issue 5 1207-1211 doi: 10.1892/0891-6640(2006)20[1207:afalio]2.0.co;2
Wagner ML, Valberg SJ, Ames EG, Bauer MM, Wiseman JA, Penedo MC, Kinde H, Abbitt B, Mickelson JR.Glycogen Branching Enzyme Deficiency (GBED), a fatal condition recently identified in fetuses and neonatal foals of the Quarter Horse and Paint Horse lineages, is caused by a nonsense mutation in codon 34 of the GBE1 gene, which prevents the synthesis of a functional GBE protein and severely disrupts glycogen metabolism. The aims of this project were to determine the mutant GBE1 allele frequency in random samples from the major relevant horse breeds, as well as the frequency with which GBED is associated with abortion and early neonatal death using the tissue archives from veterinary diagnosti...
Proglycogen, macroglycogen, glucose, and glucose-6-phosphate concentrations in skeletal muscles of horses with polysaccharide storage myopathy performing light exercise.
American journal of veterinary research    September 5, 2006   Volume 67, Issue 9 1589-1594 doi: 10.2460/ajvr.67.9.1589
Bröjer JT, Essén-Gustavsson B, Annandale EJ, Valberg SJ.To determine concentrations of proglycogen (PG), macroglycogen (MG), glucose, and glucose-6-phosphate (G-6-P) in skeletal muscle of horses with polysaccharide storage myopathy (PSSM) before and after performing light submaximal exercise. Methods: 6 horses with PSSM and 4 control horses. Methods: Horses with PSSM completed repeated intervals of 2 minutes of walking followed by 2 minutes of trotting on a treadmill until muscle cramping developed. Four untrained control horses performed a similar exercise test for up to 20 minutes. Serum creatine kinase (CK) activity was measured before and 4 hou...
Development of polyglucosan inclusions in skeletal muscle.
Neuromuscular disorders : NMD    August 21, 2006   Volume 16, Issue 9-10 603-607 doi: 10.1016/j.nmd.2006.05.259
Valentine BA, Cooper BJ.Muscle samples from 24 horses with polysaccharide storage myopathy were stained with periodic acid-Schiff (PAS) stain and were immunostained for ubiquitin. Abnormalities detected with PAS stain were coarse granular cytoplasmic aggregates of amylase sensitive glycogen, subsarcolemmal aggregates of glycogen, central amylase sensitive bodies, and a variety of subsarcolemmal to intracytoplasmic amylase resistant polyglucosan inclusions. All amylase resistant inclusions were positive for ubiquitin. Ubiquitin was also detected in many amylase sensitive inclusions. Based on morphologic findings and p...
Ubiquitin expression in muscle from horses with polysaccharide storage myopathy.
Veterinary pathology    May 5, 2006   Volume 43, Issue 3 270-275 doi: 10.1354/vp.43-3-270
Valentine BA, Flint TH, Fischer KA.Serial sections of formalin-fixed, paraffin-embedded muscle biopsy specimens from 28 Quarter Horse, Paint, and draft-related breeds, aged 0.5-23 years, were treated with periodic acid-Schiff (PAS) stain for glycogen and were immunostained to detect ubiquitin expression. On the basis of findings in PAS-stained sections, a diagnosis of equine polysaccharide storage myopathy (EPSSM) was made in 22 horses aged 2-23 years (mean, 9.4 years); samples from 6 horses aged 0.5-15 years (mean, 7.3 years) had a normal PAS staining pattern, with no relevant lesions. Ubiquitin expression was detected in all ...
Ingestion of starch-rich meals after exercise increases glucose kinetics but fails to enhance muscle glycogen replenishment in horses.
Veterinary journal (London, England : 1997)    April 21, 2006   Volume 171, Issue 3 468-477 doi: 10.1016/j.tvjl.2005.02.002
Jose-Cunilleras E, Hinchcliff KW, Lacombe VA, Sams RA, Kohn CW, Taylor LE, Devor ST.Fatiguing exercise substantially decreases muscle glycogen concentration in horses, impairing athletic performance in subsequent exercise bouts. Our objective was to determine the effect of ingestion of starch-rich meals after exercise on whole body glucose kinetics and muscle glycogen replenishment. In a randomized, cross-over study seven horses with exercise-induced muscle glycogen depletion were either not fed for 8 h, fed half of the daily energy requirements ( approximately 15 Mcal DE) as hay, or fed an isocaloric amount of corn 15 min and 4 h after exercise. Starch-rich meals fed after e...
Neuromuscular disease associated with glycogen storage in a Spanish-bred filly.
The Veterinary record    April 18, 2006   Volume 158, Issue 15 513-516 doi: 10.1136/vr.158.15.513
Gil F, Alemán M, Rivero MA, Latorre R, Carrión MA, Aguirre C, Ruíz I, Ayala I.No abstract available
Histology, immunohistochemistry and ultrastructure of the tonsil of the soft palate of the horse.
Anatomia, histologia, embryologia    January 26, 2006   Volume 35, Issue 1 1-6 doi: 10.1111/j.1439-0264.2005.00622.x
Kumar P, Timoney JF.The tonsil of the soft palate was an oval, flat structure located centro-rostrally on the oral surface of the soft palate. Its stratified squamous non-keratinized epithelium was perforated by holes or small crypts the deeper parts of which were loosely spongiform inter-digitated with lymphoid tissue. These unusual features have not previously been reported in tonsils of any species. Crypts and reticulated epithelium as found in the lingual and palatine tonsils were not observed. Lectins showed varying affinities for specific layers of the epithelium. M cells were not observed. A few Langerhans...
Incidence of polysaccharide storage myopathy: necropsy study of 225 horses.
Veterinary pathology    November 23, 2005   Volume 42, Issue 6 823-827 doi: 10.1354/vp.42-6-823
Valentine BA, Cooper BJ.Muscle samples were obtained at necropsy from 225 horses and ponies 1 year of age or older. Samples were processed in routine manner and were stained with hematoxylin and eosin and with periodic acid-Schiff for glycogen. Sections were examined for abnormal glycogen content and amylase-resistant complex polysaccharide and for chronic myopathic change (excessive fiber size variation, increase in number of internal nuclei). A total of 101 horses and ponies with lesions of polysaccharide storage myopathy were identified. Age of affected horses ranged from one to 30 years, with a mean of 14.7 years...
Recruitment pattern of muscle fibre type during high intensity exercise (60-100% VO2max) in thoroughbred horses.
Research in veterinary science    June 29, 2005   Volume 80, Issue 1 109-115 doi: 10.1016/j.rvsc.2005.04.006
Yamano S, Eto D, Hiraga A, Miyata H.To consider the optimal training programme for Thoroughbred horses, we examined the recruitment pattern of muscle fibres including hybrid muscle fibres in well-trained Thoroughbred horses. The horses performed exercise at three different intensities and durations; i.e., 100% VO2max for 4 min, 80% and 60% VO2max for 8 min on a treadmill with 10% incline. Muscle samples were obtained from the middle gluteal muscle before, during (4 min at 80% and 60% VO2max), and after exercise. Four muscle fibre types (types I, IIA, IIA/IIX, and IIX) were immunohistochemically identified, and optical density of...
The opioid haemorphin-7 in horses during low-speed and high-speed treadmill exercise to fatigue.
Journal of veterinary medicine. A, Physiology, pathology, clinical medicine    May 11, 2005   Volume 52, Issue 4 162-165 doi: 10.1111/j.1439-0442.2005.00712.x
Collinder E, Nyberg F, Sanderson-Nydahl K, Gottlieb-Vedi M, Lindholm A.The opioid neuropeptide haemorphin-7 was measured, by immunoreactivity, in Standardbred horses during low-speed (7 m/s) and high-speed (10 m/s) endurance exercises, lasting 49-58 and 12-16 min respectively. In parallel, heart rate, muscle temperature and plasma lactate concentrations were measured. The profile of the low-speed exercise showed significantly increased heart rate after 10 min [154 beats per minute (bpm)]. After the exercise, muscle temperature (42.1 degrees C) and plasma lactate (4.8 mmol/l) were significantly increased. The profile of the high-speed exercise was comparatively ch...
Expression of equine glucose transporter type 4 in skeletal muscle after glycogen-depleting exercise.
American journal of veterinary research    April 13, 2005   Volume 66, Issue 3 379-385 doi: 10.2460/ajvr.2005.66.379
Jose-Cunilleras E, Hayes KA, Toribio RE, Mathes LE, Hinchcliff KW.To clone and sequence cDNA for equine insulin-responsive glucose transporter (glucose transporter type 4 [GLUT-4]) and determine effects of glycogen-depleting exercise and meal type after exercise on GLUT-4 gene expression in skeletal muscle of horses. Methods: Muscle biopsy specimens from 7 healthy adult horses. Methods: Total RNA was extracted from specimens, and GLUT-4 cDNA was synthesized and sequenced. Horses were exercised on 3 consecutive days. On the third day of exercise, for 8 hours after exercise, horses were either not fed, fed half of daily energy requirements as hay, or fed an is...
The effect of varying dietary starch and fat content on serum creatine kinase activity and substrate availability in equine polysaccharide storage myopathy.
Journal of veterinary internal medicine    January 11, 2005   Volume 18, Issue 6 887-894 doi: 10.1892/0891-6640(2004)182.0.co;2
Ribeiro WP, Valberg SJ, Pagan JD, Gustavsson BE.The effect of dietary starch and fat content on serum creatine kinase (CK) activity and substrate availability was evaluated in 4 mares of Quarter Horse-related breeds with polysaccharide storage myopathy (PSSM). Four isocaloric diets ranging in digestible energy (DE) from 21.2% (diet A), 14.8% (B), 8.4% (C), to 3.9% (D) for starch, and 7.2% DE (diet A), 9.9% (B), to 12.7% DE (diet C and D) for fat were fed for 6-week periods (4 weeks with exercise) using a 4 X 4 Latin square design. Postprandial glucose and insulin responses were measured, and 4 hours postexercise, serum CK activity, glucose,...
Insulin sensitivity and skeletal muscle glucose transport in horses with equine polysaccharide storage myopathy.
Neuromuscular disorders : NMD    September 8, 2004   Volume 14, Issue 10 666-674 doi: 10.1016/j.nmd.2004.05.007
Annandale EJ, Valberg SJ, Mickelson JR, Seaquist ER.Equine polysaccharide storage myopathy (PSSM) is an inherited disorder characterized by the accumulation of glycogen and abnormal polysaccharide in muscle with normal glyco(geno)lytic enzyme activities. The purpose of this study was to evaluate in vivo insulin sensitivity and glucose excursion in PSSM using a euglycemic hyperinsulinemic clamp. In addition, the content of muscle glucose transporters (GLUT1 and GLUT4) and the insulin receptor was determined in muscle biopsies using Western blot analysis. The glycogen content was 1.8-fold higher, and isolated polysaccharide analyzed by iodine abs...
Effects of feeding meals with various soluble-carbohydrate content on muscle glycogen synthesis after exercise in horses.
American journal of veterinary research    July 30, 2004   Volume 65, Issue 7 916-923 doi: 10.2460/ajvr.2004.65.916
Lacombe VA, Hinchcliff KW, Kohn CW, Devor ST, Taylor LE.To determine effects of feeding diets with various soluble-carbohydrate (CHO) content on rates of muscle glycogen synthesis after exercise in horses. Methods: 7 fit horses. Methods: In a 3-way crossover study, horses received each of 3 isocaloric diets (a high soluble CHO [HC] diet, a low soluble CHO [LC] diet, or a mixed soluble CHO [MC] diet). For each diet, horses were subjected to glycogen-depleting exercise, followed by feeding of the HC, LC, or MC diet at 8-hour intervals for 72 hours. Results: Feeding the HC diet resulted in a significantly higher glycemic response for 72 hours and sign...
Genetic mapping of GBE1 and its association with glycogen storage disease IV in American Quarter horses.
Cytogenetic and genome research    February 19, 2004   Volume 102, Issue 1-4 201-206 doi: 10.1159/000075749
Ward TL, Valberg SJ, Lear TL, Guérin G, Milenkovic D, Swinburne JE, Binns MM, Raudsepp T, Skow L, Chowdhary BP, Mickelson JR.Comparative biochemical and histopathological data suggest that a deficiency in the glycogen branching enzyme (GBE) is responsible for a fatal neonatal disease in Quarter Horse foals that closely resembles human glycogen storage disease type IV (GSD IV). Identification of DNA markers closely linked to the equine GBE1 gene would assist us in determining whether a mutation in this gene leads to the GSD IV-like condition. FISH using BAC clones as probes assigned the equine GBE1 gene to a marker deficient region of ECA26q12-->q13. Four other genes, ROBO2, ROBO1, POU1F1, and HTR1F, that flank GB...
Effects of exercise and glucose administration on content of insulin-sensitive glucose transporter in equine skeletal muscle.
American journal of veterinary research    December 16, 2003   Volume 64, Issue 12 1500-1506 doi: 10.2460/ajvr.2003.64.1500
Lacombe VA, Hinchcliff KW, Devor ST.To characterize insulin-sensitive glucose-transporter (GLUT-4) protein in equine tissues and determine effects of exercise and glucose administration on content of GLUT-4 protein in equine skeletal muscle. Methods: Tissue samples from 9 horses. Methods: Western blot analyses were performed on crude membrane preparations of equine tissues to characterize GLUT-4. In a crossover, randomized study, horses were strenuously exercised for 3 consecutive days and then administered 13.5% glucose or isotonic saline (0.9% NaCl; control) solution, i.v., at similar infusion rates for 12.1 hours. Samples wer...
Interactions of substrate availability, exercise performance, and nutrition with muscle glycogen metabolism in horses.
Journal of the American Veterinary Medical Association    December 11, 2003   Volume 223, Issue 11 1576-1585 doi: 10.2460/javma.2003.223.1576
Lacombe VA, Hinchcliff KW, Taylor LE.No abstract available