Muscle‐specific VEGF deficiency greatly reduces exercise endurance in mice

Vascular endothelial growth factor (VEGF) is required for vasculogenesis and angiogenesis during embryonic and early postnatal life. However the organ‐specific functional role of VEGF in adult life, particularly in skeletal muscle, is less clear. To explore this issue, we engineered skeletal muscle‐targeted VEGF deficient mice (mVEGF−/−) by crossbreeding mice that selectively express Cre recombinase in skeletal muscle under the control of the muscle creatine kinase promoter (MCKcre mice) with mice having a floxed VEGF gene (VEGFLoxP mice). We hypothesized that VEGF is necessary for regulating both cardiac and skeletal muscle capillarity, and that a reduced number of VEGF‐dependent muscle capillaries would limit aerobic exercise capacity. In adult mVEGF−/− mice, VEGF protein levels were reduced by 90 and 80% in skeletal muscle (gastrocnemius) and cardiac muscle, respectively, compared to control mice (P < 0.01). This was accompanied by a 48% (P < 0.05) and 39% (P < 0.05) decreases in the capillary‐to‐fibre ratio and capillary density, respectively, in the gastrocnemius and a 61% decrease in cardiac muscle capillary density (P < 0.05). Hindlimb muscle oxidative (citrate synthase, 21%; β‐HAD, 32%) and glycolytic (PFK, 18%) regulatory enzymes were also increased in mVEGF−/− mice. However, this limited adaptation to reduced muscle VEGF was insufficient to maintain aerobic exercise capacity, and maximal running speed and endurance running capacity were reduced by 34% and 81%, respectively, in mVEGF−/− mice compared to control mice (P < 0.05). Moreover, basal and dobutamine‐stimulated cardiac function, measured by transthoracic echocardiography and left ventricular micromanomtery, showed only a minimal reduction of contractility (peak +dP/dt) and relaxation (peak –dP/dt, τE). Collectively these data suggests adequate locomotor muscle capillary number is important for achieving full exercise capacity. Furthermore, VEGF is essential in regulating postnatal muscle capillarity, and that adult mice, deficient in cardiac and skeletal muscle VEGF, exhibit a major intolerance to aerobic exercise.

[1]  S. Jalava,et al.  Exercise-induced expression of angiogenic growth factors in skeletal muscle and in capillaries of healthy and diabetic mice , 2008, Cardiovascular diabetology.

[2]  M. Polkey,et al.  Cytokine profile in quadriceps muscles of patients with severe COPD , 2007, Thorax.

[3]  Kenneth P. Roos,et al.  Autocrine VEGF Signaling Is Required for Vascular Homeostasis , 2007, Cell.

[4]  M. Polkey,et al.  CYTOKINE PROFILE IN QUADRICEPS MUSCLES OF PATIENTS WITH SEVERE CHRONIC OBSTRUCTIVE PULMONARY DISEASE , 2007 .

[5]  Betty Y. Y. Tam,et al.  VEGF-dependent plasticity of fenestrated capillaries in the normal adult microvasculature. , 2006, American journal of physiology. Heart and circulatory physiology.

[6]  H. T. Yang,et al.  What makes vessels grow with exercise training? , 2004, Journal of applied physiology.

[7]  K. Tang,et al.  Capillary regression in vascular endothelial growth factor-deficient skeletal muscle. , 2004, Physiological genomics.

[8]  Gavin Thurston,et al.  Age-Related Changes in Vascular Endothelial Growth Factor Dependency and Angiopoietin-1–Induced Plasticity of Adult Blood Vessels , 2004, Circulation research.

[9]  Yusu Gu,et al.  The cardiovascular physiologic actions of urocortin II: acute effects in murine heart failure. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[10]  N. Ferrara,et al.  The biology of VEGF and its receptors , 2003, Nature Medicine.

[11]  R. A. Howlett,et al.  Selected contribution: skeletal muscle capillarity and enzyme activity in rats selectively bred for running endurance. , 2003, Journal of applied physiology.

[12]  H. T. Yang,et al.  Exercise-Induced Vascular Remodeling , 2003, Exercise and sport sciences reviews.

[13]  P. Wagner,et al.  Skeletal muscle capillarity and angiogenic mRNA levels after exercise training in normoxia and chronic hypoxia. , 2001, Journal of applied physiology.

[14]  Yusu Gu,et al.  A cardiac myocyte vascular endothelial growth factor paracrine pathway is required to maintain cardiac function , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[15]  J. Gea,et al.  Metabolic characteristics of the deltoid muscle in patients with chronic obstructive pulmonary disease. , 2001, The European respiratory journal.

[16]  J. DiMaio,et al.  Adaptive Mechanisms That Preserve Cardiac Function in Mice Without Myoglobin , 2001, Circulation research.

[17]  Christopher J. Robinson,et al.  The splice variants of vascular endothelial growth factor (VEGF) and their receptors. , 2001, Journal of cell science.

[18]  P. Wagner,et al.  Structural basis of muscle O(2) diffusing capacity: evidence from muscle function in situ. , 2000, Journal of applied physiology.

[19]  S. Mudaliar,et al.  Human VEGF gene expression in skeletal muscle: effect of acute normoxic and hypoxic exercise. , 1999, American journal of physiology. Heart and circulatory physiology.

[20]  U. Flögel,et al.  Disruption of myoglobin in mice induces multiple compensatory mechanisms. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[21]  M Aguet,et al.  VEGF is required for growth and survival in neonatal mice. , 1999, Development.

[22]  T. Gustafsson,et al.  Exercise-induced expression of angiogenesis-related transcription and growth factors in human skeletal muscle. , 1999, American journal of physiology. Heart and circulatory physiology.

[23]  D. Pode,et al.  Selective ablation of immature blood vessels in established human tumors follows vascular endothelial growth factor withdrawal. , 1999, The Journal of clinical investigation.

[24]  N. Ferrara,et al.  Role of Vascular Endothelial Growth Factor in Regulation of Angiogenesis , 1999 .

[25]  C. Kahn,et al.  A muscle-specific insulin receptor knockout exhibits features of the metabolic syndrome of NIDDM without altering glucose tolerance. , 1998, Molecular cell.

[26]  Daniel J. Garry,et al.  Mice without myoglobin , 1998, Nature.

[27]  J. Ross,et al.  Transthoracic echocardiography in models of cardiac disease in the mouse. , 1996, Circulation.

[28]  P. Wagner,et al.  Angiogenic growth factor mRNA responses in muscle to a single bout of exercise. , 1996, Journal of applied physiology.

[29]  Lieve Moons,et al.  Abnormal blood vessel development and lethality in embryos lacking a single VEGF allele , 1996, Nature.

[30]  Kenneth J. Hillan,et al.  Heterozygous embryonic lethality induced by targeted inactivation of the VEGF gene , 1996, Nature.

[31]  K. Groebe,et al.  Calculated intra- and extracellular PO2 gradients in heavily working red muscle. , 1990, The American journal of physiology.

[32]  J. Billadello,et al.  Tissue-specific distribution and developmental regulation of M and B creatine kinase mRNAs. , 1990, Biochimica et biophysica acta.

[33]  Daniel L. Feeback,et al.  A metachromatic dye-ATPase method for the simultaneous identification of skeletal muscle fiber types I, IIA, IIB and IIC. , 1990, Stain technology.

[34]  T. Scherstén,et al.  Muscle enzyme adaptation in patients with peripheral arterial insufficiency: spontaneous adaptation, effect of different treatments and consequences on walking performance. , 1989, Clinical science.

[35]  J. Derenne,et al.  Metabolic enzymatic activities in the intercostal and serratus muscles and in the latissimus dorsi of middle-aged normal men and patients with moderate obstructive pulmonary disease. , 1988, The European respiratory journal.

[36]  C. Sylvén,et al.  Calf muscle adaptation in intermittent claudication. Side-differences in muscle metabolic characteristics in patients with unilateral arterial disease. , 1988, Clinical physiology.

[37]  M. Grim,et al.  Enzymatic heterogeneity of the capillary bed of rat skeletal muscles. , 1986, The American journal of anatomy.

[38]  C. Honig,et al.  O2 gradients from sarcolemma to cell interior in red muscle at maximal VO2. , 1986, The American journal of physiology.

[39]  E. Coyle,et al.  Adaptations of skeletal muscle to endurance exercise and their metabolic consequences. , 1984, Journal of applied physiology: respiratory, environmental and exercise physiology.

[40]  O. H. Lowry,et al.  Enzyme patterns in single human muscle fibers. , 1978, The Journal of biological chemistry.

[41]  J P Jacky,et al.  A plethysmograph for long-term measurements of ventilation in unrestrained animals. , 1978, Journal of applied physiology: respiratory, environmental and exercise physiology.

[42]  M. Danson,et al.  Citrate synthase. , 2020, Current topics in cellular regulation.

[43]  J. Folkman The vascularization of tumors. , 1976, Scientific American.

[44]  J. Holloszy Adaptations of muscular tissue to training. , 1976, Progress in cardiovascular diseases.

[45]  J. Holm,et al.  Enzyme activities in skeletal muscles from patients with peripheral arterial insufficiency. , 1976, European journal of clinical investigation.

[46]  P. Srere,et al.  [1] Citrate synthase. [EC 4.1.3.7. Citrate oxaloacetate-lyase (CoA-acetylating)] , 1969 .

[47]  W. O. Fenn,et al.  A barometric method for measuring ventilation in newborn infants. , 1955, Pediatrics.