Abnormal Cardiac Development in the Absence of Heart Glycogen

REFERENCES

• Altman, P. L., and Dittmer D. S.. 1962. Growth including reproduction and morphological development. Federation of American Societies for Experimental Biology, Washington, D.C.
   Google Scholar
• Arad, M., Benson D. W., Perez-Atayde A. R., McKenna W. J., Sparks E. A., Kanter R. J., McGarry K., Seidman J. G., and Seidman C. E.. 2002. Constitutively active AMP kinase mutations cause glycogen storage disease mimicking hypertrophic cardiomyopathy. J. Clin. Investig. 109:357–362.
   PubMed Web of Science ®Google Scholar
• Arad, M., Moskowitz I. P., Patel V. V., Ahmad F., Perez-Atayde A. R., Sawyer D. B., Walter M., Li G. H., Burgon P. G., Maguire C. T., Stapleton D., Schmitt J. P., Guo X. X., Pizard A., Kupershmidt S., Roden D. M., Berul C. I., Seidman C. E., and Seidman J. G.. 2003. Transgenic mice overexpressing mutant PRKAG2 define the cause of Wolff-Parkinson-White syndrome in glycogen storage cardiomyopathy. Circulation 107:2850–2856.
   PubMed Web of Science ®Google Scholar
• Azpiazu, I., Saltiel A. R., DePaoli-Roach A. A., and Lawrence J. C.. 1996. Regulation of both glycogen synthase and PHAS-I by insulin in rat skeletal muscle involves mitogen-activated protein kinase-independent and rapamycin-sensitive pathways. J. Biol. Chem. 271:5033–5039.
   PubMedGoogle Scholar
• Bergmeyer, H. U., Berndt E., Schmidt F., and Stork H.. 1974. Glucose determination with hexokinase and glucose-6-phosphate dehydrogenase, p. 1196–1201. In Bergmeyer H. U. (ed.), Methods of enzymatic analysis, 2nd ed., vol. 3. Academic Press, Inc., New York, N.Y.
   Google Scholar
• Bernard, C. 1859. De la matiere glycogene consideree comme condition de developpement de certains tissues chez le foetus avant l'apparition de la fonction glycogenique de foie. C. R. Acad. Sci. 48:673–684.
   Google Scholar
• Bhavnani, B. R. 1983. Ontogeny of some enzymes of glycogen metabolism in rabbit fetal heart, lungs, and liver. Can. J. Biochem. Cell Biol. 61:191–197.
   PubMedGoogle Scholar
• Biggers, J. D., and Stern S.. 1973. Metabolism of the preimplantation mammalian embryo. Adv. Reprod. Physiol. 6:1–59.
   PubMedGoogle Scholar
• Bradford, M. M. 1976. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem. 72:248–254.
   PubMed Web of Science ®Google Scholar
• Butler, H., and Juurlink B. H. J.. 1987. An atlas for staging mammalian and chick embryos. CRC Press, Inc., Boca Raton, Fla.
   Google Scholar
• Clark, E. B. 2001. Etiology of congenital cardiovascular malformation: epidemiology and genetics, p. 2–9. In Allen H. D., Gutgesell H. G., Clark E. B., and Driscoll D. J. (ed.), Moss and Adams' heart disease in infants, children, and adolescents: including the fetus and young adult, 6th ed. Lippincott Williams & Wilkins, Philadelphia, Pa.
   Google Scholar
• Collins-Nakai, R. L., Noseworthy D., and Lopaschuk G. D.. 1994. Epinephrine increases ATP production in hearts by preferentially increasing glucose metabolism. Am. J. Physiol. 267:H1862–H1871.
   PubMedGoogle Scholar
• Crystal, R. G. 1997. The lung: scientific foundations, 2nd ed. Lippincott-Raven, Philadelphia, Pa.
   Google Scholar
• Dawes, G. S., Mott J. C., and Shelley H. J.. 1959. The importance of cardiac glycogen for the maintenance of life in foetal lambs and newborn animals during anoxia. J. Physiol. (London) 146:516–538.
   Google Scholar
• Dawes, G. S., and Shelley H. J.. 1968. Physiological aspects of carbohydrate metabolism in the foetus and newborn, p. 87–121. In Dickens F., Randle P. J., and Whelan W. S. (ed.), Carbohydrate metabolism and its disorders, vol. 2. Academic Press, Inc., New York, N.Y.
   Google Scholar
• Depre, C., Vanoverschelde J. L., and Taegtmeyer H.. 1999. Glucose for the heart. Circulation 99:578–588.
   PubMed Web of Science ®Google Scholar
• DiMauro, S., and Lamperti C.. 2001. Muscle glycogenoses. Muscle Nerve 24:984–999.
   PubMed Web of Science ®Google Scholar
• Edwards, J. A. 1968. The external development of the rabbit and rat embryo. Adv. Teratol. 3:239–262.
   Google Scholar
• Elpeleg, O. N. 1999. The molecular background of glycogen metabolism disorders. J. Pediatr. Endocrinol. Metab. 12:363–379.
   PubMedGoogle Scholar
• Elsasser, A., Schlepper M., Klovekorn W. P., Cai W. J., Zimmermann R., Muller K. D., Strasser R., Kostin S., Gagel C., Munkel B., Schaper W., and Schaper J.. 1997. Hibernating myocardium: an incomplete adaptation to ischemia. Circulation 96:2920–2931.
   PubMed Web of Science ®Google Scholar
• Fletterick, R. J., and Madsen N. B.. 1980. The structures and related functions of phosphorylase a. Annu. Rev. Biochem. 49:31–61.
   PubMed Web of Science ®Google Scholar
• Gilboe, D. P., Larson K. L., and Nuttall F. Q.. 1972. Radioactive method for the assay of glycogen phosphorylases. Anal. Biochem. 47:20–27.
   PubMed Web of Science ®Google Scholar
• Girard, J., Ferre P., Pegorier J. P., and Duee P. H.. 1992. Adaptations of glucose and fatty acid metabolism during perinatal period and suckling-weaning transition. Physiol. Rev. 72:507–562.
   PubMed Web of Science ®Google Scholar
• Goodwin, G. W., Ahmad F., Doenst T., and Taegtmeyer H.. 1998. Energy provision from glycogen, glucose, and fatty acids on adrenergic stimulation of isolated working rat hearts. Am. J. Physiol. 274:H1239–H1247.
   PubMed Web of Science ®Google Scholar
• Goodwin, G. W., Ahmad F., and Taegtmeyer H.. 1996. Preferential oxidation of glycogen in isolated working rat heart. J. Clin. Investig. 97:1409–1416.
   PubMed Web of Science ®Google Scholar
• Gutierrez-Correa, J., Hod M., Passoneau J. V., and Freinkel N.. 1991. Glycogen and enzymes of glycogen metabolism in rat embryos and fetal organs. Biol. Neonate 59:294–302.
   PubMedGoogle Scholar
• Henning, S. L., Wambolt R. B., Schonekess B. O., Lopaschuk G. D., and Allard M. F.. 1996. Contribution of glycogen to aerobic myocardial glucose utilization. Circulation 93:1549–1555.
   PubMedGoogle Scholar
• Hlastala, M. P., and Berger A. J.. 1996. Physiology of respiration. Oxford University Press, New York, N.Y.
   Google Scholar
• Hoffman, J. I., and Kaplan S.. 2002. The incidence of congenital heart disease. J. Am. Coll. Cardiol. 39:1890–1900.
   PubMed Web of Science ®Google Scholar
• Kaslow, H. R., and Lesikar D. D.. 1984. Isozymes of glycogen synthase. FEBS Lett. 172:294–298.
   PubMedGoogle Scholar
• Kaslow, H. R., Lesikar D. D., Antwi D., and Tan A. W.. 1985. L-type glycogen synthase. Tissue distribution and electrophoretic mobility. J. Biol. Chem. 260:9953–9956.
   PubMedGoogle Scholar
• Krege, J. H., Hodgin J. B., Hagaman J. R., and Smithies O.. 1995. A noninvasive computerized tail-cuff system for measuring blood pressure in mice. Hypertension 25:1111–1115.
   PubMed Web of Science ®Google Scholar
• Manchester, J., Skurat A. V., Roach P., Hauschka S. D., and Lawrence J. C., Jr. 1996. Increased glycogen accumulation in transgenic mice overexpressing glycogen synthase in skeletal muscle. Proc. Natl. Acad. Sci. USA 93:10707–10711.
   PubMed Web of Science ®Google Scholar
• Meeson, A. P., Radford N., Shelton J. M., Mammen P. P., DiMaio J. M., Hutcheson K., Kong Y., Elterman J., Williams R. S., and Garry D. J.. 2001. Adaptive mechanisms that preserve cardiac function in mice without myoglobin. Circ. Res. 88:713–720.
   PubMed Web of Science ®Google Scholar
• Roach, P. J., Skurat A. V., and Harris R. A.. 2001. Regulation of glycogen metabolism, p. 609–647. In Cherrington A. D. and Jefferson L. S. (ed.), The endocrine pancreas and regulation of metabolism, vol. 2. Oxford University Press, New York, N.Y.
   Google Scholar
• Rottman, J. N., Ni G., Khoo M., Wang Z., Zhang W., Anderson M. E., and Madu E. C.. 2003. Temporal changes in ventricular function assessed echocardiographically in conscious and anesthetized mice. J. Am. Soc. Echocardiogr. 16:1150–1157.
   PubMedGoogle Scholar
• Shelley, H. J. 1961. Cardiac glycogen in different species before and after birth. Br. Med. Bull. 17:137–156.
   Web of Science ®Google Scholar
• Skurat, A. V., Peng H. L., Chang H. Y., Cannon J. F., and Roach P. J.. 1996. Rate-determining steps in the biosynthesis of glycogen in COS cells. Arch. Biochem. Biophys. 328:283–288.
   PubMedGoogle Scholar
• Snyder, T. E., Weitlauf H. M., and Nelson S. R.. 1971. Comparison of the glycogen content of eggs in the uteri and oviducts of intact and hypophysectomized mice. Biol. Reprod. 5:314–318.
   PubMedGoogle Scholar
• Stern, S., and Biggers J. D.. 1968. Enzymatic estimation of glycogen in the cleaving mouse embryo. J. Exp. Zool. 168:61–66.
   PubMedGoogle Scholar
• Suzuki, Y., Lanner C., Kim J. H., Vilardo P. G., Zhang H., Yang J., Cooper L. D., Steele M., Kennedy A., Bock C. B., Scrimgeour A., Lawrence J. C., Jr., and DePaoli-Roach A. A.. 2001. Insulin control of glycogen metabolism in knockout mice lacking the muscle-specific protein phosphatase PP1G/RGL. Mol. Cell. Biol. 21:2683–2694.
   PubMed Web of Science ®Google Scholar
• Taegtmeyer, H. 1994. Energy metabolism of the heart: from basic concepts to clinical applications. Curr. Probl. Cardiol. 19:59–113.
   PubMed Web of Science ®Google Scholar
• Theiler, K. 1972. The house mouse: development and normal stages from fertilization to 4 weeks of age. Springer-Verlag KG, Berlin, Germany.
   Google Scholar
• Thomas, J. A., Schlender K. K., and Larner J.. 1968. A rapid filter paper assay for UDPglucose-glycogen glucosyltransferase, including an improved biosynthesis of UDP-14C-glucose. Anal. Biochem. 25:486–499.
   PubMed Web of Science ®Google Scholar
• Zambrowicz, B. P., Abuin A., Ramirez-Solis R., Richter L. J., Piggott J., BeltrandelRio H., Buxton E. C., Edwards J., Finch R. A., Friddle C. J., Gupta A., Hansen G., Hu Y., Huang W., Jaing C., Key B. W., Jr., Kipp P., Kohlhauff B., Ma Z. Q., Markesich D., Payne R., Potter D. G., Qian N., Shaw J., Schrick J., Shi Z. Z., Sparks M. J., Van Sligtenhorst I., Vogel P., Walke W., Xu N., Zhu Q., Person C., and Sands A. T.. 2003. Wnk1 kinase deficiency lowers blood pressure in mice: a gene-trap screen to identify potential targets for therapeutic intervention. Proc. Natl. Acad. Sci. USA 100:14109–14114.
   PubMed Web of Science ®Google Scholar
• Zambrowicz, B. P., Friedrich G. A., Buxton E. C., Lilleberg S. L., Person C., and Sands A. T.. 1998. Disruption and sequence identification of 2,000 genes in mouse embryonic stem cells. Nature 392:608–611.
   PubMed Web of Science ®Google Scholar