Temporary Suppression of the Hyperglycemic Response to 2-Deoxy-d-Glucose by Blinding

References

• Nagai K., Yamamoto H., Nakagawa H. Time-dependent hyperglycemic actions of centrally administered 2-deoxy-d-glucose, d-mannitol, and d-glucose. Biomedical Res 1982; 3: 288–293
   Google Scholar
• Mori T., Nagai K., Hara M., Nakagawa H. Time-dependent effect of insulin in suprachiasmatic nucleus on blood glucose. Am J Physiol 1985; 249: R23–R30
   Google Scholar
• Yamamoto H., Nagai K., Nakagawa H. Role of the suprachiasmatic nucleus in glucose homeostasis. Biomedical Res 1984; 5: 55–60
   Google Scholar
• Yamamoto H., Nagai K., Nakagawa H. Additional evidence that the suprachiasmatic nucleus is the center for regulation of insulin secretion and glucose homeostasis. Brain Res 1984; 304: 237–241
   PubMed Web of Science ®Google Scholar
• Rusak B., Zucker I. Neural regulation of circadian rhythm. Phsyiol Rev 1979; 59: 449–526
   PubMed Web of Science ®Google Scholar
• Moore-Ede M. C., Sulzman F. M., Fuller C. A. The Clocks That Time Us: Physiology of the Circadian Timing System. Harvard University Press, Cambridge 1982
   Google Scholar
• Nagai K., Nishio T., Nakagawa H., Nakamura S., Fukuda Y. Effect of bilateral lesions of the suprachiasmatic nuclei on the circadian rhythm of food-intake. Brain Res 1978; 142: 384–389
   PubMed Web of Science ®Google Scholar
• Altaffer F. B., De Balbian Verster F., Hall S., Long C. J., D'encarnacao P. A simple and inexpensive cannula technique for chemical stimulation of the brain. Physiol Behav 1970; 5: 119–121
   PubMed Web of Science ®Google Scholar
• Steffens A. B. A method for frequent sampling of blood and continuous infusion of fluids in the rat without disturbing the animal. Physiol Behav 1969; 4: 833–836
   Web of Science ®Google Scholar
• Yamamoto H., Nagai K., Nakagawa H. Bilateral lesions of the suprachiasmatic nucleus enhance glucose tolerance in rats. Biomedical Res 1984; 5: 47–54
   Google Scholar
• Yamamoto H., Nagai K., Nakagawa H. Bilateral lesions of the SCN abolish lipolytic and hyperphagic responses to 2DG. Physiol Behav 1984; 32: 1017–1020
   PubMed Web of Science ®Google Scholar
• Yamamoto H., Nagai K., Nakagawa H. Lesions involving the suprachiasmatic nucleus eliminate the glucagon response to intracranial injection of 2-deoxy-d-glucose. Endocrinology 1985; 117: 468–473
   PubMed Web of Science ®Google Scholar
• Stephan F. K., Zucker I. Circadian rhythms in drinking behavior and locomotor activity of rats are eliminated by hypothalamic lesions. Proc Natl Acad Sci USA 1972; 69: 1583–1586
   PubMed Web of Science ®Google Scholar
• Moore R. Y., Eichler V. B. Loss of a circadian adrenal corticosterone rhythm following suprachiasmatic lesions in the rat. Brain Res 1972; 42: 201–206
   PubMed Web of Science ®Google Scholar
• Inouye S. T., Kawamura H. Persistence of circadian rhythmicity in a mammalian hypothalamic “island” containing the suprachiasmatic nucleus. Proc Natl Acad Sci USA 1979; 76: 5962–5966
   PubMed Web of Science ®Google Scholar
• Nagai K., Mori T., Nakagawa H. Application of an immunological technique to behavioral studies: Anti-supra- chiasmatic nucleus γ-globulin induced loss of the circadian rhythm. Biomed Res 1982; 3: 294–302
   Web of Science ®Google Scholar
• Schwartz W. J., Gainer H. Suprachiasmatic nucleus: Use of 14C-labeled deoxyglucose uptake as a functional marker. Science 1977; 197: 1089–1091
   PubMed Web of Science ®Google Scholar
• Shibata S., Liou S. Y., Ueki S., Oomura Y. Influence of environmental light-dark cycle and enucleation on activity of suprachiasmatic neurons in slice preparations. Brain Res 1984; 302: 75–81
   PubMed Web of Science ®Google Scholar
• Nakagawa H., Nagai K., Kida K., Nishio T. Control mechanism of circadian rhythms of feeding behavior and metabolism influenced by food intake. Biological Rhythms and Their Central Mechanism, M. Suda, O. Hayaishi, H. Nakagawa. Elsevier/North-Holland Biomedical Press, Amsterdam 1979; 283–294
   Google Scholar
• Nishio T., Shiosaka S., Nakagawa H., Sakumoto T., Satoh K. Circadian feeding rhythm after hypothalamic knifecut isolating suprachiasmatic nucleus. Physiol Behav 1979; 23: 763–769
   PubMed Web of Science ®Google Scholar
• Kita H., Shibata S., Oomura Y., Ohki K. Excitatory effects fo the suprachiasmatic nucleus on the ventromedial nucleus in the rat hypothalamic slice. Brain Res 1982; 235: 137–141
   PubMed Web of Science ®Google Scholar
• Oomura Y., Ono T., Nishino H., Kita H., Shimizu N., Ishizuka S., Sasaki K. Hypothalamic control of feeding behavior: Modulation by the suprachiasmatic nucleus. Biological Rhythms and Their Central Mechanism, M. Suda, O. Hayaishi, H. Nakagawa. Elsevier//North-Holland Biomedical Press, Amsterdam 1979; 283–294
   Google Scholar
• Bray G. A., York D. A. Hypothalamic and genetic obesity in experimental animals: An autonomic and endocrine hypothesis. Physiol Rev 1979; 59: 719–809
   PubMed Web of Science ®Google Scholar
• Frohman L. A. Hypothalamic control of metabolism. Handbook of The Hypothalamus, P. J. Morgane, J. Panksepp. Marcel Dekker, New York and Basel 1980; Vol. 2: 519–555, Physiology of the Hypothalamus
   Google Scholar
• Rohner-Jeanrenaud F., Bobioni E., Ionescu E., Sauter J-F., Jeanrenaud B. Central nervous system regulation of insulin secretion. Advances in Metabolic Disorders, A. J. Szabo. Academic Press, New York 1983; Vol. 10: 193–220, CNS Regulation of Carbohydrate Metabolism.
   Google Scholar
• Shimazu T. Reciprocal innervation of the liver: Its significance in metabolic control. Advances in Metabolic Disorders, A. J. Szabo. Academic Press, New York 1983; Vol. 10: 355–384, CNS Regulation of Carbohydrate Metabolism.
   Google Scholar
• Moore R. Y., Lenn N. J. A retinohypothalamic projection in the rat. J Comp Neurol 1972; 146: 1–14
   PubMed Web of Science ®Google Scholar
• Shibata S., Oomura Y., Kita H., Liou S. Y., Ueki S. Field potentials in the suprachiasmatic nucleus of rat hypo-thalmic slice produced by optic nerve stimulation. Brain Res Bull 1984; 12: 377–379
   PubMed Web of Science ®Google Scholar