INFLUENCE OF ACUTE HYPERGLYCAEMIA ON THE AMPLITUDE OF NOCICEPTIVE SPINAL EVOKED POTENTIALS IN HEALTHY RATS

REFERENCES

• Chey Wx˙ D., Kim M., Hasler Wx˙ L., Owyang C. Hyperglycemia alters perception of rectal distension and blunts the rectoanal inhibitory reflex in healthy volunteers. Gastroenterology 1995; 108(6)1700–1708
   PubMedGoogle Scholar
• Chistyakov A., Soustiel J. F., Hafner H., Kaplan B., Feinsod M. The value of motor and somatosensory evoked potentials in evaluation of cervical myelopathy in the presence of peripheral neuropathy. Spine 2004; 29(12)E239–E247
   PubMedGoogle Scholar
• Dull S. T., Konrad P. E., Taker W. A., Jr. Amplitude and latency characteristics of spinal cord motor evoked potentials in rat. Electroencephalography and Clinical Neurophysiology 1990; 77(1)68–76
   PubMedGoogle Scholar
• Dyck P. J., Lambert E. H., Windebank A. J., Lais A. A., Sparks M. F., Karnes J., Sherman W. R., Hallcher L. M., Low P. A., Service F. J. Acute hyperosmolar hyperglycemia causes axonal shrinkage and reduced nerve conduction velocity. Experimental Neurology 1981; 71(3)507–514
   PubMedGoogle Scholar
• Galik J., Conway C. Evoked potentials: Principles and techniques. Kopf Carrier 1997, February; 48: 1–5
   Google Scholar
• Gilmore J., Fedirchuk B. The excitability of lumbar motoneurones in the neonatal rat is increased by a hyperpolarization of their voltage threshold for activation by descending serotonergic fibres. The Journal of Physiology 2004; 558: 213–224
   PubMedGoogle Scholar
• Halonen J. P., Rönnemaa T. Peripheral nerve conduction in healthy subjects during short-term hyperglycemia. Electromyography and Clinical Neurophysiology 1998; 38(6)355–358
   PubMedGoogle Scholar
• Kikkawa Y., Misawa S., Tamura N., Kitano Y., Ogawara K., Hattori T. The acute effects of glycemic control on nerve conduction in human diabetics. Clinical Neurophysiology 2005; 116(2)270–274
   PubMedGoogle Scholar
• Kitano Y., Kuwabara S., Misawa S., Ogawara K., Kanai K., Kikkawa Y., Yagui K, Hattori T. The acute effects of glycemic control on axonal excitability in human diabetics. Annals of Neurology 2004; 56(4)462–467
   PubMedGoogle Scholar
• Maruyama Y., Shimoji K., Shimizu H., Kuribayashi H., Fujioka H. Human spinal cord potentials evoked by different sources of stimulation and conduction velocities along the cord. Journal of Neurophysiology 1982; 48(5)1098–1107
   PubMedGoogle Scholar
• McGovern P. J., Jr, Machiedo G. W., Rush B. F., Jr. The effect of pH of resuscitative fluids in treatment of severe hemorrhagic shock. Advances in Shock Research 1981; 5: 133–141
   PubMedGoogle Scholar
• Mercado F., Vega R., Soto E. Ion channels that are sensitive to the extracellular concentration of protons: Their structure, function, pharmacology and pathophysiology. Revista de Neurologia 2005; 41(11)667–675
   PubMedGoogle Scholar
• Misawa S., Kuwabara S., Ogawara K., Kitano Y., Hattori T. Strength-duration properties and glycemic control in human diabetic motor nerves. Clinical Neurophysiology 2005; 116(2)254–258
   PubMedGoogle Scholar
• Ola M. S., Berkich D. A., Xu Y., King M. T., Gardner T. W., Simpson I., Lanoue K. F. Analysis of glucose metabolism in diabetic rat retinas. American Journal of Physiology, Endocrinology and Metabolism 2005; 290(6)E1057–1067
   Google Scholar
• Orskov L., Worm M., Schmitz O., Mengel A., Sidenius P. Nerve conduction velocity in man: Influence of glucose, somatostatin and electrolytes. Diabetologia 1994; 37(12)1216–1220
   PubMedGoogle Scholar
• Padnick-Silver L., Linsenmeier R. A. Effect of hypoxemia and hyperglycemia on pH in the intact cat retina. Archives Ophthalmology 2005; 123(12)1684–1690
   PubMedGoogle Scholar
• Pleasure D. E. Biochemistry of neuropathy. Basic neurochemistry, G. J. Siegel, B. W. Agranoff, R. W. Albers, P. B. Molinoff. Raven Press, New York 1993; 768–769
   Google Scholar
• Quasthoff S. The role of axonal ion conductances in diabetic neuropathy: A review. Muscle & Nerve 1998; 21(10)1246–1255
   PubMedGoogle Scholar
• Ramakrishnan R., Sheeladevi R., Suthanthirarajan N., Namasivayam A. An acute hyperglycemia or acidosis-induced changes of indolamines level correlates with PKC-alpha expression in rat brain. Brain Research Bulletin 2005; 67(1–2)46–52
   PubMedGoogle Scholar
• Russo A., Smout A. Jx˙ Px˙ M., Kositchaiwat C., Rayner C., Sattawatthamrong Y., Semmler J., Horowitz M., Sun W. M. The effect of hyperglycaemia on cerebral potentials evoked by rapid rectal distension in healthy humans. European Journal of Clinical Investigation 1999; 29(6)512–518
   PubMedGoogle Scholar
• Sannita W. G., Fatone M., Garbarino S., Giglioli D., Massimilla S., Riela S. Effects of physiological changes of serum glucose on the pattern-VEP of healthy volunteers. Physiology & Behavior 1995; 58(5)1021–1026
   PubMedGoogle Scholar
• Shimoji K. Origins and properties of spinal cord evoked potentials. Atlas of human spinal cord evoked potentials, M. R. Dimitrijević, J. A. Halter. Butterworth-Heinemann, Washington 1995; 1–25
   Google Scholar
• Sindrup S. H., Ejlertsen B., Gjessing H., Froland A., Sindrup E. H. Peripheral nerve function during hyperglycemic clamping in healthy subjects. Acta Neurologica Scandinavica 1988; 78(2)141–145
   PubMedGoogle Scholar
• Waldmann R., Bassilana F., Heurteaux C., Lazdunski M. A proton-gated cation channel involved in acid-sensing. Nature 1997; 386(6621)173–177
   PubMed Web of Science ®Google Scholar
• Yeap B. B., Russo A., Fraser R. J., Wittert G. A., Horowitz M. Hyperglycemia affects cardiovascular autonomic nerve function in normal subjects. Diabetes Care 1996; 19(8)880–882
   PubMedGoogle Scholar