Role of excitatory aminoacids in neonatal hypoglycemia

Pediatrics International

Volumn 40, Issue 4, 1998, Pages 303-306

  Aral, Yusuf Ziya ^a   GÜcÜyener, Kİvİlcİm ^c   Atalay, YİLdİZ ^a   HasanoǦLu, Alev ^a   TÜRkyilmaz, Canan ^a   Sayal, Ahmet ^b   BiberoǦLu, GÜRsel ^a  

^a GAZI UNIVERSITY   (Turkey)

^b GULHANE SCHOOL OF MEDICINE   (Turkey)

^c NONE

Author keywords

Cerebrospinal fluid; Excitatory amino acids; Hypoglycemia; N methyl D aspartate; Newborn; Trace minerals

Indexed keywords

ASPARTIC ACID; COPPER ION; EXCITATORY AMINO ACID; GLUTAMIC ACID; MAGNESIUM ION; N METHYL DEXTRO ASPARTIC ACID RECEPTOR; ZINC ION;

ARTICLE; ATOMIC ABSORPTION SPECTROMETRY; BRAIN METABOLISM; CEREBROSPINAL FLUID LEVEL; CLINICAL ARTICLE; CONTROLLED STUDY; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; HYPOGLYCEMIA; NEUROTOXICITY; NEWBORN; NEWBORN DISEASE; PRIORITY JOURNAL;

ASPARTIC ACID; COPPER; EXCITATORY AMINO ACIDS; GLUTAMIC ACID; HUMANS; HYPOGLYCEMIA; INFANT, NEWBORN; MAGNESIUM; ZINC;

EID: 0031848637     PISSN: 13288067     EISSN: 1442200X     Source Type: Journal    
DOI: 10.1111/j.1442-200X.1998.tb01936.x     Document Type: Article

References (37)

1. Mann Li Developmental aspects and the effect of carbon dioxide tension on fetal cephalic blood flow. Exp. Neurol. 1970; 26: 136–41.
2. Jones Md, Burd Li, Makowski Ei, Meschia G., Battaglia Fc. Cerebral metabolism in sheep: A comparative study of the adult, the lamb and the fetus. Am. J. Phvsiol. 1975; 229: 235–9.
3. Levitsky Ll, Fisher De, Paton Kjb, Delonnoy Cw, Fasting plasma levels of glucose, acetoacetate, P-hydroxybutyrate, glycerol and lactate in the baboon infant: Correlation with cerebral uptake of substrates and oxygen. Pediatr. Res. 1977; 11: 198–202.
4. Gregoire Nm, Gjedde A., Plum F., Duffy Te. Cerebral blood flow and cerebral metabolic rates for oxygen, glucose and ketone bodies in newborn dogs. J. Neurochem. 1978; 30: 63–9.
5. Hernandez Mj, Brennan Rw, Vannucci Rc, Bowman Gs. Cerebral blood flow and oxygen consumption in the newborn dog. Am. J. Physiol. 1978; 234: R209–15.
6. Volpe Jj. Neurology of the Newborn. WB Saunders, Philadelphia, 1995; 467–89.
7. Vannucci Rc. Acute perinatal brain injury: Hypoxic ischemia. In: Cohen Wr, Acher Db, Friedman Ea (eds). Management of Labour. Rockville, Aspen Publishers, 1989; 183–244.
8. Dwek Hs, Cassady G. Glucose intolerance of infants of very low birth weight. Pediatrics 1974; 53: 189–95.
9. Cornblath M., Schwartz R. Disorders of Carbohydrate Metabolism in Infancy. WB Saunders, Philadelphia, 1976.
10. Choi Dw. Glutamate neurotoxicity and diseases of the nervous system. Neuron 1988; 1: 623–34.
11. Simon Rp, Schmidley Jw, Meldrum Bs, Swan Jh. Chapman Ag. Excitotoxic mechanisms in hypoglycaemic hippocampal injury. Neuropathol. Appl. Neurobiol. 1986; 12: 567–76.
12. Sandberg M., Butcher Sp, Hagberg H. Extracellular overflow of neuroactive amino acids during severe insulin-induced hypoglycemia: In vivo dialysis of the rat hippocampus. J. Neurochem. 1986; 47: 178–84.
13. Barks Jd, Silverstein Fs, Sims K., Greenamyre T., Johnston Mv. Glutamate recognition sites in human fetal brain. Neurosci. Lett. 1988; 84: 131–6.
14. Slater P. Simpson Mdl. Gilchrist Ac. Age-related changes in binding to excitatory amino acid uptake site in temporal cortex of human brain. Dev. Brain Res. 1992; 65: 157–60.
15. D'Souza Sw. Mcconnell S., Slater P. Barson Aj. N-methyl D aspartate binding sites in neonatal and adult brain. Lancet 1992; 339: 1240.
16. Greenamyre T., Penney Jb, Young Ab, Hudson C., Silverstein Fs, Johnston Mv. Evidence for transient perinatal glutamatergic innervation of globus pallidus. J. Neurosci. 1987; 7: 10 022–30.
17. Riikonen Rs. Kero Po, Simmcl Og. Excitatory amino acids in cerebrospinal fluid in neonatal asphyxia. Pediatr. Neurol. 1992; 8: 37–40.
18. Hagberg H. Thornberg E. Blennaw M. et al. Excitatory amino acids in the cerebrospinal fluid of asphyxiated infants: Relationship to hypoxic ischemic encephalopathy. Acta Paediatr. 1993; 82: 925–9.
19. Davey Jf. Ersser Rs. Amino acid analysis of physiological fluids by high performance liquid chromatography. J. Chroinatogr. 1990:528: 9–23.
20. Mckenzie T. Analytical data of the GTA 95. In: Rothery Analytical Methods for Graphite Tube Atomizer. Varian Tech-tron. Mulgrave. Australi. 1982: 25–48.
21. Sandberg M. NystÖM B. Hamberger A. Metabolically derived aspartate elevated extracellular levels in vivo in iodoacetate poisoning. J. Neurosci. Res. 1985; 13: 489–95.
22. Fagg Ge. Lane Jd. The uptake and release of putative amino-acid neurotransmitters. Neuroscience 1979; 4: 1015–36.
23. Wielsch T. Harris Rj. Symon L. SiesjÖ Bk. Influence of severe hypoglycemia on brain extracellular calcium and potassium activities, energy and phospholipid metabolism J. Neurochem. 1984:43: 160–8.
24. Drejer J. Beneveniste H., Diemer Nh, Schousboe E. Cellular origin of ischemia induced glutamate release from brain tissue in vivo and in vitro. J. Neurochem. 1985; 45: 145–51.
25. Agardh Cd, Westerberg E. SiesjÖ Bk. Severe hypoglycemia leads to accumulation of arachidonic acid in brain tissue. Acta Physiol. Stand. 1980; 109: 115–16.
26. Rhoads De. Osburn Lp. Peterson Na. Raghupathy E. Release of neurotransmitter amino acids from synaptosome enhancement of calcium-independent efflux of oleic and arachidonic acids. J. Neurochem. 1983; 41: 531–7.
27. Pery Tl, Hansen S., Kennedy I. CSF aminoacids and plasma-CSF amino acid ratios in adults. J. Neurochem. 1975; 24: 587–9.
28. ÖZta B., KÜÇÜK M., Sandalci U. Effect of insulin induced hypoglycemia on blood-brain barrier permeability. Exp. Neurol. 1985; 87: 129–36.
29. Hagberg H., Lehmann A., Sadberg M., NystrÖM B., Jacobson L., Hamberger A. Ischemia induced shift of inhibitory and excitatory amino acids from intra to extracellular compartments. J. Cereb. Blood Flow Metab. 1985; 5: 413–19.
30. Nadler Jv, Everson Da, Cuthbertson Gj. Comparative toxicity of kainic acid and other acidic aminoacids toward rat hippo-campal neurons Neuroscience 1981; 6: 2505–17.
31. Wieloch T. The aminoacid antagonist 2 amino-7-phosphono-heptanoic acid neuronal damage in the striatum due to hypoglycemia. Acta Physiol. Scand. 1995; 125 (Suppl.): 542.
32. Wieloch T., Engelsen B., Westerberg E., Auer R. Lesions of the glutamatergic cortio-striatal projections ameliorate hypoglycemic brain damage in the striatum. Neurosci. Lett. 1985; 58: 25–30.
33. Choi Dw. NMDA receptors and AMPA/kainate receptors mediate parallel injury oxygen-glucose deprivation. Progr. Brain Res. 1993:96: 137–43.
34. Novak L., Bregestovski P., Ascher P., Herbet A., Prochiantz A. Magnesium gates glutamate-activated channels in mouse central neurons. Nature 1984; 307: 462–5.
35. 2+ block at the N-methyl-D-aspartate receptor underlies receptor activation during inhibition of neuronal metabolism. J. Neurochem. 1992; 59: 1211–20.
36. 2+ toxicity is blocked by the N-methyl-D-aspartate antagonist MK-801 Proc. Natl Acad. Sci. USA 1988;85: 6556–60.
37. Burnashev N., Schoepfer R., Monyer H. Control by asparagine residues of calcium permeability and magnesium blockade in the NMDA receptor. Science 1992; 257: 1415–19.