Manganese and Epilepsy: Brain Glutamine Synthetase and Liver Arginase Activities in Genetically Epilepsy Prone and Chronically Seizured Rats

Summary: Low blood manganese (Mn2+) concentration is associated with epilepsy in humans and rats. The low Mn2+ concentration is attributed by some investigators to the seizure activity associated with the epilepsy, whereas others propose that the low Mn2+ concentration may be secondary to genetic mechanisms underlying the epilepsy. To begin to differentiate between these possibilities, Mn2+‐binding enzymes of liver and brain (i.e., arginase and glutamine synthetase, respectively) were assayed in rats exposed to chronically induced seizures and in genetically epilepsy‐prone rats (GEPRs). Chronic seizures caused a decrease in whole blood Mn2+ levels but did not affect brain Mn2+ concentrations. Arginase activity was increased in livers of rats with chronic seizure as compared with controls, but this difference was eliminated when Mn2+ was added to the assay. Brain glutamine synthetase activity was unaffected by chronic seizures, but the activity of this enzyme was significantly lower in GEPR brain than in control brain. Liver arginase activity tended to be lower in GEPRs, although the difference was not statistically significant. These data indicate that seizures affect liver arginase activity through changes in liver Mn2+ concentration, but GEPRs show abnormalities in Mn2+ ‐dependent enzymes apparently independent of seizure activity.

[1]  C. Keen,et al.  Analysis of whole blood manganese by flameless atomic absorption spectrophotometry and its use as an indicator of manganese status in animals. , 1986, Analytical biochemistry.

[2]  P. Laming,et al.  Seizures in the Mongolian gerbil are related to a deficiency in cerebral glutamine synthetase. , 1989, Comparative biochemistry and physiology. C, Comparative pharmacology and toxicology.

[3]  P. Laming,et al.  Do glia contribute to behaviour? A neuromodulatory review. , 1989, Comparative biochemistry and physiology. A, Comparative physiology.

[4]  P. Timiras,et al.  Influence of manganese on susceptibility of rats to convulsions. , 1963, The American journal of physiology.

[5]  Y. Tanaka,et al.  Blood manganese levels in children with convulsive disorder. , 1985, Biochemical medicine.

[6]  N. Buchanan,et al.  What is the clinical significance of reduced manganese and zinc levels in treated epileptic patients? , 1989, The Medical journal of Australia.

[7]  B. Gallagher,et al.  Association of low blood manganese concentrations with epilepsy , 1986, Neurology.

[8]  A. Meister,et al.  Glutamine synthetase from mammalian tissues. , 1985, Methods in enzymology.

[9]  P. Jobe,et al.  The genetically epilepsy-prone rat: an overview of seizure-prone characteristics and responsiveness to anticonvulsant drugs. , 1986, Life sciences.

[10]  G. Holmes,et al.  Effect of kainate-induced seizures on tissue trace element concentrations in the rat , 1989, Neuroscience.

[11]  G. Holmes,et al.  Genetically Epilepsy‐Prone Rats are Characterized by Altered Tissue Trace Element Concentrations , 1990, Epilepsia.

[12]  M. Failla,et al.  Elevated manganese concentration and arginase activity in livers of streptozotocin-induced diabetic rats. , 1983, The Journal of biological chemistry.

[13]  U. Rüegg,et al.  A rapid and sensitive assay for arginase. , 1980, Analytical biochemistry.

[14]  S. Miller,et al.  Generalized seizures alter the cerebral and peripheral metabolism of essential metals in mice , 1983, Experimental Neurology.

[15]  M. Maurizi,et al.  Mg2+ is bound to glutamine synthetase extracted from bovine or ovine brain in the presence of L-methionine-S-sulfoximine phosphate. , 1986, Archives of biochemistry and biophysics.

[16]  F. Sharp,et al.  Methionine sulfoximine reduces cortical infarct size in rats after middle cerebral artery occlusion. , 1990, Stroke.