Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/5754
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Type: Journal article
Title: Magnesium gluconate offers no more protection than magnesium sulphate following diffuse traumatic brain injury in rats
Author: Turner, R.
Da Silva, K.
O'Connor, C.
Van Den Heuvel, C.
Vink, R.
Citation: Journal of the American College of Nutrition, 2004; 23(5):541S-544S
Publisher: Amer Coll Nutrition
Issue Date: 2004
ISSN: 0731-5724
1541-1087
Statement of
Responsibility: 
Renee J. Turner, K. W. DaSilva, C. O’Connor, Corinna van den Heuvel, and Robert Vink
Abstract: Objective: Previous studies have demonstrated that magnesium salts, including the sulphate and chloride forms, are neuroprotective following traumatic brain injury (TBI). Recently, studies in cardiac ischaemia/reperfusion injury have demonstrated that the gluconate salt of magnesium may provide superior protection against oxidative damage and postischaemic dysfunction than MgSO4. We have therefore compared the efficacy of both MgSO4 and magnesium gluconate (MgGl2) on outcome following diffuse TBI in rats. Methods: Adult male Sprague-Dawley rats were injured using the 2-metre impact acceleration model of diffuse TBI. At 30 min after injury, animals were administered with either 250µmoles/kg i.v. MgSO4, MgGl2, or equal volume saline vehicle. Thereafter, animals were assessed for motor and cognitive outcome using the rotarod and Barnes maze, respectively, or their brains removed at 3 days after TBI and used for histological examination. Results: Treatment with either magnesium salt significantly improved functional outcome as compared to vehicle treated controls. Similarly, treatment with either magnesium salt attenuated the degree of histological dark cell change at 3 days after TBI relative to the vehicle treated animals. There were no significant differences between the magnesium treated groups. Conclusions: We conclude that MgSO4 and MgGl2 are equally neuroprotective following TBI. Our results suggest that MgGl2 may only be more effective in conditions that produce ischaemia, where high concentrations of reactive oxygen species are generated.
Keywords: ischaemia; rat; neuroprotection; traumatic brain injury; reactive oxygen species; magnesium salts
Description: Copyright © 2004 by the American College of Nutrition.
RMID: 0020041477
DOI: 10.1080/07315724.2004.10719399
Published version: http://www.jacn.org/cgi/content/full/23/5/541S
Appears in Collections:Pathology publications

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