Abstract:OBJECTIVE: Some research has shown that learning and memory function impairments in rats with hypothyroidism are associated with triiodothyronine (T3) deficiency in neurons. This study aimed to investigate the effects of L-T3 administration on learning and memory behaviors in neonatal mice with excitotoxic brain damage. METHODS: Seventy-one 5-day-old ICR neonatal mice were randomly assigned to five groups: controls that received intracerebral and intraperitoneal injections of phosphate buffered saline (PBS) (n=14); a group that received intracerebral injections of ibotenic acid (IA) and intraperitoneal injection of PBS (n=14); 3 groups that received intracerebral injections of IA and intraperitoneal injection of L-T3 at 0.2, 0.5, and 1 μg/kg, respectively (n=14-15). Intraperitoneal injections were done 1, 24, 48, 72 and 96 hrs after intracerebral injections. Learning and memory functions were evaluated by the Y-maze discrimination learning test on postnatal days 33-34. RESULTS: The learning and memory functions in the highest L-T3 dose group were significantly better than those in the IA, and the lower L-T3 dose groups, presenting with decreased number of trials to criterion [15.8±4.5 vs 21.3±6.3 (IA group), 20.5±6.0 (0.2 μg/kg L-T3 group) or 21.0±6.5 (0.5 μg/kg L-T3 group); P<0.05], and achieving a higher correct percentage [91.4±9.5% vs 79.3±10.0% (IA group), 77.9±14.2% (0.2 μg/kg L-T3 group) or 80.7±12.2% (0.5μg/kg L-T3 group); P<0.05]. CONCLUSIONS: High-dose L-T3 (1 μg/kg) may improve learning and memory functions in mice following excitotoxic brain damage.[Chin J Contemp Pediatr, 2010, 12 (4):284-286]
WU Gen-Feng,HE Xiang-Ying,LI Qi et al. Effects of triiodothyronine on the learning and memory behaviors in neonatal mice following excitotoxic brain damage[J]. CJCP, 2010, 12(04): 284-286.
[3]Marret S, Mukendi R, Gadisseux JF, Gressens P, Evrard P. Effect of ibotenate on brain development:an excitotoxic mouse model of microgyria and posthypoxic-like lesions[J]. Neuropathol Exp Neurol, 1995, 54(3):358-370.
[4]Xu XH, Zhao TQ. Effects of puerarin on D-galactose-induced memory deficits in mice[J].Acta Pharmacol Sin, 2002, 23(7):587-590.
[5]Patkai J, Mesples B, Dommergues MA, Fromont G, Thornton EM, Renauld JC, et al. Deleterious effects of IL-9 activated mast cell and neuroprotection by antihistamine drugs in the developing mouse brain[J]. Pediatr Res, 2001, 50(2):222-230.
[6]Johnston MV, Frescher WH, Ishida A, Nakajima W. Novel treatments after experimental brain injury[J].Semin Neonatal, 2000, 5(1):75-86.
[7]Bernal J. Thyroid hormones and brain development[J]. Vitam Horm, 2005, 71(4):95-122.
[8]Gerges NZ, Alzoubi KH, Park CR, Diamond DM, Alkadhi KA. Adverse effect of the combination of hypothyroidism and chronic psychosocial stress on hippocampus-dependent memory in rats[J]. Behav Brain Res, 2004, 155(1):77-84.
[9]Sárk-zy G, Griesmaier E, He X. T3 replacement does not prevent excitotoxic cell death but reduces developmental neuronal apoptosis in newborn mice[J]. Eur J Paediatr Neurol, 2007, 11(3):129-135.
[10]Palha JA, Nissanov J, Fernandes RJC. Sousa JC, Bertra L, Dratman MB, et al. Thyroid hormone distribution in the mouse brain: the role of transthyretin[J]. Neuroscience, 2002, 113(4):837-847.