» Articles » PMID: 27324790

D-Galactose Causes Motor Coordination Impairment, and Histological and Biochemical Changes in the Cerebellum of Rats

Abstract

Classical galactosemia is an inborn error of carbohydrate metabolism in which patients accumulate high concentration of galactose in the brain. The most common treatment is a galactose-restricted diet. However, even treated patients develop several complications. One of the most common symptoms is motor coordination impairment, including affected gait, balance, and speech, as well as tremor and ataxia. In the present study, we investigated the effects of intracerebroventricular galactose administration on motor coordination, as well as on histological and biochemical parameters in cerebellum of adult rats. Wistar rats received 5 μL of galactose (4 mM) or saline by intracerebroventricular injection. The animals performed the beam walking test at 1 and 24 h after galactose administration. Histological and biochemical parameters were performed 24 h after the injections. The results showed motor coordination impairment at 24 h after galactose injection. Galactose also decreased the number of cells in the molecular and granular layers of the cerebellum. The immunohistochemistry results suggest that the cell types lost by galactose are neurons and astrocytes in the spinocerebellum and neurons in the cerebrocerebellum. Galactose increased active caspase-3 immunocontent and acetylcholinesterase activity, decreased acetylcholinesterase immunocontent, glutathione, and BDNF levels, as well as caused protein and DNA damage. Our results suggest that galactose induces histological and biochemical changes in cerebellum, which can be associated with motor coordination impairment.

Citing Articles

Galactose Impairs Motor Performance and Cerebellar Signaling in Young Male Wistar Rats.

Ferreira B, Paz-Simoes T, Melo T, Goncalves P, Kubrusly R, de Melo Reis R Mol Neurobiol. 2025; .

PMID: 39913017 DOI: 10.1007/s12035-024-04684-6.


Classical Hereditary galactosemia: findings in patients and animal models.

Teixeira L, Prauchner G, Gusso D, Wyse A Metab Brain Dis. 2023; 39(1):239-248.

PMID: 37702899 DOI: 10.1007/s11011-023-01281-9.


BDNF and Cerebellar Ataxia.

Lalonde R, Hernandez M, Strazielle C Curr Drug Res Rev. 2023; 16(3):300-307.

PMID: 37609676 DOI: 10.2174/2589977515666230811093021.

References
1.
Schulpis K, Michelakakis H, Tsakiris T, Tsakiris S . The effect of diet on total antioxidant status, erythrocyte membrane Na+,K+-ATPase and Mg2+-ATPase activities in patients with classical galactosaemia. Clin Nutr. 2005; 24(1):151-7. DOI: 10.1016/j.clnu.2004.09.001. View

2.
Schreiner B, Romanelli E, Liberski P, Ingold-Heppner B, Sobottka-Brillout B, Hartwig T . Astrocyte Depletion Impairs Redox Homeostasis and Triggers Neuronal Loss in the Adult CNS. Cell Rep. 2015; 12(9):1377-84. DOI: 10.1016/j.celrep.2015.07.051. View

3.
Schmahmann J . Disorders of the cerebellum: ataxia, dysmetria of thought, and the cerebellar cognitive affective syndrome. J Neuropsychiatry Clin Neurosci. 2004; 16(3):367-78. DOI: 10.1176/jnp.16.3.367. View

4.
Rodrigues A, Roecker R, Junges G, de Lima D, da Cruz J, Wyse A . Hypoxanthine induces oxidative stress in kidney of rats: protective effect of vitamins E plus C and allopurinol. Cell Biochem Funct. 2014; 32(4):387-94. DOI: 10.1002/cbf.3029. View

5.
Apps R, Garwicz M . Anatomical and physiological foundations of cerebellar information processing. Nat Rev Neurosci. 2005; 6(4):297-311. DOI: 10.1038/nrn1646. View