EFEITO DA SINVASTATINA NO TESTE DO COMPORTAMENTO ROTATÓRIO APÓS DESAFIO COM APOMORFINA EM UM MODELO ANIMAL DA DOENÇA DE PARKINSON

Authors

  • Edmar Miyoshi Universidade Estadual de Ponta Grossa
  • Marissa Giovanna Schamne Universidade Estadual de Ponta Grossa / Mestrado em Ciências Farmacêuticas
  • Marcela Vaz Kuhn Minardi Universidade Estadual de Ponta Grossa
  • Marcelo Machado Ferro Universidade Estadual de Ponta Grossa / Departamento de Biologia Geral

Keywords:

doença de Parkinson, sinvastatina, neuroinflamação.

Abstract

A doença de Parkinson (DP) é a segunda doença neurodegenerativa mais comum na atualidade, e ainda não há nenhuma terapia eficaz para controlar a sua progressão, os tratamentos atuais apenas aliviam os sintomas. O objetivo desse trabalho foi avaliar o efeito da sinvastatina no comportamento rotatório de ratos com lesão unilateral pela 6-hidroxidopamina (6-OHDA). Ratos Wistar machos adultos receberam infusão unilateral de 6-OHDA no feixe prosencefálico medial (FPM) através de cirurgia estereotáxica. Em seguida, diferentes grupos de animais receberam diferentes doses de sinvastatina (1, 5 ou 25 mg/Kg) ou veículo, por via oral, diariamente por 28 dias. No 28° dia após a cirurgia, todos os animais foram submetidos ao teste do comportamento rotatório, induzido pela administração subcutânea (s.c.) de apomorfina (1 mg/Kg), no qual foram avaliados o número de rotações ipsi e contralaterais ao lado lesionado. Os animais do grupo 6-OHDA+veículo apresentaram um número maior de rotações contralaterais que os animais do grupo SHAM+veículo. Os animais dos grupos 6-OHDA+sinvastatina 1 mg/Kg e 6-OHDA+sinvastatina 5 mg/Kg apresentaram um menor número de rotações contralaterais, quando comparados com os animais do grupo 6-OHDA+veículo. Estes resultados sugerem que a sinvastatina pode diminuir ou impedir a morte de neurônios dopaminérgicos, portanto, possuir um efeito benéfico na doença de Parkinson. Este efeito pode estar ligado à conhecida ação anti-inflamatória da sinvastatina.

ABSTRACT

Parkinson's disease (PD) is currently the second most common neurodegenerative disease, and yet there is no effective therapy to control its progression, as current treatments only relieve symptoms. The aim of this study was to evaluate the simvastatin’s pharmacological effect on the rotational behavior in rats unilaterally lesioned by 6-hydroxydopamine (6-OHDA). Male adult Wistar rats received unilateral administration of 6-OHDA into de medial forebrain bundle, performed by stereotaxic surgery. Then, different groups received different doses of simvastatin (1, 5 and 25 mg/Kg) or vehicle, orally administrated on a daily basis for 28 days. On the 28th day after surgery, all animals were submitted to the turning behavior test, induced by subcutaneous administration of apomorphine (1 mg/Kg), in which the number of ipsilateral and contralateral rotations to the lesioned side rotations were analyzed. The 6-OHDA+vehicle animals showed an increased number of contralateral rotations when compared with SHAM+vehicle animals. The 6-OHDA+simvastatin 1 mg/Kg and 6-OHDA+simvastatin 5 mg/Kg animals showed a lower number of contralateral rotations compared to 6-OHDA+vehicle animals. These results suggest that simvastatin can reduce or prevent the death of dopaminergic neurons, and thus, have a beneficial effect on Parkinson’s disease. This effect may be related to the well-known simvastatin anti-inflammatory action.

Author Biography

Edmar Miyoshi, Universidade Estadual de Ponta Grossa

Possui graduação em Farmácia pela Universidade Federal do Paraná (1998), mestrado em Farmacologia pela Universidade Federal do Paraná (2001) e doutorado em Farmacologia pela Universidade Federal do Paraná (2009). Atualmente é professor adjunto da Universidade Estadual de Ponta Grossa.

References

OBESO, J. A., et al. Pathophysiology of the basal ganglia in Parkinson’s disease. Trends in Neurosciences v. 23, p. s8-s19, 2000.

SULZER, D. Multiple hit hypotheses for dopamine neuron loss in Parkinson's disease. Trends in Neurosciences v.30, n.5, p.244-50. 2007.

DA CUNHA, C., et al. Pre-training to find a hidden platform in the Morris water maze can compensate for a deficit to find a cued platform in a rat model of Parkinson's disease. Neurobiology of Learning and Memory, v. 87, n. 4, p. 451-63, 2007.

DA CUNHA, C., et al. Learning processing in the basal ganglia: a mosaic of broken mirrors. Behavioural Brain Research, v. 199, n. 1, p. 157-70, 2009.

PADOVANI, A. C., et al. Parkinson’s disease and dementia. Neurological Sciences, v. 27, p. 40-43, 2006.

MELLO, L. M., BARBOSA, E. R., CARAMELLI, P. Declínio cognitivo e demência associados à doença de Parkinson: características clínicas e tratamento. Revista de Psiquiatria Clínica., vol. 34, n. 4, p. 176-183, 2007.

FRANCARDO, V., et al. Impact of the lesion procedure on the profiles of motor impairment and molecular responsiveness to L-DOPA in the 6-hydroxydopamine mouse model of Parkinson’s disease. Neurobiology of Disease, v. 42, p. 327-340, 2011.

BEZARD, E, et al. Relationship between the appearance of symptoms and the level of nigrostriatal degeneration in a progressive 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-lesioned macaque model of Parkinson’s disease. Journal of Neuroscience v. 21, p. 6853-6861, 2001.

DEUMENS, R, et al. Modeling Parkinson’s disease in rats: An evaluation of 6-OHDA lesions of the nigrostriatal pathway experimental. Neurology, v.175, p. 303–317, 2002.

BOKA, G., et al. Immunocytochemical analysis of tumor necrosis factor and its receptors in Parkinson's disease. Neuroscience Letters, v. 172, n. 1-2, p.151-154, 1994.

HUNOT, S., et al. FcepsilonRII/CD23 is expressed in Parkinson's disease and induces, in vitro, production of nitric oxide and tumor necrosis factor-alpha in glial cells. Journal of Neuroscience, v. 19, n. 9, p. 3440-3447, 1999.

DAUER, W.; PRZEDBORSKI, S. Parkinson’s Disease: Mechanisms and models. Neuron, v. 39, p. 889-909, 2003.

HERNÁNDEZ-ROMERO, M.C., et al. Simvastatin prevents the inflammatory process and the dopaminergic degeneration induced by the intranigral injection of lipopolysaccharide. Journal of Neurochemical, v. 105, p. 445-459, 2008.

SANTOS, C.M.M. New agents promote neuroprotection in Parkinson's disease models. CNS & Neurological Disorders - Drug Targets, v. 11, p. 410-418, 2012.

VAN DER MOST, P. J.; et al. Statins: Mechanisms of neuroprotection. Progress in Neurobiology, v. 88, p. 64-75, 2009.

WANG, Q., et al. Statins: Multiple neuroprotective mechanisms in neurodegenerative diseases. Experimental Neurology, v. 230, p. 27-34, 2011.

ROY, A., PAHAN, K. Prospects of statins in Parkinson disease. The Neuroscientist, v. 17, no 3, p. 244-255, 2011.

GOSH, A., et al. Simvastatin inhibits the activation of p21ras and prevents the loss of dopaminergic neurons in a mouse model of Parkinson’s disease. Journal of Neuroscience, v. 29, p. 13543-13556, 2009.

ZACCO, A., et al. 3-Hydroxy-3-methylglutaryl coenzyme A reductase inhibitors protect cortical neurons from excitotoxicity. Journal of Neuroscience, v. 23, p. 11104-11111, 2003.

WOLOZIN, B., et al. Simvastatin is associated with a reduced incidence of dementia and Parkinson's disease. BMC Medicine, v. 5, 2007.

KAHLE, P.J., et al. Structure/function of alpha-synuclein in health and disease: rational development of animal models for Parkinson´s and related disease. Journal of Neurochemistry, v. 82, p. 449-457, 2002.

YONG, Y., et al. Lithium fails to protect dopaminergic neurons in the 6-OHDA model of Parkinson’s disease. Neurochemistry, v. 36, p. 367-374, 2011.

THOENEN, H., TRANZER, J. P. The pharmacology of 6-hydroxydopamine. Revist of Pharmacology, v. 13, p. 169-180, 1973.

BLUM, D., et al. Molecular pathways involved in the neurotoxicity of 6-OHDA, dopamine and MPTP: contribution to the apoptotic theory in Parkinson’s disease. Progress in Neurobiology, v. 65, p. 135-172, 2001.

BERNSTEIN, A. I., et al. 6-OHDA generated ROS induces DNA damage and p53-and PUMA-dependent cell death. BMC Medicine, 2011.

PRZEDBORSKI, S., et al. Dose-dependent lesions of the dopaminergic nigrostriatal pathway induced by intrastriatal injection of 6-hydroxydopamine. Neuroscience, v. 67, n. 3, p. 631-47, 1995.

SCHWARTING, R. K., HUSTON, J. P. Unilateral 6-hydroxydopamine lesions of the meso-striatal dopaminergic neurons and their physiological sequelae. Progress in Neurobiology, v. 49, p. 215-66, 1996.

DA CUNHA, C., et al. Hemiparkinsonian rats rotate toward the side with the weaker dopaminergic neurotransmission. Behavioural Brain Research, v. 189, p. 364-372, 2008.

PAXINOS, G; WATSON, C. The rat brain in stereotaxic coordinates. San Diego: Academic Press, 5 ed., 2005.

GERLACH, M.; RIEDERER, P. Animal models of Parkinson´s disease: an empirical comparison with the phenomenology of the disease in man. Journal of Neural Transmission, v. 103, p. 987-1041, 1996.

BETARBET, R.; SHERER, T.B.; GREENAMYRE, J.T. Animal models of Parkinson´s disease. Bioessays, v. 24, p. 308-318, 2002.

WANG, Q., et al. Simvastatin reverses the dowregulation of dopamine D1 and D2 receptor expression in the prefrontal cortex of 6-hydroxydopamine-induced Parkisonian rats. Brain Research, vol. 1045, p. 229-233, 2005.

KUMAR, A., et al. Neuroprotective potential of atorvastatin and simvastatin (HMG-CoA reductase inhibitors) against 6-hydroxydopamine (6-OHDA) induced Parkinson-like symptoms. Brain Research, v. 1471, p. 13-22, 2012.

SELLEY, M.L. Simvastatin prevents 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced striatal dopamine depletion and protein tyrosine nitration in mice. Brain Research, v. 1037, p. 1–6, 2005.

KALONIA, H., et al. Comparative neuroprotective profile of statins in quinolinic acid induced neurotoxicity in rats. Behavioral Brain Research, v. 216, p. 220- 228, 2011.

Published

2014-11-27

How to Cite

Miyoshi, E., Schamne, M. G., Minardi, M. V. K., & Ferro, M. M. (2014). EFEITO DA SINVASTATINA NO TESTE DO COMPORTAMENTO ROTATÓRIO APÓS DESAFIO COM APOMORFINA EM UM MODELO ANIMAL DA DOENÇA DE PARKINSON. SaBios- Journal of Health and Biology, 9(3), 62–68. Retrieved from http://68.183.29.147/revista/index.php/sabios/article/view/1772

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