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1.
Indian J Biochem Biophys ; 2014 Dec ; 51 (6): 567-573
Artigo em Inglês | IMSEAR | ID: sea-156538

RESUMO

There are several reports on herbicide paraquat (PQ)-induced Parkinsonian-like pathology in different animal models, including Drosophila melanogaster. Also, the role of some inflammatory factors, such as nitric oxide is reported in PQ-induced neuroinflammation of Drosophila. Although invertebrate model is valuable to study the conserved inflammatory pathway at the time of neurodegeneration, but neuroinflammation during PQ-mediated neurodegeneration has not been studied explicitly in Drosophila. In this study, the inflammatory response was examined in Drosophila model during PQ-induced neurodegeneration. We found that after exposure to PQ, survivability and locomotion ability were affected in both sexes of Drosophila. Behavioural symptoms indicated similar physiological features of Parkinson’s disease (PD) in different animal models, as well as in humans. Our study revealed alteration in proinflamatory factor, TNF-α and Eiger (the Drosophila homologue in TNF superfamily) was changed in PQ-treated Drosophila both at protein and mRNA level during neurodegeneration. To ensure the occurrence of neurodegeneration, tyrosine hydroxylase (TH) positive neuronal cell loss was considered as a hallmark of PD in the fly brain. Thus, our result revealed the conserved inflammatory events in terms of expression of TNF-α and Eiger present during a sublethal dose of PQ-administered neurodegeneration in male and female Drosophila with significant variation in proinflamatory factor level among both the sexes.


Assuntos
Animais , Apoptose/efeitos dos fármacos , Apoptose/imunologia , Relação Dose-Resposta a Droga , /imunologia , Feminino , Herbicidas , Masculino , Neurite (Inflamação)/induzido quimicamente , Neurite (Inflamação)/imunologia , Doenças Neurodegenerativas/induzido quimicamente , Doenças Neurodegenerativas/imunologia , Neurônios/imunologia , Neurônios/patologia , Paraquat , Caracteres Sexuais , Tirosina 3-Mono-Oxigenase/imunologia
2.
Braz. j. med. biol. res ; 34(9): 1191-1195, Sept. 2001. graf
Artigo em Inglês | LILACS | ID: lil-290409

RESUMO

Neonatal handling has long-lasting effects on behavior and stress reactivity. The purpose of the present study was to investigate the effect of neonatal handling on the number of dopaminergic neurons in the hypothalamic nuclei of adult male rats as part of a series of studies that could explain the long-lasting effects of neonatal stimulation. Two groups of Wistar rats were studied: nonhandled (pups were left undisturbed, control) and handled (pups were handled for 1 min once a day during the first 10 days of life). At 75-80 days, the males were anesthetized and the brains were processed for immunohistochemistry. An anti-tyrosine hydroxylase antibody and the avidin-biotin-peroxidase method were used. Tyrosine hydroxylase-immunoreactive (TH-IR) neurons were counted bilaterally in the arcuate, paraventricular and periventricular nuclei of the hypothalamus in 30-æm sections at 120-æm intervals. Neonatal handling did not change the number of TH-IR neurons in the arcuate (1021 + or - 206, N = 6; 1020 + or - 150, N = 6; nonhandled and handled, respectively), paraventricular (584 + or - 85, N = 8; 682 + or - 62, N = 9) or periventricular (743 + or - 118, N = 7; 990 + or - 158, N = 7) nuclei of the hypothalamus. The absence of an effect on the number of dopaminergic cells in the hypothalamus indicates that the reduction in the amount of neurons induced by neonatal handling, as shown by other studies, is not a general phenomenon in the brain


Assuntos
Animais , Masculino , Feminino , Ratos , Comportamento Animal/fisiologia , Manobra Psicológica , Hipotálamo Anterior/fisiologia , Neurônios/fisiologia , Tirosina 3-Mono-Oxigenase/metabolismo , Animais Recém-Nascidos , Núcleo Hipotalâmico Anterior/enzimologia , Núcleo Hipotalâmico Anterior/fisiologia , Dopamina/fisiologia , Hipotálamo Anterior/enzimologia , Neurônios/imunologia , Estimulação Física , Ratos Wistar , Estresse Psicológico , Tirosina 3-Mono-Oxigenase/imunologia
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