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Physiol Behav ; 104(3): 417-22, 2011 Sep 01.
Artigo em Inglês | MEDLINE | ID: mdl-21570993

RESUMO

Prenatal lipopolysaccharide (LPS) exposure causes reproductive, behavioral and neurochemical defects in both dams and pups. The present study evaluated male rats prenatally treated with LPS for behavioral and neurological effects related to the olfactory system, which is the main sensorial path in rodents. Pregnant Wistar rats received 100 µg/kg of LPS intraperitoneally (i.p.) on gestational day (GD) 9.5, and maternal behavior was evaluated. Pups were evaluated for (1) maternal odor preference, (2) aversion to cat odor, (3) monoamine levels and turnover in the olfactory bulb (OB) and (4) protein expression (via immunoblotting) within the OB dopaminergic system and glial cells. Results showed that prenatal LPS exposure impaired maternal preference and cat odor aversion and decreased dopamine (DA) levels in the OB. This dopaminergic impairment may have been due to defects in another brain area given that protein expression of the first enzyme in the DA biosynthetic pathway was unchanged in the OB. Moreover, there was no change in the protein expression of the DA receptors. The fact that the number of astrocytes and microglia was not increased suggests that prenatal LPS did not induce neuroinflammation in the OB. Furthermore, given that maternal care was not impaired, abnormalities in the offspring were not the result of reduced maternal care.


Assuntos
Lipopolissacarídeos/toxicidade , Percepção Olfatória/efeitos dos fármacos , Transtornos da Percepção/etiologia , Efeitos Tardios da Exposição Pré-Natal/fisiopatologia , Fatores Etários , Análise de Variância , Animais , Animais Recém-Nascidos , Monoaminas Biogênicas/metabolismo , Antígeno CD11b/metabolismo , Feminino , Proteína Glial Fibrilar Ácida/metabolismo , Masculino , Comportamento Materno/efeitos dos fármacos , Odorantes , Bulbo Olfatório/metabolismo , Transtornos da Percepção/patologia , Gravidez , Efeitos Tardios da Exposição Pré-Natal/induzido quimicamente , Ratos , Receptores Dopaminérgicos/metabolismo
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