RESUMO
Clinical evidence suggests that early malnutrition promotes symptoms related to psychiatric disorders later in life. Nevertheless, the molecular mechanisms underpinning nutritional injury induce depression remains unknown. The purpose of the present study was to evaluate whether perinatal protein restriction increases vulnerability to developing depressive-like behavior in adulthood by focusing on anhedonia, a core symptom of depression. To this, male adult Wistar rats submitted to a protein restriction schedule at perinatal age (PR-rats), were subjected to the sucrose preference test (SPT), the novel object recognition test (NORT), the forced swim test (FST), and the elevated plus maze (EPM), and compared to animals fed with a normoprotein diet. To investigate neurobiological substrates linked to early protein undernutrition-facilitated depressive-like behavior, we assessed the levels of brain-derived neurotrophic factor (BDNF) and its receptor TrkB in the nucleus accumbens (NAc), and evaluated the reversal of anhedonic-like behavior by infusing ANA-12. We found that early malnutrition decreased sucrose preference, impaired performance in the NORT and increased immobility time in the FST. Furthermore, perinatal protein-restriction-induced anhedonia correlated with increased BDNF and p-TrkB protein levels in the NAc, a core structure in the reward circuit linked with anhedonia. Finally, bilateral infusion of the TrkB antagonist ANA-12 into the NAc shell ameliorated a reduced sucrose preference in the PR-rats. Altogether, these findings revealed that protein restriction during pregnancy and lactation facilitates depressive-like behavior later in life and may increase the risk of developing anhedonia by altering BDNF-TrkB in the NAc shell.
Assuntos
Anedonia , Fator Neurotrófico Derivado do Encéfalo , Núcleo Accumbens , Ratos Wistar , Receptor trkB , Transdução de Sinais , Animais , Núcleo Accumbens/metabolismo , Núcleo Accumbens/efeitos dos fármacos , Fator Neurotrófico Derivado do Encéfalo/metabolismo , Masculino , Anedonia/fisiologia , Ratos , Receptor trkB/metabolismo , Feminino , Transdução de Sinais/fisiologia , Transdução de Sinais/efeitos dos fármacos , Gravidez , Dieta com Restrição de Proteínas , Efeitos Tardios da Exposição Pré-Natal/metabolismo , Depressão/metabolismo , Depressão/psicologia , Azepinas , BenzamidasRESUMO
BACKGROUND: Post-translational modifications are key factors in the modulation of nuclear protein functions controlling cell physiology and an individual's health. OBJECTIVES: This study examined the influence of protein restriction during the perinatal period on the nuclear O-N-acetylgalactosamine (O-GalNAc) glycosylation of cells from the liver and parts of the brain in the rat. METHODS: Pregnant Wistar rats were divided into 2 groups on day 14 of pregnancy and fed ad libitum 1 of 2 isocaloric diets containing 24% (well-fed) or 8% (protein-restricted diet) casein until the end of the experiment. Male pups were studied after weaning at 30 d of life. Animals and their organ/tissues (liver, cerebral cortex, cerebellum and hippocampus) were weighed. Cell nuclei were purified, and the presence in nucleus and cytoplasm of all factors required for the initiation of O-GalNAc glycan biosynthesis, i.e., the sugar donor (UDP-GalNAc), enzyme activity (ppGalNAc-transferase) and the glycosylation product (O-GalNAc glycans), were evaluated by western blotting, fluorescent microscopy, enzyme activity, enzyme-lectin sorbent assay and mass spectrometry. RESULTS: The perinatal protein deficit reduced progeny weight, as well as the cerebral cortex and cerebellum weight. UDP-GalNAc levels in the cytoplasm and nuclei of the liver, the cerebral cortex, cerebellum, or hippocampus were not affected by the perinatal dietary protein deficits. However, this deficiency affected the ppGalNAc-transferase activity localized in the cerebral cortex and hippocampus cytoplasm as well as in the liver nucleus, thus reducing the "writing" ppGalNAc-transferase activity of O-GalNAc glycans. In addition, liver nucleoplasm from protein-restricted offspring revealed a significant reduction in the expression of O-GalNAc glycans on important nuclear proteins. CONCLUSIONS: Our results report an association between the consumption of a protein-restricted diet by the dam and her progeny with the modulation in the offspring' liver nuclei O-GalNAc glycosylation, which may ultimately regulate nuclear protein functions.
Assuntos
Núcleo Celular , Dieta com Restrição de Proteínas , Masculino , Ratos , Animais , Glicosilação , Ratos Wistar , Polissacarídeos , Fígado , Proteínas Nucleares , Encéfalo , Transferases , Difosfato de UridinaRESUMO
It is known that a consolidated memory can return to a labile state and become transiently malleable following reactivation. This instability is followed by a restabilization phase termed reconsolidation. In this work, we explored whether an unrelated appetitive experience (voluntary consumption of diluted sucrose) can affect a contextual fear memory in rats during the reactivation-induced destabilization phase. Our findings show that exposure to an appetitive experience following reactivation can diminish fear retention. This effect persisted after 1 wk. Importantly, it was achieved only under conditions that induced fear memory destabilization. This result could not be explained as a potentiated extinction, because sucrose was unable to promote extinction. Since GluN2B-containing NMDA receptors in the basolateral amygdala complex (BLA) have been implicated in triggering fear memory destabilization, we decided to block pharmacologically these receptors to explore the neurobiological bases of the observed effect. Intra-BLA infusion with ifenprodil, a GluN2B-NMDA antagonist, prevented the fear reduction caused by the appetitive experience. In sum, these results suggest that the expression of a fear memory can be dampened by an unrelated appetitive experience, as long as memory destabilization is achieved during reactivation. Possible mechanisms behind this effect and its clinical implications are discussed.
Assuntos
Comportamento Apetitivo , Complexo Nuclear Basolateral da Amígdala/fisiologia , Medo , Consolidação da Memória/fisiologia , Receptores de N-Metil-D-Aspartato/fisiologia , Retenção Psicológica/fisiologia , Animais , Antagonistas de Aminoácidos Excitatórios/administração & dosagem , Masculino , Piperidinas/administração & dosagem , Ratos Wistar , Receptores de N-Metil-D-Aspartato/antagonistas & inibidoresRESUMO
Gangliosides are compounds that are abundant throughout the CNS, participating actively in neuroplasticity. We previously described that exogenous GM1 ganglioside pretreatment enhances the rewarding properties of cocaine, evidenced by a lower number of sessions and/or dosage necessary to induce conditioned place preference (CPP). Since GM1 pretreatment did not modify cocaine's pharmacokinetic parameters, we suspected that the increased rewarding effect found might be mediated by BDNF, a neurotrophic factor closely related to cocaine addiction. This study was performed to investigate the possibility that GM1 may induce changes in BDNF levels in the nucleus accumbens (NAc), a core structure in the brain's reward circuitry, of rats submitted to three conditioning sessions with cocaine (10 mg/kg, i.p.). The results demonstrate that GM1 administration, which showed no rewarding effect by itself in the CPP, induced a significant increase of BDNF protein levels in the NAc, which may account for the increased rewarding effect of cocaine shown in the CPP paradigm.
Assuntos
Fator Neurotrófico Derivado do Encéfalo/metabolismo , Cocaína/farmacologia , Condicionamento Operante/efeitos dos fármacos , Gangliosídeo G(M1)/farmacologia , Núcleo Accumbens/metabolismo , Recompensa , Animais , Gangliosídeo G(M1)/administração & dosagem , Masculino , Ratos , Ratos WistarRESUMO
GM1 pretreatment enhanced the rewarding properties of cocaine as assessed in the conditioned place preference paradigm. This effect was shown by the lower dosage of cocaine necessary to induce conditioning compared with rats receiving cocaine alone, as well as by the fewer number of sessions necessary to induce place preference. GM1 pretreatment did not modify the plasma level of cocaine, but it induced a significant increase in the brain cocaine level compared with animals receiving cocaine alone. In order to evaluate the possibility that GM1 pretreatment may alter the pharmacokinetic parameters of cocaine, the brain and plasma esterase activities, the plasma bound/free cocaine ratio and the brain blood barrier permeability to i.v. Evans Blue administration were assessed. None of these parameters was modified by the GM1 administration. In addition, GM1 (100microM) did not alter the dopamine transporter inhibition induced by cocaine (10(-7)-10(-5)M), as determined by the uptake of [(3-)H]-dopamine in the microsacs of nucleus accumbens. In conclusion, GM1 pretreatment, which did not have any effect per se, increased the rewarding effect of cocaine, a phenomenon correlated with a significant increase in the brain cocaine levels. The different pharmacokinetic parameters evaluated, as well as the inhibitory effect of cocaine on the dopamine transporter, were not modified by GM1, but it modifies the brain cocaine disposition. Thus, the mechanisms by which GM1 enhanced the rewarding effects of cocaine merit further study.
Assuntos
Comportamento Animal/efeitos dos fármacos , Cocaína/farmacologia , Condicionamento Operante/efeitos dos fármacos , Gangliosídeo G(M1)/farmacologia , Animais , Masculino , Ratos , Ratos WistarRESUMO
The influence of neuronal alterations induced by early undernutrition on the stimulant effect of cocaine was assessed in adult rats submitted to a protein deprivation schedule at perinatal age. To evaluate the sensitization phenomenon induced by repeated cocaine administration, different groups of control (C) and deprived (D) rats received a daily injection of cocaine (5, 10 or 15 mg/kg, i.p.) for 16 days. Behavioral parameters were assessed every two days in an open-field. Dose-response curves obtained with different doses of cocaine used revealed a shift to the left in the locomotor activity curves of D rats compared to controls. Thus, D animals showed a clear behavioral sensitization to the lower dose of cocaine, whereas this phenomenon was only observed in C rats for the higher dose used. To correlate this differential development of sensitization with neurochemical parameters, we assessed extracellular dopamine (DA) levels in nucleus accumbens (core and shell) and in the dorsal caudate-putamen, using a microdialysis technique. A challenge with cocaine in cocaine pre-exposed animals produced a different increase in DA output only in nucleus accumbens "core" of D animals. Comparable DA levels were observed in nucleus accumbens shell and in dorsal caudate-putamen of both groups. These results demonstrate that D rats had a lower threshold developing a progressive behavioral sensitization following repeated cocaine administration, as well as higher responsiveness of the nucleus accumbens (core) expressed by increased DA release.
Assuntos
Cocaína/farmacologia , Dopamina/metabolismo , Desnutrição/metabolismo , Atividade Motora/efeitos dos fármacos , Esquema de Reforço , Animais , Animais Recém-Nascidos , Encéfalo/efeitos dos fármacos , Encéfalo/metabolismo , Proteínas Alimentares/administração & dosagem , Feminino , Masculino , Desnutrição/psicologia , Atividade Motora/fisiologia , Gravidez , Ratos , Ratos WistarRESUMO
We have previously described an increased locus coeruleus activity in perinatally protein-deprived rats. Since locus coeruleus dysfunction has been involved in different types of anxiety disorders and considering the modulating action of serotonergic transmission on locus coeruleus activity, we assessed the effect of fluoxetine, a selective serotonin reuptake inhibitor (SSRI), on locus coeruleus activity as measured by the firing rate and the number of spontaneously active cells/track. Repeated fluoxetine administration reduced locus coeruleus activity in both control and protein-deprived rats, although the reduction was greater in protein-deprived rats. Dose-response curves for the inhibitory effect of clonidine showed subsensitivity of alpha2-adrenergic autoreceptors in protein-deprived rats, a phenomenon reversed by fluoxetine treatment. Dose-response curves for the inhibitory effect of 2,5-dimethoxy-4-iodoamphetamine (DOI) were similar in both groups of rats. Following fluoxetine administration, subsensitivity to this effect developed in control but not in protein-deprived rats. Extracellular noradrenaline level in the prefrontal cortex, as measured by microdialysis procedure, was higher in protein-deprived rats compared to controls, and this difference was reduced after fluoxetine administration. A challenge with yohimbine increased the extracellular noradrenaline level in control but not in protein-deprived rats, suggesting subsensitivity of alpha2-adrenergic autoreceptors in early protein malnourished animals. These results stress the complexity of plastic changes induced by early protein malnutrition and sustain the hypothesis that perinatally protein-deprived rats may represent a useful animal model for screening antipanic agents.
Assuntos
Antidepressivos de Segunda Geração/farmacologia , Fluoxetina/farmacologia , Locus Cerúleo/fisiologia , Desnutrição Proteico-Calórica/fisiopatologia , Inibidores Seletivos de Recaptação de Serotonina/farmacologia , Agonistas alfa-Adrenérgicos/farmacologia , Antagonistas Adrenérgicos alfa/farmacologia , Anfetaminas/farmacologia , Animais , Monoaminas Biogênicas/metabolismo , Clonidina/farmacologia , Relação Dose-Resposta a Droga , Eletrofisiologia , Espaço Extracelular/efeitos dos fármacos , Espaço Extracelular/metabolismo , Feminino , Locus Cerúleo/citologia , Locus Cerúleo/efeitos dos fármacos , Microdiálise , Neurônios/efeitos dos fármacos , Neurônios/metabolismo , Neurônios/fisiologia , Norepinefrina/metabolismo , Norepinefrina/fisiologia , Córtex Pré-Frontal/efeitos dos fármacos , Córtex Pré-Frontal/metabolismo , Gravidez , Ratos , Ratos Wistar , Agonistas do Receptor de Serotonina/farmacologia , Ioimbina/farmacologiaRESUMO
Se realizaron estudios de la reactividad conductual de receptores serotoninérgicos de tipo 5-HTl y 5-HT2, en ratas "Killer" (K) y "non-Killer" (NK), obtenidos por aislamiento social o por lesión de los núcleos dorsal y medial del rafe. La reactividad de los receptores tipo 5-HTl fue medida en una escala de intensidad arbitraria para los síntomas de "forepaw treading" y "hindlimb abduction" luego de la administración de 5-MeODMT, mientras que la reactividad de los sitios 5-HT2 fue determinada a través del comportamiento de "wet dog shake", inducido por la administración de 5-hidroxitriptófano. No se observaron diferencias en las conductas mediadas por los sitios 5-HTl y 5-HT2 entre los animales aislados. De igual manera, se obtuvieron valores similares en el "wet dog shake" de ratas lesioandas K y NK. Por el contrario, 5- MeODMT indujo una menor respuesta conductual en las ratas lesionadas K en comparación con las lesionadas NK. Esta alteración en la respuesta conductual no es consecuencia de una desnervación neuronal diferente en el sistema serotoninérgico central, ya que no hubo modificaciones en el "uptake" de 5-Ht en las estructuras cerebrales analizadas entre estos dos grupos experimentales de ratas. Esta menor reactividad de los sitios 5-HTl podría reflejar una neurotransmisión serotoninérgica disminuida y aportaría una probable explicación a la aparición de la actvidad muricida en algunos pero no en todos los animales lesionados
Assuntos
Ratos , Animais , Masculino , Comportamento Animal , Núcleos da Rafe/fisiologia , Receptores de Serotonina/metabolismo , Serotonina/farmacocinética , Sítios de Ligação , Metoxidimetiltriptaminas/farmacologia , Ratos Endogâmicos , Serotonina/farmacologiaRESUMO
Se realizaron estudios de la reactividad conductual de receptores serotoninérgicos de tipo 5-HTl y 5-HT2, en ratas "Killer" (K) y "non-Killer" (NK), obtenidos por aislamiento social o por lesión de los núcleos dorsal y medial del rafe. La reactividad de los receptores tipo 5-HTl fue medida en una escala de intensidad arbitraria para los síntomas de "forepaw treading" y "hindlimb abduction" luego de la administración de 5-MeODMT, mientras que la reactividad de los sitios 5-HT2 fue determinada a través del comportamiento de "wet dog shake", inducido por la administración de 5-hidroxitriptófano. No se observaron diferencias en las conductas mediadas por los sitios 5-HTl y 5-HT2 entre los animales aislados. De igual manera, se obtuvieron valores similares en el "wet dog shake" de ratas lesioandas K y NK. Por el contrario, 5- MeODMT indujo una menor respuesta conductual en las ratas lesionadas K en comparación con las lesionadas NK. Esta alteración en la respuesta conductual no es consecuencia de una desnervación neuronal diferente en el sistema serotoninérgico central, ya que no hubo modificaciones en el "uptake" de 5-Ht en las estructuras cerebrales analizadas entre estos dos grupos experimentales de ratas. Esta menor reactividad de los sitios 5-HTl podría reflejar una neurotransmisión serotoninérgica disminuida y aportaría una probable explicación a la aparición de la actvidad muricida en algunos pero no en todos los animales lesionados (AU)