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1.
Mol Psychiatry ; 28(8): 3512-3523, 2023 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-37532798

RESUMEN

Sensitive developmental periods shape neural circuits and enable adaptation. However, they also engender vulnerability to factors that can perturb developmental trajectories. An understanding of sensitive period phenomena and mechanisms separate from sensory system development is still lacking, yet critical to understanding disease etiology and risk. The dopamine system is pivotal in controlling and shaping adolescent behaviors, and it undergoes heightened plasticity during that time, such that interference with dopamine signaling can have long-lasting behavioral consequences. Here we sought to gain mechanistic insight into this dopamine-sensitive period and its impact on behavior. In mice, dopamine transporter (DAT) blockade from postnatal (P) day 22 to 41 increases aggression and sensitivity to amphetamine (AMPH) behavioral stimulation in adulthood. Here, we refined this sensitive window to P32-41 and identified increased firing of dopaminergic neurons in vitro and in vivo as a neural correlate to altered adult behavior. Aggression can result from enhanced impulsivity and cognitive dysfunction, and dopamine regulates working memory and motivated behavior. Hence, we assessed these behavioral domains and found that P32-41 DAT blockade increases impulsivity but has no effect on cognition, working memory, or motivation in adulthood. Lastly, using optogenetics to drive dopamine neurons, we find that increased VTA but not SNc dopaminergic activity mimics the increase in impulsive behavior in the Go/NoGo task observed after adolescent DAT blockade. Together our data provide insight into the developmental origins of aggression and impulsivity that may ultimately improve diagnosis, prevention, and treatment strategies for related neuropsychiatric disorders.


Asunto(s)
Proteínas de Transporte de Dopamina a través de la Membrana Plasmática , Dopamina , Ratones , Animales , Anfetamina/farmacología , Conducta Impulsiva/fisiología , Agresión
2.
Eur J Neurosci ; 55(9-10): 2455-2463, 2022 05.
Artículo en Inglés | MEDLINE | ID: mdl-33305403

RESUMEN

The amygdala is a key brain region involved in emotional memory formation. It is also responsible for memory modulation in other brain areas. Under extreme conditions, amygdala modulation may lead to the generation of abnormal plasticity and trauma-related psychopathologies. However, the amygdala itself is a dynamic brain region, which is amenable to long-term plasticity and is affected by emotional experiences. These alterations may modify the way the amygdala modulates activity and plasticity in other related brain regions, which in turn may alter the animal's response to subsequent challenges in what could be termed as "Behavioral metaplasticity."Because of the reciprocal interactions between the amygdala and other emotion processing regions, such as the medial prefrontal cortex (mPFC) or the hippocampus, experience-induced intra-amygdala metaplasticity could lead to alterations in mPFC-dependent or hippocampus-dependent behaviors. While initiated by alterations within the basolateral amygdala (BLA), such alterations in other brain regions may come to be independent of BLA modulation, thus establishing what may be termed "Trans-regional metaplasticity." In this article, we review evidence supporting the notions of intra-BLA metaplasticity and how this may develop into "Trans-regional metaplasticity." Future research is needed to understand how such dynamic metaplastic alterations contribute to developing psychopathologies, and how this knowledge may be translated into promoting novel interventions in psychopathologies associated with fear, stress, and trauma.


Asunto(s)
Extinción Psicológica , Miedo , Amígdala del Cerebelo/fisiología , Animales , Extinción Psicológica/fisiología , Miedo/fisiología , Aprendizaje/fisiología , Plasticidad Neuronal/fisiología , Corteza Prefrontal/fisiología
3.
Nat Commun ; 12(1): 6796, 2021 11 23.
Artículo en Inglés | MEDLINE | ID: mdl-34815379

RESUMEN

Septal-hypothalamic neuronal activity centrally mediates aggressive behavior and dopamine system hyperactivity is associated with elevated aggression. However, the causal role of dopamine in aggression and its target circuit mechanisms are largely unknown. To address this knowledge gap, we studied the modulatory role of the population- and projection-specific dopamine function in a murine model of aggressive behavior. We find that terminal activity of ventral tegmental area (VTA) dopaminergic neurons selectively projecting to the lateral septum (LS) is sufficient for promoting aggression and necessary for establishing baseline aggression. Within the LS, dopamine acts on D2-receptors to inhibit GABAergic neurons, and septal D2-signaling is necessary for VTA dopaminergic activity to promote aggression. Collectively, our data reveal a powerful modulatory influence of dopaminergic synaptic input on LS function and aggression, effectively linking the clinically pertinent hyper-dopaminergic model of aggression with the classic septal-hypothalamic aggression axis.


Asunto(s)
Agresión/fisiología , Conducta Animal , Dopamina/metabolismo , Tabique del Cerebro/fisiología , Área Tegmental Ventral/fisiología , Animales , Neuronas Dopaminérgicas/metabolismo , Neuronas GABAérgicas/metabolismo , Masculino , Ratones , Modelos Animales , Vías Nerviosas/fisiología , Receptores de Dopamina D2/metabolismo , Técnicas Estereotáxicas
4.
J Neurosci ; 39(39): 7664-7673, 2019 09 25.
Artículo en Inglés | MEDLINE | ID: mdl-31413075

RESUMEN

Homeostatic regulation of synaptic strength allows for maintenance of neural activity within a dynamic range for proper circuit function. There are largely two distinct modes of synaptic plasticity that allow for homeostatic adaptation of cortical circuits: synaptic scaling and sliding threshold (BCM theory). Previous findings suggest that the induction of synaptic scaling is not prevented by blocking NMDARs, whereas the sliding threshold model posits that the synaptic modification threshold of LTP and LTD readjusts with activity and thus the outcome of synaptic plasticity is NMDAR dependent. Although synaptic scaling and sliding threshold have been considered two distinct mechanisms, there are indications from recent studies that these two modes of homeostatic plasticity may interact or that they may operate under two distinct activity regimes. Here, we report using both sexes of mouse that acute genetic knock-out of the obligatory subunit of NMDAR or acute pharmacological block of NMDAR prevents experience-dependent homeostatic regulation of AMPAR-mediated miniature EPSCs in layer 2/3 of visual cortex. This was not due to gross changes in postsynaptic neuronal activity with inhibiting NMDAR function as determine by c-Fos expression and two-photon Ca2+ imaging in awake mice. Our results suggest that experience-dependent homeostatic regulation of intact cortical circuits is mediated by NMDAR-dependent plasticity mechanisms, which supports a sliding threshold model of homeostatic adaptation.SIGNIFICANCE STATEMENT Prolonged changes in sensory experience lead to homeostatic adaptation of excitatory synaptic strength in sensory cortices. Both sliding threshold and synaptic scaling models can account for the observed homeostatic synaptic plasticity. Here we report that visual experience-dependent homeostatic plasticity of excitatory synapses observed in superficial layers of visual cortex is dependent on NMDAR function. In particular, both strengthening of synapses induced by visual deprivation and the subsequent weakening by reinstatement of visual experience were prevented in the absence of functional NMDARs. Our results suggest that sensory experience-dependent homeostatic adaptation depends on NMDARs, which supports the sliding threshold model of plasticity and input-specific homeostatic control observed in vivo.


Asunto(s)
Homeostasis/fisiología , Plasticidad Neuronal/fisiología , Receptores de N-Metil-D-Aspartato/metabolismo , Corteza Visual/fisiología , Animales , Potenciales Postsinápticos Excitadores/fisiología , Femenino , Masculino , Ratones , Neuronas/fisiología
5.
Cell Rep ; 24(13): 3433-3440.e4, 2018 09 25.
Artículo en Inglés | MEDLINE | ID: mdl-30257205

RESUMEN

Plasticity of thalamocortical (TC) synapses is robust during early development and becomes limited in the adult brain. We previously reported that a short duration of deafening strengthens TC synapses in the primary visual cortex (V1) of adult mice. Here, we demonstrate that deafening restores NMDA receptor (NMDAR)-dependent long-term potentiation (LTP) of TC synapses onto principal neurons in V1 layer 4 (L4), which is accompanied by an increase in NMDAR function. In contrast, deafening did not recover long-term depression (LTD) at TC synapses. Potentiation of TC synapses by deafening is absent in parvalbumin-positive (PV+) interneurons, resulting in an increase in feedforward excitation to inhibition (E/I) ratio. Furthermore, we found that a brief duration of deafening adult mice recovers rapid ocular dominance plasticity (ODP) mainly by accelerating potentiation of the open-eye responses. Our results suggest that cross-modal sensory deprivation promotes adult cortical plasticity by specifically recovering TC-LTP and increasing the E/I ratio.


Asunto(s)
Percepción Auditiva , Potenciación a Largo Plazo , Tálamo/fisiología , Corteza Visual/fisiología , Percepción Visual , Animales , Potenciales Postsinápticos Excitadores , Femenino , Potenciales Postsinápticos Inhibidores , Interneuronas/metabolismo , Interneuronas/fisiología , Masculino , Ratones , Ratones Endogámicos C57BL , Receptores de N-Metil-D-Aspartato/metabolismo , Privación Sensorial , Tálamo/citología , Corteza Visual/citología
6.
Mol Neurobiol ; 55(9): 7317-7326, 2018 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-29404957

RESUMEN

Activation of the amygdala is one of the hallmarks of acute stress reactions and a central element of the negative impact of stress on hippocampus-dependent memory and cognition. Stress-induced psychopathologies, such as posttraumatic stress disorder, exhibit a sustained hyperactivity of the amygdala, triggered at least in part by deficits in GABAergic inhibition that lead to shifts in amygdalo-hippocampal interaction. Here, we have utilized lentiviral knock down of neurofascin to reduce GABAergic inhibition specifically at the axon initial segment (AIS) of principal neurons within the basolateral amygdala (BLA) of rats. Metaplastic effects of such a BLA modulation on hippocampal synaptic function were assessed using BLA priming prior to the induction of long-term potentiation (LTP) on dentate gyrus synapses in anesthetized rats in vivo. The knock down of neurofascin in the BLA prevented a priming-induced impairment on LTP maintenance in the dentate gyrus. At the behavioral level, a similar effect was observable, with neurofascin knock down preventing the detrimental impact of acute traumatic stress on hippocampus-dependent spatial memory retrieval in a water maze task. These findings suggest that reducing GABAergic inhibition specifically at the AIS synapses of the BLA alters amygdalo-hippocampal interactions such that it attenuates the adverse impact of acute stress exposure on cognition-related hippocampal functions.


Asunto(s)
Complejo Nuclear Basolateral/fisiopatología , Moléculas de Adhesión Celular/metabolismo , Giro Dentado/fisiopatología , Técnicas de Silenciamiento del Gen , Memoria , Factores de Crecimiento Nervioso/metabolismo , Plasticidad Neuronal , Estrés Psicológico/fisiopatología , Animales , Giro Dentado/patología , Potenciación a Largo Plazo , Masculino , Aprendizaje por Laberinto , Recuerdo Mental , Ratas Sprague-Dawley , Estrés Psicológico/patología
7.
Cereb Cortex ; 28(1): 395-410, 2018 01 01.
Artículo en Inglés | MEDLINE | ID: mdl-29136108

RESUMEN

GABAergic synapses in the basolateral amygdala (BLA) play an important role in fear memory generation. We have previously reported that reduction in GABAergic synapses innervating specifically at the axon initial segment (AIS) of principal neurons of BLA, by neurofascin (NF) knockdown, impairs fear extinction. BLA is bidirectionally connected with the medial prefrontal cortex (mPFC), which is a key region involved in extinction of acquired fear memory. Here, we showed that reducing AIS GABAergic synapses within the BLA leads to impairment of synaptic plasticity in the BLA-mPFC pathway, as well as in the ventral subiculum (vSub)-mPFC pathway, which is independent of BLA involvement. The results suggest that the alteration within the BLA subsequently resulted in a form of trans-regional metaplasticity in the mPFC. In support of that notion, we observed that NF knockdown induced a severe deficit in behavioral flexibility as measured by reversal learning. Interestingly, reversal learning similar to extinction learning is an mPFC-dependent behavior. In agreement with that, measurement of the immediate-early gene, c-Fos immunoreactivity after reversal learning was reduced in the mPFC and BLA, supporting further the notion that the BLA GABAergic manipulation resulted in trans-regional metaplastic alterations within the mPFC.


Asunto(s)
Segmento Inicial del Axón/fisiología , Complejo Nuclear Basolateral/fisiología , Plasticidad Neuronal/fisiología , Corteza Prefrontal/fisiología , Sinapsis/fisiología , Vicia faba/metabolismo , Animales , Ansiedad/patología , Ansiedad/fisiopatología , Segmento Inicial del Axón/efectos de los fármacos , Segmento Inicial del Axón/patología , Complejo Nuclear Basolateral/citología , Complejo Nuclear Basolateral/efectos de los fármacos , Complejo Nuclear Basolateral/patología , Moléculas de Adhesión Celular/antagonistas & inhibidores , Moléculas de Adhesión Celular/genética , Moléculas de Adhesión Celular/metabolismo , Condicionamiento Psicológico/fisiología , Extinción Psicológica/fisiología , Miedo/fisiología , Hipocampo/citología , Hipocampo/patología , Hipocampo/fisiología , Masculino , Memoria/fisiología , Actividad Motora/fisiología , Factores de Crecimiento Nervioso/antagonistas & inhibidores , Factores de Crecimiento Nervioso/genética , Factores de Crecimiento Nervioso/metabolismo , Vías Nerviosas/citología , Vías Nerviosas/efectos de los fármacos , Vías Nerviosas/patología , Vías Nerviosas/fisiología , Plasticidad Neuronal/efectos de los fármacos , Corteza Prefrontal/citología , Corteza Prefrontal/patología , Proteínas Proto-Oncogénicas c-fos/metabolismo , Ratas Sprague-Dawley , Aprendizaje Inverso/fisiología , Sinapsis/efectos de los fármacos , Sinapsis/patología
8.
Neuropsychopharmacology ; 42(2): 473-484, 2017 01.
Artículo en Inglés | MEDLINE | ID: mdl-27634356

RESUMEN

Inhibitory synaptic transmission in the amygdala has a pivotal role in fear learning and its extinction. However, the local circuits formed by GABAergic inhibitory interneurons within the amygdala and their detailed function in shaping these behaviors are not well understood. Here we used lentiviral-mediated knockdown of the cell adhesion molecule neurofascin in the basolateral amygdala (BLA) to specifically remove inhibitory synapses at the axon initial segment (AIS) of BLA projection neurons. Quantitative analysis of GABAergic synapse markers and measurement of miniature inhibitory postsynaptic currents in BLA projection neurons after neurofascin knockdown ex vivo confirmed the loss of GABAergic input. We then studied the impact of this manipulation on anxiety-like behavior and auditory cued fear conditioning and its extinction as BLA related behavioral paradigms, as well as on long-term potentiation (LTP) in the ventral subiculum-BLA pathway in vivo. BLA knockdown of neurofascin impaired ventral subiculum-BLA-LTP. While this manipulation did not affect anxiety-like behavior and fear memory acquisition and consolidation, it specifically impaired extinction. Our findings indicate that modification of inhibitory synapses at the AIS of BLA projection neurons is sufficient to selectively impair extinction behavior. A better understanding of the role of distinct GABAergic synapses may provide novel and more specific targets for therapeutic interventions in extinction-based therapies.


Asunto(s)
Complejo Nuclear Basolateral/fisiología , Extinción Psicológica/fisiología , Miedo/fisiología , Neuronas GABAérgicas/fisiología , Inhibición Neural , Sinapsis/fisiología , Potenciales de Acción , Animales , Ansiedad/fisiopatología , Axones/fisiología , Complejo Nuclear Basolateral/citología , Moléculas de Adhesión Celular/genética , Neuronas GABAérgicas/citología , Técnicas de Silenciamiento del Gen , Potenciación a Largo Plazo , Masculino , Potenciales Postsinápticos Miniatura , Factores de Crecimiento Nervioso/genética , Ratas Sprague-Dawley , Ratas Transgénicas , Ácido gamma-Aminobutírico/fisiología
9.
Sci Rep ; 6: 29710, 2016 07 13.
Artículo en Inglés | MEDLINE | ID: mdl-27405707

RESUMEN

Neuronal transmission is regulated by the local circuitry which is composed of principal neurons targeted at different subcellular compartments by a variety of interneurons. However, mechanisms that contribute to the subcellular localisation and maintenance of GABAergic interneuron terminals are poorly understood. Stabilization of GABAergic synapses depends on clustering of the postsynaptic scaffolding protein gephyrin and its interaction with the guanine nucleotide exchange factor collybistin. Lentiviral knockdown experiments in adult rats indicated that the receptor tyrosine kinase EphA7 is required for the stabilisation of basket cell terminals on proximal dendritic and somatic compartments of granular cells of the dentate gyrus. EphA7 deficiency and concomitant destabilisation of GABAergic synapses correlated with impaired long-term potentiation and reduced hippocampal learning. Reduced GABAergic innervation may be explained by an impact of EphA7 on gephyrin clustering. Overexpression or ephrin stimulation of EphA7 induced gephyrin clustering dependent on the mechanistic target of rapamycin (mTOR) which is an interaction partner of gephyrin. Gephyrin interactions with mTOR become released after mTOR activation while enhanced interaction with the guanine nucleotide exchange factor collybistin was observed in parallel. In conclusion, EphA7 regulates gephyrin clustering and the maintenance of inhibitory synaptic connectivity via mTOR signalling.


Asunto(s)
Dendritas/metabolismo , Giro Dentado/metabolismo , Neuronas GABAérgicas/metabolismo , Receptor EphA7/metabolismo , Transducción de Señal/fisiología , Sinapsis/metabolismo , Animales , Proteínas Portadoras/genética , Proteínas Portadoras/metabolismo , Giro Dentado/citología , Femenino , Neuronas GABAérgicas/citología , Técnicas de Silenciamiento del Gen , Proteínas de la Membrana/genética , Proteínas de la Membrana/metabolismo , Ratas , Ratas Sprague-Dawley , Receptor EphA7/genética , Serina-Treonina Quinasas TOR/genética , Serina-Treonina Quinasas TOR/metabolismo
10.
Neurobiol Dis ; 88: 139-47, 2016 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-26804028

RESUMEN

Diagnosis of psychiatric disorders in humans is based on comparing individuals to the normal population. However, many animal models analyze averaged group effects, thus compromising their translational power. This discrepancy is particularly relevant in posttraumatic stress disorder (PTSD), where only a minority develop the disorder following a traumatic experience. In our PTSD rat model, we utilize a novel behavioral profiling approach that allows the classification of affected and unaffected individuals in a trauma-exposed population. Rats were exposed to underwater trauma (UWT) and four weeks later their individual performances in the open field and elevated plus maze were compared to those of the control group, allowing the identification of affected and resilient UWT-exposed rats. Behavioral profiling revealed that only a subset of the UWT-exposed rats developed long-lasting behavioral symptoms. The proportion of affected rats was further enhanced by pre-exposure to juvenile stress, a well-described risk factor of PTSD. For a biochemical proof of concept we analyzed the expression levels of the GABAA receptor subunits α1 and α2 in the ventral, dorsal hippocampus and basolateral amygdala. Increased expression, mainly of α1, was observed in ventral but not dorsal hippocampus of exposed animals, which would traditionally be interpreted as being associated with the exposure-resultant psychopathology. However, behavioral profiling revealed that this increased expression was confined to exposed-unaffected individuals, suggesting a resilience-associated expression regulation. The results provide evidence for the importance of employing behavioral profiling in animal models of PTSD, in order to better understand the neural basis of stress vulnerability and resilience.


Asunto(s)
Trastornos Mentales/etiología , Trastornos Mentales/metabolismo , Trastornos por Estrés Postraumático/complicaciones , Análisis de Varianza , Animales , Animales Recién Nacidos , Encéfalo/metabolismo , Encéfalo/patología , Modelos Animales de Enfermedad , Conducta Exploratoria/fisiología , Reacción Cataléptica de Congelación/fisiología , Locomoción , Masculino , Aprendizaje por Laberinto/fisiología , Odorantes , Escalas de Valoración Psiquiátrica , Ratas , Ratas Sprague-Dawley , Receptores de GABA-A/metabolismo , Trastornos por Estrés Postraumático/patología
11.
J Neuroimmune Pharmacol ; 9(3): 340-53, 2014 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-24469921

RESUMEN

Neurological complications in opioid abusing Human Immunodeficiency Virus-1 (HIV-1) patients suggest enhanced neurodegeneration as compared to non-drug abusing HIV-1 infected population. Neural precursor cells (NPCs), the multipotent cells of the mammalian brain, are susceptible to HIV-1 infection and as opiates also perturb their growth kinetics, detailed mechanistic studies for their co-morbid exposure are highly warranted. Using a well characterized in vitro model of human fetal brain-derived neural precursor cells, we investigated alterations in NPC properties at both acute and chronic durations. Chronic morphine and Tat treatment attenuated proliferation in NPCs, with cells stalled at G1-phase of the cell cycle. Furthermore HIV-Tat and morphine exposure increased activation of extracellular signal-regulated kinase-1/2 (ERK1/2), enhanced levels of p53 and p21, and decreased cyclin D1 and Akt levels in NPCs. Regulated by ERK1/2 and p53, p21 was found to be indispensible for Tat and morphine mediated cell cycle arrest. Our study elaborates on the cellular and molecular machinery in NPCs and provides significant mechanistic details into HIV-drug abuse co-morbidity that may have far reaching clinical consequences both in pediatric as well as adult neuroAIDS.


Asunto(s)
Puntos de Control del Ciclo Celular/fisiología , Infecciones por VIH , Sistema de Señalización de MAP Quinasas/fisiología , Células-Madre Neurales/fisiología , Trastornos Relacionados con Sustancias , Proteína p53 Supresora de Tumor/biosíntesis , Proteínas de Unión al GTP rho/biosíntesis , Proteínas Reguladoras de la Apoptosis/toxicidad , Puntos de Control del Ciclo Celular/efectos de los fármacos , Células Cultivadas , Comorbilidad , Células Madre Fetales/efectos de los fármacos , Células Madre Fetales/fisiología , Infecciones por VIH/epidemiología , Infecciones por VIH/metabolismo , Humanos , Sistema de Señalización de MAP Quinasas/efectos de los fármacos , Morfina/toxicidad , Células-Madre Neurales/efectos de los fármacos , Proteínas Recombinantes de Fusión/toxicidad , Trastornos Relacionados con Sustancias/epidemiología , Trastornos Relacionados con Sustancias/metabolismo , Survivin , Productos del Gen tat del Virus de la Inmunodeficiencia Humana/toxicidad
12.
Niger Med J ; 54(3): 165-9, 2013 May.
Artículo en Inglés | MEDLINE | ID: mdl-23901178

RESUMEN

BACKGROUND: Dacryocystorhinostomy (DCR) consists of creating a lacrimal drainage pathway to the nasal cavity to restore permanent drainage of previously obstructed excreting system. AIM: To compare the result and advantages of both endonasal endoscopic and external DCR regarding the patency rate, patient compliance and complications. STUDY DESIGN: Prospective non-randomized comparative study. MATERIALS AND METHODS: Study was conducted for 16 months duration in a teaching hospital with 50 cases of endoscopic and 30 cases of external DCR with a follow-up of minimum 6 months. Data regarding surgical outcome and complications were analysed and compared using χ(2) test. RESULTS: Total 72 patients were included in the study with six having bilateral involvement, out of which 20 were male and 52 were female. The mean age for endoscopic and external DCR was 33.6 years and 46.0 years, respectively. Right eye (63.8%) was involved more commonly than left eye (36.2%). Epiphora was the commonest presenting symptom (63.7%). Mean duration of surgery was much lengthier in external (mean 119.6 minutes) than endoscopic (mean 49.0 minutes) DCR. Bleeding was the most common immediate postoperative complication seen in 33.3% and 10.0% of external and endoscopic DCR cases, respectively. Primary surgical success rate was 90% and 96.7% for endoscopic and external DCR, respectively (P = 0.046). Among the endoscopic DCR group, four patients underwent revision surgery giving a total successful surgical outcome of 98% at third month of follow-up. However, at 6 month of follow-up, success rate was 92% for endoscopic DCR and 93.3% for external DCR. The difference was not statistically significant (P = 0.609). CONCLUSION: Intranasal endoscopic DCR is a simple, minimally invasive, day care procedure and had comparable result with conventional external DCR.

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