RESUMEN
In Parkinson's disease patients and rodent models, dopaminergic neuron loss (DAN) results in severe motor disabilities. In contrast, general motility is preserved after early postnatal DAN loss in rodents. Here we used mice of both sexes to show that the preserved motility observed after early DAN loss depends on functional changes taking place in medium spiny neurons (MSN) of the dorsomedial striatum (DMS) that belong to the direct pathway (dMSN). Previous animal model studies showed that adult loss of dopaminergic input depresses dMSN response to cortical input, which likely contributes to Parkinson's disease motor impairments. However, the response of DMS-dMSN to their preferred medial PFC input is preserved after neonatal DAN loss as shown by in vivo studies. Moreover, their response to inputs from adjacent cortical areas is increased, resulting in reduced cortical inputs selectivity. Additional ex vivo studies show that membrane excitability increases in dMSN. Furthermore, chemogenetic inhibition of DMS-dMSN has a more marked inhibitory effect on general motility in lesioned mice than in their control littermates, indicating that expression of normal levels of locomotion and general motility depend on dMSN activity after early DAN loss. Contrastingly, DMS-dMSN inhibition did not ameliorate a characteristic phenotype of the DAN-lesioned animals in a marble burying task demanding higher behavioral control. Thus, increased dMSN excitability likely promoting changes in corticostriatal functional connectivity may contribute to the distinctive behavioral phenotype emerging after developmental DAN loss, with implications for our understanding of the age-dependent effects of forebrain dopamine depletion and neurodevelopment disorders.SIGNIFICANCE STATEMENT The loss of striatal dopamine in the adult brain leads to life-threatening motor impairments. However, general motility remains largely unaffected after its early postnatal loss. Here, we show that the high responsiveness to cortical input of striatal neurons belonging to the direct basal ganglia pathway, crucial for proper motor functioning, is preserved after early dopamine neuron loss, in parallel with an increase in these cells' membrane excitability. Chemogenetic inhibition studies show that the preserved motility depends on this direct pathway hyperexcitability/hyperconnectivity, while other phenotypes characteristic of this condition remained unaltered despite the dMSN inhibition. This insight has implications for our understanding of the mechanism underlying the behavioral impairments observed in neuropsychiatric conditions linked to early dopaminergic hypofunction.
Asunto(s)
Dopamina , Enfermedad de Parkinson , Masculino , Femenino , Ratones , Animales , Dopamina/metabolismo , Enfermedad de Parkinson/patología , Cuerpo Estriado/metabolismo , Ganglios Basales , Neuronas Dopaminérgicas/metabolismoRESUMEN
BACKGROUND: In advanced stages of Parkinson's disease (PD), dyskinesia and motor fluctuations become seriously debilitating and therapeutic options become scarce. Aberrant activity of striatal cholinergic interneurons (SCIN) has been shown to be critical to PD and dyskinesia, but the systemic administration of cholinergic medications can exacerbate extrastriatal-related symptoms. Thus, targeting the mechanisms causing pathological SCIN activity in severe PD with motor fluctuations and dyskinesia is a promising therapeutic alternative. METHODS: We used ex vivo electrophysiological recordings combined with pharmacology to study the alterations in intracellular signaling that contribute to the altered SCIN physiology observed in the 6-hydroxydopamine mouse model of PD treated with levodopa. RESULTS: The altered phenotypes of SCIN of parkinsonian mice during the "off levodopa" state resulting from aberrant Kir/leak and Kv1.3 currents can be rapidly reverted by acute inhibition of cAMP-ERK1/2 signaling. Inverse agonists that inhibit the ligand-independent activity of D5 receptors, like clozapine, restore Kv1.3 and Kir/leak currents and SCIN normal physiology in dyskinetic mice. CONCLUSION: Our work unravels a signaling pathway involved in the dysregulation of membrane currents causing SCIN hyperexcitability and burst-pause activity in parkinsonian mice treated with levodopa (l-dopa). These changes persist during off-medication periods due to tonic mechanisms that can be acutely reversed by pharmacological interventions. Thus, targeting the D5-cAMP-ERK1/2 signaling pathway selectively in SCIN may have therapeutic effects in PD and dyskinesia by restoring the normal SCIN function. © 2022 International Parkinson and Movement Disorder Society.
Asunto(s)
Discinesia Inducida por Medicamentos , Enfermedad de Parkinson , Animales , Antiparkinsonianos/farmacología , Antiparkinsonianos/uso terapéutico , Colinérgicos/metabolismo , Colinérgicos/farmacología , Colinérgicos/uso terapéutico , Cuerpo Estriado/metabolismo , Modelos Animales de Enfermedad , Discinesia Inducida por Medicamentos/patología , Interneuronas/metabolismo , Levodopa/farmacología , Levodopa/uso terapéutico , Ratones , Oxidopamina/toxicidadRESUMEN
BACKGROUND: Enhanced striatal cholinergic interneuron activity contributes to the striatal hypercholinergic state in Parkinson's disease (PD) and to levodopa-induced dyskinesia. In severe PD, dyskinesia and motor fluctuations become seriously debilitating, and the therapeutic strategies become scarce. Given that the systemic administration of anticholinergics can exacerbate extrastriatal-related symptoms, targeting cholinergic interneurons is a promising therapeutic alternative. Therefore, unraveling the mechanisms causing pathological cholinergic interneuron activity in severe PD with motor fluctuations and dyskinesia may provide new molecular therapeutic targets. METHODS: We used ex vivo electrophysiological recordings combined with pharmacological and morphological studies to investigate the intrinsic alterations of cholinergic interneurons in the 6-hydroxydopamine mouse model of PD treated with levodopa. RESULTS: Cholinergic interneurons exhibit pathological burst-pause activity in the parkinsonian "off levodopa" state. This is mediated by a persistent ligand-independent activity of dopamine D1/D5 receptor signaling, involving a cyclic adenosine monophosphate (cAMP) pathway. Dysregulation of membrane ion channels that results in increased inward-rectifier potassium type 2 (Kir2) and decreased leak currents causes the burst pause activity, which can be dampened by pharmacological inhibition of intracellular cAMP. A single challenge with a dyskinetogenic dose of levodopa is sufficient to induce persistent cholinergic interneuron burst-pause firing. CONCLUSION: Our data unravel a mechanism causing aberrant cholinergic interneuron burst-pause activity in parkinsonian mice treated with levodopa. Targeting D5-cAMP signaling and the regulation of Kir2 and leak channels may alleviate parkinsonism and dyskinesia by restoring normal cholinergic interneuron function. © 2021 International Parkinson and Movement Disorder Society.
Asunto(s)
Cuerpo Estriado , Levodopa , Animales , Colinérgicos/farmacología , Interneuronas , Levodopa/farmacología , Ratones , Oxidopamina/toxicidadRESUMEN
Parkinson's disease (PD) is characterized by a degeneration of nigrostriatal dopaminergic neurons that results in a hypercholinergic state in the striatum. This hypercholinergic state contributes to the clinical signs of PD. However, the mechanisms that underlie this state remain unknown. Cholinergic interneurons (ChIs) are the main source of acetylcholine in the striatum. Many studies have highlighted the importance of their normal physiological activity to guarantee a normal motor control and goal-directed behaviour. Moreover, recent studies with optogenetic and chemogenetic approaches have shown that reducing ChIs activity ameliorates parkinsonian symptoms and modifies L-dopa induced dyskinesia in PD animal models. Here, we review the described alterations in ChIs physiology that may contribute to a hypercholinergic state in PD. The best-established finding is an increase of ChIs intrinsic membrane excitability after dopaminergic denervation of striatum. Understanding the molecular basis of ChIs dysfunction in PD could help to develop new therapeutic tools to restore their normal activity and decrease parkinsonian symptoms, improving life quality of PD patients.
Asunto(s)
Enfermedad de Parkinson , Animales , Colinérgicos , Neuronas Colinérgicas , Cuerpo Estriado , Humanos , InterneuronasRESUMEN
In the last decade, scientific and clinical interest in the pedunculopontine nucleus (PPN) has grown dramatically. This growth is largely a consequence of experimental work demonstrating its connection to the control of gait and of clinical work implicating PPN pathology in levodopa-insensitive gait symptoms of Parkinson's disease (PD). In addition, the development of optogenetic and chemogenetic approaches has made experimental analysis of PPN circuitry and function more tractable. In this brief review, recent findings in the field linking PPN to the basal ganglia and PD are summarized; in addition, an attempt is made to identify key gaps in our understanding and challenges this field faces in moving forward.
Asunto(s)
Neuronas Colinérgicas/patología , Marcha , Enfermedad de Parkinson/patología , Núcleo Tegmental Pedunculopontino/patología , HumanosAsunto(s)
Estimulación Encefálica Profunda , Enfermedad de Parkinson/fisiopatología , Núcleo Tegmental Pedunculopontino/fisiopatología , Núcleo Subtalámico/fisiopatología , Humanos , Red Nerviosa/fisiopatología , Neuronas/fisiología , Enfermedad de Parkinson/terapia , Núcleo Tegmental Pedunculopontino/cirugía , Núcleo Subtalámico/cirugíaRESUMEN
Striatal cholinergic interneurons provide modulation to striatal circuits involved in voluntary motor control and goal-directed behaviors through their autonomous tonic discharge and their firing "pause" responses to novel and rewarding environmental events. Striatal cholinergic interneuron hyperactivity was linked to the motor deficits associated with Parkinson's disease and the adverse effects of chronic antiparkinsonian therapy like l-DOPA-induced dyskinesia. Here we addressed whether Kv7 channels, which provide negative feedback to excitation in other neuron types, are involved in the control of striatal cholinergic interneuron tonic activity and response to excitatory inputs. We found that autonomous firing of striatal cholinergic interneurons is not regulated by Kv7 channels. In contrast, Kv7 channels limit the summation of excitatory postsynaptic potentials in cholinergic interneurons through a postsynaptic mechanism. Striatal cholinergic interneurons have a high reserve of Kv7 channels, as their opening using pharmacological tools completely silenced the tonic firing and markedly reduced their intrinsic excitability. A strong inhibition of striatal cholinergic interneurons was also observed in response to the anti-inflammatory drugs diclofenac and meclofenamic acid, however, this effect was independent of Kv7 channels. These data bring attention to new potential molecular targets and pharmacological tools to control striatal cholinergic interneuron activity in pathological conditions where they are believed to be hyperactive, including Parkinson's disease.
Asunto(s)
Carbamatos/farmacología , Cuerpo Estriado/efectos de los fármacos , Diclofenaco/farmacología , Interneuronas/efectos de los fármacos , Moduladores del Transporte de Membrana/farmacología , Fenilendiaminas/farmacología , Canales de Potasio/metabolismo , Acetilcolina/metabolismo , Animales , Antiinflamatorios no Esteroideos/farmacología , Cuerpo Estriado/fisiología , Potenciales Postsinápticos Excitadores/efectos de los fármacos , Potenciales Postsinápticos Excitadores/fisiología , Interneuronas/fisiología , Masculino , Ratones Transgénicos , Bloqueadores de los Canales de Potasio/farmacología , Técnicas de Cultivo de TejidosRESUMEN
Giant, aspiny cholinergic interneurons (ChIs) have long been known to be key nodes in the striatal circuitry controlling goal-directed actions and habits. In recent years, new experimental approaches, like optogenetics and monosynaptic rabies virus mapping, have expanded our understanding of how ChIs contribute to the striatal activity underlying action selection and the interplay of dopaminergic and cholinergic signaling. These approaches also have begun to reveal how ChI function is distorted in disease states affecting the basal ganglia, like Parkinson's disease (PD). This review gives a brief overview of our current understanding of the functional role played by ChIs in striatal physiology and how this changes in PD. The translational implications of these discoveries, as well as the gaps that remain to be bridged, are discussed as well.
Asunto(s)
Neuronas Colinérgicas/fisiología , Cuerpo Estriado/fisiopatología , Interneuronas/fisiología , Enfermedad de Parkinson/fisiopatología , Animales , Cuerpo Estriado/metabolismo , Humanos , Enfermedad de Parkinson/metabolismoRESUMEN
The mechanism underlying a hypercholinergic state in Parkinson's disease (PD) remains uncertain. Here, we show that disruption of the Kv1 channel-mediated function causes hyperexcitability of striatal cholinergic interneurons in a mouse model of PD. Specifically, our data reveal that Kv1 channels containing Kv1.3 subunits contribute significantly to the orphan potassium current known as IsAHP in striatal cholinergic interneurons. Typically, this Kv1 current provides negative feedback to depolarization that limits burst firing and slows the tonic activity of cholinergic interneurons. However, such inhibitory control of cholinergic interneuron excitability by Kv1.3-mediated current is markedly diminished in the parkinsonian striatum, suggesting that targeting Kv1.3 subunits and their regulatory pathways may have therapeutic potential in PD therapy. These studies reveal unexpected roles of Kv1.3 subunit-containing channels in the regulation of firing patterns of striatal cholinergic interneurons, which were thought to be largely dependent on KCa channels.
Asunto(s)
Colinérgicos/metabolismo , Interneuronas/metabolismo , Activación del Canal Iónico , Canal de Potasio Kv1.3/metabolismo , Neostriado/metabolismo , Trastornos Parkinsonianos/metabolismo , Trastornos Parkinsonianos/fisiopatología , Envejecimiento/patología , Animales , Activación del Canal Iónico/efectos de los fármacos , Potenciales de la Membrana/efectos de los fármacos , Ratones , Oxidopamina , Fenotipo , Subunidades de Proteína/metabolismo , Venenos de Escorpión/farmacología , Sinapsis/efectos de los fármacos , Sinapsis/metabolismoRESUMEN
Sociobiology, the study of social behavior, calls for a laboratory model with specific requirements. Among the most obvious is the execution of social interactions that need to be readily observable, quantifiable and analyzable. If, in turn, one focuses on the neuroendocrinological basis of social behavior, restrictions grow even tighter. A good laboratory model should then allow easy access to its neurological and endocrine components and processes. During the last years, we have been studying the physiological foundation of social behavior on what we believe fits all the aforementioned requirements: the so called "chanchita", Cichlasoma dimerus. This Neotropical cichlid fish exhibits biparental care of the eggs and larvae and presents a hierarchical social system, established and sustained through agonistic interactions. The aim of the current article is to review new evidence on chanchita's social and reproductive behavior.
Asunto(s)
Cíclidos/fisiología , Sistema Endocrino/fisiología , Hormonas/fisiología , Conducta Sexual Animal/fisiología , Conducta Social , Agresión/fisiología , Animales , Femenino , Masculino , FotoperiodoRESUMEN
The South American cichlid fish Cichlasoma dimerus is a freshwater species that presents social hierarchies, a highly organized breeding activity, biparental care and a high frequency of spawning. Spawning is followed by a period of parental care (about 20 days in aquaria conditions) during which the cooperative pair takes care of the eggs, both by fanning them and by removing dead ones. The different spawning events in the reproductive period were classified as female reproductive stages which can be subdivided in four phases, according to their offspring degree of development: (1) female with prespawning activity (day 0), (2) female with eggs (day 1 after fertilization), (3) female with hatched larvae (day 3 after fertilization) and (4) female with swimming larvae (FSL, day 8 after fertilization). In Perciform species gonadotropin-releasing hormone type-3 (GnRH3) neurons are associated with the olfactory bulbs acting as a potent neuromodulator of reproductive behaviors in males. The aim of this study is to characterize the GnRH3 neuronal system in females of C. dimerus in relation with aggressive behavior and reproductive physiology during different phases of the reproductive period. Females with prespawning activity were the most aggressive ones showing GnRH-3 neurons with bigger nuclear and somatic area and higher optical density than the others. They also presented the highest levels of plasma androgen and estradiol and maximum gonadosomatic indexes. These results provide information about the regulation and functioning of hypothalamus-pituitary-gonads axis during reproduction in a species with highly organized breeding activity.