Cargando…

Wildtype peers rescue social play and 50-kHz ultrasonic vocalization deficits in juvenile female Cacna1c heterozygous rats

BACKGROUND: Healthy brain development depends on early social practices and experiences. The risk gene CACNA1C is implicated in numerous neuropsychiatric disorders, in which key characteristics include deficits in social functioning and communication. Recently, we reported sex-dependent impairments...

Descripción completa

Detalles Bibliográficos
Autores principales:	Bogdan, Rebecca, Kayumova, Rukhshona, Schwarting, Rainer K. W., Wöhr, Markus, Kisko, Theresa M.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2023
Materias:	Neuroscience
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10435996/ https://www.ncbi.nlm.nih.gov/pubmed/37600756 http://dx.doi.org/10.3389/fnbeh.2023.1190272

Ejemplares similares

Cacna1c haploinsufficiency leads to pro-social 50-kHz ultrasonic communication deficits in rats
por: Kisko, Theresa M., et al.
Publicado: (2018)

Response Calls Evoked by Playback of Natural 50-kHz Ultrasonic Vocalizations in Rats
por: Berz, Annuska C., et al.
Publicado: (2022)

Environmental and Pharmacological Modulation of Amphetamine-Induced 50-kHz Ultrasonic Vocalizations in Rats
por: Rippberger, Henrike, et al.
Publicado: (2015)

Ultrasonic Communication in Rats: Can Playback of 50-kHz Calls Induce Approach Behavior?
por: Wöhr, Markus, et al.
Publicado: (2007)

Playback of 50-kHz ultrasonic vocalizations overcomes psychomotor deficits induced by sub-chronic haloperidol treatment in rats
por: Melo-Thomas, Liana, et al.
Publicado: (2020)

Social Behavior and Ultrasonic Vocalizations in a Genetic Rat Model Haploinsufficient for the Cross-Disorder Risk Gene Cacna1c
por: Wöhr, Markus, et al.
Publicado: (2021)

Pro-social 50-kHz ultrasonic communication in rats: post-weaning but not post-adolescent social isolation leads to social impairments—phenotypic rescue by re-socialization
por: Seffer, Dominik, et al.
Publicado: (2015)

Specific 50-kHz vocalizations are tightly linked to particular types of behavior in juvenile rats anticipating play
por: Burke, Candace J., et al.
Publicado: (2017)

The Effects of Electrical and Optical Stimulation of Midbrain Dopaminergic Neurons on Rat 50-kHz Ultrasonic Vocalizations
por: Scardochio, Tina, et al.
Publicado: (2015)

Changes in Rat 50-kHz Ultrasonic Vocalizations During Dopamine Denervation and Aging: Relevance to Neurodegeneration
por: Johnson, Aaron M., et al.
Publicado: (2015)

Modulation of Rat 50-kHz Ultrasonic Vocalizations by Glucocorticoid Signaling: Possible Relevance to Reward and Motivation
por: Simola, Nicola, et al.
Publicado: (2017)

50‐kHz ultrasonic vocalizations do not signal social anhedonia in transgenic DISC1 rats
por: Seidisarouei, Mohammad, et al.
Publicado: (2023)

Limited generalizability, pharmacological modulation, and state-dependency of habituation towards pro-social 50-kHz calls in rats
por: Berz, Annuska, et al.
Publicado: (2021)

Predator odour but not TMT induces 22-kHz ultrasonic vocalizations in rats that lead to defensive behaviours in conspecifics upon replay
por: Fendt, Markus, et al.
Publicado: (2018)

Social Transmission of Fear in Rats: The Role of 22-kHz Ultrasonic Distress Vocalization
por: Kim, Eun Joo, et al.
Publicado: (2010)

Alimentation 50 kHz Pulsee
por: Bourgeois, Μ
Publicado: (1974)

Involvement of Glutamate NMDA Receptors in the Acute, Long-Term, and Conditioned Effects of Amphetamine on Rat 50kHz Ultrasonic Vocalizations
por: Costa, Giulia, et al.
Publicado: (2015)

Anticipatory 50-kHz Precontact Ultrasonic Vocalizations and Sexual Motivation: Characteristic Pattern of Ultrasound Subtypes in an Individual Analyzed Profile
por: Bogacki-Rychlik, Wiktor, et al.
Publicado: (2021)

Introduction of gloved hand to cage induces 22-kHz ultrasonic vocalizations in male albino rats
por: Hwang, Seo-Kyoung, et al.
Publicado: (2022)

Extracellular Dopamine Levels in Nucleus Accumbens after Chronic Stress in Rats with Persistently High vs. Low 50-kHz Ultrasonic Vocalization Response
por: Kõiv, Kadri, et al.
Publicado: (2021)

Contingent Social Interaction Does Not Prevent Habituation towards Playback of Pro-Social 50-kHz Calls: Behavioral Responses and Brain Activation Patterns
por: Berz, Annuska, et al.
Publicado: (2022)

Poor sensitization of 50-kHz vocalization response to amphetamine predicts rat susceptibility to self-administration of the drug
por: Taracha, Ewa, et al.
Publicado: (2016)

Distinct Profiles of 50 kHz Vocalizations Differentiate Between Social Versus Non-social Reward Approach and Consumption
por: Seidisarouei, Mohammad, et al.
Publicado: (2021)

New Insights from 22-kHz Ultrasonic Vocalizations to Characterize Fear Responses: Relationship with Respiration and Brain Oscillatory Dynamics
por: Dupin, Maryne, et al.
Publicado: (2019)

Acute and subchronic toxicity of 20 kHz and 60 kHz magnetic fields in rats
por: Nishimura, Izumi, et al.
Publicado: (2015)

Rat 50 kHz Trill Calls Are Tied to the Expectation of Social Interaction
por: Burke, Candace J., et al.
Publicado: (2021)

Inter-individual diversity and intra-individual stability of amphetamine-induced sensitization of frequency-modulated 50-kHz vocalization in Sprague–Dawley rats
por: Taracha, Ewa, et al.
Publicado: (2012)

Contextual Modulation of Vocal Behavior in Mouse: Newly Identified 12 kHz “Mid-Frequency” Vocalization Emitted during Restraint
por: Grimsley, Jasmine M. S., et al.
Publicado: (2016)

Rat 50 kHz calls reflect graded tickling-induced positive emotion
por: Hinchcliffe, Justyna K., et al.
Publicado: (2020)

Stable long-term individual differences in 50-kHz vocalization rate and call subtype prevalence in adult male rats: Comparisons with sucrose preference
por: Sundarakrishnan, Adithi, et al.
Publicado: (2022)

Estación de radio AM comercial en la banda 535 kHz a 1605 kHz /
por: Diantes Loya, Lizette
Publicado: (2005)

Testing the potential of 50 kHz rat calls as a species-specific rat attractant
por: Davidson, Nicola B., et al.
Publicado: (2019)

Effect of 60 kHz and 150 kHz Femtosecond Lasers on Corneal Stromal Bed Surfaces: A Comparative Study
por: Monterosso, Cristina, et al.
Publicado: (2013)

Review of Studies Concerning Electromagnetic Field (EMF) Exposure Assessment in Europe: Low Frequency Fields (50 Hz–100 kHz)
por: Gajšek, Peter, et al.
Publicado: (2016)

Can an average of thresholds at 2 kHz and 4 kHz substitute for the threshold at 3 kHz in pure tone audiometry? A study based on the Korean National Health and Nutrition Examination Survey 2010–2012
por: Kim, Ju Yeon, et al.
Publicado: (2018)

Calcium Handling Remodeling Underlies Impaired Sympathetic Stress Response in Ventricular Myocardium from Cacna1c Haploinsufficient Rats
por: Fender, Hauke, et al.
Publicado: (2023)

kHz-precision wavemeter based on reconfigurable microsoliton
por: Niu, Rui, et al.
Publicado: (2023)

Psychiatric risk gene Cacna1c determines mitochondrial resilience against oxidative stress in neurons
por: Michels, Susanne, et al.
Publicado: (2018)

Acupuncture Alleviates Anxiety and 22-kHz Ultrasonic Vocalizations in Rats Subjected to Repeated Alcohol Administration by Modulating the Brain-Derived Neurotrophic Factor/Corticotropin-Releasing Hormone Signaling Pathway
por: Seo, Su Yeon, et al.
Publicado: (2021)

Sex differences in 50 kHz call subtypes emitted during tickling-induced playful behaviour in rats
por: Tivey, Emma K. L., et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_ua9ah1o33metdrb63es1b6ubo6