NEUROBIOLOGICAL UNDERPINNINGS OF LANGUAGE IN AUTISM SPECTRUM DISORDERS

As a neurodevelopmental disorder, autism is characterized by impairments and differences at the levels of both brain and behavior. Communicative impairments in autism are a core feature of the disorder, and a rapidly expanding literature is exploring language in autism using the tools of cognitive neuroscience, particularly electroencephalography and brain imaging. Recent research indicates consistent differences in the degree to which language-specific processes are lateralized in the brain, and it also suggests that language impairments are linked to differences in brain structure that may lead to inefficient coordination of activity between different neural assemblies to achieve a complex cognitive task, defined as functional connectivity. We review findings from current work and suggest that neurobiological data are critical in our ability to understand the mechanisms underlying behavioral differences in communicative skills. Going beyond simple dichotomies between delayed versus deviant development, we can use such data to ask whether behavior reflects processes that are merely inefficient or, instead, whether impairments at the behavioral level reflect fundamental differences in brain organization and the networks involved in various tasks.

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Epilepsy: A Stigma More than Disease

Annals of Advanced Biomedical Sciences ◽

10.23880/aabsc-16000131 ◽

2019 ◽

Vol 2 (1) ◽

Author(s):

Rana Khalid Iqbal

Keyword(s):

Genetic Basis ◽

Neurodevelopmental Disorder ◽

Health Conditions ◽

Attitudes And Beliefs ◽

Negative Attitudes ◽

Male And Female ◽

Ancient Times ◽

Brain And Behavior ◽

And Behavior ◽

The Brain

Epilepsy is a common neurological disorder that occurs from ancient times and accompanying with convulsions or seizures. Epilepsy has revealed a genetic basis. Epilepsy which is considered as a neurodevelopmental disorder has reduced the life expectancy and associated with various stigmatized attitudes or beliefs. Epilepsy and seizures can develop in any person both in male and female at any age. Head trauma and brain strokes are the major causes of epilepsy in adults. Epilepsy accompanied by changes in behavior, personality, and cognition. Several aspects of epilepsy can affect the brain and behavior. Stigma is a reality for a lot of people with a mental disorder. It is a mark of disgrace which sets a person apart from others. Negative attitudes and beliefs create prejudice which leads to negative actions and discrimination. Stigma and social exclusions are stereotyped characteristics of epilepsy. Someone with a mental illness known to be a dangerous and senseless rather than saying in poor health conditions. There are no effective cures for an epileptic people. Besides, many epileptic therapies or cures are still available for the diagnosis and prevention of people with epilepsy. Epilepsy treatment entails how epilepsy is treated and which techniques and antiepileptic drugs are used.

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Behavioral Alterations and Decreased Number of Parvalbumin-Positive Interneurons in Wistar Rats after Maternal Immune Activation by Lipopolysaccharide: Sex Matters

International Journal of Molecular Sciences ◽

10.3390/ijms22063274 ◽

2021 ◽

Vol 22 (6) ◽

pp. 3274

Author(s):

Iveta Vojtechova ◽

Kristyna Maleninska ◽

Viera Kutna ◽

Ondrej Klovrza ◽

Klara Tuckova ◽

...

Keyword(s):

Immune Activation ◽

Autism Spectrum ◽

Startle Reaction ◽

Adult Offspring ◽

Behavioral Alterations ◽

Maternal Immune Activation ◽

Brain And Behavior ◽

Communication Impairments ◽

And Behavior ◽

The Brain

Maternal immune activation (MIA) during pregnancy represents an important environmental factor in the etiology of schizophrenia and autism spectrum disorders (ASD). Our goal was to investigate the impacts of MIA on the brain and behavior of adolescent and adult offspring, as a rat model of these neurodevelopmental disorders. We injected bacterial lipopolysaccharide (LPS, 1 mg/kg) to pregnant Wistar dams from gestational day 7, every other day, up to delivery. Behavior of the offspring was examined in a comprehensive battery of tasks at postnatal days P45 and P90. Several brain parameters were analyzed at P28. The results showed that prenatal immune activation caused social and communication impairments in the adult offspring of both sexes; males were affected already in adolescence. MIA also caused prepulse inhibition deficit in females and increased the startle reaction in males. Anxiety and hypolocomotion were apparent in LPS-affected males and females. In the 28-day-old LPS offspring, we found enlargement of the brain and decreased numbers of parvalbumin-positive interneurons in the frontal cortex in both sexes. To conclude, our data indicate that sex of the offspring plays a crucial role in the development of the MIA-induced behavioral alterations, whereas changes in the brain apparent in young animals are sex-independent.

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Review of Self-regulation of the Brain and Behavior.

Contemporary Psychology ◽

10.1037/023440 ◽

1985 ◽

Vol 30 (12) ◽

pp. 999-999

Author(s):

Gerald S. Wasserman

Keyword(s):

Self Regulation ◽

Brain And Behavior ◽

And Behavior ◽

The Brain

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FOXP1 syndrome: a review of the literature and practice parameters for medical assessment and monitoring

Journal of Neurodevelopmental Disorders ◽

10.1186/s11689-021-09358-1 ◽

2021 ◽

Vol 13 (1) ◽

Author(s):

Reymundo Lozano ◽

Catherine Gbekie ◽

Paige M. Siper ◽

Shubhika Srivastava ◽

Jeffrey M. Saland ◽

...

Keyword(s):

Neurodevelopmental Disorder ◽

Autism Spectrum ◽

Medical Assessment ◽

Forkhead Box ◽

Organ Systems ◽

Practice Parameters ◽

Assessment And Monitoring ◽

Multidisciplinary Group ◽

The Brain

AbstractFOXP1 syndrome is a neurodevelopmental disorder caused by mutations or deletions that disrupt the forkhead box protein 1 (FOXP1) gene, which encodes a transcription factor important for the early development of many organ systems, including the brain. Numerous clinical studies have elucidated the role of FOXP1 in neurodevelopment and have characterized a phenotype. FOXP1 syndrome is associated with intellectual disability, language deficits, autism spectrum disorder, hypotonia, and congenital anomalies, including mild dysmorphic features, and brain, cardiac, and urogenital abnormalities. Here, we present a review of human studies summarizing the clinical features of individuals with FOXP1 syndrome and enlist a multidisciplinary group of clinicians (pediatrics, genetics, psychiatry, neurology, cardiology, endocrinology, nephrology, and psychology) to provide recommendations for the assessment of FOXP1 syndrome.

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LSD1 enzyme inhibitor TAK-418 unlocks aberrant epigenetic machinery and improves autism symptoms in neurodevelopmental disorder models

Science Advances ◽

10.1126/sciadv.aba1187 ◽

2021 ◽

Vol 7 (11) ◽

pp. eaba1187

Author(s):

Rina Baba ◽

Satoru Matsuda ◽

Yuuichi Arakawa ◽

Ryuji Yamada ◽

Noriko Suzuki ◽

...

Keyword(s):

Gene Expression ◽

Enzyme Activity ◽

Neurodevelopmental Disorders ◽

Neurodevelopmental Disorder ◽

Specific Inhibitor ◽

Autism Spectrum ◽

Poly I:C ◽

Control Of Gene Expression ◽

Epigenetic Machinery ◽

The Brain

Persistent epigenetic dysregulation may underlie the pathophysiology of neurodevelopmental disorders, such as autism spectrum disorder (ASD). Here, we show that the inhibition of lysine-specific demethylase 1 (LSD1) enzyme activity normalizes aberrant epigenetic control of gene expression in neurodevelopmental disorders. Maternal exposure to valproate or poly I:C caused sustained dysregulation of gene expression in the brain and ASD-like social and cognitive deficits after birth in rodents. Unexpectedly, a specific inhibitor of LSD1 enzyme activity, 5-((1R,2R)-2-((cyclopropylmethyl)amino)cyclopropyl)-N-(tetrahydro-2H-pyran-4-yl)thiophene-3-carboxamide hydrochloride (TAK-418), almost completely normalized the dysregulated gene expression in the brain and ameliorated some ASD-like behaviors in these models. The genes modulated by TAK-418 were almost completely different across the models and their ages. These results suggest that LSD1 enzyme activity may stabilize the aberrant epigenetic machinery in neurodevelopmental disorders, and the inhibition of LSD1 enzyme activity may be the master key to recover gene expression homeostasis. TAK-418 may benefit patients with neurodevelopmental disorders.

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Song competition changes the brain and behavior of a male songbird

Journal of Experimental Biology ◽

10.1242/jeb.028456 ◽

2009 ◽

Vol 212 (15) ◽

pp. 2411-2418 ◽

Cited By ~ 7

Author(s):

K. W. Sockman ◽

K. G. Salvante ◽

D. M. Racke ◽

C. R. Campbell ◽

B. A. Whitman

Keyword(s):

Brain And Behavior ◽

And Behavior ◽

The Brain

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The brain and behavior of the fowl

General Pharmacology The Vascular System ◽

10.1016/0306-3623(84)90107-1 ◽

1984 ◽

Vol 15 (2) ◽

pp. 175

Keyword(s):

Brain And Behavior ◽

And Behavior ◽

The Brain

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Müllerian inhibiting substance contributes to sex-linked biases in the brain and behavior

Proceedings of the National Academy of Sciences ◽

10.1073/pnas.0902253106 ◽

2009 ◽

Vol 106 (17) ◽

pp. 7203-7208 ◽

Cited By ~ 45

Author(s):

Pei-Yu Wang ◽

Anna Protheroe ◽

Andrew N. Clarkson ◽

Floriane Imhoff ◽

Kyoko Koishi ◽

...

Keyword(s):

Motor Neurons ◽

Reproductive Tract ◽

Behavioral Traits ◽

Spinal Motor Neurons ◽

Müllerian Inhibiting Substance ◽

Males And Females ◽

Brain And Behavior ◽

And Behavior ◽

The Brain ◽

Mullerian Inhibiting Substance

Many behavioral traits and most brain disorders are common to males and females but are more evident in one sex than the other. The control of these subtle sex-linked biases is largely unstudied and has been presumed to mirror that of the highly dimorphic reproductive nuclei. Sexual dimorphism in the reproductive tract is a product of Müllerian inhibiting substance (MIS), as well as the sex steroids. Males with a genetic deficiency in MIS signaling are sexually males, leading to the presumption that MIS is not a neural regulator. We challenge this presumption by reporting that most immature neurons in mice express the MIS-specific receptor (MISRII) and that male Mis−/− and Misrii−/− mice exhibit subtle feminization of their spinal motor neurons and of their exploratory behavior. Consequently, MIS may be a broad regulator of the subtle sex-linked biases in the nervous system.

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Sex differences in neural and behavioral signatures of cooperation revealed by fNIRS hyperscanning

Scientific Reports ◽

10.1038/srep26492 ◽

2016 ◽

Vol 6 (1) ◽

Cited By ~ 57

Author(s):

Joseph M. Baker ◽

Ning Liu ◽

Xu Cui ◽

Pascal Vrticka ◽

Manish Saggar ◽

...

Keyword(s):

Sex Differences ◽

Temporal Cortex ◽

Neural Correlates ◽

Behavioral Signatures ◽

Computer Based ◽

Males And Females ◽

Brain And Behavior ◽

The Right ◽

And Behavior ◽

The Brain

Abstract Researchers from multiple fields have sought to understand how sex moderates human social behavior. While over 50 years of research has revealed differences in cooperation behavior of males and females, the underlying neural correlates of these sex differences have not been explained. A missing and fundamental element of this puzzle is an understanding of how the sex composition of an interacting dyad influences the brain and behavior during cooperation. Using fNIRS-based hyperscanning in 111 same- and mixed-sex dyads, we identified significant behavioral and neural sex-related differences in association with a computer-based cooperation task. Dyads containing at least one male demonstrated significantly higher behavioral performance than female/female dyads. Individual males and females showed significant activation in the right frontopolar and right inferior prefrontal cortices, although this activation was greater in females compared to males. Female/female dyad’s exhibited significant inter-brain coherence within the right temporal cortex, while significant coherence in male/male dyads occurred in the right inferior prefrontal cortex. Significant coherence was not observed in mixed-sex dyads. Finally, for same-sex dyads only, task-related inter-brain coherence was positively correlated with cooperation task performance. Our results highlight multiple important and previously undetected influences of sex on concurrent neural and behavioral signatures of cooperation.

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