Oxytocin and Vasopressin: Mechanisms for Potential Sex Differences Observed in Autism Spectrum Disorders

Author(s):  
C. Sue Carter ◽  
Suma Jacob

The effects of oxytocin and vasopressin on the brain and behavior can be sexually dimorphic, especially during the course of development (Bales, Kim, et al., 2004; Bales, Pfeifer, et al., 2004; Bales, Plotsky, et al., 2007; Bielsky et al., 2005a; Carter, 2003; Thompson et al., 2006; Yamamoto et al., 2005; Yamamoto et al., 2004). Given the sexual discrepancy observed in autism spectrum disorders (ASDs), these two neuropeptides, oxytocin (OT) and arginine vasopressin (AVP), have received attention for their potential role in ASDs (Green and Hollander, 2010; Insel et al., 1999; Leckman & Herman, 2002; Welch et al., 2005; Winslow, 2005; Young et al., 2002). Changes in either OT or AVP and their receptors could be capable of influencing symptom domains or behaviors associated with ASDs. Arginine vasopressin is androgen dependent in some brain regions (De Vries & Panzica, 2006), and males are more sensitive to AVP, especially during development. We hypothesize here that AVP, which has a unique role in males, must be present in optimal levels to be protective against ASDs. Either excess AVP or disruptions in the AVP system could play a role in development of the traits found in ASDs. In contrast, OT may possibly be secreted in response to adversity, especially in females, serving as a protective factor.

2020 ◽  
Vol 10 (7) ◽  
pp. 435
Author(s):  
Andrea Caria ◽  
Luciana Ciringione ◽  
Simona de Falco

An accumulating body of evidence indicates a tight relationship between the endocrine system and abnormal social behavior. Two evolutionarily conserved hypothalamic peptides, oxytocin and arginine-vasopressin, because of their extensively documented function in supporting and regulating affiliative and socio-emotional responses, have attracted great interest for their critical implications for autism spectrum disorders (ASD). A large number of controlled trials demonstrated that exogenous oxytocin or arginine-vasopressin administration can mitigate social behavior impairment in ASD. Furthermore, there exists long-standing evidence of severe socioemotional dysfunctions after hypothalamic lesions in animals and humans. However, despite the major role of the hypothalamus for the synthesis and release of oxytocin and vasopressin, and the evident hypothalamic implication in affiliative behavior in animals and humans, a rather small number of neuroimaging studies showed an association between this region and socioemotional responses in ASD. This review aims to provide a critical synthesis of evidences linking alterations of the hypothalamus with impaired social cognition and behavior in ASD by integrating results of both anatomical and functional studies in individuals with ASD as well as in healthy carriers of oxytocin receptor (OXTR) genetic risk variant for ASD. Current findings, although limited, indicate that morphofunctional anomalies are implicated in the pathophysiology of ASD and call for further investigations aiming to elucidate anatomical and functional properties of hypothalamic nuclei underlying atypical socioemotional behavior in ASD.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Jason L. He ◽  
Georg Oeltzschner ◽  
Mark Mikkelsen ◽  
Alyssa Deronda ◽  
Ashley D. Harris ◽  
...  

AbstractIndividuals on the autism spectrum are often reported as being hyper- and/or hyporeactive to sensory input. These sensory symptoms were one of the key observations that led to the development of the altered excitation-inhibition (E-I) model of autism, which posits that an increase ratio of excitatory to inhibitory signaling may explain certain phenotypical expressions of autism spectrum disorders (ASD). While there has been strong support for the altered E-I model of autism, much of the evidence has come from animal models. With regard to in-vivo human studies, evidence for altered E-I balance in ASD come from studies adopting magnetic resonance spectroscopy (MRS). Spectral-edited MRS can be used to provide measures of the levels of GABA + (GABA + macromolecules) and Glx (glutamate + glutamine) in specific brain regions as proxy markers of inhibition and excitation respectively. In the current study, we found region-specific elevations of Glx in the primary sensorimotor cortex (SM1) in ASD. There were no group differences of GABA+ in either the SM1 or thalamus. Higher levels of Glx were associated with more parent reported difficulties of sensory hyper- and hyporeactivity, as well as reduced feed-forward inhibition during tactile perception in children with ASD. Critically, the finding of elevated Glx provides strong empirical support for increased excitation in ASD. Our results also provide a clear link between Glx and the sensory symptoms of ASD at both behavioral and perceptual levels.


2018 ◽  
Vol 40 (3) ◽  
pp. 142-151 ◽  
Author(s):  
Belinda L. Daughrity

This current study explores parent perceptions of barriers to friendship development for highly verbal children with autism spectrum disorders (ASD) in mainstream academic settings. Participants were 10 parents of school-age children with ASD in mainstream classrooms. Findings from semistructured interviews and qualitative analysis pointed to five central themes regarding barriers to friendship development: propinquity, attempts at social exposure, common social problems within ASD, siblings as a protective factor, and parent networks. Results suggest parent networks among parents with mainstreamed children may help to facilitate social opportunities both in and out of school. Further investigation is needed to explore possible solutions to help parents to better support friendship development.


2019 ◽  
Vol 8 (4) ◽  
pp. 487 ◽  
Author(s):  
Billeci ◽  
Calderoni ◽  
Conti ◽  
Lagomarsini ◽  
Narzisi ◽  
...  

Autism Spectrum Disorders (ASD) is a group of neurodevelopmental disorders that is characterized by an altered brain connectivity organization. Autistic traits below the clinical threshold (i.e., the broad autism phenotype; BAP) are frequent among first-degree relatives of subjects with ASD; however, little is known regarding whether subthreshold behavioral manifestations of ASD mirror also at the neuroanatomical level in parents of ASD probands. To this aim, we applied advanced diffusion network analysis to MRI of 16 dyads consisting of a child with ASD and his father in order to investigate: (i) the correlation between structural network organization and autistic features in preschoolers with ASD (all males; age range 1.5–5.2 years); (ii) the correlation between structural network organization and BAP features in the fathers of individuals with ASD (fath-ASD). Local network measures significantly correlated with autism severity in ASD children and with BAP traits in fath-ASD, while no significant association emerged when considering the global measures of brain connectivity. Notably, an overlap of some brain regions that are crucial for social functioning (cingulum, superior temporal gyrus, inferior temporal gyrus, middle frontal gyrus, frontal pole, and amygdala) in patients with ASD and fath-ASD was detected, suggesting an intergenerational transmission of these neural substrates. Overall, the results of this study may help in elucidating the neurostructural endophenotype of ASD, paving the way for bridging connections between underlying genetic and ASD symptomatology.


Author(s):  
Alinne Lorrany Gomes Dos Santos ◽  
Ellen Rose Leandro Ponce de Leão ◽  
Larissa Victória Barra de Moura ◽  
Dilza Souza ◽  
Daniel Guerreiro Diniz ◽  
...  

2021 ◽  
Author(s):  
Yvonne M.Y. Han ◽  
Suk Yu Yau ◽  
Melody M.Y. Chan ◽  
Chun Kwok Wong ◽  
Agnes S. Chan

Abstract Previous studies have shown that immunological factors are involved in the pathogenesis of autism spectrum disorders (ASDs). The present study examined whether immunological abnormalities are associated with cognitive deficits and problem behaviors in children with ASD and whether children with ASD show different immunological biomarkers and brain-derived neurotrophic factor BDNF levels than typically developing (TD) children. Sixteen TD and 18 children with ASD, aged 6–18 years, voluntarily participated in the study. Participants’ executive functions were measured using neuropsychological tests, and behavioral measures were measured using parent ratings. Immunological measures were assessed by measuring the levels of chemokine ligand 2 (CCL2) and chemokine ligand 5 (CCL5) in participants’ blood serum. Children with ASD showed greater deficits in cognitive functions as well as altered levels of immunological measures when compared to TD children, and their cognitive functions and behavior deficits were significantly associated with increased CCL5 levels and decreased BDNF levels. These results provide evidence to support the notion that altered immune functions are associated with neuronal deficits, are indexed by decreased levels of BDNF and manifest as selective cognitive and behavioral symptoms in individuals with ASD.


2020 ◽  
Author(s):  
Jinglun Li ◽  
Xiu Chen ◽  
Ruwen Zheng ◽  
Ai Chen ◽  
Yan Zhou ◽  
...  

Abstract BackgroundAutism Spectrum Disorders (ASD) is a neurodevelopment disorder. The cerebellum has been reported to be one of the key regions involved in ASD. However, the associations between the cerebellum and clinical traits remain unclear. MethodsHere we performed Amplitude of Low Frequency Fluctuations (ALFF) analysis to detect the alterations of brain spontaneous activity in ASDs and explore the associations between spontaneous brain activity and clinical traits. ResultsCompared with normal controls, cerebellum crus 2 showed significantly weaker average ALFF values. Other regions such as left cerebellum 6, cerebellum vermis 4 5, putamen, SMA and thalamus showed increased mean ALFF values. In ASD patients with SRS total score T above 59, the mean ALFF values of cerebellum vermis 4 5 was significantly correlated with SRS total score T (r=0.175, P=0.031), SRS cognition score T (r=0.169, P=0.036) and SRS motivation score T (r=0.176, P=0.028).ConclusionsThese findings were not observed in other brain regions and in normal controls. Our study suggests a role of cerebellum in cognitive impairments in ASD and supports a mechanistic basis for the targeted treatment of ASD disorders.Trial registrationNot applicable.


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