https://time.com/6551520/loneliness-autism-essay/
Victor Pineda the new head of CIL
Excellent news about Victor Pineda getting to be the new head of Center for Independent Living.
Great pick for CIL. I remember former CIL head James Stuart referring to Victor as a "Super Crip".
- https://uniquelyhari.blogspot.com/2019/04/dr-victor-pineda.html
- https://uniquelyhari.blogspot.com/2019/02/role-of-disability-in-society.html
- https://uniquelyhari.blogspot.com/2019/02/lives-worth-living_2.html
- https://uniquelyhari.blogspot.com/2019/09/word-enabled-summer-internship.html
- https://uniquelyhari.blogspot.com/2020/04/a-chilling-waiting-game-disability-and.html
The Cocktail Party Effect
The cocktail party effect refers to the brain's ability to focus on a specific auditory stimulus, such as a single conversation, in a noisy environment. In autism, difficulties with this selective auditory attention may contribute to sensory overload and challenges in social communication.
PlainSpeak: The cocktail party effect is the ability to tune into one conversation in a noisy room. Many autistic individuals may find this difficult, leading to sensory overload and making social situations challenging.
Read more on the Cocktail Party Effect:
Impact of language choices in scientific publication on representation of autistic researchers.
The impact manifests in several key ways.
- Inclusivity and Accessibility. Language that is clear, direct, and jargon-free is more accessible to a wider audience. Which means a wider spectrum of autistics can engage more fully with scientific content, whether they are authors, reviewers, or readers.
- Bias and stigma.
- Representation. Who is getting left out and who is getting included.
- Authorship and collaboration. Autistics may face barriers in scientific publishing due to implicit biases in what is considered rigorous or appropriate academic language. This can discourage participation or lead to under representation in authorship and peer review processes.
- Ethical considerations. Engaging the autistic community ensures that scientific discourse does not inadvertently marginalize or misrepresent groups.
- Policy and guidelines. Journals and publishers can influence language norms through their style guides and editorial policies. By adopting guidelines that favor inclusive and respectful language, publishers can lead the shift towards more equitable representation in scientific literature.
Even after being told to stop
I submitted an Abstract
Decoding the Excitatory-Inhibition Imbalance in Autism
The Excitatory-Inhibition (E-I) Imbalance hypothesis posits that an imbalance between excitatory and inhibitory signaling in the brain contributes to the sensory, cognitive, and behavioral features of autism.
Factors that contribute to the E-I imbalance.
Elevated Glutamate and Hyperactive Glutamatergic Neurons
Glutamate is the primary excitatory neurotransmitter in the brain, and its excessive release or receptor overactivation can lead to heightened neuronal excitability. Research indicates that autistics have increased glutamate concentrations in certain brain regions, suggesting a hyper-excitable state that disrupts normal neural communication and network dynamics. This over-excitation can manifest in the form of heightened sensitivity to sensory stimuli and difficulties in cognitive processing.
GABAergic Signaling Deficit
GABA is the primary inhibitory neurotransmitter, crucial for counterbalancing excitation. In autism, there is often a reduction in GABAergic signaling, whether through decreased GABA levels, impaired GABA receptor function, or reduced GABAergic neuron activity. This means that the inhibitory 'brake' on neuronal activity is weakened, failing to counteract the excessive excitation from glutamate, thus exacerbating the E-I imbalance.
Imbalance in Pyramidal Neurons and Interneurons
Pyramidal neurons are the primary excitatory cells in the cortex, while interneurons provide the necessary inhibitory control. In autism, there are differences in the density, function, and connectivity of these neuron types eg: alterations in the number or function of specific types of inhibitory interneurons, such as parvalbumin-positive (PV+) interneurons. These changes disrupt the local circuitry, leading to an overall increase in excitation and reduced inhibition.
Critical Developmental Periods
E-I imbalance is particularly impactful during critical developmental periods when the brain is highly plastic and sensitive to changes. Early disruptions in E-I balance can have long-lasting effects on brain development and function. During these periods, the maturation of both excitatory and inhibitory circuits is crucial for establishing proper neural networks. If the E-I balance is skewed, it can impair synaptic plasticity, cortical maturation, and the formation of functional neural circuits, contributing to the developmental trajectory of autism.
Alterations in Synaptic Proteins
Changes in the expression or function of synaptic proteins play a critical role in E-I imbalance. Proteins such as neuroligins and neurexins, which are involved in synaptic adhesion and signaling, have been implicated in autism. Mutations or dysregulation of these proteins can lead to atypical synapse formation and function, contributing to an imbalance between excitatory and inhibitory synapses.
Ion Channel Dysfunction
Ion channels are essential for maintaining the proper function of neurons. Dysfunctions in ion channels, such as those involving sodium, potassium, and calcium, can alter neuronal excitability. In autism, mutations in genes encoding these ion channels (e.g., SCN2A, KCNQ2) have been identified, leading to altered action potential generation and propagation, thereby affecting the E-I balance.
Impaired Synaptic Plasticity
Synaptic plasticity, the ability of synapses to strengthen or weaken over time, is crucial for learning and memory. Long-term potentiation (LTP) and long-term depression (LTD) are key mechanisms of synaptic plasticity that depend on a delicate E-I balance. In autism, impairments in LTP and LTD have been observed, suggesting that the capacity for synaptic change is disrupted, further contributing to cognitive and behavioral challenges.
Role of Astrocytes and Microglia
Astrocytes and microglia, types of glial cells, also play significant roles in maintaining E-I balance. Astrocytes regulate neurotransmitter levels, including glutamate and GABA, by uptake and recycling processes. Dysregulation of astrocyte function can lead to excess glutamate and insufficient GABA, exacerbating E-I imbalance. Microglia, the brain's immune cells, are involved in synaptic pruning during development. Abnormal microglial activity can lead to either excessive or insufficient synaptic pruning, disrupting the E-I balance and normal brain connectivity.
Genetic and Epigenetic Factors
Genetic mutations and epigenetic modifications can influence E-I balance. Numerous genes associated with autism are involved in synaptic function, neurotransmitter systems, and neuronal development. Additionally, epigenetic changes, such as DNA methylation and histone modification, can alter gene expression patterns related to E-I balance. These genetic and epigenetic factors contribute to the heterogeneity observed in autism, affecting the degree and nature of E-I imbalance across individuals.
Environmental Influences
Environmental factors, including prenatal exposure to toxins, infections, and stress, can impact E-I balance. These factors can alter the development of neural circuits and neurotransmitter systems, leading to long-term changes in excitatory and inhibitory signaling. Understanding the interaction between genetic predisposition and environmental influences is crucial for comprehending the full picture of E-I imbalance in autism.
- 2 versions of this post:
- For the Scientific/Academic Audience
- PlainSpeak / Plain Language for the Lay Reader
Keynote at Duke ACE
Rewind: Interactions with Planet X
Rewinding to something I wrote many years ago in high school.
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Interactions with Planet X
Words matter: Reframing neurodivergence in science, medicine and society
How we write and think about neurodiversity can have a profound effect on people’s lives; watch the webinar hosted by Cell Press and The Lancet.
Weak Central Coherence Theory of Autism
Autism Lexicon: Weak Central Coherence (WCC) Theory
The WCC Theory is a cognitive theory of autism (cognitive theories try to explain how autistics think).
It suggests that autistics focus on noticing details but might struggle with seeing the bigger picture. This affects how they see and understand the world around them. This unique way of thinking brings both strengths and challenges, affecting everyday tasks, social interactions, and work or hobbies.
Read about WCC in more detail
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Vanderbilt Brain Institute Graduate Student Directory
https://medschool.vanderbilt.edu/brain-institute/about-us/team-directories/#h2-graduate-student-directory