summary lectures molecular principles of brain disorders, including workgroup (article) and pictures
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Molecular Principles of Brain Disorders (AB1049)
Instelling
Vrije Universiteit Amsterdam (VU)
a summery of the lectures of 'molecular principles of brain disorders'. this is part of the minor 'topics in biomedical science' and 'Biomolecular Science and Neuroscience - Track Neurosciences'. it includes the slides, additional explanation, pictures and a list of the learning outcomes.
MOLECULAR PRINCIPLES OF BRAIN DISORDERS
Contents
MODULE 1: PSYCHIATRIC DISORDERS ..................................................................................................... 2
Lecture 1 + 2: Etiology of mental traits and conditions ...................................................................... 2
Lecture 3 + 4 + 5: depression .............................................................................................................. 7
Part 1 ............................................................................................................................................... 7
Part 2 (6-9 of the current ideas etiology depression) ................................................................... 11
Workgroup 1: article “Epigenetic programming by maternal behavior” .......................................... 15
lecture 16: ADHD ............................................................................................................................... 17
Lecture 17: neurodiversity for ASD & ADHD ..................................................................................... 21
Lecture 18: schizophrenia ................................................................................................................. 23
Lecture 19: Bright side of mental illness: creativity and psychiatric conditions ............................... 28
Part 2: the neurobiology of resilience ........................................................................................... 30
learning outcomes: ............................................................................................................................ 34
MODULE 2: NEURODEGENERATIVE DISORDERS ................................................................................... 37
Lecture 6: general mechanisms in neuro-degeneration ................................................................... 37
Lecture 7: dementia 1, Alzheimer’s disease ...................................................................................... 41
Lecture 8: dementia 2, frontotemporal dementia ............................................................................ 44
Lecture 9: synucleopathies ................................................................................................................ 47
Lecture 10: Prion disease and Prion like mechanisms ...................................................................... 50
Lecture 11: stem cell technology in neurodegenerative disease ...................................................... 52
Lecture 12: therapy 1, treatment for neurodegenerative disease ................................................... 55
Lecture 13: therapy 2, targeting amyloid beta in Alzheimer’s disease ............................................. 57
Lecture 14: therapy 3, disease modifying therapy. The UPR as target ............................................. 60
Lecture 15: the genomes behind the 100+ study.............................................................................. 62
Learning outcomes: ........................................................................................................................... 64
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,MODULE 1: PSYCHIATRIC DISORDERS
Lecture 1 + 2: Etiology of mental traits and conditions
Behavior traits: impulsivity, mood, social behavior, stress-sensitivity, resilience and vulnerability.
- Each trait exists along a spectrum
o Example: Impulsivity (extremely thoughtful, difficulties decision taking – extremely
impulsive)
- What creates a trait? Is there a border between normal and abnormal behavior?
- Other traits: iq, extraversion, blood pressure
- Disorders: diabetes, obesities, autism (?), depression, schizophrenia
What factors can contribute to traits / (mental) characteristics and brain disorders
- Genetics
- Environmental factors
o Stress, infection, food, pregnancy, alcohol, trauma, family situation, etc.
Nature – nurture discussion:
- Past: tendency to explain disease via nurture concept.
o Autism = refrigerator mother
o Homosexual orientation= overly present mother
- Later: role biological factors more clear (nature)
- Hard reductionism: all psychiatric illness is best explained solely in terms of molecular
neuroscience
- Etiological models for psychiatric disease need to be pluralistic (= trueth is more than reality,
with a multiplicity of principles) or multilevel
- Best understood from biological, psychological and sociocultural, economic perspectives
- Break down dichotomy between nature-nurture, but view brain as in constant interaction
with environment, society and culture via plasticity.
Most brain disorders are complex, multifactorial disoders
- Both genetic and environmental factors involved in etiology.
- Often complex interactions and causal loops, Complex puzzle
- Genes and environmental factors
- How can environmental factors exert their influence?
o Altered expression via
▪ Stress system
▪ Epigenetics
- Interactions gene-environment
Genes
- From twin + adoption studies: several behavioral traits and psychiatric diseases moderate /
high heritability
- Heritability: proportion of variance in symptoms (of a certain condition) that is explained by
the variance in genetic factors
o Major depression 40-50%
o ADHD: 75%
2
, o Autism, bipolar disorder, schizophrenia around 80%
o NOT: when your parents have ADHD, you have 75% change getting it. trueth: you can
explain a trait (impulsivity) 75% by the genetics.
- In post – humane genome project era
o Expectation: easy to find risk genes
o Contrary: it was very difficult to identify the risk genes; ‘Missing heritability’
o Model of single / few risk genes = overly simplistic paradigm. (genetic risk is not
really a thing. It increases the risk only by a tiny amount. It is difficult to spot this).
Genes and psychiatry
- Classic theory: Single abnormal gene → abnormal gene product → neuronal malfunction →
mental illness
o Single abnormal gene is not sufficient to cause mental conditions
o What is pathway from gene to mental conditions?
- New explanations, new hypotheses, new models for pathway ‘genotype to phenotype’.
o 1. ‘Complex genetics’ or ‘diathesis-stress model’ (explained in lecture etiology)
o 2. ‘Differential susceptibly to environment hypothesis’ (explained in lecture
neurobiology of resilience)
o 3. ‘balancing selection hypothesis’ (explained in lecture mental illness & creativity)
- new hypotheses and new models are complex
- new ways of doing research and unravel these pathways from genotype to phenotype:
‘endophenotype approach’
- hypothesis: mental conditions are caused by multiple small contributions from several genes,
all interacting with environmental stressors.
- ‘Complex genetics’
o Complex set of risk factors that bias person toward condition/illness but do not cause
it (inherits risk not disease). it is about probability. Every risk factor is tiny.
o Reachting tipping point: high probability developing condition/disorder. (critical
point in an evolving situation that leads to a new and irreversible development)
o Concept also applies to hypertension, obesity, diabetes, etc.
Endophenotype approach: from genotype to phenotype
- path from gene → mental illness
- new ways of doing research and unravel’ these pathways from ‘genotype to phenotype’:
endophenotype approach
- pathway genotype to phenotype is much more complex!
- solution: important intermediaries between gene (genotype) and
disease/behavior(phenotype)
- endophenotypes:
o measurable, inheritable and closely linked to disease condition
o more precisely measurable than disease/condition
o two types:
▪ biological endophenotypes (more close to genotype site)
▪ symptom/system endophenotypes (more close to the phenotype site)
o electrophysiological response to startle
o neuroimaging response to information processing
o activation of certain brain circuit
symptom/system endophenotypes: single symptoms associated with mental disease/condition:
o insomnia
o executive dysfunction
o hallucinations
o poor fear conditioning
o anhedonia (easily with a questionnaire)
genes and psychiatry
- gene → molecules → circuits → information processing (biological phenotype) → single
symptom (system endophenotype) → full syndrome or mental condition/disorder
o closer to the gene on pathway → more readily linked to gene (so the link gene to
endophenotype is easier than to the condition / disease)
o genes only loosely linked to psychiatric conditions/disorders, therefore hard to
identify
psychopathology and brain circuits
- etiology of psychiatric conditions is moving beyond receptors, enzymes and other molecules
as causes. (depression is often explained by to low numbers of serotonin, this is not etiology
good explained).
- New paradigm: psychiatric symptoms are increasingly linked to malfunctioning specific brain
circuits
- Genes + environmental risk factors conspire to produce inefficient information processing in
neuronal circuitry
- Brain imaging → focus on brain circuits
Why are subtle molecular abnormalities not more ‘penetrant ‘at behavioral level?
- Multiple genes complementary / redundant effects ‘healthy compensatory backup system’.
- Risk genes are not necessary sufficient to cause mental conditions / disorders
- Combination with environmental risk factors (stress, life events, biological stressors such as
viruses, toxins…)!!!
Socio-ecological framework: no single factor can explain
- There is a dynamic interplay of multiple risk and protective factors.
o Risk and protective factors are along a social ecology continuum: (small to big)
▪ Individual (also genes belong to this) – Relationship - Cultural /
environmental
o Environmental:
▪ Pre/peri natal risk factors: maternal stress during pregnancy, maternal
nutritional deficiency, maternal use of tobacco / alcohol / drugs /
medication.
▪ Birth complications
▪ Perinatal nutrition deficiency, maternal separation
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