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Experience-dependent brain change
Environmental features can change the hardwiring of the brain (neuronal structures), producing stable changes within the person
Epigenetic mechanisms
Environment changes gene expression, NOT the DNA sequence
Reciprocal gene-environment relationship
Genes affect responses to environments; environments change gene expression, brain structure, and physiology, which change behavior
Glucocorticoids (GCs)
Stress hormones such as cortisol; sustained high levels have negative health effects and can impair the hippocampus
Hippocampus
Brain structure crucial for learning and memory (especially spatial memory)
Stress and the hippocampus
Chronic stress → high cortisol → reduced hippocampal volume (impairs learning and new memory formation)
seen in depression and PTSD
DNA sequence is NOT changed
Depression duration and the hippocampus
Longer time spent depressed is associated with smaller left hippocampal volume
Maguire et al. (2000)
London taxi drivers had a larger posterior hippocampus than controls; learning the city's layout → spatial memory formation and retrieval
Stress vs. learning effects on the hippocampus
Sustained stress hormones shrink it; repeated active use and learning grow it
Level of arousal (LOA)
Physiological arousal level in the brain; differs between extraverts and introverts
ARAS
Ascending reticular activation system in the brainstem
regulates attention, arousal, vigilance, and sleep-wake cycles
ARAS in introverts vs extraverts
Introverts: even small amounts of stimulation overstimulate the ARAS → distress and withdrawal
Extraverts: large amounts of stimulation are needed to activate the ARAS → seek more engaging activities
Optimal level of arousal (OLA)
arousal level most appropriate for doing a task effectively
too much or too little undermines performance
Yerkes-Dodson law
Inverted-U relation between arousal and performance:
low arousal → boredom/inattention
moderate → optimal
high → anxiety impairs performance
Introvert vs Extravert OLA
Introvert: lower optimal level of arousal → perform better in less stimulating environments
Extravert: higher optimal level of arousal → bored easily, seek stimulation
Geen's findings
Introverts preferred lower levels of stimulation and performed worse than extraverts under high stimulation
Behavioral Inhibition System (BIS)
Causes withdrawal from undesirable stimuli
avoidance and hypervigilance
punishment-avoiding
right frontal activity
linked to introversion and anxiety
magnifies reactions to negative events
Behavioral Activation System (BAS)
Directs approach toward desirable goals/incentives
reward-seeking
left frontal activity
greater activity in extraverts (NEO-PI-R)
magnifies reactions to positive events
BIS/BAS independence
BIS and BAS are functionally independent neurological systems
BIS/BAS Scale
measures BIS plus three BAS subscales: reward responsiveness, drive, fun seeking
Carver & White (1994)
Gable's BIS/BAS findings
BAS sensitivity magnified reactions to positive events and correlated with higher positive affect
BIS sensitivity magnified reactions to negative events
Sensation Seeking Scale (SSS)
tedb
4 aspects
thrill and adventure seeking
experience seeking
disinhibition
boredom susceptibility
Sensation seekers
Restless and upset when stimulation is lacking
correlated with a high optimal level of arousal
low scorers get stressed when closely confined with another person
High sensation seeker traits
Risk-taking (sex, drugs, driving, sports)
prefer complexity, tolerate ambiguity, more original and creative
liberal/nonconforming
prefer high-stimulation jobs
may view love as a game
Neurotransmitters
Chemicals in nerve cells that transmit impulses from cell to cell across synapses
Monoamine oxidase (MAO)
Enzyme that breaks down serotonin, dopamine, norepinephrine, and epinephrine after use
high sensation seekers tend to have LOW MAO → higher NT levels
MAO is NOT the sole cause
No one-to-one mapping
A single physiological pathway rarely maps onto a single personality trait; neural correlates of thoughts, feelings, and behaviors are complex
Endocrine glands
Secrete hormones into the bloodstream to maintain homeostasis
Hormones vs. neurotransmitters
Hormones travel through the blood and act slower, more widespread, and longer-term; neurotransmitters act quickly across synapses (nervous system)
Purely endocrine organs
Organs dedicated solely to hormone secretion: pituitary, pineal, thyroid, parathyroid, adrenal glands (cortex and medulla)
Organs with endocrine cells
Organs that also contain endocrine cells: pancreas, thymus, gonads, hypothalamus
Pituitary gland
"Master gland"; releases hormones that signal other glands
Steroid hormones
Lipid-soluble hormones produced from cholesterol (estrogen, progesterone, testosterone, cortisol); the ONLY hormones that cross the cell membrane; bind receptors inside the cell and affect transcription
Water-soluble hormones
Amino acid-based hormones; cannot cross the cell membrane, so they bind receptors on the cell surface
Cortisol
Glucocorticoid (steroid hormone) released from the adrenal glands; key in the stress response
HPA axis
Hypothalamus releases CRH → pituitary releases ACTH → adrenal gland releases cortisol → short-term stress responses (fight, flight, freeze); hypothalamus responds to cortisol level (feedback)
Testosterone and antisocial behavior
High testosterone correlated with assault, going AWOL, substance abuse, multiple sex partners; correlational only; amplifies dominance-related behavior depending on environment; interacts with social factors such as education
fMRI
Functional magnetic resonance imaging; traces relations between brain activity (blood flow) and what a person is doing, thinking, or feeling
PET
Positron emission tomography; records radioactivity after a nontoxic radioactively-labeled glucose tracer is injected, measuring metabolic activity
Amygdala
Small almond-shaped forebrain region under the prefrontal cortex; reacts instantly to danger (behavioral, autonomic, endocrine responses); fear learning and threat detection; also involved in appetitive responses
Kagan and the amygdala
Amygdala overactivity is linked to temperamental inhibition (caution, fearfulness, withdrawal) and shyness
Schwartz et al. (2003)
Infants classified as inhibited vs. uninhibited at age 2; at age 22 under fMRI, formerly inhibited adults showed greater amygdala activation to novel vs. familiar faces
Blood flow as proxy
In fMRI studies, greater blood flow to a structure is assumed to mean greater activation (a simplification)
Reif et al. (2011) NOS1 study
Estonian youth; NOS1 promoter polymorphism × adverse environment (maternal rejection, stressful life events, family relationships) on impulsivity; s/s with more rejection showed highest impulsivity
NOS1
Nitric oxide synthase gene; deletion associated with impulsivity in animals; influences the serotonergic system
BIS-11
Barratt Impulsiveness Scale (outcome in NOS1 study; NOT the Behavioral Inhibition System)
AMIS
Adaptive-Maladaptive Impulsivity Scale (outcome in NOS1 study)
Chang et al. OXTR study
OXTR rs53576 A/G polymorphism, oxytocin, dopamine, neuroticism in healthy adults (SPECT, n=82); AA had higher striatal DAT than G-carriers; in G-carriers higher DAT linked to lower oxytocin; DAT correlated with neuroticism only in AA with lower oxytocin
OXTR
Oxytocin receptor gene; rs53576 A/G polymorphism (G-carriers vs. AA)
DAT
Dopamine transporter; striatal DAT availability measured by SPECT
Maudsley Personality Inventory
Neuroticism measure used in the OXTR study
Donaldson & Young study
Oxytocin, vasopressin, and the neurogenetics of sociality; vasopressin receptor levels in reward regions (VP) linked to social bonding
Oxytocin and vasopressin
Hypothalamic hormones released from the pituitary; involved in social behavior; have homologs across species
Prairie vs. meadow voles
Prairie voles are monogamous with more vasopressin receptors in VP; meadow voles are polygamous; meadow voles given extra receptors via AAV showed partner preference
avpr1a / AVPR1A microsatellite
Length variation upstream of the vasopressin receptor gene; in humans, long alleles → more mRNA and greater amygdala activation to faces; linked to relationship quality and autism
Poole, Jetha & Schmidt study
Retrospective childhood behavioral inhibition (social vs. non-social), adult shyness, salivary cortisol; social inhibition correlated with adult shyness; in females, high cortisol + high social inhibition → highest shyness; no significant results in males
Chein et al. (Steinberg) study
Peers increase adolescent risk taking via reward circuitry; stoplight driving task under fMRI; adolescents made more risky decisions and crashes with peers watching
LPFC
Lateral prefrontal cortex; activity increased with age (main effect of age); cognitive control
VS and OFC
Ventral striatum and orbitofrontal cortex; reward regions showing an age × social context interaction (adolescents most active with peers)