Chapter 3 Flashcards
Historically; what are the 3 main approaches to studying the brain from oldest to most recent?
Phrenology: assessed bumps on the head and attributed various personality and intellectual characteristics
Brain damage: study psychological functioning following damage to specific brain regions
Electrical stimulation and recording of NS activity: idea of brain cells sending information through electrical activity arose (send signals to and record electrical activity from the brain)
What are some flaws of phrenology, brain damage, and electrical stimulation?
Phrenology
1. Patients with damage to specific brain areas didn’t experience the psychological deficits phrenologists had predicted
2. Shape of outer skull doesn’t match that of the underlying brain
Brain damage
1. Minority groups could differ from normative sample in social and economic determinants of brain health → available norms may not apply to their test performance
Electrical stimulation and recording
1. Show neural activity that reaches the surface of the scalp → tell us little, if anything about what is happening inside
What is the difference between CT and MRI scan?
Computer tomography: 3D reconstruction of multiple X-rays taken through a part of the body
Magnetic resonance imaging; measures the release of energy from water in biological tissues following exposure to a magnetic field (superior by detecting soft tissues - tumors)
→ Limitations: show only brain structure, not activity
What is the difference between a PET, fMRI, and MEG?
Positron Emission Tomogaphy (PET): measures changes in the brain’s activity in response to stimuli
→ Brain cells increase their intake of glucose when they are active
→ Injection of radioactive glucose-like molecules and the scanner measures where in the brain most of these glucose-like molecules are, allowing to determine which regions are most active
Functional MRI (fMRI): increase in oxygenated blood flowing to areas in response to the increased demand for O by the cells in a region
→ Measures the change in blood O2 level = indirect indicator of brain activity
Magnetoencephalography (MEG): detects electrical activity in the brain by measuring tiny magnetic fields in order to reveal patterns of magnetic fields on the skull’s surface → reveal which areas are becoming active in response to stimuli
What is the difference between deep and transcranial brain stimulation?
Deep brain stimulation: neurosurgical procedure that implants battery-powered electrodes within the brain to provide electrical stimulation directly at specific areas
Transcranial magnetic stimulation: applies strong and quickly changing magnetic fields to the surface of the skull to create electric fields in the brain that can enhance/interrupt brain function
Glutamate
- Most common excitatory neurotransmitter in CNS
- Associated with enhanced learning and memory (when abnormally high, may contribute to schizophrenia and other mental disorders → over stimulates receptors)
GABA
- Most common inhibitory neurotransmitter in CNS
- Critical role in learning, memory, and sleep
ACh
- Plays a role in arousal, selective attention, memory, and sleep
- NMJ releases ACh as well triggering movement
MONOAMINES
NE, dopamine, and serotonin (contain 1 amino acid)
1. Dopamine
- Plays a critical role in motivation and rewarding experiences (reward system)
2. NE and serotonin
- Activate/deactivate various parts of the brain = influence consciousness, arousal, movement, and readiness to respond to stimuli (state of arousal)
NEUROPEPTIDES
- Endorphins
- Play a role in pain reduction
→ Neuropeptides play a role in hunger and satiety and others can alter learning and memory
What is a psychoactive drug? What are the 2 main types of psychoactive drugs that we can find?
Drugs that target the production or inhibition of neurotransmitters
Agonists (codeine and morphine): increase or mimic the effect of a neurotransmitter
Reduce emotional response to painful stimuli by binding to opioid receptors and mimic endorphins
Others block the reuptake of a neurotransmitter (antidepressants - serotonin)
Antagonist: block or decrease the effect of a neurotransmitter (pretend to be a neurotransmitter without exerting the effects of this)
What does neural plasticity refer to?
Brain’s adaptability to almost any environment (brain is most adaptable during early development since our brains don’t mature fully until late adolescence/early childhood)
What are the 4 ways in which a neuron network can change over development?
- Growth of dendrites and axons
- Synaptogenesis (formation of new synapses)
- Pruning (death of certain neurons and the retraction of axons to remove connections that aren’t useful)
- Myelination (insulation of axons with myelin sheath
→ Brains change as we learn, such changes may arise from:
- New synapses
- Increased connections among neurons
- Strengthening of existing synaptic connections (neurotransmitters released into synapses produce stronger and more prolonged response) → “potentiation”
→ “Structural plasticity”: changes in the shape of neurons is critical for learning (axonal expansion or dendritic reshaping)
Does PNS and CNS heal the same way following an injury?
→ CNS display limited regeneration following an injury or serious illness (still, certain brain regions can take over the functions previously performed by others)
Neurogenesis: creation of new neurons