What is electrical brain stimulation?
A technique that stimulates neurons electrically using a bipolar electrode (two insulated wires). Weak pulses make neurons near the tip fire more.
Why is electrical stimulation important in research?
Helps identify the function of a brain area.
Usually produces behavioral effects opposite to lesions in the same area.
Can elicit behaviors like eating, drinking, attacking, mating, or sleeping.
Effects depend on location of electrode, current parameters, and environment.
Who is usually tested with electrical brain stimulation?
Mostly nonhuman animals because it’s invasive.
Sometimes conscious humans for therapeutic purposes.
What are the four invasive recording methods?
Intracellular unit recording – records graded changes in a single neuron’s membrane potential.
Extracellular unit recording – records firing of a neuron from outside the cell.
Multiple-unit recording – records combined activity from many neurons.
Invasive EEG – EEG recorded inside the brain using implanted electrodes.
What is intracellular unit recording?
Records moment-by-moment changes in one neuron’s membrane potential.
Usually done in immobilized animals, but new tech allows freely moving animals.
What is extracellular unit recording?
Electrode tip is in the fluid near a neuron.
Records neuron firing but not membrane potential.
Can now record up to ~1,000 neurons at once using multiple electrodes.
What is multiple-unit recording?
Electrode tip is larger → picks up many neurons’ signals.
Signals are added together to show total firing per time unit.
What is invasive EEG recording?
Electrodes are implanted in the brain rather than on the scalp.
Cortical EEG: often via skull screws.
Subcortical EEG: via implanted wire electrodes.
How are drugs commonly administered in psychopharmacology experiments?
What are selective neurotoxic lesions and why are they used?
Target specific neurons rather than all neurons in an area.
Use neurotoxins that destroy certain cells while leaving others intact.
Examples:
Kainic acid or ibotenic acid: destroys cell bodies near the injection site; axons passing through remain.
6-hydroxydopamine (6-OHDA): destroys only neurons that release dopamine or norepinephrine; other neurons are unaffected.
What is the 2-deoxyglucose (2-DG) technique?
Inject animal with radioactive 2-DG, which is like glucose. Active neurons absorb it but don’t metabolize it. Brain is removed, sliced, and processed with autoradiography. Active areas appear as dark spots, which can be color-coded to show activity.
What is cerebral dialysis?
Measures extracellular neurochemicals in behaving animals. Implant a fine tube with a semipermeable section in a brain area. Chemicals diffuse into the tube for collection or analysis. Can be analyzed later or sent directly to a chromatograph.
How does immunocytochemistry locate neurotransmitters/receptors?
Uses antibodies labeled with dye or radioactivity. Antibodies bind to neuroproteins or enzymes needed for neurotransmitter synthesis. Exposing brain slices to these labeled antibodies shows where proteins are located.
How does in situ hybridization locate neurotransmitters/receptors?
In situ hybridization uses a labeled DNA or RNA probe that binds to specific mRNA, showing where certain neurotransmitters or receptors are being made in the brain.
What are the three main genetic methods used in biopsychology?
Gene knockout – remove a specific gene.
Gene knockin – add or replace a gene.
Gene editing – precisely edit genes (e.g., CRISPR/Cas9).
What is a gene knockout technique and an example?
Removes a gene to see its role in behavior.
Example: Melanopsin knockout mice – gene deleted → mice had impaired circadian rhythms, but other mechanisms also contributed.
What is a gene knockin technique and an example?
Adds or replaces a gene in an organism.
Example: Transgenic mice with a human schizophrenia gene → showed brain abnormalities (smaller cortex, enlarged ventricles) and abnormal behaviors.
What is gene editing and how is CRISPR/Cas9 used?
Edits genes at specific times during development.
CRISPR/Cas9 method: Cas9 protein + guide-RNA → targets specific DNA. Can be delivered via virus peripherally (whole organism) or intracranially (specific brain region). Cas9 can activate, inhibit, or reversibly control gene expression.
What is Green Fluorescent Protein (GFP) and why is it useful in neuroscience?
GFP is a protein that glows green under blue light. It can be expressed in specific cells to visualize them. First used in C. elegans neurons to see touch receptor neurons. Allows tracing of neurons, labeling neurotransmitters, synaptic vesicles, and visualizing postsynaptic potentials.
What is the Brainbow technique?
Modifies GFP to create multiple colors (cyan, yellow, blue). Each neuron gets a unique color, making it easier to trace neural pathways. Helps map the brain’s complex network of neurons.
What are opsins and how are they used in neuroscience?
Opsins are light-sensitive ion channels from bacteria/algae. Light opens them → ions enter → neurons depolarize or hyperpolarize. Inserting opsin genes into neurons allows control of specific neuron activity with light.
How does optogenetics work in living animals?
Virus carries opsin gene → targets specific neurons. Optical fiber implanted → light activates opsins. Can increase or suppress activity of targeted neurons. Wireless tech allows use in freely moving animals.
What is the purpose of neuropsychological testing?
Assist in diagnosing neural disorders, especially when imaging/EEG is inconclusive.
Guide counseling and patient care.
Evaluate treatment effectiveness and side effects.