Behavioural neuroscience Flashcards
(76 cards)
What is Behavioural Neuroscience?
-A scientific study of the role of the central nervous system in behaviour
-Combines psychology and neuroscience
Allied disciplines:
Physiological psychology
Psychopharmacology
Neuropsychology
Psychophysiology
Cognitive neuroscience
Historical limits to understanding the link between mind and brain
-Initially, heart was believed to be the seat of the mind
-Changes to our understanding of the brain were limited by:
religious or moral views
limited methods
reliance on chance discoveries (serendipity)
scientific conservatism
The brain is proposed to control the body – Hippocrates 460 BCE
- Our brain is the command centre of body (not heart)
- Noted the behavioural effects of brain damage
- Dissection not allowed in Greece
- Observed anatomy through open wounds after traumatic head injury
Nerves connect the brain to the body – Galen 130 CE
-Used vivisection to study anatomy of the nervous system
-Distinguished between sensory and motor nerves
-Proposed the idea of pneumata (‘spirits’)
Thought that animal spirits travelled through the hollow nerves to and from the ventricles
-No method or data to support or refute the pneumata theory
Structure of the brain mapped in detail- Andreas Vesalius 1514 CE
- Revived dissection and vivisection after the Dark Ages
- Detailed drawings substantially advanced knowledge of brain structure but detailed anatomical understanding failed to illuminate brain function
- So the pneumata theory of animal spirits flowing through nerves persisted…
Nerve signals are electrical (not fluid) - Luigi Galvani 1737
- Rejected the idea of animal spirits flowing through hollow nerves
- Found that an electrical charge applied to a frog’s leg made the muscle contract
- Suggested that nerves must be coated in fat to prevent electricity from leaking out
The idea of a modular brain is proposed - Franz Joseph Gall 1758
- Influenced by physiognomy the art of ascribing personality characteristics to facial features
- Proposed that the brain was composed of several distinct ‘organs of thought’or faculties reflected by characteristic patterns of bumps on the skull
- skull maps could be used to “read” a person’s character
- Gall’s Phrenology is flawed
- but Gall introduced the important notion of cortical localisation of function
The first solid evidence of brain modularity - Paul Broca 1861
-Paul Broca described a patient
unable to speak after damage to the left frontal lobe (Broca’s area)
-Normal chewing, comprehension
Electrical stimulation of animal brains revealed precise localisation of cortical function
- In 1870, Fritsch & Hitzig (Germany) electrically stimulated part of the frontal cortex in dogs; induced contractions of specific muscles on the opposite side of the body
- Surgical removal of these ‘motor’ regions of cortex caused impairments of actions performed by the relevant limb
Ablation studies
Ablation studies in non human primates reveals the hippocampus’ role in memory
Role of CT and MRI
They both help to reveals brain structure
Functional Magnetic Resonance Imaging (fMRI)
-Cognitive processes use energy
-The production of energy uses oxygen from hemoglobin (blood)
Oxygenated blood
-Weakly diamagnetic
-Doesn’t distort surrounding magnetic field
Deoxygenated blood
-Paramagnetic
-Distorts surrounding magnetic field
First observed by Seiji Ogawa in 1990
blood vessels became more visible as blood oxygen decreased
Basis for the BOLD effect
The blood oxygen level dependent effect (BOLD)
reflects anticipated brain activity
-the flow of oxygenated blood is monitor through fMRI the see which part of the brain is active for a particular task
transcranial magnetic stimulation (TMS)
- In TMS, a coil carrying an electrical current is held over the scalp, and a brief, focal magnetic pulse is generated which activates a small region of cortex (approximately 10 – 15 mm, depending on the size of the coil) underlying the coil. The activation acts like a ‘virtual lesion’,
- If a particular brain region is critically involved in a task, then TMS of that region should affect performance.
Limitations of clinical neuropsychology
Patients often difficult to test intensively
Problem of replicability in single cases
Assumes local lesions have local effects
No control of lesion size or location in the brain – ‘experiments of nature’
neuron
Neurons come in many different shapes and sizes. Almost all have four basic structures or regions:
Cell body– contains the nucleus (genetic material) and internal organelles necessary for cell maintenance.
Dendrites – the tree-like branches that allow neurons to communicate with one another. Dendrites receive information from other neurons.
Axon – a long, slender fibre that carries signals from the cell body. The signal carried by an axon is an action potential,
Glial cells
- provide physical support
- assist with chemical transport to and from neurons
- provide insulation
- destroy and remove neurons that have died from injury or old age
Resting membrane potential
the inside of an axon is more negatively charged than the outside. This difference, known as the resting membrane potential, is about -70 millivolts (mV, a thousandth of a volt).
Depolarisation
-A very rapid reversal (depolarisation) of the membrane potential of an axon is called an action potential. The action potential constitutes the basic message that is transmitted down an axon from the cell body to the terminal buttons.
The action potential (AP) – ion exchange across the axon
Normally the cell membrane is not very permeable to sodium Na+. But if the membrane were suddenly to became permeable to sodium Na+, sodium Na+ ions tend to rush into the cell, causing a sudden increase in the concentration of positively charged ions and changing the membrane potential. This change in membrane permeability is precisely what causes an action potential.
Certain protein molecules in the cell membrane, known as ion channels, provide an opening through which ions can rapidly enter or leave the cell. When ion channels for sodium Na+ open, sodium Na+ ions rush into the cell. Shortly thereafter, ion channels specific to potassium K+ open, allowing potassium K+ ions to rush out of the cell.
AP
An action potential can be described as the following sequence of events:
1) Once a neuron’s threshold for excitation is reached, sodium channels in the cell membrane open and there is a rapid influx of positively charged sodium Na+ ions. This produces a sudden change in the membrane potential, from –70 mV to +40 mV (depolarisation).
2) Shortly afterwards (less 1 millisecond), the potassium channels also open, allowing positively charged potassium ions to leave the axon (repolarisation).
3) At the peak of the action potential (about 1 millisecond) the sodium channels close and cannot re-open until the membrane reaches its resting potential again (refractory period).
4) As potassium ions are moved out of the axon, the membrane slightly overshoots its resting value (hyperpolarisation) before returning to its resting level (–70 mV ).
Saltatory conduction of the AP
Rather than moving as a single continuous wave down the axon, action potentials ‘jump’ into the gaps (Nodes of Ranvier) between segments of myelin that are wrapped around the axon (oligodendrocytes and Schwann cells).
Because an action potential is generated by the rapid influx of sodium Na+ ions into the cell, this process can only occur where the axon membrane is in direct contact with the extracellular fluid (i.e., at the Nodes of Ranvier). Within the myelinated portion of the axon, the electrical signal is conducted passively (like electricity down a wire) until it gets to the next Node, at which point another action potential is generated. Although the strength of the electrical potential decreases as it moves along myelinated portions of the axon, it is still large enough to trigger a new action potential at the next Node.
This jumping of the action potential along myelinated axons has two advantages. First, it saves energy because sodium-potassium transporters only have to work within the Nodes. Second, it increases the speed of neural signalling, and thus the speed with which we perceive, react and think.
All-or-none law of the AP
Neurons have a threshold for excitation, above which an action potential will reliably be triggered. In other words, an action potential either occurs or it does not occur – the all-or-none law.
Once triggered an action potential remains at the same amplitude (i.e., its membrane reaches the same level of depolarisation), and travels down the axon to its end.
Rate law of the AP
Variable information is signalled by the number of action potentials produced by a neuron (i.e., the neuron’s rate of firing). A strong muscle contraction is caused by a high rate of firing of a motor neuron; similarly, a loud sound is represented by a high rate of firing of an auditory nerve fibre.
Thus, the basic unit of information carried by axons is their rate of firing (known as the rate law).