Lecture 4 Flashcards

1
Q

Advantages of using rats for neuroscience

A
  1. Cheap housing/maintenance/breeding
  2. Friendly disposition and easy to train
  3. Intelligent and agile
  4. Resistant to infection
  5. Many inbred strains available
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2
Q

Neuroscience manipulation techniques

A
  1. Lesions: mechanical, chemical, electrolysis
  2. Electrical stimulation (excite or inhibit neural function)
  3. Pharmacological: injection, osmotic pumps, microdialysis
  4. Genetic manipulation
  5. Behavioural manipulation
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3
Q

Neuroscience monitoring techniques

A
  • In vivo:
    1. Electrophysiology
    2. Microdialysis
    3. Behavioural evaluation

Ex vivo:
1. Localization of tissue components: Histology, Immunohistochemistry, Hybridization for mRNA or DNA
2. Quantification of components in tissue homogenates

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4
Q

Stereotaxic surgery

A

Microinjections
Lesions
Cannula placement
Microdialysis
Electrodes
Headsets

Are all used in stereotaxic surgery

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5
Q

Microdialysis

A

A catheter is injected into or near to the cell which acts as a blood capillary. Extracellular substances diffuse accross the membrane of the catheter into the perfusion liquid inside the catheter.
Substances inside the catheter can also flow out.
The absolute recovery of a substance depends on the size of the pores of the membrane, length of the membrane, flow rate of the perfusion fluid and the diffusion coefficient of the compound.

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6
Q

Microdialysis applications

A
  • Continuous monitoring of chemical events in living tissue
  • Continuous drug delivery
  • Contemporaneous drug delivery and monitoring of drug effects
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7
Q

Levels of electrophysiology

A
  • Single ion channel
  • Single unit (cell)
  • Multi unit
  • Field potentials
  • Brain potentials (ECG, EEG, MEG)
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8
Q

Patch clamp recording

A

Micro pipette clamps on to part of the cell body and can monitor a single ion channel and has very stable intracellular recording compared to conventional electrode recording

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9
Q

Intracellular recording

A

This measures the voltage across the membrane of the cell.
Sharp electrode penetrates cell membrane.
Has extracellular reference electrode in a bath

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10
Q

Extracellular recordings

A
  • One cell
  • Recording electrode close to the cell
  • Commonly in vivo
  • Reference electrode = ground
  • Multi unit recording
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11
Q

Field potentials

A

Extracellular field potentials are local current sinks or sources that are generated by collective activity of many cells.
Two electrodes are implanted, one inside the cell and one outside. The intracellular one records change in membrane potential caused by influx of positive sodium ions. The extracellular electrode measures the outside getting more negative.

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12
Q

EEG

A

This measures correlated synaptic activity caused by post-synaptic potential of cortical neurons.
The ionic currents from action potentials don’t contribute much to EEG recording. Rather the extracellular ionic currents caused by dendritic electrical activity are what gives the signal.
Post-synaptic potentials give the signal.
Oscillations are synchronized activity over a network of neurons.

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13
Q

fMRI

A
  • Based on blood oxygenation (Blood-oxygen-level-dependent imaging)
  • Theory: increased flow of oxyhemoglobin-rich blood to ‘active’ brain
  • Disadvantage: Does not measure neural activity directly. Can only measure changes in BOLD signal
  • Advantage: can measure subcortical structures
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14
Q

Genetic engineering

A

The proteins occuring in an organism are altered by altering the DNA.

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15
Q

The transgene

A

A piece of foreign DNA carried by a transgenic organism.

Either the foreign DNA exists in the cell in the form of a plasmid (prokaryote) or the foreign DNA is integrated into the host genome (mammals)

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16
Q

Uses for genetic engineering

A
  • Modification of crops
  • Uses of GM bacteria to produce medicine
  • Produciton of transgenic mice for research
17
Q

Principle of recombinant technology (genetic engineering)

A
  1. Isolate the gene of interest
  2. Modification of the gene
  3. Insertion of the gene into a vector
  4. Insertion of the vector into cells of the organism to be modified
  5. Tests to isolate genetically modified organisms
18
Q

Application of recombinant technology in neuroscience

A
  • Loss of function experiments (Gene knock out of mice -> gene altered to cripple its function)
  • Gain of function experiments (Knock out mice -> increase function of gene)
  • Tracking experiments (when and where is protein produced)
19
Q

2 ways of producing transgenic organisms

A
  1. Microinjection of DNA into the pronuclei of fertilized oocytes
  2. Knockout: introduce DNA into embryonic stem cells. Transformed ES cells are identified and injected into a 4 day old mouse embryo