How can we classify neurons? (1)
By the shape (morphology) of the dendrites and soma
ex. pyramidal v.s. stellate neuron
- main dendrite comes up out of the apex
- dendrites come out at different places
How can we classify neurons? (2)
By the number of processes (bipolar vs. multipolar)
- unipolar (1 dendrite/axon)
- bipolar (1 dentrite, 1 axon)
- multipolar (many dendrites 1 axon)
How can we classify neurons?
By the presence of spines
- not all neurons have dendrite spines
Why are dendritic spines important?
Dendritic spine morphology
The axon: output of the neuron
Axon terminal and synapse
How can we study the structure of neurons?
Nissl stain
Golgi stain
Neuron doctrine:
Why would you choose to use a Nissl stain rather than a Golgi stain
(and vice versa)?
Immunohistochemistry
More specifically in quizlet, for pictoral studying
Golgi-stained neurons in the visual cortex
Increased branching provides:
– increased surface for synaptic contacts,
– greater potential for interneuronal interaction,
– suggests a greater capacity for information
processing.
- Enriched environments sig. increase # of dendritic spines in the somatosensory cortex in adult rats placed under experimental conditions for 3 weeks.
*details: mostly seen in pyramidal cells
What are the mechanisms for dendritic spine growth?
Glia: the “glue” of the brain
*Astrocytes
Oligodendrocytes
Schwann cells
Microglia
Astrocytes:
Astrocytes and synaptic function
Blood-brain barrier
Things that can cross the BBB:
Things that cannot cross the BBB:
-large molecules (higher than 500 daltons molecular weight)
- Antibiotics (brain infections are difficult to treat!)
- Large proteins
- Ions and charged particles
Example: L-DOPA (the precursor to dopamine) can cross the BBB, but
dopamine cannot. So Parkinson’s patients are treated with
L-DOPA, not dopamine itself.
Oligodendrocytes:
Schwann cells:
Microgila: