The Adolescent
Brain –
Some Basic
Concepts
It is so
exciting to have information that explains behaviors. The science can appear
very complicated because there are so many parts to it. Most of us have little,
if any, introduction to the details of these parts. So as we go through the
process of learning about the adolescent brain, it's important to have some
definitions. They'll be posted here as a reference page, and on a separate
webpage that will allow for frequent updating as needed. Don’t feel intimated
by the volume of information. It takes time to master this roadmap. The brain
is the most complicated computer known. But unlike the computer, the brain has
a genetic pre-disposition, and it grows, changes, and reacts to physical and
psychological exposures. This makes it
‘plastic’, which means it responds to good and bad influences.
This is a
quick, and hopefully easy, introduction to some of the basic science. (This will
be a growing page!)
The
brain is the center of the nervous system, with an estimated 120 billion neuronal (neurons) cells, and 120 billion non-neuronal (glia) cells. It's also estimated that
there are 1000 trillion connections between the neurons; they connect via
synapses. The brain is suspended in the cerebral spinal fluid, which softens
how rapid movements that might damage it. It's also protected by a very zealous
blood brain barrier that limits what can get into the central nervous system.
But that blood brain barrier is not perfect, and they cannot keep out many
drugs, alcohol, or other toxins.
The
neurons are divided into two groups – the grey matter (with no myelin), and the white matter (with the white myelin coatings – these
are similar to higher speed, larger computer cables). A neuron is a long cell that acts like a
biochemical wire – when stimulated it transmits information. Each neuron can
pick up signals from one or more other neurons, and each neuron can also send
information out to one or more other neurons. A neuron is like an arm, and the
reception and transmissions occur in areas of dendrites.
Spread your fingers open and wide – they are like the dendrites. We have recently learned that there is a
second burst of grey matter growth just before puberty.
Pruning is a natural process of removing neurons to further improve
the networking capacity of a particular area of the brain, to make circuits
less ambiguous, which is turn improves synaptic
efficiency. There are appear to be two periods of grey matter synaptic growth
followed by pruning, in early childhood and – which is new information -- in
adolescence. A 3 year old will have many more synapses that an adult. Synaptic
circuits most frequently activated will be preserved; ineffective, weak or
unused synapses will be pruned, similar to a gardener shapes a tree. For
humans, the gardener is a mixture of nature and nurture. We are rapidly learning the details of this
second pruning in adolescence.
Glia,
or glue cells, are
the non-neuronal parts. They regulate the environmental outside the neurons.
The role of glia cells has recently been much better understood, with
consideration that they may have as important a role in many conditions, such
as depression, as the neurons. The three types of glial cells produce a
healthy, protective and clean environment so the neurons can operate as best
possible.
Myelin is the product of a glial cell.
It is an electrical
insulation material that forms a sheath, around the axon. Myelin production of myelin starts in the 14th
week of fetal development, but is occurs most rapidly from birth to
adolescence. Having myelin makes it possible for neurons to more rapidly
transmit the information. Myelination reduces the loss of the electrical
current from the axon.
Two
broad classes of neurons exist, interneurons,
which form local circuits, and projection neurons,
which take information to other regions of the brain or body. Most neurons are
interneurons. All of these make up the developing
circuits and connections that we are interested in as the brain matures.
Cytoarchitecture
is the term used to explain how Korbinian Brodmann organized the cortical
neurons and glial cells into 47 areas. The organization of these areas will
become important later on as we explore the developing adolescent brain. The
highest area of computation is within the grey area of the cerebral cortex.
Neuroplasticity is
the ability of the brain to change with learning and experiences.
Neuroimaging is
the science of using x-rays, CT, MRI, PET and DTI to examine and explore the
functioning or make-up of the brain. Some studies are static – they measure the
size, location, or other structural and geographical aspects of the brain, such
as looking for bleeds, tumor, atrophy, etc., that interfere with function. Some studies are functional – they look at
blood flow, how the brain metabolizes glucose, etc. These produce pictures that ‘light up’ as the
brain becomes active. Diseases are suspected when the pictures are unusual.
DTI, or diffusion tensor imaging, enables us to see the location, orientation,
and health of the brain’s white matter tracts. This is becoming increasingly
valuable in understanding brain development and disease or injury. DTI gives
information known as the anisotropy of the white matter.
Anisotropy.
When things happen all in one direction, it is known as anisotropy. When things
happen equally in all directions, it is isotropy. Light going through a
polarizing lens is changed from isotropy into anisotropy, and that is why the glare
is reduced – less interference and confusion.
Information traveling through the white matter is best when it is
focused and on target. Damaged neurons in the white matter tracts will lessen
the strength and purity of the desired signals, so abnormal or less anisotropy
means abnormal white matter tracts. Think of it as a leaky electrical cable.
DTI, using anisotropy,
measures the degree of such leaking. This is important
information when understanding brain damage, brain growth and development, etc.
Anisotropy is usually associated with health and proper functioning; isotropy
is not.
© A. Strauss 2011
-- Posted June 1, 2011