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EFFECTS ON THE BRAIN
[ back to Brain
Injury 101 ]
The brain is "the fragile dwelling place of the soul."
When the brain becomes injured by trauma, we expect to see,
and do see, changes in how the person perceives, remembers,
thinks, feels and relates to others. Injury to the brain changes
the functioning of the individual and his identity. This should
not be surprising, since the brain is so highly vulnerable
to injury from trauma. It is a three pound mass of jelly-like
consistency made up of one hundred billion neurons and
their interconnections. It is 90% water, and cannot be expected
to retain its integrity in response to traumatic events such
as car crashes, falls or criminal assaults in which the head
is battered.
How rapidly and how completely a person recovers from brain
injury, depends on a variety of factors including severity
of initial injury, age, pre-morbid education, personality
and temperament, presence or absence of complications such
as chronic pain and/or post traumatic stress disorder, quality
of treatment, quality of social support network, and many
others. Every person has a different brain, so it is not surprising
that 100 people will respond in 100 different ways to a head
trauma of similar force, direction and impact point on their
skulls. Our brains vary anatomically on account of genetics,
age and gender. The unique developmental, educational, psychological,
nutritional, toxic exposure and trauma history of each persons'
brain affects how his brain is wired and how well or poorly
it can adapt to a particular traumatic event. Over the past
few years, Dr. Paul Thompson, a neurologist at the UCLA Lab
of Neuroimaging, has been creating a whole brain 3D atlas
of the brains of 1000s of "normal" individuals and
individuals with Alzheimer's Disease to help us better visualize
the subtle differences. A by-product of this research is visual
confirmation that every person's brain has a unique pattern
of functional organization. This correlates with neurosurgery
on epileptic and cancer patients in which mapping of the brain
functions in an awake patient with an electric disrupter tool,
shows the same unique layout of functions. In concrete terms,
this means if you strike 100 people with a blunt instrument
above and slightly behind the left ear with the same tool
at the same level of force, you will be damaging different
brain circuits and disrupting different brain functions in
each person, and each will respond differently. This is important,
because in litigation the defense medical expert will often
distort the truth by saying "most people struck in that
part of the head show a different outcome than the plaintiff;
therefore the plaintiff is faking his symptoms or they are
the result of psychological stress not organic brain damage."
The brain circuits which get disrupted by trauma are composed
of inter-connected neurons or brain cells. Neurons are nerve
cells constructed to do the specialized work of the central
nervous system. They consist of a cell body with a nucleus
and cellular processes for the reception and transmission
of nerve signals through chemical substances called "neurotransmitters".
Each neuron has a large collection of fernlike dendrites for
message reception and one large tubular axon for signaling
other neurons. Each dendrite has spines with pores called
receptor sites. Molecules of neurotransmitter are released
from pre-synaptic vesicles at the tip of the axon and flow
across the gap between nerve cells (the synapse) where they
"bind" with receptors on nearby dendrites. This
signals the receiving cell to open up its pores and allow
ion exchange with the extra-cellular environment. When this
process works as designed, the influx of ions triggers a "depolarization"
of the receiving nerve cell, which sends a mild electric current
(or "action potential") pulsing down its axon, and
triggering axonal release of more neurotransmitter. The human
brain sends messages at 1/10,000th of a second largely because
its axons are coated with a natural insulation material known
as myelin.
Trauma disrupts the normal process of communication between
nerve cells by mechanical shaking and perturbation of cell
membranes, mechanical striping away of myelin from axons,
stretching of axons which triggers obstructive swellings to
form in the axon and by triggering massive dumping of 1000s
of time the normal quantities of neurotransmitters like glutamate.
All these processes are destructive. Excess release of glutamate
can cause nerve cells to literally explode. This happens when
glutamate jams open nearby receptor sites and allows a toxic
influx of calcium into nerve cells, shutting down their mitochondria,
and depriving them of energy to work the sodium pumps to force
sodium back out of the cell, resulting in extracellular water
pouring in and bursting the cell like a balloon.
When synapses are damaged and malfunction as a result of trauma,
communication inside the brain is disturbed with evident consequences
such as slowed thinking, forgetting of intentions or difficulty
finding the right words to express oneself. Typically this
occurs when external force on the head causes the brain to
twist and bounce back and forth inside the hard, unyielding
skull case. Although surface contusions to the gray matter
may result, more often the damage is done by internal stretching
and straining of the long axons, a form of microscopic damage
not visible on MRI. Although a concussion causes an immediate
episode of dazing or confusion (which may last just seconds
or minutes), it generally takes 48 hours after the traumatic
event for stretched axons to form obstructive swellings which
block the flow of nutrients and gradually kill off the nerve
cell or decrease its connections with other neurons that are
no longer in physical communication. A randomized kill
off of synaptic connections is much like a Florida
hurricane ripping down phone lines in a helter-skelter manner.
While the phone system as a whole is intact, some messages
don't get through, others get delayed because of re-routing
and others arrive in garbled fashion.
A person who suffers a concussion from closed head trauma
will experience a momentary episode of dazing or confusion
from twisting of the brain stem or an extra heavy discharge
of neurotransmitters. This often clears by the time she is
brought to the emergency room. Diffuse strain injury to axons
produces no visible bleeding so the CT scan will be negative.
Even if a CT scan could pick up microscopic damage to axons,
it would not be visible in the ER right after the concussion,
because the process of axonal destruction takes a good 48
hours to get going. Thus an emergency room CT Scan
will pick up bleeding in the brain from a depressed skull
fracture, but cannot detect the damage done by mild brain
injury because it has not happened yet. Due to poor training,
many emergency room doctors equate a negative CT scan with
complete absence of injury to the brain.
A great many victims of mild traumatic brain injury know intuitively
that they are "different" following their accident,
and that something is wrong with them, but never get properly
diagnosed, treated, counseled, helped or rehabilitated. This
happens so frequently because microscopic damage to axons
is not detectible on standard neuroimaging techniques and
does not produce any gross disturbances of reflexes (e.g.
pupillary reflexes) that a neurologist would perceive as a
significant abnormality of the central nervous system. Although
PET scans can detect tiny disturbances of brain function,
these tests are very expensive, and most insurers refuse to
pay for them on the grounds of lack of "medical necessity."
Fortunately many persons who suffer from the "milder"
form of TBI (with no loss or only a minimal loss of consciousness
and negative CT/MRI) eventually improve on their own, especially
if they take time off work and get plenty of rest. For the
ones who get better spontaneously, most show good improvement
within three months post-accident and most, about 85%,
are symptom free within six to twelve months post -accident.
However, a minority of mild head injury, about 15%, show symptoms
on a long term, even permanent basis. Typically, there is
a mix of organic and psychological factors interacting to
perpetuate their impairments on a chronic basis. It is now
believed that at least some of these individuals have the
APOE-e4 gene for Alzheimer's Disease. It is also believed
that other consequences of mild TBI may perpetuate symptoms,
especially when untreated or undertreated. These include depression,
anxiety disorder, panic disorder, post-traumatic stress disorder,
substance abuse, pain disorder, sleep disorder and Rx
medication side effects. Undoubtedly, the amount, the intensity
and the complexity of life demands on the injured person play
a role. Someone who was retired and sedentary before the brain
injury will not experience the same level of complaints as
someone who was a mother of 3 children or a full time breadwinner
working as an accountant, software designer, attorney, engineer,
physician, architect or equally challenging position. Persons
of middle age ask a lot of themselves and become the most
frustrated when they cannot function and meet their own demands.
They also suffer from decreased neuronal reserve, i.e. they
have fewer living brain cells than they did when they were
children.
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