alertness. Some psychotropic drugs block histamine,
resulting in weight gain, sedation, and hypotension.
ACETYLCHOLINE
Acetylcholine is a neurotransmitter found in the brain,
spinalcord, and peripheral nervous system partic-
ularly at the neuromuscular junction of skeletal mus-
cle. It can be excitatory or inhibitory. It is synthesized
from dietary choline found in red meat and vegetables
and has been found to affect the sleep/wake cycle
and to signal muscles to become active. Studies have
shown that people with Alzheimer’s disease have de-
creased acetylcholine-secreting neurons, and people
with myasthenia gravis (a muscular disorder in which
impulses fail to pass the myoneural junction, which
causes muscle weakness) have reduced acetylcholine
receptors.
GLUTAMATE
Glutamate is an excitatory amino acid that, at high
levels, can have major neurotoxic effects. Glutamate
has been implicated in the brain damage caused by
stroke, hypoglycemia, sustained hypoxia or ischemia,
and some degenerative diseases such as Huntington’s
or Alzheimer’s.
GAMMA-AMINOBUTYRIC ACID (GABA)
GABA, an amino acid, is the major inhibitory neuro-
transmitter in the brain and has been found to mod-
ulate other neurotransmitter systems rather than to
provide a direct stimulus (Shank, Smith-Swintonky,
& Twyman, 2000). Drugs that increase GABA func-
24 Unit 1 CURRENTTHEORIES ANDPRACTICE
Table 2-1
MAJORNEUROTRANSMITTERS
Type Mechanism of Action Physiologic Effects
Dopamine
Norepinephrine
(noradrenaline)
Epinephrine (adrenaline)
Serotonin
Histamine
Acetylcholine
Neuropeptides
Glutamate
Gamma-aminobutyric
acid (GABA)
Controls complex movements, motivation, cognition;
regulates emotional response
Causes changes in attention, learning and memory,
sleep and wakefulness, mood
Controls fight-or-flight response
Controls food intake, sleep and wakefulness, temper-
ature regulation, pain control, sexual behaviors,
regulation of emotions
Controls alertness, gastric secretions, cardiac stimu-
lation, peripheral allergic responses
Controls sleep and wakefulness cycle; signals mus-
cles to become alert
Enhance, prolong, inhibit, or limit the effects of prin-
cipal neurotransmitters
Results in neurotoxicity if levels are too high
Modulates other neurotransmitters
Excitatory
Excitatory
Excitatory
Inhibitory
Neuromodulator
Excitatory or inhibitory
Neuromodulators
Excitatory
Inhibitory
tion, such as benzodiazepines, are used to treat anx-
iety and induce sleep.
BRAIN IMAGING TECHNIQUES
At one time, the brain could be studied only through
surgery or autopsy. Over the past 25 years, how-
ever, several brain imaging techniques developed
now allow visualization of the brain’s structure and
function. These techniques are useful for diagnos-
ing some disorders of the brain and have helped to
correlate certain areas of the brain with specific
functions. Brain imaging techniques also are useful
in research to find the causes of mental disorders.
Table 2-2 describes and compares several of these
diagnostic techniques.
Types of Brain Imaging Techniques
Computed tomography(CT, also called computed
axial tomography or CAT scan) is a procedure in
which a precise x-ray beam takes cross-sectional im-
ages (slices) layer by layer. A computer reconstructs
the images on a monitor and also stores the images
on magnetic tape or film. CT can visualize the brain’s
soft tissues; so CT is used to diagnose primary tu-
mors, metastases, and effusions and to determine the
size of the ventricles of the brain. Some people with
schizophrenia have been shown to have enlarged ven-
tricles; this finding is associated with a poorer prog-
nosis and marked negative symptoms (see Chap. 14)
(Fig. 2-5). The person undergoing a CT scan must lie
motionless on a stretcher-like table for about 20 to
40 minutes as the stretcher passes through a “ring”
while the serial x-rays are taken.