John Koo, MD
The field of mental health is in the midst of exciting the brain, such as the frontal lobes, left anterior cingu-
new developments, in both the understanding of the late gyrus, left dorsolateral prefrontal cortex, and basal
basic pathophysiology of mental disorders and the ganglia. 2,3 In schizophrenia, magnetic resonance
development of more efficacious and more "user- imaging results reveal generalized global brain dys-
friendly" psychopharmacologic agents. These devel- morphology, such as ventricular enlargement and sul-
opments, such as the application of brain imaging cal dilation, that were not appreciated on simple gross
techniques, should not only elucidate basic patho- anatomic inspection. Functional magnetic resonance
physiology or psychopathology but also make them imaging results reveal decreased metabolism and
visible to our eyes. They will undoubtedly continue blood flow in basal ganglia. 4,5 PET scans of patients
into the next millennium. As a specialty, we have a with trichotillomania also showed glucose hyperme-
choice to make. We can finally acknowledge that the tabolism as in patients with OCD but with slightly dif-
management of psychodermatologic disorders is part ferent anatomic distribution in the brain. 6 In the next
of our expertise and our responsibility and incorporate millennium, there is a real possibility that these func-
both scientific and therapeutic advances in the mental tional, noninvasive brain imaging techniques might be
health field into our own armamentarium, or we can applied to psychodermatologic conditions such as
continue to treat psychodermatology as a stepchild of delusions of parasitosis.
our specialty and remain ignorant or simply watch
from the sidelines as the progress in mental health Advances in Psychopharmacology
fields unfolds. The greatest recent advance in psychopharmacology
involves the development of psychopharmacologic
Advances in the Understanding of the agents with more benign side effect profiles but with
Pathophysiology of Mental Disorders the same, or even enhanced, efficacy. For example, the
use of tricyclic antidepressants is mostly superseded
Probably the most exciting advance in the basic sci- by the use of nontricylic agents such as fluoxetine
ence of mental disorders is the advent of functional (Prozac), sertraline (Zoloft), and paroxetine (Paxil),
neuroimaging in psychiatry. It used to be said that der- thereby obviating any concern regarding typical tri-
matology and psychiatry are like opposites: in one you cyclic side effects such as cardiac side effects, ortho-
can see everything; in the other, you can see nothing. static hypotension, anticholinergic side effects. The
This dichotomy is no longer valid with the advent of first antiobsessive-compulsive agent to be approved by
functional neuroimaging using techniques such as the Food and Drug Administration was the tricyclic
magnetic resonance spectroscopy, positive emission antidepressant clomipramine (Anafranil). However,
tomography (PET), single photon emission computed with Food and Drug Administration approval of more
tomography, and functional magnetic resonance imag- user-friendly nontricyclic selective seratonin reuptake
ing. These techniques allow psychiatrists and other inhibitors, such as fluoxetine, sertraline, and paroxe-
mental health professionals to go beyond studying the tine, clomipramine is rarely used. With antianxiety
anatomy of the brain in a cadaver to the point where agents, sedation and addiction are the major potential
functional parameters, such as cerebral blood flow and side effects of benzodiazepine. Once again, with the
cellular metabolism, can be studied noninvasively in introduction of buspirone (BuSpar), the potential for
vivo. With use of a PET scan, patients with obsessive- these serious side effects is eliminated. Last, for
compulsive disorder (OCD) clearly show hyperactivity antipsychotic agents, one of the most serious liabilities
of the orbital frontal lobes.1 In major depressive disor- involves the potential for the development of extra-
der, most studies show global or focal decreases in pyramidal (pseudoparkinsonian) side effects. The first
glucose metabolism in blood flow in various parts of "atypical" antipsychotic agent, clozapine (Clozaril),