Abnormal Psychology

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Mood Disorders and Suicide 209


dependent on others, other people may eventually criticize and even reject the


person, which could have the effect of confi rming the person’s negative view of


self and his or her prospects for the future. Consider that researchers have found


that depressed undergraduates are more likely than nondepressed undergraduates


to solicit negative information from happy people; such a tendency can lead hap-


pier people to reject the depressed questioner, confi rming negative beliefs about


himself or herself (Wenzlaff & Beevers, 1998).


In short, people’s psychological characteristics affect how they interpret events

and how they behave, which in turn infl uences how they are treated in social inter-


actions, which then infl uences their beliefs about themselves and others (Casbon et


al., 2005). And all of this is modulated by whether or not the person is neurologi-


cally vulnerable to depression. Figure 6.2 illustrates the feedback loops.


Treating Depressive Disorders


As discussed in Chapter 4, different treatments target different factors. However,


successful treatment of any one factor will affect the others. For example, improv-


ing disrupted brain functioning will alter a person’s thoughts, mood, and behav-


ior, and interactions with others.


Targeting Neurological Factors


In treating depressive disorders, clinicians rely on two major types of treatment that


directly target neurological factors: medication and brain stimulation.


Medication


Several types of medications are commonly prescribed for depression; it can take


weeks for one of these medications to bring about any change in depressed mood.


Antidepressant medications include the following:



  • Selective serotonin reuptake inhibitors (SSRIs), such as fl uoxetine (Prozac), par-


oxetine (Paxil), and sertraline(Zoloft).SSRIs slow the reuptake of serotonin from
synapses. Because these antidepressants affect only certain receptors, they have
fewer side effects than other types, which can make people less likely to stop tak-
ing them (Anderson, 2000; Beasley et al., 2000). However, SSRIs are the only type
of antidepressant to have the side effect of decreased sexual interest, which can
lead some patients to stop taking them (Brambilla et al., 2005; Gregorian et al.,
2002). Many patients also fi nd that the same dose of an SSRI brings less benefi t
over time (Arana & Rosenbaum, 2000)—an effect nicknamed Prozac poop-out.
SSRIs are also used to treat anxiety disorders, (discussed in Chapter 7), as well as
other disorders.


  • Tricyclic antidepressants (TCAs), such as amitriptyline (Elavil). TCAs are so


named because their molecular structure contains three (tri-) rings of atoms; they
have been used since the 1950s to treat depression and, until SSRIs became avail-
able, were the type of medication most commonly used for this purpose. TCAs
are generally as effective as Prozac for depression (Agency for Health Care Policy
and Research, 1999). The side effects of TCAs differ from those of SSRIs: The
most common side effects include low blood pressure, blurred vision, dry mouth,
and constipation, but diminished libido (sex drive) is not a signifi cant side effect
(Arana & Rosenbaum, 2000).


  • Monoamine oxidase inhibitors (MAOIs), such as phenelzine (Nardil). Some neu-


rotransmitters, such as serotonin, dopamine, and norepinephrine, are classifi ed
asmonoamines; monoamine oxidase is a naturally produced enzyme that breaks
down monoamines in the synapse. MAOIs inhibit this chemical breakdown, so the
net effect is to increase the amount of neurotransmitter in the synapse. MAOIs are
more effective for treating atypical depression (Cipriani et al., 2007; Prien & Kocsis,
1995) than typical depression. These medications can be dangerous when patients

Selective serotonin reuptake
inhibitors (SSRIs)
Medications that slow the reuptake of
serotonin from the synapse.

Tricyclic antidepressants (TCAs)
Older antidepressants named after the three
rings of atoms in their molecular structure.

Monoamine oxidase inhibitors (MAOIs)
Antidepressant medications that increase the
amount of monoamine neurotransmitter in
the synapse.
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