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Selective serotonin reuptake inhibitor behavioral

Beginning in the 1960s, ben2odia2epiae anxiolytics and hypnotics rapidly became the standard prescription dmg treatment. In the 1980s, buspkone [36505-84-7] (3), which acts as a partial agonist at the serotonin [50-67-9] (5-hydroxytryptamine, 5-HT) type lA receptor, was approved as treatment for generali2ed anxiety. More recently, selective serotonin reuptake inhibitors (SSRIs) have been approved for therapy of panic disorder and obsessive—compulsive behavior. [Pg.218]

Conflicting results (i.e., evidence is equivocal) , not investigated sufficiently BZD, benzodiazepines CBT, cognitive-behavioral therapy SSRl, selective serotonin reuptake inhibitors TCA, tricyclic antidepressants. [Pg.451]

Clear abnormalities of the dopamine system have not been identified in the periphery or the brain of OCD patients. Nevertheless, repetitive stereotypies and OCD-like behaviors can be produced in humans by the administration of exogenous D2 agonist or stimulants, which suggests that the dopaminergic system may be involved in some way in OCD. Conversely, antipsy-chotics can be used adjunctively in the treatment of selective serotonin reuptake inhibitor (SSRl)-resistant OCD patients with a definite benefit in a significant proportion of patients. [Pg.157]

The selective serotonin reuptake inhibitors (SSRI) have been used in adults for a wide variety of disorders, including major depression, social anxiety (social phobia), generalized anxiety disorder (GAD), eating disorders, premenstrual dysphoric disorder (PMDD), post-traumatic stress disorder (PTSD), panic, obsessive-compulsive disorder (OCD), trichotillomania, and migraine headaches. Some of the specific SSRI agents have an approved indication in adults for some of these disorders, as reviewed later in this chapter. The SSRIs have also been tried in children and in adults for symptomatic treatment of pain syndromes, aggressive or irritable ( short fuse ) behavior, and for self-injurious and repetitive behaviors. This chapter will review general aspects of the SSRIs and discuss their approved indications in children and adolescents. [Pg.274]

FIGURE 39.2 Treatment algorithm for pediatric obsessive-compulsive disorder (OCD). In adjusting cognitive behavior therapy (CBT), increase frequency or intensity, or alter the setting or format, e.g., have it be home based or day treatment. CMI, clomipramine DMI, desipramine NT, nortriptyline SSRI, selective serotonin reuptake inhibitor (fluoxetine, fluvoxamine, paroxetine, sertraline, citalopram). [Pg.521]

FIGURE 43.1 Pharmacologic treatment algorithm for full syndrome pediatric PTSD. Based on a snythesis of consensus data and clinical reports in the adult and child literature. The author hers no responsibility for the use of this guideline by third parties. SSRI, selective serotonin reuptake inhibitor NEE, nefaza-done SIB, self injurious behavior VLF, venlafaxine VPA, valproic acid. [Pg.583]

Despite the diagnostic challenges that remain in trying to understand the nature of MDD in children and adolescents, advances in its treatment has progressed considerably since the last edition of this textbook. Over this interval, selective serotonin reuptake inhibitors (SSRIs) have superseded TCAs as the treatment of first choice based both on efficacy and safety considerations. As in adults, specific psychotherapies (cognitive therapy, cognitive-behavioral therapy, and interpersonal therapy) may be as effective as antidepressant medication, at least in mild to moderate depression in children and adolescents ( 111, 112). Also, evidence indicates that depression in children and adolescents may be more influenced than is depression in adults by psychosocial variables such as peers and family, as well as other environmental factors (113). [Pg.279]

Selective serotonin reuptake inhibitors (SSRI s) like Prozac are used to treat many psychiatric disorders ranging from intermittent explosive disorder, to obsessive-compulsive disorder, to major depression and panic disorder (1), even though these disorders differ in their behavioral expression. How does one drug class treat these disparate disorders ... [Pg.537]

More recent findings suggest that the role of 5-HT reuptake in anxiety might be particularly critical during early development (26). The selective serotonin reuptake inhibitor (SSRI) fluoxetine given postnatally to wild-type mice for approximately 2 wk (between postnatal days 4 and 21) resulted in anxiety behavior when tested as adults, and this was similar to that of 5-HTT- - mice. Perhaps because these experiments were conducted in 5-HTT- mice on a 129 background, neither 5-HTT 7 nor postnatally SSRI-treated mice exhibited anxiety in the most typical measures of anxiety (see supporting online material [26]). 5-HTT- - and postnatal SSRI-treated mice did not demonstrate decreased center time in the open field or decreased open arm time or entries in the... [Pg.587]

Selective serotonin reuptake inhibitors (SSRIs) inhibit the neuronal reuptake of serotonin in the central nervous system and have shown mixed efficacy in the treatment of autistic symptoms (Moore et al., 2004). A number of studies have shown reductions in repetitive behaviors, lethargy, inappropriate speech, and improvements in the ability to relate to others, cognition, language improvement with fluoxetine (DeLong et al., 1998 Fatemi et al., 1998 Peral et al., 1999), fluvoxamine (McDougle et al., 1996b), and sertraline (Steingard et al., 1997). However, other studies have shown a lack of response with fluvoxamine (Martin et al., 2003) and citalopram (Couturier and Nicolson, 2002). [Pg.385]

When they occur, depressive symptoms should be treated actively using a combination of cognitive-behavioral therapy and an antidepressant drug. Of the available antidepressants, selective serotonin reuptake inhibitors (SSRIs) have the most favourable combination of efficacy and side-effect profile for the elderly, regardless of the presence of medical co-morbidities. Although the dual agent venlafaxine has been proposed as an alternative agent for older patients who are either non-responders or partial responders to SSRIs, the frail elderly may be particularly vulnerable to its side effects (Hayes 2004). [Pg.146]

Antidepressants. Antidepressants currently play no role in treating acute AN. Antidepressants, and in particular selective serotonin reuptake inhibitors (SSRIs), theoretically work because of their impact on serotonin, a nemotransmitter which is involved with many of the behaviors that are distmbed in AN. This recommendation is based on recent analyses of the hteratme and the most recent practice guidelines from the American Psychiatric Association. ... [Pg.1151]

FIGURE 70-2. Algorithm for management of obsessive-compulsive disorder in adults. A. Overall approach to treatment. B. Pharmacotherapeutic approach to treatment. CBT, cognitive behavioral therapy SSRI, selective serotonin reuptake inhibitor. (Derived from Expert Consensus Panel for Obsessive-Compulsive Disorder and American Pharmaceutical Association. )... [Pg.1314]

Selective serotonin reuptake inhibitors (SSRIs) A relatively new group of medicines that have been used successfully to treat emotional and behavioral problems such as depression, panic disorder, obsessive-compulsive disorder ((XID), bulimia, and posttraumatic stress disorder in adults. These medications are now being used to treat the same types of behavior in children. Some examples of SSRIs include Prozac (fluoxetine), Zoloft (sertraline), Luvox (fluvoxamine), and Paxil (paroxetine). [Pg.309]

SLC6A4 (SERT) SERT plays a role in the reuptake and clearance of serotonin in the brain. Like the other SLC6A family members, SERT transports its substrates in a Na+-dependent fashion and is dependent on CL and possibly on the countertransport of K+. Substrates of SERT include serotonin (5-HT), various tryptamine derivatives, and neurotoxins such as 3,4-methylene-dioxymethamphetamine (MDMA ecstasy) and fenfluramine. SERT is the specific target of the selective serotonin reuptake inhibitors (e.g., fluoxetine and paroxetine) and one of several targets of tricyclic antidepressants e.g., amitriptyline). Genetic variants of SERT have been associated with an array of behavioral and neurological disorders. The precise mechanism by which a reduced activity of SERT, caused by either a genetic variant or an antidepressant, ultimately affects mood and behavior is not known. [Pg.42]

CBT Cognitive-behavioral therapy MAOI Monamine oxidase inhibitor SSRI Selective serotonin reuptake inhibitor... [Pg.228]

Serotonin, also known as 5-hydroxytryptamine (5-HT) is biosynthesized from tryptophan and is a neurotransmitter. Serotonin plays an important role in many behaviors including sleep, appetite, memory, and mood [52]. People with depressive disorders exhibit low levels of serotonin in the synapses. Protonated serotonin binds to a serotonin reuptake transporter protein, sometimes referred to as the serotonin transporter (SERT) and is then moved to an inward position on the neuron and subsequently released into the cjdoplasm. Selective serotonin reuptake inhibitors (SSRI) bind with high affinity to the serotonin binding site of the transporter. This leads to antidepressant effects by increasing extracellular serotonin levels which in turn enhances serotonin neurotransmission [53]. The SSRI class of antidepressants has fewer side effects than the monoamine oxidase inhibitors. [Pg.199]


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