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Trauma and the Developing Brain - College of Education & Human ...

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H<strong>and</strong>out for <strong>Trauma</strong>, The <strong>Developing</strong> <strong>Brain</strong>, Healing <strong>and</strong> Emotional Regulation Seminars<br />

Karina A. Forrest-­‐Perkins MHR LADC, 2011<br />

The Neurobiological Responses to Threat<br />

When a child is threatened, various neurophysiological <strong>and</strong> neuroendocrine responses are<br />

initiated. If <strong>the</strong>y persist, <strong>the</strong>re will be ‘use-­‐dependent’ alterations in <strong>the</strong> key neural systems<br />

involved in <strong>the</strong> stress response. These include <strong>the</strong> hypothalamic-­‐pituitary-­‐adrenal (HPA) axis.<br />

In animal models, chronic activation <strong>of</strong> <strong>the</strong> HPA system in response to stress has negative<br />

consequences. Chronic activation may "wear out" parts <strong>of</strong> <strong>the</strong> body including <strong>the</strong> hippocampus,<br />

a key area involved in memory, cognition <strong>and</strong> arousal. This may be occurring in traumatized<br />

children as well. Dr. Martin Teicher <strong>and</strong> colleagues have demonstrated hippocampal/limbic<br />

abnormalities in a sample <strong>of</strong> abused children.<br />

Ano<strong>the</strong>r set <strong>of</strong> neural systems that become sensitized by repetitive stressful experiences are<br />

<strong>the</strong> catecholamine systems including <strong>the</strong> dopaminergic <strong>and</strong> noradrenergic systems. These key<br />

neurochemical systems become altered following traumatic stress. The result is a cascade <strong>of</strong><br />

associated changes in attention, impulse control, sleep, fine motor control <strong>and</strong> o<strong>the</strong>r<br />

functions mediated by <strong>the</strong> catecholamines.<br />

As <strong>the</strong>se catecholamines <strong>and</strong> <strong>the</strong>ir target regions (e.g., amygdaloid nuclei) also mediate a<br />

variety <strong>of</strong> o<strong>the</strong>r emotional, cognitive <strong>and</strong> motor functions, sensitization <strong>of</strong> <strong>the</strong>se systems by<br />

repetitive re-­‐experiencing <strong>of</strong> <strong>the</strong> trauma leads to dysregulation in many functions.<br />

A traumatized child may, <strong>the</strong>refore, exhibit motor hyperactivity, anxiety, behavioral impulsivity,<br />

sleep problems, tachycardia <strong>and</strong> hypertension. In preliminary studies by our group, we have<br />

seen altered cardiovascular regulation (e.g., increased resting heartrate) suggesting altered<br />

autonomic regulation at <strong>the</strong> level <strong>of</strong> <strong>the</strong> brainstem. In o<strong>the</strong>r studies, clonidine, an alpha2<br />

adrenergic receptor partial agonist has been demonstrated to be an effective<br />

pharmaco<strong>the</strong>rapeutic agent, presumably by altering <strong>the</strong> sensitivity <strong>of</strong> <strong>the</strong> noradrenergic<br />

systems.<br />

Implications <strong>of</strong> <strong>Trauma</strong>-­‐related Alterations in <strong>Brain</strong> Development<br />

All experiences change <strong>the</strong> brain – yet not all experiences have equal ‘impact’ on <strong>the</strong> brain.<br />

Because <strong>the</strong> brain is organizing at such an explosive rate in <strong>the</strong> first years <strong>of</strong> life, experiences<br />

during this period have more potential to influence <strong>the</strong> brain – in positive <strong>and</strong> negative ways.<br />

<strong>Trauma</strong>tic experiences <strong>and</strong> <strong>the</strong>rapeutic experiences impact <strong>the</strong> same brain <strong>and</strong> are limited by<br />

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