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CROSS-TALK OF RETINOIC ACID AND ADRENERGIC HORMONE SIGNALING MAY INFLUENCE DEVELOPMENT OF CARDIAC CONDUCTION AND RHYTHMICITY IN UTERO
Title
CROSS-TALK OF RETINOIC ACID AND ADRENERGIC HORMONE SIGNALING MAY INFLUENCE DEVELOPMENT OF CARDIAC CONDUCTION AND RHYTHMICITY IN UTERO.
Creator
Alam, Sabikha, Ebert, Steven, University of Central Florida
Abstract / Description
Stress hormones, adrenaline and noradrenaline, have been shown to be critical for heart development. Mice lacking dopamine beta-hydroxylase (Dbh), an enzyme responsible for synthesis of these adrenergic hormones, die during mid-gestation due to cardiac failure. Prior research showed that adrenergic cells are found within the electrical conduction system of the heart, and adrenergic deficiency leads to slowed cardiac conduction during embryogenesis. Microarray analysis of wild-type (Dbh+/+)...
Show moreStress hormones, adrenaline and noradrenaline, have been shown to be critical for heart development. Mice lacking dopamine beta-hydroxylase (Dbh), an enzyme responsible for synthesis of these adrenergic hormones, die during mid-gestation due to cardiac failure. Prior research showed that adrenergic cells are found within the electrical conduction system of the heart, and adrenergic deficiency leads to slowed cardiac conduction during embryogenesis. Microarray analysis of wild-type (Dbh+/+) and knockout (Dbh-/-) mouse hearts revealed significant differences in expression of retinoic acid (RA) signaling genes. RA signaling has also been shown to be critical for heart development. These data suggest that heart failure due to adrenergic deficiency may be dependent upon RA signaling. This led to the hypothesis that adrenergic hormones promote the development of the electrical conduction system through modulation of RA signaling. To test this, embryonic mouse hearts were cultured with LE 135, a RA receptor blocker. Heart rate, arrhythmic index (AI) and conduction time were measured. Under these conditions there was a marked increase in arrhythmias. Hearts treated with LE 135 showed a mean AI of 0.232+/-0.057 after 24 hours of treatment while when untreated had an AI of 0.083+/-0.028 (p<0.05;n=15). In contrast, there was no significant change in heart rate or conduction speed after 24 hours with or without the retinoic acid receptor blocker. To determine if adrenergic stimulus influences retinoic acid response, an established RA-sensitive reporter cell line was employed. These F9-RARE-LacZ cells were treated with forskolin (cAMP regulator) and isoproterenol (beta-agonist) to measure changes in RA signaling. Evaluation of RA signaling showed an increase in retinoic acid responsiveness when treated with an adrenergic signaling agonist. These results suggest that proper retinoic acid signaling is essential for maintaining cardiac rhythmicity during embryonic development and adrenergic stimulation can influence this response.
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Date Issued
2011
Identifier
CFH0003831, ucf:44726
Format
Document (PDF)
PURL
http://purl.flvc.org/ucf/fd/CFH0003831
Does Virtual Reality Elicit Physiological Arousal in Social Anxiety Disorder
Title
Does Virtual Reality Elicit Physiological Arousal in Social Anxiety Disorder.
Creator
Owens, Maryann, Beidel, Deborah, Cassisi, Jeffrey, Bowers, Clint, Neer, Sandra, University of Central Florida
Abstract / Description
The present study examined the ability of a Virtual Reality (VR) public speaking task to elicit physiological arousal in adults with SAD (n=25) and Controls (n=25). A behavioral assessment paradigm was employed to address three study objectives: (a) to determine whether the VR task can elicit significant increases in physiological response over baseline resting conditions (b) to determine if individuals with SAD have a greater increase from baseline levels of physiological and self-reported...
Show moreThe present study examined the ability of a Virtual Reality (VR) public speaking task to elicit physiological arousal in adults with SAD (n=25) and Controls (n=25). A behavioral assessment paradigm was employed to address three study objectives: (a) to determine whether the VR task can elicit significant increases in physiological response over baseline resting conditions (b) to determine if individuals with SAD have a greater increase from baseline levels of physiological and self-reported arousal during the in vivo speech task as opposed to the VR speech task and (c) to determine whether individuals with SAD experience greater changes in physiological and self-reported arousal during each speech task compared to controls. Results demonstrated that the VR task was able to elicit significant increases in heart rate, skin conductance, and respiratory sinus arrhythmia, but did not elicit as much physiological or self-reported arousal as the in vivo speech task. In addition, no differences were found between groups. Clinical implications of these findings are discussed.
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Date Issued
2013
Identifier
CFE0004906, ucf:49624
Format
Document (PDF)
PURL
http://purl.flvc.org/ucf/fd/CFE0004906