Central Components of the Orienting Response (EEG Reactivity) in Acute and Former Schizophrenics, Neurotics, and Normals

2015 ◽  
pp. 20-27 ◽  
Author(s):  
Martha Koukkou ◽  
Marianne Bigler ◽  
D. Lehmann
Keyword(s):  
Orienting Response ◽  
Eeg Reactivity

Application of Information Introduced to Dynamic Message Processing and Enjoyment

2018 ◽  
Vol 30 (4) ◽  
pp. 196-206 ◽  
Author(s):  
Byungho Park ◽  
Rachel L. Bailey
Keyword(s):  
Resource Allocation ◽  
Recognition Memory ◽  
Emotional Processing ◽  
Orienting Response ◽  
Structural Features ◽  
Cognitive Resources ◽  
Coding System ◽  
Message Complexity ◽  
Cognitive Resource ◽  
Cognitive Overload

Abstract. In an effort to quantify message complexity in such a way that predictions regarding the moment-to-moment cognitive and emotional processing of viewers would be made, Lang and her colleagues devised the coding system information introduced (or ii). This coding system quantifies the number of structural features that are known to consume cognitive resources and considers it in combination with the number of camera changes (cc) in the video, which supply additional cognitive resources owing to their elicitation of an orienting response. This study further validates ii using psychophysiological responses that index cognitive resource allocation and recognition memory. We also pose two novel hypotheses regarding the confluence of controlled and automatic processing and the effect of cognitive overload on enjoyment of messages. Thirty television advertisements were selected from a pool of 172 (all 20 s in length) based on their ii/cc ratio and ratings for their arousing content. Heart rate change over time showed significant deceleration (indicative of increased cognitive resource allocation) for messages with greater ii/cc ratios. Further, recognition memory worsened as ii/cc increased. It was also found that message complexity increases both automatic and controlled allocations to processing, and that the most complex messages may have created a state of cognitive overload, which was received as enjoyable by the participants in this television context.

Primacy Effect in Orienting Responses to Auditory Stimuli of Tones and Music

1976 ◽  
Vol 42 (3) ◽  
pp. 919-928 ◽  
Author(s):  
Eleanor B. Simon
Keyword(s):  
College Students ◽  
Orienting Response ◽  
Primacy Effect ◽  
Factorial Experiment ◽  
Auditory Stimuli ◽  
Adaptation Period ◽  
Soft Or ◽  
Interstimulus Intervals ◽  
Music Stimulus

This 26 factorial experiment investigated the primacy effect in the orienting response. The type of stimuli (tone or “music”), stimulus intensities (loud or soft), length of adaptation period (same, 5 or 30 sec.; or different, 5 min.), interstimulus intervals (5 or 30 sec.), and sex were studied. College students, 32 males and 32 females were randomly assigned to each group. In the same condition, the tone (or music) was soft (or loud) for 5 sec. (or 30 sec.) in adaptation and was then changed alternately without interruption to loud, soft, etc. (or soft, loud, etc.) for 5 sec. (or 30 sec.). The different condition was identical except for the length of the adaptation period in which the stimuli sounded continuously for 5 min. Analyses of the GSR manifestation of the orienting responses indicated: (a) an over-all primacy effect with the auditory stimuli and (b) the primacy effect occurred in the 5-sec.-same but not in the 30-sec.-same condition as predicted.

Heart-rate change as a component of the orienting response.

1966 ◽  
Vol 65 (5) ◽  
pp. 305-320 ◽  
Author(s):  
Frances K. Graham ◽  
Rachel K. Clifton
Keyword(s):  
Heart Rate ◽  
Orienting Response ◽  
Heart Rate Change ◽  
Rate Change

The orienting response of Lake Michigan mottled sculpin is mediated by canal neuromasts

2001 ◽  
Vol 204 (2) ◽  
pp. 337-348 ◽  
Author(s):  
S. Coombs ◽  
C.B. Braun ◽  
B. Donovan
Keyword(s):  
Time Course ◽  
Lake Michigan ◽  
Cell Damage ◽  
Aminoglycoside Antibiotic ◽  
Response Rates ◽  
Orienting Response ◽  
Sensory Epithelium ◽  
Live Prey ◽  
Mottled Sculpin ◽  
Pre Treatment

Lake Michigan mottled sculpin, Cottus bairdi, exhibit a naturally occurring and unconditioned orienting response that can be triggered by both live prey and chemically inert vibrating spheres, even in blinded animals. CoCl(2)-induced reductions of the orienting response demonstrate that the lateral line is required for this behavior in the absence of non-mechanosensory cues (such as vision), but shed no light on the relative contributions of superficial and canal neuromasts to this behavior. To determine the relative roles of these two subsystems, we measured the frequency with which mottled sculpin oriented towards a small vibrating sphere before and after two treatments: (i) immersion of fish in a solution of gentamicin, an aminoglycoside antibiotic that damages hair cells in canal, but not superficial, neuromasts; and (ii) scraping the skin of the fish, which damages the superficial, but not the canal, neuromasts. To ensure that both superficial and canal neuromasts were adequately stimulated, we tested at different vibration frequencies (10 and 50 Hz) near or at the best frequency for each type of neuromast. At both test frequencies, response rates before treatment were greater than 70 % and were significantly greater than ‘spontaneous’ response frequencies measured in the absence of sphere vibration. Response rates fell to spontaneous levels after 1 day of gentamicin treatment and did not return to pre-treatment levels for 10–15 days. In contrast, response rates stayed approximately the same after superficial neuromasts had been damaged by skin abrasion. Scanning electron microscopy confirmed hair cell damage (loss of apical cilia) in canal, but not superficial, neuromasts of gentamicin-treated animals after as little as 24 h of treatment. The sensory epithelium of canal neuromasts gradually returned to normal, following a time course similar to behavioral loss and recovery of the orienting response, whereas that of superficial neuromasts appeared normal throughout the entire period. This study shows that the orienting response of the mottled sculpin is mediated by canal neuromasts.

Covert orienting of attention in macaques. I. Effects of behavioral context

1993 ◽  
Vol 70 (1) ◽  
pp. 431-443 ◽  
Author(s):  
E. M. Bowman ◽  
V. J. Brown ◽  
C. Kertzman ◽  
U. Schwarz ◽  
D. L. Robinson
Keyword(s):  
Cognitive Processes ◽  
Reaction Times ◽  
Orienting Response ◽  
Validity Effect ◽  
Experimental Conditions ◽  
Covert Orienting ◽  
Cognitive Influences ◽  
Attentional Effect ◽  
Peripheral Cues ◽  
Neurophysiological Studies

1. A task was used by Posner (1980) to measure shifts of attention that occurred covertly, in the absence of an eye movement or other orienting response. This paradigm was used here to assess the nature of covert attentional orienting in monkeys to develop an animal model for neurophysiological studies. Shifts of attention were measurable in monkeys and were consistent across a variety of experimental conditions. 2. The paradigm required that monkeys fixate and release a bar at the appearance of a target, which was preceded by a cue. Reaction times to targets that followed peripheral cues at the same location (validly cued) were significantly faster than those that followed cues in the opposite visual field (invalidly cued). This difference was defined as the validity effect, which as in humans, is used as the measure of a covert attentional shift. 3. When the proportion of validly to invalidly cued targets was decreased, no change was seen in the validity effect of the monkeys. This is in contrast to humans, for whom the ratio of validly to invalidly cued targets affected the magnitude of the validity effect. When 80% of the targets were preceded by cues at the same location, the validity effect was greatest. The effect was reversed when the proportions were reversed. From this result, it is concluded that cognitive processes can affect covert orienting to peripheral cues in humans, whereas in trained monkeys, performance was automatic. 4. To test whether cognitive influences on attention could be demonstrated in the monkey, an animal was taught to use symbolic, foveal signals to covertly direct attention. The magnitude of this validity effect was greater than that obtained with peripheral cues. 5. The effects of motivational and perceptual processes were tested. Although overall reaction times could be modified, the facilitating effects of the cues persisted. This constancy across motivational and perceptual levels supports the notion that the monkeys were performing the task in an automatic way, under the exogenous control of peripheral cues. 6. Most visual cuing has been tested with visual landmarks at the locations of cues and targets. These monkeys were trained with such landmarks, and when tested without them, the attentional effect of the cues was nearly abolished. These data suggest that local visual features can be important for covert orienting. 7. To determine the spatial extent of the effect of the cue, monkeys and humans were tested with four cue-target distances (0-60 degrees).(ABSTRACT TRUNCATED AT 400 WORDS)

Involvement of SA channels in orienting response of cultured endothelial cells to cyclic stretch

1998 ◽  
Vol 274 (5) ◽  
pp. H1532-H1538 ◽  
Author(s):  
Keiji Naruse ◽  
Takako Yamada ◽  
Masahiro Sokabe
Keyword(s):  
Endothelial Cells ◽  
Cell Elongation ◽  
Umbilical Vein ◽  
Orienting Response ◽  
Cyclic Stretch ◽  
Silicone Membrane ◽  
Cell Orientation ◽  
Human Umbilical Vein ◽  
Intracellular Ca ◽  
Dependent Cell

The present work was designed to elucidate the involvement of Ca2+-permeable stretch-activated (SA) channels in the orienting response of endothelial cells to uniaxial cyclic stretch. Endothelial cells from human umbilical vein were cultured on an elastic silicone membrane and subjected to uniaxial cyclic stretch (120% in length, 1 Hz). The cells started to change their morphology 15 min after the onset of stretch, and >90% of the cells oriented perpendicularly to the stretch axis after 2 h. Associated with the orienting response, cell elongation proceeded with a slower rate. Both of the orientating and elongating responses were largely inhibited by the removal of external Ca2+ or by Gd3+, a potent blocker for the SA channel, but not by nifedipine. Intracellular Ca2+ concentration ([Ca2+]i) transiently increased in response to uniaxial stretch, and the basal [Ca2+]igradually increased during cyclic stretch. This Ca2+ response was inhibited by the removal of extracellular Ca2+ or by the addition of Gd3+. These results suggest that stretch-dependent Ca2+ influx through SA channels is essential in the stretch-dependent cell orientation and elongation.

Orienting Response

2013 ◽  
pp. 2099-2100
Author(s):  
Suzanne Macari ◽  
Ruth Eren ◽  
Louise Spear-Swerling ◽  
John T. Danial ◽  
Lawrence David Scahill ◽  
...  
Keyword(s):  
Orienting Response
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