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Second Department of Physiology, Showa University School of Medicine, Tokyo 142, Japan
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ABSTRACT |
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 TOP
 ABSTRACT
 INTRODUCTION
METHODS
RESULTS
DISCUSSION
REFERENCES
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We have previously found that individual anxiety
levels influence respiratory rates in physical load and mental stress
(Y. Masaoka and I. Homma. Int. J. Psychophysiol. 27: 153-159, 1997). On the basis of
that study, in the present study we investigated the metabolic outputs
during tests and analyzed the respiratory timing relationship between
inspiration and expiration, taking into account individual anxiety
levels. Disregarding anxiety levels, there were correlations between
O2 consumption
(
O2) and minute ventilation (E) and between
O2 and tidal volume in the
physical load test, but no correlations were observed in the noxious
audio stimulation test. There was a volume-based increase in
respiratory patterns in physical load; however,
E increased not only for the adjustment
of metabolic needs but also for individual mental factors; anxiety
participated in this increase. In the high-anxiety group, the
E-to-O2
ratio, indicating ventilatory efficiency, increased in both tests. In
the high-anxiety group, increases in respiratory rate contributed to a
E increase, and there were negative
correlations between expiratory time and anxiety scores in both tests.
In an awake state, the higher neural structure may dominantly affect
the mechanism of respiratory rhythm generation. We focus on the
relationship between expiratory time and anxiety and show diagrams of
respiratory output, allowing for individual personality.
physical load; mental stress; respiratory rate; expiratory time; anxiety
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INTRODUCTION |
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TOP
ABSTRACT
INTRODUCTION
METHODS
RESULTS
DISCUSSION
REFERENCES
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BREATHING APPEARS TO BE REGULATED in the brain stem for metabolic, homeostatic purposes. During a physical workload, increases in tidal volume (VT) and respiratory rate (RR) contribute to a rise in ventilation (13). The reflexes of respiratory drive have been shown in the VT-inspiratory time (TI) relationship (6); in addition, certain stimuli alter respiratory drive (9).
In the awake state, the breathing pattern comes from the complex interaction between matching for metabolic requirements and the nonhomeostatic demands. It has been reported that auditory or visual input alters the breathing patterns under the condition of rest (23), and the production of various emotions affects breathing patterns (4); furthermore, different personality factors have affected different responses of sensitivity toward carbon dioxide (24). Research on ventilation, taking into consideration the personality factor, has been evaluated by a number of studies. People breathe in different ways in defining a resting state, and these patterns of breathing, referred to as "ventilation personality," are reproduced over long periods of time (22). Breathing patterns in patients with chronic anxiety have showed irregularities of rhythm (29), and our previous study demonstrated that individual anxiety levels greatly influence respiratory patterns, in particular the RR (18). Curiously, our study found that significant correlations were not observed between the scores that indicated how the subjects feel and variables of breathing parameters, but significant correlations were found between RR and state anxiety scores in the isometric leg exercise (indicated as "physical load" in the following pages) and between RR and trait anxiety scores in the mental stress test. It was Sigmund Freud who first proposed a role for anxiety in personality theory, and anxiety was described as "a specific unpleasant emotional state or condition of the human organism" (27). Since 1950, research on human anxiety has been facilitated by using scales that have been created for measuring anxiety, and the concept of state and trait anxiety was introduced in the 1960's (26, 27).
Each person has his or her own personality traits; therefore, the psychological or physiological response toward stimulation may depend on the individual. In physiology, research on the relationship between psychological factors and respiratory parameters has not been carried out. Psychological symptoms such as fear of dying or anxiety are common feelings in patients complaining of dyspnea or a feeling of breathlessness. It has been reported that anxious patients' perceptions were less sensitive toward added loads (28). Another study suggested that defensive subjects tend to impair accurate respiratory sensation (15). The study of the relationship between anxiety levels and respiratory parameters and between anxiety levels and sensation could assist the understanding of symptoms reported from patients.
In a pilot study, a correlation between state anxiety and RR in a physical load test, and between trait anxiety and RR in a mental stress test, was found in 10 normal subjects (18). In this study, in a new set of experiments, we tested the hypothesis that exceeding increases in RR are not related to differences in the metabolic rate but are caused by individual anxiety that enhances the respiratory drive.
We investigated breath-by-breath metabolic outputs during physical load, comparing the outputs during noxious audio stimulation and identifying the relationship between these respiratory timings and metabolic outputs between two groups of subjects, one with high anxiety and one with low anxiety.
Because our previous study found the state anxiety scores related to the RR in physical load and the trait anxiety scores related to the RR in mental stress, we focused on the influences of both state anxiety levels on respiratory parameters in physical load and of trait anxiety levels on respiratory parameters in noxious audio stimulation.
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METHODS |
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TOP
ABSTRACT
INTRODUCTION
METHODS
RESULTS
DISCUSSION
REFERENCES
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Subjects
Ten undergraduate students (all men; mean age 21 ± 1.6 yr), who were naive to the purpose of the study, participated. Before the experiments the subjects signed an informed consent, and all were tested for anxiety levels by using Spielberger's State-Trait Anxiety Inventory (STAI) (26).Two sets of experiments were carried out in each subject, a study of physical load and a study of noxious audio stimulation. The subjects were examined twice for each study, and the raw data of trial 1 and trial 2 were combined statistically.
Measurements
STAI. Before they entered a dark, soundproof room, subjects' anxiety levels were evaluated by Spielberger's STAI (26) translated into Japanese (19). The reliability and validity of this version have been evaluated by many researchers (26). The STAI is designed to be self-administered and consists of two anxiety scales, state anxiety and trait anxiety. Each test form has 20 statements and requires ~15 min to complete both. The state anxiety scale is used to evaluate how people feel ("right now") in a variety of situations. For example, the scale has been used to assess the level of state anxiety induced by a stressful experimental situation or an important school test. The trait anxiety scale is used to assess how people generally feel, referring to stable individual differences in proneness to anxiety. Accordingly, the trait anxiety scores are generally not influenced by any conditions. The purpose of using this scale is to measure the state and trait anxieties separately. Because the experiment was performed in a laboratory situation, the subjects might be in a nervous state or be sensitive toward these procedures. Therefore, we wanted to understand how the subjects were feeling right then at the moment. In addition, in a future study we intend to investigate different state anxieties in individuals and whether the anxieties affect subjects' respiratory parameters.
O2 consumption
(O2) and
CO2 production
(CO2) during tests.
Other measurements were made in the dark, sound- proof
room separated from the investigator. The subjects were seated on a chair, wore a face mask, and kept their eyes open; a 10-min rest period
was allowed for them to adapt to the apparatus. An aeromoniter (AE280,
Minato Medical Science, Osaka, Japan) (16) was installed outside the
soundproof room. The AE280 consists of a microcomputer, a hot-wire
flowmeter, O2 and
CO2 analyzers, (Zr element-based O2 analyzer and infrared
CO2 analyzer). Gas was sampled by
pumping it through a filter into the analyzers at the rate of 220 ml/min. On a breath-by-breath basis, the AE280 continuously calculated minute ventilation (E),
VT, RR,
O2,
CO2, end-tidal fraction of
CO2
(FETCO2),
TI, and expiratory time
(TE). The system was
calibrated before each study. The accuracy of the system measuring the
breath-by-breath calculation of
O2 and
CO2 was confirmed with the
same results in measuring
O2 obtained by
the gas-collection method (20).
Physical load. For physical load (isometric leg exercise), a Velcro belt attached to a spring balance was wrapped around the subjects' knees; the subjects were asked to stretch their knees, holding a 7-kg load, in an outer direction. The reason for choosing this physical load is that a prior exercise study reported that breathing frequency is entrained by the rhythm of the exercise (3), so we omitted this factor.
Noxious audio stimulation. For noxious audio stimulation, subjects wore headphones to deliver noxious sounds: incessant sawmill noise from a compact disk of environmental sounds, with a volume set at 73 dBA (King Record). The sound was delivered by a digital portable stereo compact disk system (Panasonic RX DT7). Through a study of aggregation of noise (7), 73 dBA is a level characterized as "moderately loud."
Measurement during the resting state for a baseline over 3 min during physical load or over 2 min during noxious audio stimulation, and 3 min after the tests were over, was monitored after a 10-min interval for subjects to adapt to the apparatus. As mentioned above (see Subjects), subjects were tested twice for each study, and results of the two trials were combined statistically. In one report, only 2 min of noxious stimulation were administered for fear of causing adaptation to the stimulation (17). We used this time period for one trial, and the trial was recorded twice because we wanted to have more data to analyze each subject. In addition, we wanted to avoid emotional factors that might arise if one trial were over a long period of time, such as, for example, fatigue toward the physical load or any feeling caused by the subjects not being acclimatized to the apparatus. Statistically, 20 breaths before each test were reserved for baseline and 20 breaths during the test for the physical load or noxious audio stimulation.Statistical Analysis
Differences between the raw data before and during the manipulations were analyzed by a repeated-measures ANOVA. To calculate repeated-measures ANOVA, we entered each subject's raw breath-by-breath data, not the means. The probability values applying the Greenhouse-Geisser correction procedure for ANOVA were used to control for possible violations of the assumption of homogeneity of variance. We calculated a correlation coefficient for the linear regression analysis. Data are reported as means ± SD in Tables 1-4, and the scatterplots indicate mean value of each subject in Figs. 1-5.
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RESULTS |
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TOP
ABSTRACT
INTRODUCTION
METHODS
RESULTS
DISCUSSION
REFERENCES
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Age and individual STAI scores are shown in Table 1. In the STAI, subjects blacken a number beside each item that best describes their feelings. The scores for state anxiety and trait anxiety were obtained by adding the weighted scores of the 20 items. STAI scores were graded on a scale of five according to the normalization for the Japanese version evaluated by Mizuguchi et al. (19). Trait anxiety scores were divided into I ("very low," <23), II ("low," 24-32), III ("normal," 33-43), IV ("high," 44-52), and V ("very high," >53). State anxiety scores were also divided into I (very low, <22), II (low, 23-31), III (normal, 32-40), IV (high, 41-49), and V (very high, >50). As shown in Table 1, the subjects were divided into groups with high state anxiety or high trait anxiety (denoted by brackets) and groups with low state anxiety or low trait anxiety (denoted by bold numbers).
Effect of Physical Load and Noxious Audio Stimulation on Respiratory Parameters
Comparison between parameters for the baseline period and during physical load in each group are presented in Table 2. As metabolism changed inO2 and
CO2
(P < 0.001 in both groups), E (P < 0.001 in each group) increased. Both
VT
(P < 0.001) and RR
(P < 0.05 in the low-state-anxiety
group, P < 0.001 in the high-state-anxiety group) increased to contribute to the increase in
E. In subjects with low state anxiety,
FETCO2
increased (P < 0.05) and
TI and
TE remained unchanged. On the
contrary, FETCO2
decreased (P < 0.05) and significant
decreases in TI and
TE were observed in the
high-state-anxiety group.
O2/kg increased in both
groups (P < 0.001) in the physical
load test. With regard to the effect of physical load, differences in
the ventilatory response between the high-state-anxiety and the
low-state-anxiety groups were not observed, except for
changes in
FETCO2, TI, and
TE.
Table 3 shows that noxious audio
stimulation affected VT
(P < 0.05) and RR
(P < 0.05) in the
low-trait-anxiety group, but the increase in
E was not significant.
FETCO2
(P < 0.001) significantly increased,
whereas
FETCO2
(P < 0.05) decreased in the
high-trait-anxiety group. This decrease was caused by an increase in RR
(P < 0.001) as a result of both
TI
(P < 0.05) and
TE
(P < 0.001) decreases. Although an
increase in O2/kg was observed in the high-trait-anxiety group,
E increased not only for the
fulfillment of the metabolic demand but also for the trait anxiety
factor involved as a result of dominant RR increases reflected by
TI and
TE decreases.
Correlation Between Both Anxiety and
O2 and Respiratory
Parameters
E and
O2 in both tests,
disregarding anxiety levels (Fig. 1), showed linear relationships between the baseline of E and
O2
(r = 0.6505, P < 0.05, 
and solid line) and
between E and
O2
(r = 0.6571, P < 0.05, 
and dashed line)
during the physical load (Fig.
1A). On the other hand, a
correlation between E and
O2 was observed during the
baseline period (r = 0.6664, P < 0.05, and solid line), but
only E increased while
O2 remained unchanged during
the noxious audio stimulation test (r = 0.2268, P < 0.05, and dashed line) (Fig. 1B).
There was a nonlinear relationship between
E and
O2 during noxious audio
stimulation. This increase in E was not
caused by an increase in metabolic demand. Relationships between
metabolic output, RR, VT, and
anxiety scores are indicated in Figs. 2 and 3.
During physical load, as a whole
VT and
O2 correlated positively and
significantly (r = 0.448, P < 0.05). There were no correlations between RR and
O2
(r = 0.129) and between
O2/kg and state anxiety
scores (r = 0.367); however, during
noxious audio stimulation, there were no correlations between these
variables as shown in Fig. 3.
Ventilatory Efficiency Observed in Subjects with Low and High Anxiety
A rise inE over the metabolic
demand in the high-anxiety group during the physical load test
and the noxious audio stimulation test was also observed compared with
baseline and during physical load of the
E-to-O2
(E/O2)
and
E-to-CO2
(E/CO2) ratio (Table 4). In the high-anxiety group, the
E/O2
ratio (P < 0.001 in physical load,
P < 0.05 in noxious audio
stimulation) and
E/CO2
ratio (P < 0.001 in physical load,
P < 0.05 in noxious audio
stimulation) increased.
Analysis of Respiratory Timing Relationship Between Both TI and TE and Anxiety Scores
Figure 4 shows the relationship between decreases in TI ( and dashed line) and
TE ( and solid line) and
state anxiety scores during physical load
(top) and between
TI and
TE and trait anxiety scores
during noxious audio stimulation
(bottom). Taking into consideration
the individual anxiety level, the difference between TE during baseline and
TE during physical load and the
state anxiety scores had a negative correlation
(r = 
0.5930,
P < 0.05) (Fig. 4,
top); in addition, a negative
correlation was observed in the noxious audio stimulation test, but it
was of a trait anxiety score (r = 0.4936, P < 0.05) (Fig. 4,
bottom). Thus an increase in RR in
people with high anxiety is related to a decrease in TE.
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DISCUSSION |
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TOP
ABSTRACT
INTRODUCTION
METHODS
RESULTS
DISCUSSION
REFERENCES
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A previous study showed that there was no correlation between emotion scores (feeling of unpleasantness or difficulty continuing the task) and respiratory parameters, but there was a correlation between anxiety level and RR in the physical load and the noxious audio- stimulation tests (18). In addition, interestingly, this study found that significant correlations were found between RR and state anxiety scores in the physical load test and between RR and trait anxiety scores in the mental stress test.
As we hypothesized, from the viewpoint of Spielberger's concept that explains the distinction between state and trait anxiety, an increase in RR in the physical load may change if a subject is in a different anxiety state, but an increase in RR with mental stress may not change because trait anxiety is conceptualized by a potential tendency (18). We did not examine the effect of different state anxieties on respiration for each subject; however, from this result, we could suggest that emotional state caused by a particular situation or physical condition may affect respiratory patterns in physical workload. Spielberger (26) proposed that physiological indexes are likely to be affected by state anxiety rather than trait anxiety, but we also found that an increase in RR was related to trait anxiety in the noxious audio stimulation test. Therefore, our result suggests that the effect of psychological stimulation may be involved in a potential anxiety trait.
The present study focused on the relationship between the level of
either individual state or trait anxiety and RR; we analyzed whether
anxiety participates in metabolic output, whether this exceeding
increase in RR was not caused to fulfill the metabolic demand, and
whether the respiratory timing relationship is related to anxiety. In
observing the data of physical load in Table 2, we saw that there was a
similarity in most parameters comparing the high-state-anxiety and
low-state-anxiety groups. However, in the high-state-anxiety group,
FETCO2
decreased significantly and TI
and TE shortened. As a whole,
there was a VT-based increase in
respiratory patterns reflected by a correlation between
E and
O2 and between
VT and
O2. However, the
result indicates that E increased not
only for the metabolic demand, indicating an increase in the
E/O2
ratio expressed as ventilatory efficiency during physical load. In
Table 2, O2/kg is shown to
have increased in the high-state-anxiety group; however, there was no
correlation between metabolic output and individual state anxiety
scores. In COPD patients, the
E/O2
ratio increased as a result of a decrease in ventilatory efficiency
(25). An increase in ventilatory efficiency was influenced by
individual high state anxiety even in normal subjects as a result of a
dominant increase in RR reflected by a fall in
FETCO2.
Analysis of the increase in RR in the physical load test shows there
was no correlation between TI
and state anxiety scores, but there was a correlation between TE and state anxiety scores. It
has been reported that breathing frequency is entrained by
the rhythm of exercise (3), but in this study the physical load test
was performed without the rhythmic factor.
An increase in E with a nonmetabolic
purpose was also observed in the noxious audio-stimulation test. In the
noxious audio-stimulation test, constancy of
O2 with noxious audio
stimulation suggests that a E increase is
not due to increased metabolism. As also shown in ventilatory
efficiency, an increase in the
E/O2
ratio was observed in the high-trait-anxiety and not in the
low-trait-anxiety group; there was an RR-based increase in
E without any metabolic factor. RR
increased as a result of TI and
TE decreases, whereas VT was unchanged in high trait
anxiety; a correlation between TE and trait anxiety scores was
also observed in the noxious audio-stimulation test.
A number of investigators have presented irregular breathing patterns
during auditory stimulation (12). The increase in E was achieved by RR without a
VT increase in audiovisual
stimulation, whereas increases in both
VT and RR were observed in
noxious audio stimulation (17). Our study suggests that an increase in
E is related not only to a fulfillment of
the metabolic demand but also to the mental factor, in particular
anxiety. Fear and anxiety behaviors are associated with elicitation of
physiological changes such as increases in blood pressure and
respiration (11). Gardner (10) suggested a shortening of
TE caused by anxiety in their subjects in a steady state. Another study demonstrated that anxiety affects both TI and
TE (2). Although there was a
difference between state anxiety and trait anxiety in each test result,
this study confirmed that the anxiety level is related to the RR,
particularly to TE.
Shea and Guz (22) suggested that wakeful perception, like unpleasantness or comfort, is not an essential factor in the genesis of the breathing pattern in the normal individual. We found that change in respiratory parameters did not correlate with scores indicating how subjects feel but did correlate with anxiety levels: RR and TE are changed not by sensation or emotion caused by sensory experience but by a factor more central, one related to the core of the human condition.
We hypothesized that, in subjects in the awake state, the mechanism of
determination of TE or
determination of initiation of inspiration is greatly influenced by the
individual anxiety level. Homma (14) showed, in humans, the mechanism
determining the rate of increase in inspiratory activity by
VT-TI
and
VT-TE relationships during rebreathing, which were indicated by slopes of
regression lines. In Fig. 5, we drew the regression lines of the
VT-TE
relationship during the physical load and the noxious audio-stimulation
tests, which accounted for the individual anxiety level. In the
physical load, there was an increase in E
achieved by VT in people with
low state anxiety; on the other hand, integration of
VT and
TE contributed to an increase in
E in people with high state
anxiety. In the noxious audio-stimulation test, there was little effect
on E and respiratory patterns in people
with low trait anxiety, but, in people with trait anxiety, an increase of E was achieved by a TE
decrease with unchanged VT.
In a consideration of different baselines in high- and low-anxiety levels, it could be suggested that the anticipation of stimulation affects the RR even in a steady, nonstimulation state. It has been reported that respiratory center drive is enhanced before actual exercise (30). Because this study was performed in a laboratory situation, the state anxiety level would most likely increase in an anxious subject before the beginning of stimulation. According to Spielberger (26), the state anxiety score is higher under stressful conditions than normal conditions.
It is also possible that there was discomfort with the instrumentation, thus causing anxiety (21). In this study, the subjects were tested twice for each 2-min test. These repeated measurements may have caused the problem of adaptation. It would be interesting to examine the relationship between personality and the effect of each test, taking adaptation into account; however, we did not study this in detail.
In summary, we demonstrated that there were negative correlations between anxiety levels and decrease in TE in both the physical load test and the noxious audio- stimulation test. In an early study by Euler's group (5), respiratory patterns changed because of the different metabolic demand as shown in VT-TI or VT-TE relationships; it was suggested that the VT-TI curve fluctuated, possibly by the general state of "arousal." In our study, the VT-TE curves shifting to the left were reflected by individual anxiety levels. Respiration is regulated by the automatic metabolic system in the brain stem (8) and is still referred to as "the black box" (1), an area between the forebrain or the cortical structure and respiratory outputs. Our study suggests that the higher neural center may dominantly affect the RR, especially the TE in an awake state.
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ACKNOWLEDGEMENTS |
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We thank Suzanne Knowlton for preparation of the manuscript.
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FOOTNOTES |
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The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. §1734 solely to indicate this fact.
Address for reprint requests and other correspondence: I. Homma, Second Dept. of Physiology, Showa Univ. School of Medicine, Hatanodai 1-5-8, Shinagawa-ku, Tokyo 142, Japan.
Received 9 March 1998; accepted in final form 15 December 1998.
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REFERENCES |
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TOP
ABSTRACT
INTRODUCTION
METHODS
RESULTS
DISCUSSION
REFERENCES
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1.
Asmussen, E.
Regulation of respiration: "the black box."
Acta Physiol. Scand.
99:
85-90,
1977[Medline].
2.
Bechbache, R. R.,
H. H. K. Chow,
J. Duffin,
and
E. C. Orsini.
The effects of hypercapnia, hypoxia, exercise and anxiety on the pattern of breathing in man.
J. Physiol. (Lond.)
293:
285-300,
1979
3.
Bechbache, R. R.,
and
J. Duffin.
The entrainment of breathing frequency by exercise rhythm.
J. Physiol. (Lond.)
272:
553-561,
1971
4.
Boiten, F. A.,
N. H. Frijda,
and
C. J. E. Wientjes.
Emotions and respiratory patterns: review and critical analysis.
Int. J. Psychophysiol.
17:
103-128,
1994[Medline].
5.
Bradley, G. W.,
C. von Euler,
I. Marttila,
and
B. Roos.
Steady state effects of CO2 and temperature on the relationship between lung volume and inspiratory duration (Hering-Breuer threshold curve).
Acta Physiol. Scand.
92:
351-363,
1974[Medline].
6.
Clark, F. J.,
and
C. von Euler.
On the regulation of depth and rate of breathing.
J. Physiol. (Lond.)
222:
267-295,
1972
7.
Cohen, A.,
J. R. Anticaglia,
and
H. H. Jones.
Noise-induced hearing loss.
Arch. Environ. Health
20:
614-623,
1970[Medline].
8.
von Euler, C.
Brainstem mechanisms for generation and control of breathing pattern.
In: Handbook of Physiology. The Respiratory System. Control of Breathing. Bethesda, MD: Am. Physiol. Soc., 1986, vol. 3, pt. 1, p. 1-67.
9.
von Euler, C.,
and
M. Katz-Salamon
(Editors).
Respiratory Psychophysiology. New York: Stockton, 1986von Euler, C., and M. Katz-Salamon (Editors).
Respiratory Psychophysiology. New
York: Stockton, 1986.
10.
Gardner, W. N.
The relation between tidal volume and inspiratory and expiratory times during steady-state carbon dioxide inhalation in man.
J. Physiol. (Lond.)
272:
591-611,
1977
11.
Goddard, A. W., and D. S. Charney.
Toward an integrated neurobiology of panic disorder.
J. Clin. Psychiatry 58, Suppl. 2: 4-11, 1997.
12.
Haas, F.,
S. Distenfeld,
and
K. Axen.
Effects of perceived musical rhythm on respiratory pattern.
J. Appl. Physiol.
61:
1185-1191,
1986
13.
Hey, E. N.,
B. B. Lloyd,
D. J. C. Cunningham,
M. G. M. Jukes,
and
D. P. G. Bolton.
Effects of various respiratory stimuli on the depth and frequency of breathing in man.
Respir. Physiol.
1:
193-205,
1966[Medline].
14.
Homma, I.
Inspiratory inhibitory reflex caused by the chest wall vibration in man.
Respir. Physiol.
39:
345-353,
1980[Medline].
15.
Isenberg, S.,
P. Lehrer,
and
S. Hochron.
Defensiveness and perception of external inspiratory resistive loads in asthma.
J. Behav. Med.
20:
461-472,
1997[Medline].
16.
Koike, A.,
T. Yajima,
H. Adachi,
N. Shimizu,
H. Kano,
K. Sugimoto,
A. Niwa,
F. Marumo,
and
M. Hiroe.
Evaluation of exercise capacity using submaximal exercise at a constant work rate in patients with cardiovascular disease.
Circulation
91:
1719-1724,
1995
17.
Mador, M. J.,
and
M. J. Tobin.
Effect of alterations in mental activity on the breathing pattern in healthy subjects.
Am. Rev. Respir. Dis.
144:
481-487,
1991[Medline].
18.
Masaoka, Y.,
and
I. Homma.
Anxiety and respiratory pattern: their relationship during mental stress and physical load.
Int. J. Psychophysiol.
27:
153-159,
1997[Medline].
19.
Mizuguchi, T.,
J. Shimonaka,
and
K. Nakazato.
The Japanese Version of STAI. Kyoto, Japan: Sankyoubou, 1991.
20.
Noguchi, H.,
Y. Oguchi,
I. Yoshiya,
N. Itakura,
and
H. Yamabayashi.
Breath-by-breath CO2 and O2 require compensation for transport delay and dynamic response.
J. Appl. Physiol.
52:
79-84,
1982
21.
Perez, W.,
and
M. J. Tobin.
Separation of factors responsible for change in breathing pattern induced by instrumentation.
J. Appl. Physiol.
59:
1515-1520,
1985
22.
Shea, S. A.,
and
A. Guz.
Personnalit ventilatoire
an overview.
Respir. Physiol.
87:
275-291,
1992[Medline].
23.
Shea, S. A.,
J. Walter,
C. Pelley,
K. Murphy,
and
A. Guz.
The effect of visual and auditory stimuli upon resting ventilation in man.
Respir. Physiol.
68:
345-357,
1987[Medline].
24.
Shershow, J. G.,
A. King,
and
S. Robinson.
Carbon dioxide sensitivity and personality.
Psychosom. Med.
35:
155-160,
1973
25.
Shindoh, C.,
W. Hida,
Y. Kikuchi,
O. Taguchi,
H. Miki,
T. Takishima,
and
K. Shirato.
Oxygen consumption of respiratory muscles in patients with COPD.
Chest
105:
790-797,
1994
26.
Spielberger, C. D.
Manual for the State-Trait Anxiety Inventory. Palo Alto, CA: Consulting Psychologists, 1983.
27.
Spielberger, C. D.
Theory and research on anxiety, edited by C. D. Spielberger.
In: Anxiety and Behavior. New York: Academic, 1966.
28.
Tiller, J.,
M. Pain,
and
N. Biddle.
Anxiety disorder and perception of inspiratory resistive loads.
Chest
4:
547-551,
1987.
29.
Tobin, M. J.,
T. S. Chadha,
G. Jenouri,
S. J. Birch,
H. B. Gazeroglu,
and
M. A. Sackner.
Breathing pattern 2. Diseased subjects.
Chest
84:
286-294,
1983
30.
Tobin, M. J.,
W. Perez,
S. M. Guenther,
G. D'Alonzo,
and
R. Dantzker.
Breathing pattern and metabolic behavior during anticipation of exercise.
J. Appl. Physiol.
60:
1306-1312,
1986
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, baseline period; 
, values during physical
load (left) and during noxious audio
stimulation (right) in subjects with
low anxiety;