- Open Access
Changes in salivary physiological stress markers induced by muscle stretching in patients with irritable bowel syndrome
BioPsychoSocial Medicinevolume 2, Article number: 20 (2008)
Psychophysiological processing has been reported to play a crucial role in irritable bowel syndrome (IBS) but there has been no report on modulation of the stress marker chromogranin A (CgA) resulting from muscle stretching. We hypothesized that abdominal muscle stretching as a passive operation would have a beneficial effect on a biochemical index of the activity of the sympathetic/adrenomedullary system (salivary CgA) and anxiety.
Fifteen control and eighteen untreated IBS subjects underwent experimental abdominal muscle stretching for 4 min. Subjects relaxed in a supine position with their knees fully flexed while their pelvic and trunk rotation was passively and slowly moved from 0 degrees of abdominal rotation to about 90 degrees or the point where the subject reported feeling discomfort.
Changes in the Gastrointestinal Symptoms Rating Scale (GSRS), State Trait Anxiety Inventory (STAI), Self-rating Depression Scale (SDS), ordinate scale and salivary CgA levels were compared between controls and IBS subjects before and after stretching. A three-factor analysis of variance (ANOVA) with period (before vs. after) as the within-subject factor and group (IBS vs. Control), and sex (men vs. female) as the between-subject factors was carried out on salivary CgA.
CgA showed significant interactions between period and groups (F[1, 31] = 4.89, p = 0.03), and between groups and sex (F[1, 31] = 4.73, p = 0.03). Interactions between period and sex of CgA secretion were not shown (F[1, 3] = 2.60, p = 0.12). At the baseline, salivary CgA in IBS subjects (36.7 ± 5.9 pmol/mg) was significantly higher than in controls (19.9 ± 5.5 pmol/mg, p < 0.05). After the stretching, salivary CgA significantly decreased in the IBS group (25.5 ± 4.5 pmol/mg), and this value did not differ from that in controls (18.6 ± 3.9 pmol/mg).
Our results suggest the possibility of improving IBS pathophysiology by passive abdominal muscle stretching as indicated by CgA, a biochemical index of the activity of the sympathetic/adrenomedullary system.
Paying attention to the gut may magnify perceptions of abdominal symptoms and symptom related emotion [1, 2]. Irritable bowel syndrome (IBS) is associated with an increased incidence of psychological disorder in patient populations , and while the cause and nature of this association are a matter of discussion, several possible mechanisms, both psychological and physiological, have been proposed to account for the finding [4–6]. Although there are many treatment strategies , traditional IBS therapy is mainly symptom oriented and often unsatisfactory. Increasing knowledge of brain-gut physiology , mechanisms, and neurotransmitters and receptors  involved in gastrointestinal motor and sensory function have led to the development of several new therapeutic approaches [10, 11].
No single medication has proven to be universally effective, and the multiple therapeutic approach of gastrointestinal neurophysiology has led to promising advances in medical and non-medical approaches to IBS. Most studies have examined the association between mood state and IBS symptom severity using between-subjects design. The mechanisms involved suggest an association between mood state and IBS symptom severity within the individual. For example, although self-report measures of symptom severity cannot distinguish between the effect of mood state on physiology and on symptom perception, both mechanisms would lead to a situation in which a worsening of mood would occur before a worsening of IBS symptoms when both are measured longitudinally.
Autonomic imbalance has been proposed as a pathophysiological factor of IBS. Adrenergic neural activity and rectal sensitivity are more pronounced in IBS patients than in normal controls . The stress response system includes the sympathetic/adrenomedullary (S/A) system and the hypothalamic-pituitary-adrenal (HPA) axis. The activities of the HPA axis and the S/A system can be biochemically evaluated by measuring catecholamines and cortisol, and we can measure these hormones as objective markers of stress. Recently, as a result of investigating the derivatives of catecholamines that are detectable in saliva, chromogranin A (CgA) was determined to be a useful index of psychological stress. CgA is a member of a family of highly acidic proteins, chromogranins, which are co-stored in the adrenergic neurons and paraneurons and co-released with adrenaline and noradrenaline in response to stimulation [13, 14]. The changes in salivary CgA secretion resulting from exposure to a cognitive task may indicate psychological stress in humans .
Colonic stimulation results in brain activation of the somatosensory, insular, anterior cingulate and prefrontal cortices . The somatosensory cortex receives direct anatomical projections from the ventral posterior thalamic nucleus, it is generally assumed that the somatosensory cortex is involved in parallel processing of tactile sensory information derived from this thalamic source of input . In contrast, psychological stress influences pain thresholds via activation of the prefrontal cortices. Corticotropin releasing hormone is released from the hypothalamus, binding to visceral muscles and causing abnormal movement of the colon [9, 17]. A stress marker of the S/A system, CgA, is released in saliva due to negative feelings such as aversive stimuli and psychological stress [15, 18]. Mental activity may modulate gut perception [18, 19] and override the effect of somatic stimulation on gut perception. For example, afferent signals from muscle stretching might modulate visceral perception and emotion via the spinothalamic pathway.
Skeletal muscle stretching is a unique method for relaxation [20–22]. The effect of hypnotherapy on IBS has been well documented , but specific psychotherapy usually needs long-range training for therapists at much cost. On the other hand, skeletal muscle stretching is simple and applicable in daily practice. Skeletal muscle stretching improved subjective pain scores of the patients with low back pain, and salivary cortisol concentrations were also significantly decreased during exercise . However, the effects of skeletal muscle stretching on IBS are still unknown.
We hypothesized that IBS subjects would show abnormal salivary CgA and that skeletal muscle stretching would have beneficial effects on the pathophysiology of IBS.
This study was approved by the Ethics Committee of Niigata University of Health and Welfare. All subjects gave their written informed consent. The subjects were university students, including 15 healthy volunteers as controls (7 males, 8 females: university students at Niigata University of Health and Welfare) and 18 subjects with IBS (not receiving medical treatment for IBS, 7 males, 11 females) aged 20 to 23 years old. The IBS subjects were 20 subjects selected from 245 volunteers selected through a pre-designed questionnaire based on the Rome III criteria  for functional gastrointestinal diseases. Two IBS subjects were excluded from the results because of incomplete examinations due to cold and headache.
As recommended by the Rome III committees , patients with IBS were classified by the predominant stool pattern: IBS with diarrhea (IBS-D) was defined as loose (mushy) or watery stool >25% and hard or lumpy stool <25% of bowel movements; and IBS with constipation (IBS-C) as hard or lumpy stool 25% and loose or watery stool <25% of bowel movements. Based on questions about the proportion of bowel movements that were either loose or watery, or hard or like a ball (lumpy), IBS subjects were classified by Rome III criteria  as IBS-D (n = 4), IBS-C (n = 8), IBS-M (n = 2) and IBS-U (n = 4).
Stretching of the abdominal muscles
Subjects attended a preliminary test session that included the measurement of psychological characteristics and maximal abdominal muscle stretch. Subjects relaxed in a supine position with their knees fully flexed while their pelvis and trunk were passively and slowly moved from 0 degrees of abdominal rotation to about 90 degrees or until the subject reported feeling discomfort.
Participants attended one of several 30-minute experimental stretch sessions that were conducted at the same time of day. Subjects were instructed not to begin a stretching program session and to reschedule their session, if symptoms of their IBS prevented the stretching. During the session, subjects engaged in a 1-minute cyclic stretching protocol, 2 times right and left side rotation of their pelvis and trunk, and a 4-minute static stretching protocol. For the 4-minute static stretching protocol, the subject's knees were moved at a rate of 30°/s from 90 degrees of trunk and pelvic rotation (neutral) to a static hold at 80% of the subject's maximal passive rotation angle for one minute . Immediately following the static stretching, the knees were returned to neutral, then moved to 80% of maximal angle on the other side, and again returned back to neutral . The last stretching sequence was necessary so that measurements of stiffness and abdominal discomfort before the stretching could be compared with measurements of sensation and emotion after the stretching.
Measurement of symptoms and psychological status
Before the experiment, gastrointestinal (GI) symptoms and psychological status were evaluated using the Gastrointestinal Symptoms Rating Scale (GSRS) , Zung's Self-rating Depression Scale (SDS) , and the State-Trait Anxiety Inventory (STAI) . In addition, the subjects were asked to report the following seven items of visceral sensation or emotion : abdominal discomfort, abdominal distention, abdominal pain, urgency for defecation, perceived stress, sleepiness, and anxiety before and after perceived stretching. Each sensation was evaluated on a scale from 0 (no sensation) to 10 (maximal sensation) as previously described [2, 31].
GSRS is a 15-item instrument designed to assess the symptoms associated with common GI disorders. It has five subscales (Reflux, Diarrhea, Constipation, Abdominal Pain, and Indigestion Syndrome). Subscale scores range from 1 to 7 and higher scores represent more discomfort. A total score is derived by summing the individual item scores, and ranges from 15 to 105 .
SDS is a 20-item self-report questionnaire. Each item is scored on a Likert scale ranging from 1 to 4. A total score ranges from 20 to 80. Most people with depression score between 50 and 69, while a score of 70 and above indicates severe depression .
Mean scores of STAI for normal subjects were substantially lower than those reported in the English STAI Manual (State 24.95 ± 11.36 vs. 36.54 ± 10.22 and the Trait score was 27.88 ± 11.43 vs. 35.55 ± 9.76). The reported scores for depressed patients were 56.22 ± 8.86 and 53.83 ± 10.87, The state score for healthy subjects was 34.30 ± 10.79 and the Trait score was 36.07 ± 10.47 .
Salivary CgA sampling
Salivary samples were collected immediately before and after stretching. Saliva samples were extracted from cotton wads that subjects held in their mouths for 2 min by centrifuging at 3,000 rpm for 15 min. The tactile stimulation of the presence of the cotton wad in the oral cavity tends to stimulate a rather uniform salivary flow . During collection, the cotton wad was rolled around like a hard candy in the oral cavity. The samples were stored at -20°C until the assay. Salivary CgA levels were determined using an enzyme-linked immunosorbent assay (EIA) kit (YK070 Human Chromogranin A EIA, Yanaihara Institute, Inc., Shizuoka, Japan), using the method of Yanaihara et al.  of Yanaihara Laboratories (Fujinomiya, Shizuoka, Japan). The corrected values of CgA (pmol/mg) were calculated by dividing by the raw results of EIA with the protein concentration of the saliva in the samples (pg/mg).
Levels of salivary CgA were evaluated, according to a previously described method [35, 37, 38]. Salivary CgA levels are reported as being within the range of 50.0 ± 40.0 pmol/mg (protein corrected) in healthy subjects . Salivary CgA might be a sensitive and promising index for psychosomatic stress. Therefore, an understanding of the circadian rhythm of salivary CgA in normal humans is important. According to a recent report, CgA does not show any obvious circadian rhythm. Salivary CgA levels peak upon awakening, and then quickly decrease to the nadir after 1 hour and maintain a low level throughout the day . The circadian variation of CgA is still not fully established.
A three-factor analysis of variance (ANOVA) with period (before vs. after) as the within-subject factor and group (IBS vs. Normal) and sex (men vs. female) as the between-subject factors, was carried out on salivary CgA. Changes in revised salivary CgA levels between before and after stretching sessions for each group were analyzed statistically by related-measures 3-factor ANOVA, followed by Bonferroni protected least significant difference for multiple comparisons; values of p < 0.05 were considered significant.
Values of visceral perception and emotion were compared between groups with the Mann-Whitney U test. Spearman's rank correlation was used for evaluating the intragroup correlation coefficient between CgA and psychological status and perceptional/emotional ratings; values of p < 0.05 were accepted as significant.
GI symptoms and psychological status
Table 1 shows the scores for GI symptoms and psychological status in the Normal and IBS groups. The GSRS score of IBS subjects was significantly higher than that of Normal subjects (Mann-Whitney's U test, p = 0.01). State anxiety and trait anxiety scores of STAI of IBS subjects were significantly higher than those of normal subjects (p < 0.01). SDS scores did not significantly differ between Normal and IBS subjects.
Abdominal discomfort in IBS subjects before and after stretching was significantly higher than in Normal subjects (p = 0.03) (Table 2). After stretching, there was no difference in abdominal discomfort between the groups. Anxiety was significantly decreased by stretching in Normal subjects (p = 0.04).
Two-way ANOVA of abdominal discomfort showed that there were significant period × group interactions (F [3, 62] = 6.82, p = 0.005). Before stretching, abdominal discomfort in IBS subjects (1.84 ± 0.43) was significantly higher than in Normal subjects (0.27 ± 0.12, post-hoc, p = 0.02). After stretching, abdominal discomfort in IBS subjects (1.74 ± 0.37) was significantly higher than in Normal subjects (0.20 ± 0.11, post-hoc, p = 0.01). Abdominal discomfort changes between before and after stretching in Normal controls were not significant (post-hoc, p = 0.89). There were no changes in the other scales before and after stretching or between normal controls and IBS subjects.
Changes of salivary CgA
For multiple group comparisons, homogeneity of variance was assessed by the Levene test. Three-way repeated-measures ANOVA of CgA showed significant interactions between period and groups (F[1, 31] = 4.89, p = 0.03), and between groups and sex (F[1, 31] = 4.73, p = 0.03). Interactions between period and sex of CgA secretion were not significant (F[1, 3] 2.60, p = 0.12). Before stretching, salivary CgA in IBS subjects (36.7 ± 5.9 pmol/mg) was significantly higher than in Normal subjects (19.9 ± 5.5 pmol/mg, post-hoc, p = 0.006) (Fig. 1). CgA changes before and after stretching in Normal subjects were not significant (post-hoc, p = 0.60). In contrast, CgA was significantly decreased after stretching in IBS subjects (22.5 ± 4.5 pmol/mg, post-hoc, p = 0.02). After stretching, there was no significant difference in CgA between Normal and IBS subjects (post-hoc, p = 0.22).
The Spearman rank correlation coefficient showed a significantly positive correlation between CgA secretion before stretching and SDS score in IBS (r = 0.51, p = 0.03) (Table 3). The change in CgA after stretching compared with before stretching was positively correlated to the SDS score in both groups (IBS: r = 0.52, p = 0.03. Normal: r = 0.53, p = 0.04). In ratings of perception and emotion, perceived stress to stretching was negatively correlated with CgA secretion in the Normal group (r = -0.66, p = 0.007).
This is the first study to demonstrate that the salivary CgA level of IBS subjects is higher than that of normal subjects. We also demonstrated that, after stretching, the CgA level of IBS subjects became comparable with that of normal subjects. CgA is a major soluble protein in adrenal medullary chromaffin granules and adrenergic neurons and is co-released with catecholamines, which are considered to be a good index of sympathetic activity [41, 42]. In particular, salivary CgA is reported to be a sensitive and substantial marker of psychological stress, which does not respond well to physical stress . The results of this study suggest that abdominal muscle stretching may improve sympathetic arousal in IBS subjects.
Patients with IBS show more psychiatric disorders and pathologic behavioral patterns than normal subjects [4, 43]. A correlation between CgA secretion and the depression score was observed in this study. This result suggests a potential mechanism connecting events in the nervous system (central or enteric) with IBS symptoms. Noradrenaline in the brain plays a crucial role in anxiety, and colorectal distention induces noradrenaline release in the hippocampus . Not only central but also peripheral adrenergic/noradrenergic functions may contribute to the pathophysiology of IBS. Elsenbruch et al. reported that IBS patients demonstrated significantly greater postprandial increases in plasma noradrenaline and systolic blood pressure . In inflammatory bowel diseases, disturbed adrenergic regulation of interleukin-10 (IL-10) could be part of the mechanism underlying the modulation of disease activity due to psychological stress . Disturbed autonomic or neuroendocrine modulation of cytokine production, may play a role in the pathogenesis of IBS . Increased salivary CgA in IBS subjects suggests that IBS subjects have sympathetic arousal due to increased signaling to the gut afferent neurons.
IBS symptoms are generally worsened by stress and often improve with physical exercise and medications affecting serotonin function [47–49]. Sugano et al. reported that the skeletal muscle stretching program improved subjective pain scores of the patients with low back pain and that salivary cortisol concentrations were also significantly decreased up to 90 min after exercise . Exercise may have beneficial effects on IBS symptoms .
CgA secretion before stretching was negatively correlated with the stress score of normal subjects. Additionally, the anxiety score was reduced after stretching in the normal subjects. Psychological factors influencing symptom reporting have been identified in the constructs of visceral perceptional amplification and alexithymia . From a psychological viewpoint, IBS may be conceived as an abnormal cognitive processing of emotional stimuli, via verbal responses, and a tendency to perceive somatic stimuli as evidence of symptoms of disease.
Ghoncheh et al. examined the psychological and physical effect of passive muscle stretching and yoga stretching exercises for relaxation . Muscle relaxation displayed higher levels of relaxation states, physical relaxation, disengagement and higher levels of joy as a post-training effect . Muscle stretching provides sensation contrasts for learning relaxation in addition to fostering relaxation through the stretching of muscles . Muscle stretching for patients with IBS may be of benefit to the patients and could be used as part of a multi-component approach to the treatment of IBS.
Evidence of a physiological component of IBS is based on gender differences in GI symptoms, central nervous system pain processing, and specific effects of estrogen and progesterone on gut function [54, 55]. Additional factors may play a role, including gender-related differences in neuroendocrine, S/A system, and stress reactivity, which are related to bowel function and pain. Although gender differences in the therapeutic benefits of serotonergic agents have been observed , less is known about potential differences in responsiveness to non-drug therapies for IBS. Multiple comparisons between CgA and gender related information suggest that stretch intervention may have gender dependent effects on IBS.
The following three points can be cited as limitations of this study. The first is that sample size was very small. The levels of CgA found in our subjects were somewhat different from the reported mean value , and our findings could not exclude the effect of the sample size. Additionally, we could not examine the effects on subtypes of IBS (i.e. constipation-predominant or diarrhea-predominant), because the sample sizes of the subtypes were too small to analyze them separately. However, a long follow-up study  proved the inconsistency of IBS subtypes, suggesting that whole IBS analysis is more important than subtype analysis. The second limitation is that the duration of muscle stretching might be too short. The duration of the effect of contraction-relaxation stretching on range of motion (ROM) in the lower extremities is 15 min and the increase in ROM usually remains for 90 min . Proprioceptive neuromuscular facilitation (PNF) stretching techniques produced greater increases in ROM than static or dynamic stretching exercises. The stretching hold time at the hip is 3–10 sec in one hold-relax PNF stretch . There is no study that clarifies the stretch duration required of the abdominal muscle for relaxation. Thus, it will be necessary to examine how long we should stretch the abdominal muscles for IBS treatment. Lastly, we could not analyze the effect of lifestyle and medical history on CgA in this study. Many stress-related biomarkers are affected by lifestyle or medical history . Such relationships might contribute to increased knowledge about strategies to prevent progression of IBS.
Our results suggested that it is possible to improve IBS pathophysiology by passive abdominal muscle stretching using a biochemical index of the activity of the S/A system (salivary CgA). In this study, we verified only the effects of stretching and presence of IBS on CgA levels. Further study of the S/A system and muscle stretching in IBS is warranted.
irritable bowel syndrome
Gastrointestinal Symptoms Rating Scale
State Trait AnxietyInventory
Self-rating Depression Scale
Kanazawa M, Endo M, Yamaguchi K, Hamaguchi T, Whitehead WE, Itoh M, Fukudo S: Classical conditioned response of rectosigmoid motility and regional cerebral activity in humans. Neurogastroenterol Motil 2005, 17: 705-713.
Hamaguchi T, Kano M, Rikimaru H, Kanazawa M, Itoh M, Yanai K, Fukudo S: Brain activity during distention of the descending colon in humans. Neurogastroenterol Motil 2004, 16: 299-309.
Creed F, Guthrie E: Psychological factors in the irritable bowel syndrome. Gut 1987, 28: 1307-1318.
Drossman DA: Personality and psychological factors in the irritable bowel syndrome. Gastroenterol Clin Biol 1990, 14: 49C-53C.
Ditto B, Miller SB, Barr RG: A one-hour active coping stressor reduces small bowel transit time in healthy young adults. Psychosom Med 1998, 60: 7-10.
Mayer EA, Craske M, Naliboff BD: Depression, anxiety, and the gastrointestinal system. J Clin Psychiatry 2001,62(Suppl 8):28-36.
Andresen V, Camilleri M: Irritable bowel syndrome: recent and novel therapeutic approaches. Drugs 2006, 66: 1073-1088.
Kano M, Fukudo S, Kanazawa M, Endo Y, Narita H, Tamura D, Hongo M: Changes in intestinal motility, visceral sensitivity and minor mucosal inflammation after fasting therapy in a patient with irritable bowel syndrome. J Gastroenterol Hepatol 2006, 21: 1078-1079.
Fukudo S: Role of corticotropin-releasing hormone in irritable bowel syndrome and intestinal inflammation. J Gastroenterol 2007,42(Suppl 17):48-51.
Sagami Y, Shimada Y, Tayama J, Nomura T, Satake M, Endo Y, Shoji T, Karahashi K, Hongo M, Fukudo S: Effect of a corticotropin releasing hormone receptor antagonist on colonic sensory and motor function in patients with irritable bowel syndrome. Gut 2004, 53: 958-964.
Mertz H: Psychotherapeutics and serotonin agonists and antagonists. J Clin Gastroenterol 2005, 39: S247-250.
Park JH, Rhee PL, Kim HS, Lee JH, Kim YH, Kim JJ, Rhee JC, Kang EH, Yu BH: Increased beta-adrenergic sensitivity correlates with visceral hypersensitivity in patients with constipation-predominant irritable bowel syndrome. Dig Dis Sci 2005, 50: 1454-1460.
Majdoubi ME, Metz-Boutigue MH, Garcia-Sablone P, Theodosis DT, Aunis D: Immunocytochemical localization of chromogranin A in the normal and stimulated hypothalamo-neurohypophysial system of the rat. J Neurocytol 1996, 25: 405-416.
Sato F, Kanno T, Nagasawa S, Yanaihara N, Ishida N, Hasegawa T, Iwanaga T: Immunohistochemical localization of chromogranin a in the acinar cells of equine salivary glands contrasts with rodent glands. Cells Tissues Organs 2002, 172: 29-36.
Kanamaru Y, Kikukawa A, Shimamura K: Salivary chromogranin-A as a marker of psychological stress during a cognitive test battery in humans. Stress 2006, 9: 127-131.
Zhang HQ, Murray GM, Coleman GT, Turman AB, Zhang SP, Rowe MJ: Functional characteristics of the parallel SI- and SII-projecting neurons of the thalamic ventral posterior nucleus in the marmoset. J Neurophysiol 2001, 85: 1805-1822.
Saito K, Kasai T, Nagura Y, Ito H, Kanazawa M, Fukudo S: Corticotropin-releasing hormone receptor 1 antagonist blocks brain-gut activation induced by colonic distention in rats. Gastroenterology 2005, 129: 1533-1543.
Watanabe S, Hattori T, Kanazawa M, Kano M, Fukudo S: Role of histaminergic neurons in hypnotic modulation of brain processing of visceral perception. Neurogastroenterol Motil 2007, 19: 831-838.
Watanabe S, Fukudo S: Abnormal relationship between dissociation and hypnotic susceptibility in irritable bowel syndrome. Scand J Gastroenterol 2006, 41: 757-758.
Carlson CR, Collins FL Jr, Nitz AJ, Sturgis ET, Rogers JL: Muscle stretching as an alternative relaxation training procedure. J Behav Ther Exp Psychiatry 1990, 21: 29-38.
Carlson CR, Curran SL: Stretch-based relaxation training. Patient Educ Couns 1994, 23: 5-12.
Ghoncheh S, Smith JC: Progressive muscle relaxation, yoga stretching, and ABC relaxation theory. J Clin Psychol 2004, 60: 131-136.
Whorwell PJ, Prior A, Faragher EB: Controlled trial of hypnotherapy in the treatment of severe refractory irritable-bowel syndrome. Lancet 1984, 2: 1232-1234.
Sugano A, Nomura T: Influence of water exercise and land stretching on salivary cortisol concentrations and anxiety in chronic low back pain patients. J Physiol Anthropol Appl Human Sci 2000, 19: 175-180.
Longstreth GF, Thompson WG, Chey WD, Houghton LA, Mearin F, Spiller RC: Functional bowel disorders. Gastroenterology 2006, 130: 1480-1491.
Roberts JM, Wilson K: Effect of stretching duration on active and passive range of motion in the lower extremity. Br J Sports Med 1999, 33: 259-263.
Sullivan MK, Dejulia JJ, Worrell TW: Effect of pelvic position and stretching method on hamstring muscle flexibility. Med Sci Sports Exerc 1992, 24: 1383-1389.
Svedlund J, Sjodin I, Dotevall G: GSRS – a clinical rating scale for gastrointestinal symptoms in patients with irritable bowel syndrome and peptic ulcer disease. Dig Dis Sci 1988, 33: 129-134.
Zung WW: A Self-Rating Depression Scale. Arch Gen Psychiatry 1965, 12: 63-70.
Spielberger CD: Manual for the State-Trait Anxiety Inventory (STAI). Palo Alto, CA: Consulting Psychologists Press; 1983.
Talley N: Optimal design of treatment trials. In The Functional Gastrointestinal Disorders: Diagnosis, Pathophysiology, and Treatment. Edited by: Drossman D, Richter J, Talley N, Thompson WEC, Whitehead W. Boston: Little, Brown and Company; 1994:265-310.
Machnicki G, Pefaur J, Gaite L, Linchenco AM, Raimondi C, Schiavelli R, Otero A, Margolis MK: Gastrointestinal (GI)-Specific patient reported outcomes instruments differentiate between renal transplant patients with or without GI symptoms: results from a South American cohort. Health Qual Life Outcomes 2008, 6: 53.
Gabrys JB, Peters K: Reliability, discriminant and predictive validity of the Zung Self-rating Depression Scale. Psychol Rep 1985, 57: 1091-1096.
Fountoulakis KN, Papadopoulou M, Kleanthous S, Papadopoulou A, Bizeli V, Nimatoudis I, Iacovides A, Kaprinis GS: Reliability and psychometric properties of the Greek translation of the State-Trait Anxiety Inventory form Y: preliminary data. Ann Gen Psychiatry 2006, 5: 2.
Guinard JX, Zoumas-Morse C, Walchak C: Relation between parotid saliva flow and composition and the perception of gustatory and trigeminal stimuli in foods. Physiol Behav 1997, 63: 109-118.
Yanaihara H, Hata M, Nishikawa Y, Hoshino M, Yanaihara N, Murai M: Application of region-specific immunoassay for human chromogranin A: substantial clue for detection and measurement of chromogranin A in human plasma. Regul Pept 1999, 80: 83-90.
Toda M, Morimoto K, Nagasawa S, Kitamura K: Change in salivary physiological stress markers by spa bathing. Biomed Res 2006, 27: 11-14.
Toda M, Morimoto K: Effect of lavender aroma on salivary endocrinological stress markers. Arch Oral Biol 2008, 53: 964-968.
Fujimoto S, Nomura M, Niki M, Motoba H, Ieishi K, Mori T, Ikefuji H, Ito S: Evaluation of stress reactions during upper gastrointestinal endoscopy in elderly patients: assessment of mental stress using chromogranin A. J Med Invest 2007, 54: 140-145.
Den R, Toda M, Nagasawa S, Kitamura K, Morimoto K: Circadian rhythm of human salivary chromogranin A. Biomed Res 2007, 28: 57-60.
Kanno T, Asada N, Yanase H, Iwanaga T, Yanaihara N: Salivary secretion of chromogranin A. Control by autonomic nervous system. Adv Exp Med Biol 2000, 482: 143-151.
Winkler H, Fischer-Colbrie R: The chromogranins A and B: the first 25 years and future perspectives. Neuroscience 1992, 49: 497-528.
Drossman DA, McKee DC, Sandler RS, Mitchell CM, Cramer EM, Lowman BC, Burger AL: Psychosocial factors in the irritable bowel syndrome. A multivariate study of patients and nonpatients with irritable bowel syndrome. Gastroenterology 1988, 95: 701-708.
Saito K, Kanazawa M, Fukudo S: Colorectal distention induces hippocampal noradrenaline release in rats: an in vivo microdialysis study. Brain Res 2002, 947: 146-149.
Elsenbruch S, Holtmann G, Oezcan D, Lysson A, Janssen O, Goebel MU, Schedlowski M: Are there alterations of neuroendocrine and cellular immune responses to nutrients in women with irritable bowel syndrome? Am J Gastroenterol 2004, 99: 703-710.
Lucas A, Cobelens PM, Kavelaars A, Heijnen CJ, Holtmann G, Haag S, Gerken G, Langhorst J, Dobos GJ, Schedlowski M, Elsenbruch S: Disturbed in vitro adrenergic modulation of cytokine production in inflammatory bowel diseases in remission. J Neuroimmunol 2007, 182: 195-203.
Talley NJ: Serotoninergic neuroenteric modulators. Lancet 2001, 358: 2061-2068.
Bellini M, Rappelli L, Blandizzi C, Costa F, Stasi C, Colucci R, Giannaccini G, Marazziti D, Betti L, Baroni S, et al.: Platelet serotonin transporter in patients with diarrhea-predominant irritable bowel syndrome both before and after treatment with alosetron. Am J Gastroenterol 2003, 98: 2705-2711.
Atkinson W, Lockhart S, Whorwell PJ, Keevil B, Houghton LA: Altered 5-hydroxytryptamine signaling in patients with constipation- and diarrhea-predominant irritable bowel syndrome. Gastroenterology 2006, 130: 34-43.
Levy RL, Linde JA, Feld KA, Crowell MD, Jeffery RW: The association of gastrointestinal symptoms with weight, diet, and exercise in weight-loss program participants. Clin Gastroenterol Hepatol 2005, 3: 992-996.
Kano M, Hamaguchi T, Itoh M, Yanai K, Fukudo S: Correlation between alexithymia and hypersensitivity to visceral stimulation in human. Pain 2007.
Engel L, Andersen LB: Effects of body-mind training and relaxation stretching on persons with chronic toxic encephalopathy. Patient Educ Couns 2000, 39: 155-161.
Carlson CR, Ventrella MA, Sturgis ET: Relaxation training through muscle stretching procedures: a pilot case. J Behav Ther Exp Psychiatry 1987, 18: 121-126.
Fukudo S: Sex and gender in irritable bowel syndrome. J Gastroenterol 2006, 41: 608-610.
Chang L, Toner BB, Fukudo S, Guthrie E, Locke GR, Norton NJ, Sperber AD: Gender, age, society, culture, and the patient's perspective in the functional gastrointestinal disorders. Gastroenterology 2006, 130: 1435-1446.
Gershon MD, Tack J: The serotonin signaling system: from basic understanding to drug development for functional GI disorders. Gastroenterology 2007, 132: 397-414.
Drossman DA: The functional gastrointestinal disorders and the Rome III process. Gastroenterology 2006, 130: 1377-1390.
Moller M, Ekstrand J, Oberg B, Gillquist J: Duration of stretching effect on range of motion in lower extremities. Arch Phys Med Rehabil 1985, 66: 171-173.
Bonnar BP, Deivert RG, Gould TE: The relationship between isometric contraction durations during hold-relax stretching and improvement of hamstring flexibility. J Sports Med Phys Fitness 2004, 44: 258-261.
Schell E, Theorell T, Hasson D, Arnetz B, Saraste H: Stress biomarkers' associations to pain in the neck, shoulder and back in healthy media workers: 12-month prospective follow-up. Eur Spine J 2008, 17: 393-405.
The authors would like to thank Professor Yasuo Hotta, Department of Health and Nutrition, and Ms. Kazeumi Aoki, Ms. Hitomi Ito, Ms. Yui Tanabe, Ms. Yoshie Kondo, Ms. Ritsuko Mizusawa and Mr. Kenta Kato, Department of Occupational Therapy, Niigata University of Health and Welfare, for their help with this study.
This study was supported by Grant-in-Aid for Scientific Research Nos. 33111-17700461 and 22401-20700440 from the Ministry of Education, Culture, Sports, Science and Technology of Japan, and a Research Grant from Niigata University Health and Welfare.
The authors declare that they have no competing interests.
TH was the main investigator and wrote the first draft of the manuscript. SF supervised the study, analyzed the data and wrote the final draft of the manuscript. MT and TT supervised the study. KS, MO and KS contributed to the study design. KS contributed to the data collection. All authors contributed to the preparation of the article and approved the final manuscript.
Authors’ original submitted files for images
Below are the links to the authors’ original submitted files for images.
About this article
- Irritable Bowel Syndrome
- Irritable Bowel Syndrome Patient
- State Trait Anxiety Inventory
- Irritable Bowel Syndrome Symptom