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Updated: Feb 28, 2026

In vitro Functional Characterization of Mouse Colorectal Afferent Endings
Published on: January 21, 2015
[Visceral sensitivity, gut barrier function and autonomic nerve function in patients with diarrhea-predominant
Xiaojuan Xu1, Liang Liu2, Shukun Yao1
1Chinese Academy of Medical Sciences, Graduate School of Peking Union Medical College, Beijing 100730; Department of Gastroenterology, China-Japan Friendship Hospital, Beijing 100029, China.
Objective:
To evaluate visceral sensitivity, gut barrier function and autonomic nerve function (ANF) in patients with diarrhea-predominant irritable bowel syndrome (IBS-D), and to explore their roles in IBS-D pathophysiology. Methods: A total of 46 IBS-D patients (IBS-D group) were selected from the Department of Gastroenterology of China-Japan Friendship Hospital from October 2015 to March 2016, and 20 healthy volunteer were served as a control group (HC group). Clinical and psychological symptoms were evaluated by questionnaire, and visceral sensitivity to rectal balloon distention, gut barrier function and autonomic nerve function (ANF) were examined. The difference in the above-mentioned indexes were compared between the 2 groups, and the correlations in the parameters were analyzed in the IBS-D group. Results: The scores of IBS symptom severity scale (IBS-SSS), Hamilton anxiety scale (HAMA), Hamilton depression scale (HAMD) and visceral sensitivity index (VSI) were significantly higher in the IBS-D group than those in the HC group (P<0.01). In the visceral sensitivity test, maximum tolerable threshold in the IBS-D group was significantly decreased compared to that in the HC group (P<0.01); there was no significant difference in first sensation threshold and defecating sensation threshold between the two groups (P>0.05). As gut barrier function markers, the serum diamine oxidase (DAO) and d-lactate were significantly increased in the IBS-D group (P<0.05). In ANF test, the total score and parasympathetic score as well as the proportion of abnormal scores in the IBS-D group were significantly higher than those in the HC group (P<0.05). In IBS-D group, the HAMA, VSI and serum DAO were positively correlated with IBS-SSS (r=0.528, 0.575, 0.507; P<0.01), while the 3 visceral sensitivity thresholds were negatively correlated with IBS-SSS (r= -0.636, -0.476, -0.697; P<0.01); in addition to the IBS-SSS, the HAMA, HAMD, VSI and serum DAO were also significant negatively correlated with the visceral sensitivity thresholds (all P<0.05); no significant correlations were found between the ANF and the other parameters. Conclusion: IBS-D patients show psychological symptoms, visceral hypersensitivity, impaired gut barrier function and abnormal ANF characterized by parasympathetic dysfunction; the former 3 factors are all associated with disease severity, and thus may play vital roles in IBS-D pathophysiology.
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