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1.
Am J Physiol Gastrointest Liver Physiol ; 310(11): G989-98, 2016 06 01.
Article in English | MEDLINE | ID: mdl-27056723

ABSTRACT

UNLABELLED: Anxiety, depression, and altered memory are associated with intestinal diseases, including inflammatory bowel disease (IBD). Understanding the link between these behavioral changes and IBD is important clinically since concomitant mood disorders often increase a patient's risk of requiring surgery and developing secondary functional gastrointestinal diseases. Anxiety-like behavior (light/dark box test) and recognition memory (novel object recognition task) were determined at the peak and during resolution of inflammation in the dextran sodium sulfate (DSS) mouse model of acute colitis. DSS (5 days) was administered via drinking water followed by 3 or 9 days of normal drinking water to assess behavior during active or resolving inflammation, respectively. Disease (weight, colon length, and histology) was assessed and the composition of the gut microbiota was characterized by using qPCR on fecal pellet DNA. In a subset of mice, pretreatment with probiotics was started 1 wk prior to commencing DSS. During active inflammation (8 days), mice demonstrated impaired recognition memory and exhibited anxiety-like behavior vs. CONTROLS: These behavioral defects were normalized by 14 days post-DSS. Shifts in the composition of the gut microbiota were evident during active inflammation, notably as decreases in lactobacilli and segmented filamentous bacteria, which were also reversed once the disease had resolved. Administration of probiotics could prevent the behavioral defects seen in acute DSS. Taken together, our findings indicate that changes in mood and behavior are present during acute inflammation in murine IBD and associated with dysbiosis and that these outcomes can be prevented by the administration of probiotics.


Subject(s)
Anxiety/therapy , Colitis, Ulcerative/therapy , Probiotics/therapeutic use , Animals , Anxiety/etiology , Anxiety/microbiology , Brain/physiopathology , Colitis, Ulcerative/complications , Colitis, Ulcerative/microbiology , Female , Intestines/microbiology , Intestines/pathology , Male , Memory , Mice , Mice, Inbred C57BL
2.
Am J Physiol Gastrointest Liver Physiol ; 307(8): G793-802, 2014 Oct 15.
Article in English | MEDLINE | ID: mdl-25190473

ABSTRACT

The gut-brain-microbiota axis is increasingly recognized as an important regulator of intestinal physiology. Exposure to psychological stress causes activation of the hypothalamic-pituitary-adrenal (HPA) axis and causes altered intestinal barrier function, intestinal dysbiosis, and behavioral changes. The primary aim of this study was to determine whether the effects of psychological stress on intestinal physiology and behavior, including anxiety and memory, are mediated by the adaptive immune system. Furthermore, we wanted to determine whether treatment with probiotics would normalize these effects. Here we demonstrate that B and T cell-deficient Rag1(-/-) mice displayed altered baseline behaviors, including memory and anxiety, accompanied by an overactive HPA axis, increased intestinal secretory state, dysbiosis, and decreased hippocampal c-Fos expression. Both local (intestinal physiology and microbiota) and central (behavioral and hippocampal c-Fos) changes were normalized by pretreatment with probiotics, indicating an overall benefit on health conferred by changes in the microbiota, independent of lymphocytes. Taken together, these findings indicate a role for adaptive immune cells in maintaining normal intestinal and brain health in mice and show that probiotics can overcome this immune-mediated deficit in the gut-brain-microbiota axis.


Subject(s)
Adaptive Immunity , Hypothalamo-Hypophyseal System/microbiology , Intestines/microbiology , Microbiota , Probiotics/pharmacology , Animals , Anxiety/immunology , Anxiety/microbiology , Anxiety/physiopathology , Female , Homeodomain Proteins/genetics , Homeodomain Proteins/metabolism , Hypothalamo-Hypophyseal System/immunology , Hypothalamo-Hypophyseal System/metabolism , Intestinal Mucosa/metabolism , Intestines/immunology , Lymphocytes/drug effects , Lymphocytes/immunology , Lymphocytes/metabolism , Male , Memory , Mice , Mice, Inbred C57BL , Proto-Oncogene Proteins c-fos/genetics , Proto-Oncogene Proteins c-fos/metabolism , Stress, Psychological/immunology , Stress, Psychological/microbiology , Stress, Psychological/physiopathology
3.
Tomography ; 8(2): 550-559, 2022 02 23.
Article in English | MEDLINE | ID: mdl-35314622

ABSTRACT

This study aimed to assess the accuracy of a method of predicting post-movement root position during orthodontic treatment using a 3D digital crown/root model (3DCRM) created with pre-movement records of both cone-beam computed tomography (CBCT) and dental arch digital scans. Pre- and post-movement CBCT scans and dental arch digital scans of five patients who had completed orthodontic treatments were used in this study. The 3DCRM was superimposed onto the post-movement scanned dental arch to identify the post-movement root position (test method). Post-movement CBCT (referenced as the current method) served as the control to identify the actual post-movement root position. 3D-coordinate analysis revealed no significant differences between the test and current methods along the X and Y axes. However, the discrepancy on the Z axis (especially in cases of intrusion) was greater than that in all other directions for all three tooth types examined (p < 0.05). A strong positive correlation between the degree of discrepancy and the distance of tooth movement was observed on the Z axis (r = 0.71). The 3DCRM method showed promising potential to accurately predict root position during orthodontic treatments without the need for a second CBCT. However, root resorption, which affected the Z axis prediction, needs to be closely monitored using periapical radiographs to complement this method.


Subject(s)
Root Resorption , Tooth , Cone-Beam Computed Tomography/methods , Crowns , Humans , Root Resorption/diagnostic imaging , Tooth Crown/diagnostic imaging
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