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1.
Brain Behav Immun ; 93: 226-237, 2021 03.
Article in English | MEDLINE | ID: mdl-33516921

ABSTRACT

While toll-like receptors (TLRs), which mediate innate immunity, are known to play an important role in host defense, recent work suggest their involvement in some integrated behaviors, including anxiety, depressive and cognitive functions. Here, we investigated the potential involvement of the flagellin receptor, TLR5, in anxiety, depression and cognitive behaviors using male TLR5 knock-out (KO) mice. We aobserved a specific low level of basal anxiety in TLR5 KO mice with an alteration of the hypothalamo-pituitary axis (HPA) response to acute restraint stress, illustrated by a decrease of both plasma corticosterone level and c-fos expression in the hypothalamic paraventricular nucleus where TLR5 was expressed, compared to WT littermates. However, depression and cognitive-related behaviors were not different between TLR5 KO and WT mice. Nor there were significant changes in the expression of some cytokines (IL-6, IL-10 and TNF-α) and other TLRs (TLR2, TLR3 and TLR4) in the prefrontal cortex, amygdala and hippocampus of TLR5 KO mice compared to WT mice. Moreover, mRNA expression of BDNF and glucocorticoid receptors in the hippocampus and amygdala, respectively, was not different. Finally, acute intracerebroventricular administration of flagellin, a specific TLR5 agonist, or chronic neomycin treatment did not exhibit a significant main effect, only a significant main effect of genotype was observed between TLR5 KO and WT mice. Together, those findings suggest a previously undescribed and specific role of TLR5 in anxiety and open original prospects in our understanding of the brain-gut axis function.


Subject(s)
Anxiety , Toll-Like Receptor 5 , Animals , Anxiety/genetics , Anxiety Disorders , Corticosterone , Male , Mice , Mice, Knockout , Toll-Like Receptor 5/genetics
2.
Article in English | MEDLINE | ID: mdl-27997083

ABSTRACT

BACKGROUND: Sacral nerve stimulation (SNS) is a surgical treatment of fecal and urinary incontinence that consists of inserting a stimulating electrode into one of the s3 or s4 sacral holes. In addition to the benefit of SNS in the treatment of incontinence, recent studies showed that SNS is effective in the treatment of irritable bowel syndrome as well as bladder pain syndrome. The aim of this study was to evaluate the effect of SNS on visceral mechanosensitivity in a cross-organ sensitization rat model. METHODS: Hypersensitive model was obtained by instillation of acetic acid into the bladder of rats during 5 minutes, 30 minutes before the start of the experiments. Visceral sensitivity was assessed by monitoring the change in mean arterial pressure in response to graded isobaric colorectal distension series. To decipher the mechanisms underlying SNS effect, rats were administered intravenously either a nonselective opioid receptor antagonist (naloxone) or a nitric oxide synthesis antagonist (L-NAME). Neuronal activation in the dorsal horn of the sacral spinal cord was measured by counting c-fos immunoreactive cells in response to colorectal distension and NMS. KEY RESULTS: Intravesical acetic acid instillation increased mean arterial pressure variation in response to colorectal distension when compared to saline group. SNS reduced the variation in arterial pressure. Colorectal distension induced a rise in c-fos immunoreactive cells in the dorsal horn of the spinal cord. This effect was reduced by SNS. CONCLUSIONS & INFERENCES: SNS reduces visceral mechanosensitivity in a cross-organ sensitization model.


Subject(s)
Colon/physiology , Mechanotransduction, Cellular/physiology , Rectum/physiology , Sacrum/physiology , Spinal Nerves/physiology , Visceral Pain/physiopathology , Animals , Colon/drug effects , Colon/innervation , Electric Stimulation/methods , Enzyme Inhibitors/pharmacology , Male , Mechanotransduction, Cellular/drug effects , Narcotic Antagonists/pharmacology , Rats , Rats, Sprague-Dawley , Rectum/drug effects , Rectum/innervation , Sacrum/drug effects , Sacrum/innervation , Visceral Pain/drug therapy
3.
Sci Rep ; 6: 19399, 2016 Jan 18.
Article in English | MEDLINE | ID: mdl-26775847

ABSTRACT

Visceral pain and intestinal dysbiosis are associated with Irritable Bowel Syndrome (IBS), a common functional gastrointestinal disorder without available efficient therapies. In this study, a decrease of Faecalibacterium prausnitzii presence has been observed in an IBS-like rodent model induced by a neonatal maternal separation (NMS) stress. Moreover, it was investigated whether F. prausnitzii may have an impact on colonic sensitivity. The A2-165 reference strain, but not its supernatant, significantly decreased colonic hypersensitivity induced by either NMS in mice or partial restraint stress in rats. This effect was associated with a reinforcement of intestinal epithelial barrier. Thus, F. prausnitzii exhibits anti-nociceptive properties, indicating its potential to treat abdominal pain in IBS patients.


Subject(s)
Faecalibacterium prausnitzii/physiology , Intestinal Mucosa , Irritable Bowel Syndrome/etiology , Animals , Colon/immunology , Colon/metabolism , Colon/microbiology , Disease Models, Animal , Irritable Bowel Syndrome/metabolism , Irritable Bowel Syndrome/microbiology , Male , Maternal Deprivation , Mice , Permeability , Stress, Physiological
4.
Neurogastroenterol Motil ; 27(6): 816-23, 2015 Jun.
Article in English | MEDLINE | ID: mdl-25808214

ABSTRACT

BACKGROUND: Sacral nerve stimulation (SNS) is an alternative surgical treatment of refractory urge incontinence and/or fecal incontinence. Despite its clinical efficacy, the mechanisms of action of SNS remain poorly understood. The aim of this experimental study was to evaluate the effect of SNS on visceral mechanosensitivity in rats. METHODS: Anesthetized Sprague-Dawley rats were treated with SNS or sham stimulation. SNS was performed by implanting an electrode close to the sacral nerve root S1. Rats were administered either a non-selective opioid receptor antagonist (naloxone) or a nitric oxide synthase inhibitor (L-NAME). Colonic mechanosensitivity was evaluated using the variation of arterial blood pressure as a spino-bulbar reflex in response to graded isobaric colorectal distension (CRD). C-fos immunoreactive neurons were quantified in spinal and supraspinal sites. µ-opioid receptor (MOR) internalization was counted in the sacral spinal cord with sham or effective SNS in response to CRD. KEY RESULTS: SNS reduced visceral mechanosensitivity in response to CRD. This effect was reversed by intrathecal and intraveinous naloxone administration. In both models, CRD induced increased c-fos immunoreactivity in the dorsal horn neurons of the sacral spinal cord and supraspinal areas. This increase was prevented by SNS. MOR internalization was significantly higher in stimulated group. CONCLUSIONS & INFERENCES: SNS impacts on visceral mechanosensitivity by decreasing the spino-bulbar reflex in response to CRD. Spinal opioid receptors are likely involved in this effect.


Subject(s)
Electric Stimulation , Hyperalgesia/metabolism , Lumbosacral Plexus , Posterior Horn Cells/metabolism , Receptors, Opioid, mu/metabolism , Spinal Cord/metabolism , Visceral Pain/metabolism , Animals , Arterial Pressure/drug effects , Colon , Dilatation , Enzyme Inhibitors/pharmacology , NG-Nitroarginine Methyl Ester/pharmacology , Naloxone/pharmacology , Narcotic Antagonists/pharmacology , Neurons/drug effects , Neurons/metabolism , Nitric Oxide Synthase/antagonists & inhibitors , Posterior Horn Cells/drug effects , Proto-Oncogene Proteins c-fos , Rats , Rats, Sprague-Dawley , Receptors, Opioid/metabolism , Reflex , Sacrococcygeal Region , Sensory Thresholds/drug effects , Spinal Cord/drug effects
5.
Neurogastroenterol Motil ; 25(11): e740-54, 2013 Nov.
Article in English | MEDLINE | ID: mdl-23902154

ABSTRACT

BACKGROUND: Irritable bowel syndrome (IBS) is a functional gastrointestinal disorder associated with idiopathic colonic hypersensitivity (CHS). However, recent studies suggest that low-grade inflammation could underlie CHS in IBS. The pro-inflammatory mediator nerve growth factor (NGF) plays a key role in the sensitization of peripheral pain pathways and several studies have reported its contribution to visceral pain development. NGF modulates the expression of Acid-Sensing Ion Channels (ASICs), which are proton sensors involved in sensory neurons sensitization. This study examined the peripheral contribution of NGF and ASICs to IBS-like CHS induced by butyrate enemas in the rat colon. METHODS: Colorectal distension and immunohistochemical staining of sensory neurons were used to evaluate NGF and ASICs contribution to the development of butyrate-induced CHS. KEY RESULTS: Systemic injection of anti-NGF antibodies or the ASICs inhibitor amiloride prevented the development of butyrate-induced CHS. A significant increase in NGF and ASIC1a protein expression levels was observed in sensory neurons of rats displaying butyrate-induced CHS. This increase was specific of small- and medium-diameter L1 + S1 sensory neurons, where ASIC1a was co-expressed with NGF or trkA in CGRP-immunoreactive somas. ASIC1a was also overexpressed in retrogradely labeled colon sensory neurons. Interestingly, anti-NGF antibody administration prevented ASIC1a overexpression in sensory neurons of butyrate-treated rats. CONCLUSIONS & INFERENCES: Our data suggest that peripheral NGF and ASIC1a concomitantly contribute to the development of butyrate-induced CHS NGF-ASIC1a interplay may have a pivotal role in the sensitization of colonic sensory neurons and as such, could be considered as a potential new therapeutic target for IBS treatment.


Subject(s)
Acid Sensing Ion Channels/metabolism , Ganglia, Spinal/metabolism , Hyperalgesia/etiology , Irritable Bowel Syndrome/metabolism , Nerve Growth Factor/metabolism , Acid Sensing Ion Channel Blockers/pharmacology , Amiloride/pharmacology , Animals , Disease Models, Animal , Ganglia, Spinal/drug effects , Hyperalgesia/metabolism , Hyperalgesia/physiopathology , Irritable Bowel Syndrome/physiopathology , Male , Nerve Growth Factor/pharmacology , Pain Measurement , Rats , Rats, Sprague-Dawley
6.
Aliment Pharmacol Ther ; 36(11-12): 1009-31, 2012 Dec.
Article in English | MEDLINE | ID: mdl-23066886

ABSTRACT

BACKGROUND: Irritable bowel syndrome (IBS), one of the most common gastrointestinal disorders, markedly impairing patients' quality of life. Drug development for IBS treatment has been hampered by the lack of understanding of IBS aetiology. In recent years, numerous data have emerged that suggest the involvement of immune activation in IBS, at least in a subset of patients. AIM: To determine whether immune activation and intestinal permeabilisation are more frequently observed in IBS patients compared with healthy controls. METHODS: The scientific bibliography was searched using the following keywords: irritable bowel syndrome, inflammation, immune activation, permeabilisation, intestine, assay, histology and human. The retrieved studies, including blood, faecal and histological studies, were analysed to provide a comprehensive and structured overview of the available data including the type of assay, type of inflammatory marker investigated or intestinal segment studied. RESULTS: Immune activation was more frequently observed in IBS patients than in healthy controls. An increase in the number of mast cells and lymphocytes, an alteration in cytokine levels and intestinal permeabilisation were reported in IBS patients. No consistent changes in the numbers of B cells or enterochromaffin cells or in mucosal serotonin production were demonstrated. CONCLUSIONS: The changes observed were modest and often heterogeneous among the studied population. Only appropriate interventions improving irritable bowel syndrome symptoms could highlight and confirm the role of immune activation in this pathophysiology.


Subject(s)
Cytokines/immunology , Intestinal Mucosa/immunology , Irritable Bowel Syndrome/immunology , Lymphocytes/immunology , Mast Cells/immunology , Case-Control Studies , Humans , Intestines/physiology , Permeability
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