Cold stress induces colitis-like phenotypes in mice by altering gut microbiota and metabolites

doi:10.21203/rs.3.rs-1400518/v1

PDF

Research Article

Cold stress induces colitis-like phenotypes in mice by altering gut microbiota and metabolites

https://doi.org/10.21203/rs.3.rs-1400518/v1

This work is licensed under a CC BY 4.0 License

Version 1

posted 31 Mar, 2022

You are reading this older preprint version

Read the latest preprint version →

Objective: The westernized lifestyle has been paralleled by an epidemic of inflammatory bowel disease (IBD). Excessive consumption of cold beverages is especially common among the modern humans. However, whether cold stress contributes directly to the gut barrier and gut-brain axis is not clear. We investigated whether the cold stress affect gut inflammation or not.

Material: 16 male mice were used in this study.

Treatment: The mice were treated with 14 consecutive days of intragastric cold or common water administration.

Methods: We observed changes in gut transit and gut barrier in the colon.We also employed RNA sequencing-based transcriptomic analysis to identify the genes potentially driving gut injury, and simultaneously examined the gut microbiota and metabolites in the feces.

Results: Cold stress inhibited the colonic motility and increased gut permeability. A set of core genes related to immune responses were consistently overexpressed in the cold stress group. Additionally, cold stress induced decreased bacterial diversity, ecological network, and increased pathogens mainly belonging to Proteobacteria. The dopamine signaling pathway-related metabolites were largely reduced in the cold stress group.

Conclusion: This study revealed that cold stress could trigger an IBD-like phenotype in mice, implying that cold stress is a possible risk factor for IBD development.

cold stress

inflammatory bowel disease

gut microbiota

gut-brain axis

The westernized lifestyle has been paralleled by an epidemic of several gastrointestinal diseases worldwide beginning in the 1980s, including irritable bowel disease (IBD) characterized by gut barrier dysfunction (1, 2). Especially, the incidence of IBD is continuously rising among young people (3). Patients with IBD present symptoms similar to those of patients with irritable bowel syndrome (IBS) to some extent, including anxiety and depression (4). These findings suggest a potential link between westernized lifestyle, gut barrier, and gut–brain interaction.

Excessive consumption of cold beverages is highly prevalent in modern population subsets, especially in the youth. Mounting evidence has shown that sweeteners, food additives, and other food ingredients in beverages play important roles in IBD (5). However, whether some other related factors (for instance, cold stress in the gut) might affect IBD occurrence or not, is still not quietly clear. A study has reported that cold meal intake inhibits contractile activity of the gastric (6). Another study has showed that women who consumed excessive cold drinks exhibits an abnormal intestinal response to stress (7).

Interestingly, industrial and domestic refrigeration development is regarded as a key environmental factor in the etiology of IBD since it increases the chance for exposure of human populations to psychrotrophic bacteria (such as Yersinia), which exacerbate intestinal inflammation (8). However, only approximately 10% of patients with IBD were found to harbor Yersinia in their gut (9); therefore, the theory of psychrotrophic bacteria cannot explain these conditions completely. Consequently, some other related factors (for instance, cold stress in the gut) might affect IBD occurrence.

To untangle the link between cold stress, gut barrier, and the gut–brain interaction, we mimicked excess cold beverage consumption in a mouse model. Metabolic syndrome is a potentially important confounder factor, which can indirectly affect the gut–brain axis by changing a myriad of physiological and endocrine systems in the gut, liver, pancreas, muscle, adipose tissue, and brain. To uncouple the metabolic effects directly caused by excess calorie intake from the beverage rather than the cold stress, we treated mice with cold water intragastrically for 14 consecutive days. We then evaluated the gastrointestinal physiology and stress-related behavior in mice. Moreover, we investigated whether cold water could affect the microbiota and metabolites of fecal contents since gut microbiota and metabolites are essential for bidirectional interactions within the gut–brain axis. These findings could highlight a link between cold beverage consumption on gut barrier dysfunction, gut microbiota, and metabolite disturbance, providing new preventive strategies to quell the creeping up in the incidence of IBD.

Animals

The C57BL/6 mice (8 week, male) were used in this study. 16 mice were divided into two groups: The mice in the control group (n = 8) were subjected to gastric instillation with a total of 1.0 mL water at threes (from 8 am to 10 am) with room temperature (20–25 ℃). The experience group (n = 8) was subjected to gastric instillation with a total 1.0 mL water at threes (from 8 am to 10 am) with low temperature (0–4 ℃). In addition, regular drinking water and food were available to the mice at all times. Gut function tests and behavioral tests were carried out after intragastric administration for 2 weeks. During the procedure, the body weight was measured on the same day every week.

Fecal output, fecal moisture content evaluation, and Bristol score

All mice were transferred into separate clean cages, and the feces were numbered and collected for 4 h between 8 am, and 12 am. All the feces during the procedure were collected and placed in tubes, then tubes were weighed and the wet weight were recorded, dried overnight at 60 ℃, then reweighed and the dry weight were recorded. At last the water content was calculated. The criteria for Bristol score was evaluated as described in previous study(10).

Bead discharge test and Gut peristalsis

Assessment of gut transit was performed using a bead discharge test. A 2 mm steel bead was lubricated with petroleum jelly and put into the anus (3 cm distance to the anus) using a smooth rod. The mice were placed in the cage, then the evacuation time of the steel bead was monitored and recorded. Gut peristalsis was assessed as described previously (11). In brief, 0.6 g of carmine was dissolved in 0.5% hydroxymethyl cellulose solution to obtain a 6% carmine solution. A 200 μL aliquot of the 6% carmine solution was administered to mice by gavage. The mice were then placed in separate cages. Gut peristalsis activity was defined as the time between intragastric administration and the first red bolus excreted.

Histological analysis and DAI (disease activity index) score

Hematoxylin-eosin staining of the ileum and colon was performed. Intestinal inflammation was assessed by observing ulcer formation, epithelial cell changes (goblet cells), lymphocyte infiltration, and lymph node formation, according to a previous report (12). DAI score is evaluated according the stool consistency, blood and weight loss as previously described (13).

Western blot and Immunofluorescence

The total protein was extracted, separated, transferred and detected as previously described(14). The antibodies against E-cadherin (1:1000; BD Biosciences,); Occludin (1:1000; ThermoFisher); Claudin 3 (1:1000; ThermoFisher); ZO-2 (1:1000; Cell Signaling Technology) and ZO-1 (1:1000; ThermoFisher) were used. The paraffin section of colon tissue were used for immunofluorescence, the antibody ZO-2 (1:100; Cell Signaling Technology) were used overnight, then secondary antibodies (1:300; Servicebio) for 1 h.

Depression- and anxiety-like behaviors test

The tail suspension test (TST) were used to evaluate depression- like behaviors. As described previously (15, 16), the mice were admitted to suspend for 6 min. All sessions were video-recorded. The time spent struggling in TST within a 6-min session were recorded and evaluated as behaviors for survival. The behaviors with reduced time for struggling were regarded as depression-like behaviors. Additionally, anxiety-like behaviors were examined using Open Field Test (OFT) as described previously (17). Their locomotor activity were monitored for 15 min. The time spent in the central area were recorded as indicators of exploratory behavior. The behaviors with reduced time in the center were regarded as anxiety-like behaviors.

Feces collection, 16S rDNA Sequencing and Untargeted metabolomic analysis

Collection of fecal samples was performed during 8 am and 11 am in the day before euthanasia. The pellets collected were stored at −80 °C. The feces DNA extraction, polymerase chain reaction, library construction and sequencing were performed as previously described(18). Diversity indices were calculated using QIIME2. Principal coordinate analysis was performed using Calypso online tools. The relative abundances, Spearman correlation coefficients, and heatmap were calculated and compared using T packages. Spearman’s rank correlations at the genus level were calculated as our previous study(19).

The liquid chromatography-mass spectrometry (LC-MS) was employed to analyze the fecal metabolome. We used the ACQUITY UPLC system (Waters Corporation, Milford, MA, USA) coupled with an AB SCIEX Triple TOF 6600 System (AB SCIEX, Framingham, MA, USA) in positive- and negative-ion modes as described previously (20, 21).

RNA sequencing and bioinformatics analysis

We used TRIzol reagent (Invitrogen, Carlsbad, CA, USA) to extract the RNA, then assess the RNA integrity by Bioanalyzer 2100 (Agilent, CA, USA). Poly(A) RNA was purified and fragmented into small pieces, and reverse-transcribed to synthesize cDNA, treated with U-labeled double-stranded DNAs with the heat-labile enzyme UDG, then amplified. Lastly, the products were sequenced on an Illumina Novaseq 6000 platform (LC-Biotechnology Co., Ltd., Hangzhou, China).

The Fastp software was used for quality control. HISAT2 was used to map the reads and the StringTie was used to assemble them. The different mRNAs were selected as the following criteria: mRNAs with fold change of >2 or <0.5 and P < 0.05 in a parametric F-test comparing nested linear models.

Statistical analysis

All data in gut function and behavioral tests were showed as the mean ± SEM. Statistical analysis was performed by using Student’s t-test for comparisons between cold water group and control group. Statistical analysis for bioinformatics data of RNA-seq, gut microbiota, and metabolites was performed using the R package vegan. The P value less than 0.05 was regarded as statistical significance.

Cold stress inhibits colonic motility and increases gut permeability in mice

A total of 15 mice (8 in control group and 7 in cold water group) were able to complete the experiment, as one mouse died from choking during intragastric administration. In the cold stress group, lower fecal output (t = 2.493, P = 0.027) (Figure 1A), lower fecal moisture percentage (t = 4.815, P < 0.001) (Figure 1B) and lower Bristol scores (t = 3.015, P = 0.010) (Figure 1C) were observed. These results suggest that cold stress induce a decreased gut motility, which are consistent with previous studies(22). Altered fecal properties, bloody stools and weight loss are the most important characteristics in IBD, then we used the DAI scores to evaluate the severity of the colitis. We found that the DAI scores in the cold water group were significantly higher than in the control group (t = -4.861, P < 0.001) (Figure 1D). Correspondingly, hematoxylin-eosin staining showed sparse intestinal villus, and edema in the intestinal villi of the jejunum (Figure 1E), a significant reduction in goblet cells, an enhanced inflammation response, and an elevated histological score in the colon (t = -2.193, P = 0.047) (Figure 1F). As to the gut barrier, we found the expression of ZO-1 and ZO-2 were lower by western blot (Figure 1G), compared to that in the control group. The immunofluorescence results confirmed the lower expression of ZO-2 in the cold water group (Figure 1H).

Cold stress exacerbates the inflammatory response of the intestinal tissue in mice

To further identify the changes in gene expression in the intestinal tissue after cold stress, we selected out 6 mice from the two groups randomly and investigated the gene expression profiles of the intestinal tissue using RNA sequencing (Figure 2A). A total of 432 genes with differential expression between groups were identified, with 330 genes upregulated and 102 genes downregulated in the cold water group when compared with the control group (Figure 2B). Gene Ontology analysis showed that all the genes most strongly enriched in immune function processes, including innate immune response and adaptive immune response, such as the B cell activation and B cell receptor complex, immunoglobulin production, immunoglobulin complex, complement activation, antigen binding and defense response to a bacterium (Figure 2C). In accordance with these findings, KEGG pathway analysis also showed that the genes were enriched in immune activation in the colon, including the primary immunodeficiency, B cell receptor signaling, intestinal immune network for IgA production, NK cell-mediated cytotoxicity pathways, leukocyte transendothelial migration, Th1, and Th2 cell differentiation, Th17 cell differentiation, cytokine–cytokine receptor interaction, chemokine and Fc gamma R-mediated phagocytosis, all of which are closely related to the immune response in the colon (Figure 2D).

To further reveal the effects of cold water on the colon, we used gene set enrichment analysis to analyze the genes which revealed substantial upregulation of genes involved in the B and T cell receptor signaling pathway, leukocyte transendothelial migration, FC epsilon RI signaling pathway, chemokine signaling pathway, and cytokine–cytokine receptor interaction (Figure 2E). These findings suggested that cold water triggers an IBD-like phenotype in mice.

Cold stress leads to low bacterial diversity and a fragile ecological network in the gut microbiota

In general, IBD is considered to occur when the immune system overreacts to the resident gut microbiota, inducing a chain of inflammatory events that can destroy the gut barrier (23). These findings prompted us to further investigate whether changes in microbiota or bacterial metabolites from the feces under cold water stimulation may regulate the gut barrier and gut–brain interactions.

Eight individual fecal samples from the control group and seven individual fecal samples from the cold stress group were collected and sequenced. The principal component plots with unweighted UniFrac distances showed a clear separation between the cold stress and control groups (Figure 3A), which suggested that cold stress led to a significant alteration in the gut microbiota composition. The Shannon index also showed a low bacterial diversity in the cold stress group (Figure 3B). At the operational taxonomic unit (OTU) level, the microbiota were significantly differed (Figure 3C). The abundances of OTU198 (Lachnospiraceae_unclassified), OTU337 (Clostridiales_Incertae_unclassified), OTU156 (Muribaculaceae_unclassified), OTU254 (Erysipelotrichaceae_unclassified), OTU88 (Duncaniella), OTU334 (Muribaculaceae_unclassified), OTU13 (Paramuribaculum), OTU433 (Proteobacteria_unclassified), OTU215 (Lachnospiraceae_unclassified), OTU258 (Firmicutes_unclassified), OTU115 (Paramuribaculum), OTU272 (Mailhella), and OTU34 (Akkermansia) were significantly increased in the cold stress group. Additionally, the abundances of OTU246 (Anaerotruncus), OTU15 (Alistipes), and OTU209 (Clostridiales_unclassified) decreased under cold stress (Figure 3D).

Linear discriminant analysis of effect size further showed that the bacteria with increased abundance in the cold stress group mainly belong to Proteobacteria (Supplementary Figure 1A). To determine the pattern of bacteria, we constructed their networks in the two group respectively, we found that the network of the cold water-treated mice had a simpler property (nodes/edges = 81/176) than the control group (nodes/edges = 80/234), indicating that cold water may induce vulnerability to environmental stress in the gut microbiota (Figure 3E).

Cold water downregulates metabolites of the dopamine-related pathway in the intestinal flora

As a microbe–host bridge, some metabolites of the intestinal flora can affect host physiology by entering the bloodstream. Therefore, we analyzed fecal metabolites using LC-MS. We found that the metabolic data clusters of the control and cold stress groups were separated from each other in both positive- and negative-ion modes by partial least-squares discriminant analysis (Figure 4A–B). The heatmap also showed that cold stress led to significant alterations in fecal metabolite levels (Figure 4C); 1179 metabolites were upregulated, and 1896 metabolites were downregulated with significant changes (Figure 4D). The most strongly impacted metabolic pathways included cocaine addiction, dopaminergic synapse, amphetamine addiction, and alcoholism addiction (Figure 4E), all of which were accompanied by a significant reduction in levels of dopamine, l-dopamine, l-tyrosine, and homovanillic acid (Figure 4F). As one of the most important neurotransmitters, decreased dopamine levels may contribute to anxiety-like and depression-like behaviors in the cold stress mice; Additionally, patients with IBD present some similar symptoms to patients with IBS, including anxiety and depression. Therefore, these behaviors were further evaluated.

Cold water increases depression-like behaviors in mice

In the tail suspended test, the struggling time was significantly decreased in the cold stress group (t = 2.618, P = 0.021) (Figure 5A), suggesting an increase in depression-like behaviors in mice exposed to cold stress. Furthermore, in the open field test, the center time (t = 2.195, P = 0.047) were reduced in the cold stress group (Figure 5C), implying a tendency of decreased exploratory behavior and increased anxiety-like behavior in the cold stress group.

Correlations of gut microbiota and metabolic changes

Finally, to explore the functional significance of the metabolite perturbations in the gut microbiota of the cold water-treated group, the 97 annotated metabolites with significant differences were selected, and their Spearman correlation coefficients with different bacteria were calculated. Significant correlations were observed between the gut microbiota and metabolites (Supplementary Figure 2A), and also observed between metabolites and gut function (Supplementary Figure 2B).

Increased beverage consumption has long been recognized to play an important role in the pathogenesis of metabolic diseases and colorectal cancer (24-26). Although food additives such as emulsifiers, food colorants, titanium dioxide, and aluminum have largely contributed to the development of these conditions, recent evidence have also identified that food additives are pathogenic factors for colitis (26, 27). In this study, we focused on the potential contribution of cold stress associated with beverage consumption to IBD development. Our results revealed that cold stress was a novel risk factor for colitis in mice, including induction of gut barrier injury, increased anxiety-like behaviors, gut microbiota disorder, and metabolite disturbance. These findings suggest that exposure to cold beverages is also a novel risk factor for IBD in humans and a potential trigger for establishing experimental IBD in mice.

Dysregulation of the gut barrier in IBD is caused by environmental factors and genetic predisposition (28), however, identifying specific environmental factors has been difficult. Several food additives are identified as environmental risk factors for IBD (27, 29). Here, we aimed to identify whether the beverage temperature directly affect the development of colitis. Similar to observations in humans, the administration of cold water to mice inhibited gut transit, additionally, the mice exhibited a colitis-like phenotype of gut barrier injury. The fact that increased cold beverage consumption is related to some gastrointestinal symptoms seemingly suggests a link between cold stress and intestinal disorders. Indeed, our results indicate that exposure to cold water not only induces gut transit disturbances but also produces low-grade inflammation. In line with these considerations, cold water exposure expectedly led to activation of ubiquitous inflammatory signaling pathways, suggesting local mucosal immune cell activation and immune cell trafficking, which are characteristics of IBD (30).

Low-grade inflammation in colitis is associated with and may be promoted by gut microbiota dysbiosis (31). The low bacterial diversity and altered gut microbiota observed in the cold stress group in this study are extremely similar to those observed in IBD. For example, microbial diversity studies have demonstrated the overgrowth of Proteobacteria in IBD patients (32). Under normal homeostasis, epithelial cells, tight junctions, and the local immune system prevent the translocation of pathogens in the gut. However, in genetically susceptible individuals, Proteobacteria expand to colonize the lumen and invade the lamina propria, further aggravating disruption of the gut barrier (33). The host recognizes Proteobacteria via nucleotide oligomerization domain-like receptors, Toll-like receptors and retinoic acid-inducible gene I-like receptors. Moreover, microbiota-derived products such as lipopolysaccharide, peptidoglycan, and flagellin from Proteobacteria trigger the activation of immune responses in the mucosa. Our study suggests that the increased abundance of pathogens accompanied by cold stress may contribute to gut barrier disruption in mice by accelerating inflammation in the gut.

Apart from the microbiota-derived products, the metabolites of the gut microbiota are also key actors in the development and exacerbation of IBD. Accumulating evidence suggests that signals from microbial metabolites affect mucosal integrity and immune homeostasis. Moreover, in IBD patients, the metabolites composition and function are disturbed seriously, including bile acids, short-chain fatty acids and tryptophan (34, 35). Significant alteration in the gut microbiota metabolites was also identified under cold stress exposure in this study. Interestingly, we found a remarkable reduction in the levels of several metabolites in the dopamine-related pathway.

Dopamine is an critical catecholaminergic neurotransmitter that present in the peripheral tissues and central nervous system simultaneously, which regulates blood pressure, sodium balance, glucose homeostasis, cognition, memory, the sympathetic nervous system, and mood (36). Dopamine is mainly synthesized in the brain, T cells, dendritic cells, and as well as by gut commensals such as members of the genus Clostridium (36). Dopamine has recently recognized as an important regulator of the immune system. Disturbance of the dopamine pathway affects both innate and adaptive immunity largely, causing the development of inflammatory pathologies (37). A significant proportion of patients with gut barrier injury suffer from anxiety and depression (38), implying a rational connection between the gut and the brain. Consistently, we examined their behaviors and found that cold water lead to a tendency to depression. Our findings suggest that cold water stress result in reduced neuro-activities in gut microbiota and enhanced pro-inflammatory activity that promotes anxiety and depression.

Nevertheless, our study has several limitations. We handled mice with cold water to explore the effect of cold stress to the gut barrier, microbiota, and metabolites. These findings acknowledge the important role of cold stress, however, it cannot mimic the condition of cold beverage consumption completely in humans because of the variety of beverages used and the differences between human and mouse physiology. In addition, although we find a significant overgrowth of pathogens and decreased dopamine-related metabolites in cold water-treated mice, we cannot completely identify that the alteration in gut microbiota causes the gut barrier injury. Further studies to investigate the role of microbiota and their metabolites with the effect on gut barrier and behavior are also needed to deeply elucidate their causal or accompanied relationships.

In summary, our study shows that exposure to cold stress promotes the development of colitis in mice. Our results may also have implications for human beings, as habit-forming consumption of cold beverages is implicated in IBD development.

IBD, irritable bowel disease; IBS, inflammatory bowel syndrome; OTU, operational taxonomic unit; Tail Suspension Test (TST); Open Field Test (OFT); Liquid Chromatography-Mass Spectrometry (LC-MS)

Data availability

The dataset of 16S rRNA gene sequencing was deposited in the Short Read Archive of NCBI under project no. PRJNA742186.

Author contributions

Jianbin Zhang designed the study; Lijuan Sun, Yue Chen and Jianxia Song performed the research and wrote the paper; Qiangqiang Yuan, Xueying Wang and Yu Zhao analyzed the data; Changting Liang, Haohao Zhang and Bo Lian contributed the methods and models

Acknowledgments

This work was supported by grants from the National Natural Science Foundation of China (No. 81900483) and the Manned Spaceflight Advance Research Program (No. 18032020103).

Conflict of interest

None declared.

Ethics statement

The protocol was approved by the Animal Research Ethics Board of The Northwest University.

Aeberli I, Gerber PA, Hochuli M, et al. Low to moderate sugar-sweetened beverage consumption impairs glucose and lipid metabolism and promotes inflammation in healthy young men: a randomized controlled trial. Am J Clin Nutr 2011;94:479-85.
de Koning L, Malik VS, Kellogg MD, Rimm EB, Willett WC, Hu FB. Sweetened beverage consumption, incident coronary heart disease, and biomarkers of risk in men. Circulation 2012;125:1735-41, S1.
Ng SC, Shi HY, Hamidi N, et al. Worldwide incidence and prevalence of inflammatory bowel disease in the 21st century: a systematic review of population-based studies. Lancet 2017;390:2769-2778.
Spiller R, Major G. IBS and IBD - separate entities or on a spectrum? Nat Rev Gastroenterol Hepatol 2016;13:613-21.
He Z, Chen L, Catalan-Dibene J, et al. Food colorants metabolized by commensal bacteria promote colitis in mice with dysregulated expression of interleukin-23. Cell Metab 2021;33:1358-1371.e5.
Verhagen MA, Luijk HD, Samsom M, Smout AJ. Effect of meal temperature on the frequency of gastric myoelectrical activity. Neurogastroenterol Motil 1998;10:175-81.
Alonso C, Guilarte M, Vicario M, et al. Maladaptive intestinal epithelial responses to life stress may predispose healthy women to gut mucosal inflammation. Gastroenterology 2008;135:163-172.e1.
Hugot JP, Dumay A, Barreau F, Meinzer U. Crohn's Disease: Is the Cold Chain Hypothesis Still Hot? J Crohns Colitis 2021;15:678-686.
Le Baut G, O'Brien C, Pavli P, et al. Prevalence of Yersinia Species in the Ileum of Crohn's Disease Patients and Controls. Front Cell Infect Microbiol 2018;8:336.
Koh H, Lee MJ, Kim MJ, Shin JI, Chung KS. Simple diagnostic approach to childhood fecal retention using the Leech score and Bristol stool form scale in medical practice. J Gastroenterol Hepatol 2010;25:334-8.
Zielinska M, Jarmuz A, Wasilewski A, Cami-Kobeci G, Husbands S, Fichna J. Methyl-orvinol-Dual activity opioid receptor ligand inhibits gastrointestinal transit and alleviates abdominal pain in the mouse models mimicking diarrhea-predominant irritable bowel syndrome. Pharmacol Rep 2017;69:350-357.
Kim JJ, Shajib MS, Manocha MM, Khan WI. Investigating intestinal inflammation in DSS-induced model of IBD. J Vis Exp 2012.
Liu YJ, Tang B, Wang FC, et al. Parthenolide ameliorates colon inflammation through regulating Treg/Th17 balance in a gut microbiota-dependent manner. Theranostics 2020;10:5225-5241.
Zhang XJ, Yuan ZW, Qu C, et al. Palmatine ameliorated murine colitis by suppressing tryptophan metabolism and regulating gut microbiota. Pharmacol Res 2018;137:34-46.
Porsolt RD, Bertin A, Jalfre M. Behavioral despair in mice: a primary screening test for antidepressants. Arch Int Pharmacodyn Ther 1977;229:327-36.
Steru L, Chermat R, Thierry B, Simon P. The tail suspension test: a new method for screening antidepressants in mice. Psychopharmacology (Berl) 1985;85:367-70.
Walsh RN, Cummins RA. The Open-Field Test: a critical review. Psychol Bull 1976;83:482-504.
Sun L, Ma L, Zhang H, et al. Fto Deficiency Reduces Anxiety- and Depression-Like Behaviors in Mice via Alterations in Gut Microbiota. Theranostics 2019;9:721-733.
Sun L, Zhang H, Cao Y, et al. Fluoxetine ameliorates dysbiosis in a depression model induced by chronic unpredicted mild stress in mice. International Journal of Medical Sciences 2019;16:1260-1270.
Yan X, Jin J, Su X, et al. Intestinal Flora Modulates Blood Pressure by Regulating the Synthesis of Intestinal-Derived Corticosterone in High Salt-Induced Hypertension. Circ Res 2020;126:839-853.
Su X, Yin X, Liu Y, et al. Gut Dysbiosis Contributes to the Imbalance of Treg and Th17 Cells in Graves' Disease Patients by Propionic Acid. J Clin Endocrinol Metab 2020;105.
Yang X, Xi TF, Li YX, et al. Oxytocin decreases colonic motility of cold water stressed rats via oxytocin receptors. World J Gastroenterol 2014;20:10886-94.
Eisenstein M. Biology: A slow-motion epidemic. Nature 2016;540:S98-S99.
Hur J, Otegbeye E, Joh HK, et al. Sugar-sweetened beverage intake in adulthood and adolescence and risk of early-onset colorectal cancer among women. Gut 2021.
Yoshida Y, Simoes EJ. Sugar-Sweetened Beverage, Obesity, and Type 2 Diabetes in Children and Adolescents: Policies, Taxation, and Programs. Curr Diab Rep 2018;18:31.
Goncalves MD, Lu C, Tutnauer J, et al. High-fructose corn syrup enhances intestinal tumor growth in mice. Science 2019;363:1345-1349.
He Z, Chen L, Catalan-Dibene J, et al. Food colorants metabolized by commensal bacteria promote colitis in mice with dysregulated expression of interleukin-23. Cell Metab 2021.
Graham DB, Xavier RJ. Pathway paradigms revealed from the genetics of inflammatory bowel disease. Nature 2020;578:527-539.
Yang H, Wang W, Romano KA, et al. A common antimicrobial additive increases colonic inflammation and colitis-associated colon tumorigenesis in mice. Sci Transl Med 2018;10.
Neurath MF. Targeting immune cell circuits and trafficking in inflammatory bowel disease. Nat Immunol 2019;20:970-979.
Levy M, Kolodziejczyk AA, Thaiss CA, Elinav E. Dysbiosis and the immune system. Nat Rev Immunol 2017;17:219-232.
Frank DN, St AA, Feldman RA, Boedeker EC, Harpaz N, Pace NR. Molecular-phylogenetic characterization of microbial community imbalances in human inflammatory bowel diseases. Proc Natl Acad Sci U S A 2007;104:13780-5.
Mukhopadhya I, Hansen R, El-Omar EM, Hold GL. IBD-what role do Proteobacteria play? Nat Rev Gastroenterol Hepatol 2012;9:219-30.
Lavelle A, Sokol H. Gut microbiota-derived metabolites as key actors in inflammatory bowel disease. Nat Rev Gastroenterol Hepatol 2020;17:223-237.
Lloyd-Price J, Arze C, Ananthakrishnan AN, et al. Multi-omics of the gut microbial ecosystem in inflammatory bowel diseases. Nature 2019;569:655-662.
Pinoli M, Marino F, Cosentino M. Dopaminergic Regulation of Innate Immunity: a Review. J Neuroimmune Pharmacol 2017;12:602-623.
Vidal PM, Pacheco R. Targeting the Dopaminergic System in Autoimmunity. J Neuroimmune Pharmacol 2020;15:57-73.
Byrne G, Rosenfeld G, Leung Y, et al. Prevalence of Anxiety and Depression in Patients with Inflammatory Bowel Disease. Can J Gastroenterol Hepatol 2017;2017:6496727.

No competing interests reported.

Supplementarymaterials.docx

PDF

Version 1

posted 31 Mar, 2022

You are reading this older preprint version

Read the latest preprint version →

Cold stress induces colitis-like phenotypes in mice by altering gut microbiota and metabolites

Status:

Version 1

Abstract

Figures

Introduction

Materials And Methods

Results

Discussion

Conclusion

Abbreviations

Declarations

References

Competing Interests

Supplementary Files

Status:

Version 1