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We began analyzing https://www.nature.com/articles/s41398-018-0240-5, but it redirected us to https://www.nature.com/articles/s41398-018-0240-5. The analysis below is for the second page.

Title[redir]:
Gut microbiota regulates mouse behaviors through glucocorticoid receptor pathway genes in the hippocampus | Translational Psychiatry
Description:
Gut microbiota has an important role in the immune system, metabolism, and digestion, and has a significant effect on the nervous system. Recent studies have revealed that abnormal gut microbiota induces abnormal behaviors, which may be associated with the hypothalamic–pituitary–adrenal (HPA) axis. Therefore, we investigated the behavioral changes in germ-free (GF) mice by behavioral tests, quantified the basal serum cortisol levels, and examined glucocorticoid receptor pathway genes in hippocampus using microarray analysis followed by real-time PCR validation, to explore the molecular mechanisms by which the gut microbiota influences the host’s behaviors and brain function. Moreover, we quantified the basal serum cortisol levels and validated the differential genes in an Escherichia coli-derived lipopolysaccharide (LPS) treatment mouse model and fecal “depression microbiota” transplantation mouse model by real-time PCR. We found that GF mice showed antianxiety- and antidepressant-like behaviors, whereas E. coli LPS-treated mice showed antidepressant-like behavior, but did not show antianxiety-like behavior. However, “depression microbiota” recipient mice exhibited anxiety- and depressive-like behaviors. In addition, six glucocorticoid receptor pathway genes (Slc22a5, Aqp1, Stat5a, Ampd3, Plekhf1, and Cyb561) were upregulated in GF mice, and of these only two (Stat5a and Ampd3) were upregulated in LPS-treated mice, whereas the shared gene, Stat5a, was downregulated in “depression microbiota” recipient mice. Furthermore, basal serum cortisol levels were decreased in E. coli LPS-treated mice but not in GF mice and “depression microbiota” recipient mice. These results indicated that the gut microbiota may lead to behavioral abnormalities in mice through the downstream pathway of the glucocorticoid receptor. Herein, we proposed a new insight into the molecular mechanisms by which gut microbiota influence depressive-like behavior.

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🏙️ Massive Traffic: 50M - 100M visitors per month


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Keywords {🔍}

mice, microbiota, pubmed, article, google, scholar, gut, genes, cas, pathway, depression, behavior, glucocorticoid, mouse, receptor, behaviors, hippocampus, brain, coli, recipient, levels, spf, cell, lpstreated, axis, stata, nature, serum, china, fig, central, cortisol, antidepressantlike, behavioral, lps, showed, depressivelike, compared, studies, basal, gene, expression, chongqing, study, analysis, upregulated, stress, increased, test, supplementary,

Topics {✒️}

supplementary figure s1 supplementary figure s2 nature portfolio s1 supplementary table privacy policy edanz editing china supplementary table supplementary method advertising medical research institute nature 464 nature 489 nature coli-derived lps-treated mice thermo fisher scientific social media editing index entire research reprints brain-gut-enteric microbiota axis open field apparatus coli lps-treated mice open field test cytokine-activated stat5 signaling34 escherichia coli–monoassociated mice20 research induces caspase-independent apoptosis n-methyl-d-aspartate2b methods animals lipopolysaccharide-induced mouse model short-chain fatty acids short–chain fatty acids escherichia coli-derived lipopolysaccharide bifidobacterium infantis-monoassociated mice initiate caspase-independent apoptosis long-chain fatty acids dopamine-beta-hydroxylase deficiency organic cation/carnitine transporter carnitine/organic cation transporters cell development s2 rights gut bacteria-derived lps aquaporin-1–mediated cerebral edema jak2-stat5 pathway cerebral ischemia‒reperfusion injury quantitative real-time pcr identified hypoxia-related genes microbiome-gut-brain axis long-term corticosterone injections

Schema {🗺️}

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         headline:Gut microbiota regulates mouse behaviors through glucocorticoid receptor pathway genes in the hippocampus
         description:Gut microbiota has an important role in the immune system, metabolism, and digestion, and has a significant effect on the nervous system. Recent studies have revealed that abnormal gut microbiota induces abnormal behaviors, which may be associated with the hypothalamic–pituitary–adrenal (HPA) axis. Therefore, we investigated the behavioral changes in germ-free (GF) mice by behavioral tests, quantified the basal serum cortisol levels, and examined glucocorticoid receptor pathway genes in hippocampus using microarray analysis followed by real-time PCR validation, to explore the molecular mechanisms by which the gut microbiota influences the host’s behaviors and brain function. Moreover, we quantified the basal serum cortisol levels and validated the differential genes in an Escherichia coli-derived lipopolysaccharide (LPS) treatment mouse model and fecal “depression microbiota” transplantation mouse model by real-time PCR. We found that GF mice showed antianxiety- and antidepressant-like behaviors, whereas E. coli LPS-treated mice showed antidepressant-like behavior, but did not show antianxiety-like behavior. However, “depression microbiota” recipient mice exhibited anxiety- and depressive-like behaviors. In addition, six glucocorticoid receptor pathway genes (Slc22a5, Aqp1, Stat5a, Ampd3, Plekhf1, and Cyb561) were upregulated in GF mice, and of these only two (Stat5a and Ampd3) were upregulated in LPS-treated mice, whereas the shared gene, Stat5a, was downregulated in “depression microbiota” recipient mice. Furthermore, basal serum cortisol levels were decreased in E. coli LPS-treated mice but not in GF mice and “depression microbiota” recipient mice. These results indicated that the gut microbiota may lead to behavioral abnormalities in mice through the downstream pathway of the glucocorticoid receptor. Herein, we proposed a new insight into the molecular mechanisms by which gut microbiota influence depressive-like behavior.
         datePublished:2018-09-07T00:00:00Z
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      headline:Gut microbiota regulates mouse behaviors through glucocorticoid receptor pathway genes in the hippocampus
      description:Gut microbiota has an important role in the immune system, metabolism, and digestion, and has a significant effect on the nervous system. Recent studies have revealed that abnormal gut microbiota induces abnormal behaviors, which may be associated with the hypothalamic–pituitary–adrenal (HPA) axis. Therefore, we investigated the behavioral changes in germ-free (GF) mice by behavioral tests, quantified the basal serum cortisol levels, and examined glucocorticoid receptor pathway genes in hippocampus using microarray analysis followed by real-time PCR validation, to explore the molecular mechanisms by which the gut microbiota influences the host’s behaviors and brain function. Moreover, we quantified the basal serum cortisol levels and validated the differential genes in an Escherichia coli-derived lipopolysaccharide (LPS) treatment mouse model and fecal “depression microbiota” transplantation mouse model by real-time PCR. We found that GF mice showed antianxiety- and antidepressant-like behaviors, whereas E. coli LPS-treated mice showed antidepressant-like behavior, but did not show antianxiety-like behavior. However, “depression microbiota” recipient mice exhibited anxiety- and depressive-like behaviors. In addition, six glucocorticoid receptor pathway genes (Slc22a5, Aqp1, Stat5a, Ampd3, Plekhf1, and Cyb561) were upregulated in GF mice, and of these only two (Stat5a and Ampd3) were upregulated in LPS-treated mice, whereas the shared gene, Stat5a, was downregulated in “depression microbiota” recipient mice. Furthermore, basal serum cortisol levels were decreased in E. coli LPS-treated mice but not in GF mice and “depression microbiota” recipient mice. These results indicated that the gut microbiota may lead to behavioral abnormalities in mice through the downstream pathway of the glucocorticoid receptor. Herein, we proposed a new insight into the molecular mechanisms by which gut microbiota influence depressive-like behavior.
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      dateModified:2018-09-07T00:00:00Z
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         Molecular neuroscience
         Medicine/Public Health
         general
         Psychiatry
         Neurosciences
         Behavioral Sciences
         Pharmacotherapy
         Biological Psychology
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