Abstract
Pingli Wei, Caitlin Keller
Abstract
Authors
Institutions
No ROR-resolved institution is linked to this work yet.
Provenance
crossref
Confidence 100%
pubmed
Confidence 98%
europepmc
Confidence 96%
unpaywall
Confidence 95%
doaj
Confidence 92%
datacite
Confidence 0%
The gut microbiome and obesity
10.1007/s11912-016-0528-7 · 2016
10.1016/j.pharmthera.2015.11.012
10.1016/j.pharmthera.2015.11.012
10.1177/1756283x13482996
10.1177/1756283x13482996
10.1097/mog.0000000000000139
10.1097/mog.0000000000000139
10.1038/nri2316
10.1038/nri2316
Gut microbiota, the immune system, and diet influence the neonatal gut–brain axis
10.1038/pr.2014.161 · 2015
10.1016/j.tins.2013.01.005
10.1016/j.tins.2013.01.005
10.1016/j.clinthera.2015.04.002
10.1016/j.clinthera.2015.04.002
10.1038/26239
10.1038/26239
Gut microbiota, intestinal permeability, obesity-induced inflammation, and liver injury
10.1177/0148607111413772 · 2011
Calcium imaging of nerve-mast cell signaling in the human intestine
10.3389/fphys.2017.00971 · 2017
The three minds of the body
2011
Principles and clinical implications of the brain–gut–enteric microbiota axis
10.1038/nrgastro.2009.35 · 2009
The gut-brain axis: interactions between enteric microbiota, central and enteric nervous systems
2015
Ontogeny of immunoreactive CCK, VIP and secretin in rat brain and gut
10.1016/0006-291x(83)91701-1 · 1983
Brain-gut interactions: brain stem neuronal response to local gastric effects of substance P
1987
The role of neuropeptides in the control of regional immunity
10.1016/j.clindermatol.2014.04.011 · 2014
The intriguing role of neuropeptides at the ocular surface
10.1016/j.jtos.2016.10.003 · 2017
Sensory neuron regulation of gastrointestinal inflammation and bacterial host defense HHS Public Access
10.1111/joim.12591 · 2017
Activation in vagal afferents and central autonomic pathways: early responses to intestinal infection with Campylobacter jejuni
10.1016/j.bbi.2004.09.002 · 2005
10.1053/j.gastro.2011.04.052
10.1053/j.gastro.2011.04.052
10.1113/jphysiol.2004.063388
10.1113/jphysiol.2004.063388
10.1016/j.ynstr.2017.03.001
10.1016/j.ynstr.2017.03.001
Microbiota and host determinants of behavioural phenotype in maternally separated mice
10.1038/ncomms8735 · 2015
Prenatal stress-induced alterations in major physiological systems correlate with gut microbiota composition in adulthood
10.1016/j.psyneuen.2015.06.002 · 2015
Effect of maternal probiotic intervention on HPA Axis, immunity and gut microbiota in a rat model of irritable bowel syndrome
10.1371/journal.pone.0046051 · 2012
Chronic early-life stress in rat pups alters basal corticosterone, intestinal permeability, and fecal microbiota at weaning: influence of sex
10.5056/jnm16105 · 2017
10.3892/etm.2016.3368
10.3892/etm.2016.3368
Capsaicin triggers immunogenic PEL cell death, stimulates DCs and reverts PEL-induced immune suppression
10.18632/oncotarget.4911 · 2015
10.1016/0024-3205(87)90405-x
10.1016/0024-3205(87)90405-x
Antimicrobial activity of neuropeptides against a range of micro-organisms from skin, oral, respiratory and gastrointestinal tract sites
10.1016/j.jneuroim.2008.05.014 · 2008
10.18632/oncotarget.17754
10.18632/oncotarget.17754
10.5056/jnm15146
10.5056/jnm15146
Immunologists getting nervous: neuropeptides, dendritic cells and T cell activation
10.1186/rr49 · 2001
10.4049/jimmunol.156.5.1810
10.4049/jimmunol.156.5.1810
The neuropeptides GnRH-II and GnRH-I are produced by human T cells and trigger laminin receptor gene expression, adhesion, chemotaxis and homing to specific organs
10.1038/nm1202-801 · 2002
Distinct distribution of CGRP-, enkephalin-, galanin-, neuromedin U-, neuropeptide Y-, somatostatin-, substance P-, VIP- and serotonin-containing neurons in the two submucosal ganglionic neural networks of the porcine small intestine
10.1007/bf00318639 · 1990
Direct and indirect antimicrobial activities of neuropeptides and their therapeutic potential
10.2174/138920312804871139 · 2012
10.1038/nri1180
10.1038/nri1180
10.1038/415389a
10.1038/415389a
Characterization of antibacterial COOH-terminal proenkephalin-A-derived peptides (PEAP) in infectious fluids. Importance of enkelytin, the antibacterial PEAP209-237 secreted by stimulated chromaffin cells
10.1074/jbc.273.45.29847 · doi-reference
10.1016/s0167-0115(03)00033-8
10.1016/s0167-0115(03)00033-8 · doi-reference
Antimicrobial effects of α-MSH peptides
10.1002/jlb.67.2.233 · doi-reference
10.1074/jbc.m114.560573
10.1074/jbc.m114.560573 · doi-reference
Antimicrobial activity of substance P and neuropeptide Y against laboratory strains of bacteria and oral microorganisms
10.1016/j.jneuroim.2006.05.011 · doi-reference
Does plasma phoenixin level associate with cognition? Comparison between subjective memory complaint, mild cognitive impairment, and mild Alzheimer’s disease
10.1017/s1041610217000825 · doi-reference
Phoenixin-14 enhances memory and mitigates memory impairment induced by Aβ1-42 and scopolamine in mice
10.1016/j.brainres.2015.10.030 · doi-reference
The role of phoenixin in behavior and food intake
10.1016/j.peptides.2019.04.002 · doi-reference
Phoenixin is negatively associated with anxiety in obese men
10.1016/j.peptides.2016.12.011 · doi-reference
Effects of Phoenixin-14 on anxiolytic-like behavior in mice
10.1016/j.bbr.2015.02.011 · doi-reference
Phoenixin-14: detection and novel physiological implications in cardiac modulation and cardioprotection
10.1007/s00018-017-2661-3 · doi-reference
10.1016/j.neuroscience.2015.09.055
10.1016/j.neuroscience.2015.09.055 · doi-reference
10.1016/j.brainres.2019.03.034
10.1016/j.brainres.2019.03.034 · doi-reference
Phoenixin-14 injected intracerebroventricularly but not intraperitoneally stimulates food intake in rats
10.1016/j.peptides.2017.08.004 · doi-reference
Central and peripheral expression sites of phoenixin-14 immunoreactivity in rats
10.1016/j.bbrc.2017.09.048 · doi-reference
The novel neuropeptide phoenixin is highly co-expressed with nesfatin-1 in the rat hypothalamus, an immunohistochemical study
10.1016/j.neulet.2015.02.060 · doi-reference
10.1016/j.neuroscience.2013.07.057
10.1016/j.neuroscience.2013.07.057 · doi-reference
Phoenixin-14 concentrations are increased in association with luteinizing hormone and nesfatin-1 concentrations in women with polycystic ovary syndrome
10.1016/j.cca.2017.06.013 · doi-reference
Regulation of Gpr173 expression, a putative phoenixin receptor, by saturated fatty acid palmitate and endocrine-disrupting chemical bisphenol A through a p38-mediated mechanism in immortalized hypothalamic neurons
10.1016/j.mce.2019.01.026 · doi-reference
The Gn RH analogues affect novel neuropeptide SMIM 20/phoenixin and GPR 173 receptor expressions in the female rat hypothalamic–pituitary–gonadal (HPG) axis
10.1111/1440-1681.13061 · doi-reference
Phoenixin expression is regulated by the fatty acids palmitate, docosahexaenoic acid and oleate, and the endocrine disrupting chemical bisphenol a in immortalized hypothalamic neurons
10.3389/fnins.2018.00838 · doi-reference
Novel regulator of vasopressin secretion: phoenixin
10.1152/ajpregu.00426.2017 · doi-reference
10.1152/ajpregu.00191.2016
10.1152/ajpregu.00191.2016 · doi-reference
A novel reproductive peptide, phoenixin
10.1111/j.1365-2826.2012.02381.x · doi-reference
Injection of corticotropin-releasing hormone into the amygdala aggravates visceral nociception and induces noradrenaline release in rats
10.1111/nmo.12462 · doi-reference
Buserelin treatment to rats causes enteric neurodegeneration with moderate effects on CRF-immunoreactive neurons and Enterobacteriaceae in colon, and in acetylcholine-mediated permeability in ileum
10.1186/s13104-015-1800-x · doi-reference
Changes in intestinal motility and gut microbiota composition in a rat stress model
10.1159/000452364 · doi-reference
10.1016/j.neuroscience.2015.09.033
10.1016/j.neuroscience.2015.09.033 · doi-reference
Microbiota modulate anxiety-like behavior and endocrine abnormalities in hypothalamic-pituitary-adrenal axis
10.3389/fcimb.2017.00489 · doi-reference
10.1371/journal.pone.0199698
10.1371/journal.pone.0199698 · doi-reference
10.1371/journal.pone.0157347
10.1371/journal.pone.0157347 · doi-reference
Psychological stress and corticotropin-releasing hormone increase intestinal permeability in humans by a mast cell-dependent mechanism
10.1136/gutjnl-2013-305690 · doi-reference
10.1080/10253890.2017.1322575
10.1080/10253890.2017.1322575 · doi-reference
10.1126/science.6267699
10.1126/science.6267699 · doi-reference
Acute restraint stress induces cholecystokinin release via enteric apelin
10.1016/j.npep.2018.11.007 · doi-reference
10.1136/gutjnl-2016-311456
10.1136/gutjnl-2016-311456 · doi-reference
The potential role of thyrotropin-releasing hormone in colonic dysmotility induced by water avoidance stress in rats
10.1016/j.npep.2018.05.005 · doi-reference
10.1016/j.npep.2015.09.008
10.1016/j.npep.2015.09.008 · doi-reference
10.1111/apha.12445
10.1111/apha.12445 · doi-reference
Traumatic stress-induced persistent changes in DNA methylation regulate neuropeptide Y expression in rat jejunum
10.1111/nmo.13074 · doi-reference