Repeated Social Defeat Stress Induces an Inflammatory Gut Milieu by Altering the Mucosal Barrier Integrity and Gut Microbiota Homeostasis

被引:3
|
作者
Yadav, Santosh K. [1 ]
Ahmad, Rizwan [1 ]
Moshfegh, Cassandra M. [2 ]
Sankarasubramanian, Jagadesan [3 ]
Joshi, Vineet [4 ]
Elkhatib, Safwan K. [2 ]
Chhonker, Yashpal Singh [4 ]
Murry, Daryl J. [4 ]
Talmon, Geoffrey A. [5 ]
Guda, Chittibabu [3 ]
Case, Adam J. [6 ,7 ]
Singh, Amar B. [1 ,8 ]
机构
[1] Univ Nebraska Med Ctr, Dept Biochem & Mol Biol, Omaha, NE 68198 USA
[2] Univ Nebraska Med Ctr, Dept Cellular & Integrat Physiol, Omaha, NE USA
[3] Univ Nebraska Med Ctr, Dept Genet Cell Biol & Anat, Omaha, NE USA
[4] Univ Nebraska Med Ctr, Dept Pharm Practice & Sci, Omaha, NE USA
[5] Univ Nebraska Med Ctr, Dept Pathol & Microbiol, Omaha, NE USA
[6] Texas A&M Univ, Dept Psychiat & Behav Sci, College Stn, TX USA
[7] Texas A&M Univ, Dept Med Physiol, College Stn, TX USA
[8] Vet Affairs Nebraska Western Iowa Hlth Care Syst, Omaha, NE 68005 USA
来源
基金
美国国家卫生研究院;
关键词
TRAUMATIC BRAIN-INJURY; CLAUDIN-2; EXPRESSION; DISORDER; IMMUNE; PERMEABILITY; DYSBIOSIS; SYMPTOMS; MARKERS; HEALTH; AXIS;
D O I
10.1016/j.bpsgos.2023.03.005
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
BACKGROUND: Posttraumatic stress disorder (PTSD) is a mental health condition triggered by exposure to traumatic events in an individual's life. Patients with PTSD are also at a higher risk for comorbidities. However, it is not well understood how PTSD affects human health and/or promotes the risk for comorbidities. Nevertheless, patients with PTSD harbor a proinflammatory milieu and dysbiotic gut microbiota. Gut barrier integrity helps to maintain normal gut homeostasis and its dysregulation promotes gut dysbiosis and inflammation. METHODS: We used a mouse model of repeated social defeat stress (RSDS), a preclinical model of PTSD. Behavioral studies, metagenomics analysis of the microbiome, gut permeability assay (on mouse colon, using an Ussing chamber), immunoblotting, and immunohistochemical analyses were performed. Polarized intestinal epithelial cells and 3-dimensional crypt cultures were used for mechanistic analysis. RESULTS: The RSDS mice harbor a heightened proinflammatory gut environment and microbiota dysbiosis. The RSDS mice further showed significant dysregulation of gut barrier functions, including transepithelial electrical resistance, mucin homeostasis, and antimicrobial responses. RSDS mice also showed a specific increase in intestinal expression of claudin-2, a tight junction protein, and epinephrine, a stress-induced neurotransmitter. Treating intestinal epithelial cells or 3-dimensional cultured crypts with norepinephrine or intestinal luminal contents (fecal contents) upregulated claudin-2 expression and inhibited transepithelial electrical resistance. CONCLUSIONS: Traumatic stress induces dysregulation of gut barrier functions, which may underlie the observed gut microbiota changes and proinflammatory gut milieu, all of which may have an interdependent effect on the health and increased risk of comorbidities in patients with PTSD.
引用
收藏
页码:824 / 836
页数:13
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