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Restraint Stress in Hypertensive Rats Activates the Intestinal Macrophages and Reduces Intestinal Barrier Accompanied by Intestinal Flora Dysbiosis.
Wang, Tiantian; Gao, Lei; Yang, Zejun; Wang, Feifei; Guo, Yuexin; Wang, Boya; Hua, Rongxuan; Shang, Hongwei; Xu, Jingdong.
Afiliación
  • Wang T; Department of Physiology and Pathophysiology, Basic Medical College, Capital Medical University, Beijing, 100069, People's Republic of China.
  • Gao L; Department of Biomedical Informatics, School of Biomedical Engineering, Capital Medical University, Beijing, 100069, People's Republic of China.
  • Yang Z; Department of Clinical Medicine, Basic Medical College, Capital Medical University, Beijing, 100069, People's Republic of China.
  • Wang F; Department of Clinical Medicine, Basic Medical College, Capital Medical University, Beijing, 100069, People's Republic of China.
  • Guo Y; Department of Oral Medicine, Basic Medical College, Capital Medical University, Beijing, 100069, People's Republic of China.
  • Wang B; Eight Program of Clinical Medicine, Peking University Health Science Center, Beijing, 100081, People's Republic of China.
  • Hua R; Department of Clinical Medicine, Basic Medical College, Capital Medical University, Beijing, 100069, People's Republic of China.
  • Shang H; Experimental Center for Morphological Research Platform, Capital Medical University, Beijing, 100069, People's Republic of China.
  • Xu J; Department of Physiology and Pathophysiology, Basic Medical College, Capital Medical University, Beijing, 100069, People's Republic of China.
J Inflamm Res ; 14: 1085-1110, 2021.
Article en En | MEDLINE | ID: mdl-33790622
ABSTRACT

PURPOSE:

Hypertension (HTN) is a major risk factor for cardiovascular disease. In recent years, there were numerous studies on the function of stress in HTN. However, the gut dysbiosis linked to hypertension in animal models under stress is still incompletely understood. Purpose of this study is to use multiple determination method to determine the juvenile stage intestinal bacteria, cytokines and changes in hormone levels.

METHODS:

Four groups of juvenile male spontaneously hypertensive rats (SHRs) and age-matched male Wistar-Kyoto (WKY) rats were randomly selected as control and experimental groups. Rats in the two stress groups were exposed to restraint stress for 3 hours per day for 7 consecutive days. In one day three times in the method of non-invasive type tail-cuff monitoring blood pressure. The detailed mechanism was illuminated based on the intestinal change using immunohistochemical and immunofluorescence staining and the stress-related hormone and inflammation factors were analyzed via ELISA method. The integrity of the epithelial barrier was assessed using FITC/HRP and the expression levels of proteins associated with the tight junction was detected by Western blot. The alteration of stress-related intestinal flora from ileocecal junction and distal colon were also analyzed using its 16S rDNA sequencing.

RESULTS:

The results indicate that acute stress rapidly increases mean arterial pressure which is positive correlation to hormone concentration, especially in SHR-stress group. Meanwhile, stress promoted the enhancement of epithelial permeability accompanied with a reduced expression of the tight junction-related protein and the macrophages (Mφ) aggregation to the lamina propria. There were remarkable significant increase of stress-related hormones and pro-inflammatory factor interleukin (IL)-6 along with a decrease in the diversity of intestinal flora and an imbalance in the F/B ratio.

CONCLUSION:

Our results reveal that stress accompanied with HTN could significantly disrupt the domino effect between intestinal flora and homeostasis.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: J Inflamm Res Año: 2021 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: J Inflamm Res Año: 2021 Tipo del documento: Article