scholarly journals Lesion Genotype Modifies High-Fat Diet Effects on Endometriosis Development in Mice

2021 ◽  
Vol 12 ◽  
Author(s):  
Melissa E. Heard-Lipsmeyer ◽  
Iad Alhallak ◽  
Frank A. Simmen ◽  
Stepan B. Melnyk ◽  
Rosalia C. M. Simmen

Endometriosis is a chronic, estrogen-dependent gynecologic disorder that affects reproductive-aged women and to a lesser extent, post-menopausal women on hormone therapy. The condition is associated with systemic and local immune dysfunctions. While its underlying mechanisms remain poorly understood, endometriosis has a genetic component and propensity for the disease is subject to environmental, nutritional, and lifestyle influences. Previously, we showed that high-fat diet (HFD) increased ectopic lesion numbers, concurrent with systemic and peritoneal changes in inflammatory and oxidative stress status, in immunocompetent recipient mice ip administered with endometrial fragments null for Krüppel-like factor 9 gene. Herein, we determined whether HFD modifies lesion parameters, when recipient peritoneal environment is challenged with ectopic wild-type (WT) endometrial fragments, the latter simulating retrograde menstruation common in women during the menstrual period. WT endometrium-recipient mice fed HFD (45% kcal from fat) showed reduced lesion incidence, numbers, and volumes, in the absence of changes in systemic ovarian steroid hormone and insulin levels, relative to those fed the control diet (CD, 17% kcal from fat). Lesions from HFD- and CD-fed recipients demonstrated comparable gene expression for steroid hormone receptors (Esr and Pgr) and cytokines (Il-6, Il-8, and CxCL4) and similar levels of DNA oxidative biomarkers. HFD moderately altered serum (3-nitrotyrosine and methionine/homocysteine) and peritoneal (reduced glutathione/oxidized glutathione) pro-oxidative status but had no effect on peritoneal inflammatory (tumor necrosis factor α and tumor necrosis factor receptor 1) mediators. Results indicate that lesion genotype modifies dietary effects on disease establishment and/or progression and if translated, could be important for provision of nutritional guidelines to women with predisposition to, or affected by endometriosis.

PLoS ONE ◽  
2018 ◽  
Vol 13 (2) ◽  
pp. e0190861 ◽  
Author(s):  
Dan Tian ◽  
Miao Tian ◽  
Leilei Zhang ◽  
Peng Zhao ◽  
Yunfeng Cui ◽  
...  

2013 ◽  
Vol 2013 ◽  
pp. 1-13 ◽  
Author(s):  
I. Rune ◽  
C. H. F. Hansen ◽  
M. Ellekilde ◽  
D. S. Nielsen ◽  
K. Skovgaard ◽  
...  

Ampicillin has been shown to improve glucose tolerance in mice. We hypothesized that this effect is present only if treatment is initiated prior to weaning and that it disappears when treatment is terminated. High-fat fed C57BL/6NTac mice were divided into groups that received Ampicillin at different ages or not at all. We found that both diet and Ampicillin significantly changed the gut microbiota composition in the animals. Furthermore, there was a significant improvement in glucose tolerance in Ampicillin-treated, five-week-old mice compared to nontreated mice in the control group. At study termination, expressions of mRNA coding for tumor necrosis factor, serum amyloid A, and lactase were upregulated, while the expression of tumor necrosis factor (ligand) superfamily member 15 was downregulated in the ileum of Ampicillin-treated mice. Higher dendritic cell percentages were found systemically in high-fat diet mice, and a lower tolerogenic dendritic cell percentage was found both in relation to high-fat diet and late Ampicillin treatment. The results support our hypothesis that a “window” exists early in life in which an alteration of the gut microbiota affects glucose tolerance as well as development of gut immunity and that this window may disappear after weaning.


Metabolism ◽  
2012 ◽  
Vol 61 (10) ◽  
pp. 1461-1472 ◽  
Author(s):  
Bodil Bjørndal ◽  
Rita Vik ◽  
Trond Brattelid ◽  
Natalya Filipchuk Vigerust ◽  
Lena Burri ◽  
...  

2018 ◽  
Vol 58 ◽  
pp. 17-27 ◽  
Author(s):  
Flavia Lambertucci ◽  
Ainelén Arboatti ◽  
María Guillermina Sedlmeier ◽  
Omar Motiño ◽  
María de Luján Alvarez ◽  
...  

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