Implication of the enteric glia in the IBS-like colonic inflammation associated with endometriosis.

IF 2.4 3区 医学 Q2 OBSTETRICS & GYNECOLOGY BMC Women's Health Pub Date : 2024-12-21 DOI:10.1186/s12905-024-03480-7
Luis A Rivera-Arce, Myrella L Cruz, Ulises Rodriguez-Cintron, James P Torres-Pirela, Caroline B Appleyard
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Abstract

Background: Endometriosis is a complex gynecological disorder characterized by the ectopic growth of endometrial tissue. Symptoms of endometriosis are known to impair the quality of life of patients, and among these are found dysmenorrhea, chronic pelvic pain, and gastrointestinal (GI) issues. GI issues such as painful bowel movements, bloating and constipation or diarrhea, are one of the common reasons for misdiagnosis with irritable bowel syndrome (IBS). Enteric glial cells (EGC) are known to play a role in pain associated with IBS, and reactive gliosis has been reported in patients with IBS, but the role of EGC in endometriosis has yet to be elucidated. We hypothesized that endometriosis will induce reactive gliosis, with increased expression of the glial fibrillary acidic protein (GFAP) and S100B, in the myenteric plexus of colonic sections in an animal model of endometriosis.

Methods: In the present study animal experiments were employed to explore the impact of endometriosis on the gastrointestinal tract. Using a surgically induced endometriosis rat model, we collected ileal and colonic segments for analysis. We used H&E to assess microscopic damage in colon and ileum, immunofluorescence to measure GFAP and S100B expression in the colon, and toluidine blue staining to measure mast cell infiltration in colon and ileum. Immunofluorescence images were captured using confocal microscope and analyzed using ImageJ software.

Results: All endometriosis animals developed vesicles. These animals had a significant increase in the colonic macroscopic damage compared to Sham and Naïve controls. Colonic and ileal sections didn't show statistical differences in microscopic damage between groups, yet endometriosis ileum had significantly increased mast cell infiltration compared to Naïve. GFAP immunostaining showed significantly increased integrated density in endometriosis when compared to Sham or Naïve, while no statistical difference was found in S100B integrated density between groups.

Conclusions: We conclude that endometriosis can alter GI homeostasis by inducing colon inflammation, reactive gliosis, and ileal mast cell infiltration. Taken together this suggests endometriosis can mimic IBS histopathology beyond the symptomatology, reinforcing this disease's complexity and the need to treat it beyond the gynecological setting.

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肠胶质细胞在ibs样结肠炎症与子宫内膜异位症相关中的意义。
背景:子宫内膜异位症是一种复杂的妇科疾病,其特征是子宫内膜组织异位生长。众所周知,子宫内膜异位症的症状会损害患者的生活质量,其中包括痛经、慢性盆腔疼痛和胃肠道(GI)问题。胃肠道问题,如排便疼痛、腹胀、便秘或腹泻,是肠易激综合征(IBS)误诊的常见原因之一。肠胶质细胞(Enteric glial cells, EGC)在IBS相关的疼痛中发挥作用,反应性胶质增生在IBS患者中也有报道,但EGC在子宫内膜异位症中的作用尚未阐明。在子宫内膜异位症动物模型中,我们假设子宫内膜异位症会诱导反应性胶质细胞增生,胶质纤维酸性蛋白(GFAP)和S100B在结肠肠系膜丛中的表达增加。方法:采用动物实验方法探讨子宫内膜异位症对胃肠道的影响。使用手术诱导的子宫内膜异位症大鼠模型,我们收集回肠和结肠段进行分析。我们使用H&E评估结肠和回肠的显微损伤,免疫荧光检测结肠中GFAP和S100B的表达,甲苯胺蓝染色检测结肠和回肠肥大细胞的浸润。共聚焦显微镜采集免疫荧光图像,ImageJ软件分析。结果:所有子宫内膜异位症动物均出现囊泡。与Sham和Naïve对照组相比,这些动物的结肠宏观损伤显著增加。结肠和回肠切片显微损伤组间无统计学差异,但回肠子宫内膜异位症肥大细胞浸润较Naïve明显增加。GFAP免疫染色显示,与Sham或Naïve相比,子宫内膜异位症的综合密度显著增加,而组间S100B综合密度无统计学差异。结论:我们认为子宫内膜异位症可以通过诱导结肠炎症、反应性胶质瘤和回肠肥大细胞浸润来改变胃肠道稳态。综上所述,这表明子宫内膜异位症可以在症状学之外模仿肠易激综合征的组织病理学,从而加强了这种疾病的复杂性,并需要在妇科之外进行治疗。
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来源期刊
BMC Women's Health
BMC Women's Health OBSTETRICS & GYNECOLOGY-
CiteScore
3.40
自引率
4.00%
发文量
444
审稿时长
>12 weeks
期刊介绍: BMC Women''s Health is an open access, peer-reviewed journal that considers articles on all aspects of the health and wellbeing of adolescent girls and women, with a particular focus on the physical, mental, and emotional health of women in developed and developing nations. The journal welcomes submissions on women''s public health issues, health behaviours, breast cancer, gynecological diseases, mental health and health promotion.
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