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High-fat diets promote peritoneal inflammation and augment endometriosis-associated abdominal hyperalgesia.
Herup-Wheeler, Tristin; Shi, Mingxin; Harvey, Madeleine E; Talwar, Chandni; Kommagani, Ramakrishna; MacLean, James A; Hayashi, Kanako.
Afiliação
  • Herup-Wheeler T; School of Molecular Bioscience, Center for Reproductive Biology, Washington State University, Pullman, WA 99614, USA.
  • Shi M; School of Molecular Bioscience, Center for Reproductive Biology, Washington State University, Pullman, WA 99614, USA.
  • Harvey ME; School of Molecular Bioscience, Center for Reproductive Biology, Washington State University, Pullman, WA 99614, USA.
  • Talwar C; Department of Pathology & Immunology, Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, TX 77030, USA.
  • Kommagani R; Department of Pathology & Immunology, Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, TX 77030, USA.
  • MacLean JA; School of Molecular Bioscience, Center for Reproductive Biology, Washington State University, Pullman, WA 99614, USA.
  • Hayashi K; School of Molecular Bioscience, Center for Reproductive Biology, Washington State University, Pullman, WA 99614, USA.
bioRxiv ; 2023 Nov 13.
Article em En | MEDLINE | ID: mdl-38014254
ABSTRACT
Immune dysfunction is one of the central components in the development and progression of endometriosis by establishing a chronic inflammatory environment. Western-style high-fat diets (HFD) have been linked to greater systemic inflammation to cause metabolic and chronic inflammatory diseases, and are also considered an environmental risk factor for gynecologic diseases. Here, we aimed to examine how HFD alter an inflammatory environment in endometriosis and discern their contribution to endometriotic-associated hyperalgesia. Our results showed that HFD-induced obesity enhanced abdominal mechanical allodynia that was induced by endometriotic lesions. Peritoneal inflammatory macrophages and cytokine levels increased by lesion induction were elevated by chronic exposure to HFD. Pain-related mediators in the dorsal root ganglia were further stimulated after lesion induction under the HFD condition. Although HFD did not affect inflammatory macrophages in the peritoneal cavity without lesion induction, the diversity and composition of the gut microbiota were clearly altered by HFD as a sign of low-grade systemic inflammation. Thus, HFD alone might not establish a local inflammatory environment in the pelvic cavity, but it can contribute to further enhancing chronic inflammation, leading to the exacerbation of endometriosis-associated abdominal hyperalgesia following the establishment and progression of the disease.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article