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Gut microbiota and metabolites drive chronic sickle cell disease pain.
Sadler, Katelyn E; Atkinson, Samantha N; Ehlers, Vanessa L; Waltz, Tyler B; Hayward, Michael; Rodríguez García, Dianise M; Salzman, Nita H; Stucky, Cheryl L; Brandow, Amanda M.
Afiliación
  • Sadler KE; Department of Neuroscience, The University of Texas at Dallas; Richardson, TX.
  • Atkinson SN; Center for Advanced Pain Studies, The University of Texas at Dallas; Richardson, TX.
  • Ehlers VL; Center for Microbiome Research, Medical College of Wisconsin; Milwaukee, WI.
  • Waltz TB; Department of Microbiology and Immunology, Medical College of Wisconsin; Milwaukee, WI.
  • Hayward M; Department of Cell Biology, Neurobiology & Anatomy, Medical College of Wisconsin; Milwaukee, WI.
  • Rodríguez García DM; Department of Cell Biology, Neurobiology & Anatomy, Medical College of Wisconsin; Milwaukee, WI.
  • Salzman NH; Center for Microbiome Research, Medical College of Wisconsin; Milwaukee, WI.
  • Stucky CL; Department of Pediatrics, Division of Gastroenterology, Medical College of Wisconsin; Milwaukee, WI.
  • Brandow AM; Department of Cell Biology, Neurobiology & Anatomy, Medical College of Wisconsin; Milwaukee, WI.
bioRxiv ; 2023 Apr 28.
Article en En | MEDLINE | ID: mdl-37163080
ABSTRACT
Pain is a debilitating symptom and leading reason for hospitalization of individuals with sickle cell disease. Chronic sickle cell pain is poorly managed because the biological basis is not fully understood. Using transgenic sickle cell mice and fecal material transplant, we determined that the gut microbiome drives persistent sickle cell pain. In parallel patient and mouse analyses, we identified bilirubin as one metabolite that induces sickle cell pain by altering vagus nerve activity. Furthermore, we determined that decreased abundance of the gut bacteria Akkermansia mucinophila is a critical driver of chronic sickle cell pain. These experiments demonstrate that the sickle cell gut microbiome drives chronic widespread pain and identify bacterial species and metabolites that should be targeted for chronic sickle cell disease pain management.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: BioRxiv Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: BioRxiv Año: 2023 Tipo del documento: Article
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