| Literature DB >> 32916104 |
Claire Chevalier1, Silas Kieser1, Melis Çolakoğlu1, Noushin Hadadi1, Julia Brun2, Dorothée Rigo1, Nicolas Suárez-Zamorano1, Martina Spiljar1, Salvatore Fabbiano1, Björn Busse3, Julijana Ivanišević4, Andrew Macpherson5, Nicolas Bonnet6, Mirko Trajkovski7.
Abstract
Osteoporosis is the most prevalent metabolic bone disease, characterized by low bone mass and microarchitectural deterioration. Here, we show that warmth exposure (34°C) protects against ovariectomy-induced bone loss by increasing trabecular bone volume, connectivity density, and thickness, leading to improved biomechanical bone strength in adult female, as well as in young male mice. Transplantation of the warm-adapted microbiota phenocopies the warmth-induced bone effects. Both warmth and warm microbiota transplantation revert the ovariectomy-induced transcriptomics changes of the tibia and increase periosteal bone formation. Combinatorial metagenomics/metabolomics analysis shows that warmth enhances bacterial polyamine biosynthesis, resulting in higher total polyamine levels in vivo. Spermine and spermidine supplementation increases bone strength, while inhibiting polyamine biosynthesis in vivo limits the beneficial warmth effects on the bone. Our data suggest warmth exposure as a potential treatment option for osteoporosis while providing a mechanistic framework for its benefits in bone disease.Entities:
Keywords: bone; metabolomics; metadata; metagenomics; microbiota; osteoporosis; ovariectomy; polyamines; post-menopause; warm
Year: 2020 PMID: 32916104 PMCID: PMC7116155 DOI: 10.1016/j.cmet.2020.08.012
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287