MicroRNA expression profiling in the adult offspring of rats with periodontal disease.

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Tác giả: Gabriele Fernandes Baliero, Bianca Elvira Belardi, Anna Clara Cachoni, Antonio Hernandes Chaves-Neto, Fernando Yamamoto Chiba, Rodrigo Martins Dos Santos, Edilson Ervolino, Flávia Lombardi Lopes, Doris Hissako Matsushita, Maria Sara de Lima Coutinho Mattera, Ana Carla Thalez Ywabuchi Nobumoto, Renato Felipe Pereira, Heloisa Macedo Sampaio, Natália Francisco Scaramele, Thaís Verônica Saori Tsosura

Ngôn ngữ: eng

Ký hiệu phân loại: 296.1146 Sources

Thông tin xuất bản: England : Archives of oral biology , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 216027

 OBJECTIVE: The present study investigated the relationship between maternal periodontal disease, insulin resistance, activation of inflammatory pathways and epigenetic modifications in adult offspring. DESIGN: Therefore, female Wistar rats were divided into control and experimental groups. Seven days after the induction of periodontal disease, female rats from both groups were mated with healthy male rats. After weaning, male offspring were divided into control offspring (CN-o) and periodontal disease offspring (PED-o) groups. Body weight was measured at 0-75 days of age. At day 75, the following were measured in the offspring: insulin resistance by the HOMA-IR index
  global miRNAs by microtranscriptome array
  validation of the selected miRNAs by quantitative real-time PCR expression
  interleukin 1 receptor associated kinase 1 (IRAK1) and tumor necrosis factor receptor-associated factor 6 (TRAF6) content in the gastrocnemius muscle tissue (GSM) by western blotting. RESULTS: Maternal periodontal disease leads to low birth weight (LBW) in the offspring and insulin resistance in adulthood
  changes in global miRNA expression (5 miRNAs upregulated and 6 downregulated)
  and increased protein expression of IRAK1 and TRAF6 in GSM. CONCLUSIONS: These findings demonstrate that maternal periodontal disease causes LBW, insulin resistance, activation of inflammatory pathways, and changes in global miRNA expression.
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