Gut-muscle axis: establishing the connection between microbial signaling and skeletal muscle function in a mouse model (mdx) of Duchenne muscular dystrophy

被引:0
|
作者
Marullo, Anthony
O'Halloran, Ken
机构
基金
爱尔兰科学基金会;
关键词
D O I
10.1152/physiol.2024.39.S1.2414
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
引用
收藏
页数:2
相关论文
共 50 条
  • [1] Resveratrol ameliorates skeletal muscle function in the mdx mouse, a model of Duchenne muscular dystrophy
    Sebori, Rio
    Kuno, Atsushi
    Hayashi, Takashi
    Hosoda, Ryusuke
    Hori, Yusuke
    Horio, Yoshiyuki
    JOURNAL OF PHARMACOLOGICAL SCIENCES, 2013, 121 : 69P - 69P
  • [2] Microbes, metabolites and muscle: Is the gut-muscle axis a plausible therapeutic target in Duchenne muscular dystrophy?
    Marullo, Anthony L.
    O'Halloran, Ken D.
    EXPERIMENTAL PHYSIOLOGY, 2023, 108 (09) : 1132 - 1143
  • [3] Sildenafil Ameliorates Skeletal Muscle Pathology in the mdx Mouse Model of Duchenne Muscular Dystrophy
    Percival, Justin
    Whitehead, Nicholas
    Siegel, Michael
    Gray, Heidi
    Adamo, Candace
    Marcinek, David
    Beavo, Joseph
    Froehner, Stanley
    FASEB JOURNAL, 2011, 25
  • [4] Respiratory Control and Diaphragm Muscle Function in the mdx Mouse Model of Duchenne Muscular Dystrophy
    Burns, D.
    O'Halloran, K. D.
    IRISH JOURNAL OF MEDICAL SCIENCE, 2016, 185 : S18 - S18
  • [5] The Effect of Vitamin D Supplementation on Skeletal Muscle in the mdx Mouse Model of Duchenne Muscular Dystrophy
    Debruin, Danielle A.
    Andreacchio, Nicola
    Hanson, Erik D.
    Timpani, Cara A.
    Rybalka, Emma
    Hayes, Alan
    SPORTS, 2019, 7 (05):
  • [6] Loss of nNOS Signaling Exacerbates Dystrophic Pathology, but not Skeletal Muscle Fatigue in the mdx Mouse Model of Duchenne Muscular Dystrophy
    Percival, Justin
    Reed, Sarah
    Bible, Ken
    Froehner, Stanley
    FASEB JOURNAL, 2010, 24
  • [7] Increasing taurine intake and taurine synthesis improves skeletal muscle function in the mdx mouse model for Duchenne muscular dystrophy
    Terrill, Jessica R.
    Pinniger, Gavin J.
    Graves, Jamie A.
    Grounds, Miranda D.
    Arthur, Peter G.
    JOURNAL OF PHYSIOLOGY-LONDON, 2016, 594 (11): : 3095 - 3110
  • [8] The location of protein oxidation in dystrophic skeletal muscle from the mdx mouse model of Duchenne muscular dystrophy
    Iwasaki, Tomohito
    Terrill, Jessica R.
    Kawarai, Kei
    Miyata, Yusei
    Tagami, Takayoshi
    Maeda, Naoyuki
    Hasegawa, Yasuhiro
    Watanabe, Takafumi
    Grounds, Miranda D.
    Arthur, Peter G.
    ACTA HISTOCHEMICA, 2022, 124 (08)
  • [9] LKB1 signaling is altered in skeletal muscle of a Duchenne muscular dystrophy mouse model
    Boccanegra, Brigida
    Mantuano, Paola
    Conte, Elena
    Cerchiara, Alessandro Giovanni
    Tulimiero, Lisamaura
    Quarta, Raffaella
    Caputo, Erika
    Sanarica, Francesca
    Forino, Monica
    Spadotto, Valeria
    Cappellari, Ornella
    Fossati, Gianluca
    Steinkuhler, Christian
    De Luca, Annamaria
    DISEASE MODELS & MECHANISMS, 2023, 16 (07)
  • [10] The D2.mdx mouse as a preclinical model of the skeletal muscle pathology associated with Duchenne muscular dystrophy
    David W. Hammers
    Cora C. Hart
    Michael K. Matheny
    Lillian A. Wright
    Megan Armellini
    Elisabeth R. Barton
    H. Lee Sweeney
    Scientific Reports, 10