
Differential adaptive responses to 1‐ or 2‐day fasting in various mouse tissues revealed by quantitative PCR analysis
Author(s) -
Yamamoto Junya,
Kamata Shotaro,
Miura Asumi,
Nagata Tomoko,
Kainuma Ryo,
Ishii Isao
Publication year - 2015
Publication title -
febs open bio
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.718
H-Index - 31
ISSN - 2211-5463
DOI - 10.1016/j.fob.2015.04.012
Subject(s) - autophagy , skeletal muscle , protein turnover , lysosome , biology , kidney , endocrinology , medicine , spleen , catabolism , apoptosis , metabolism , biochemistry , protein biosynthesis , enzyme
Dietary or caloric restriction confers various clinical benefits. Short‐term fasting of mice is a common experimental procedure that may involve systemic metabolic remodeling, which may significantly affect experimental outputs. This study evaluated adaptive cellular responses after 1‐ or 2‐day fasting in 13 mouse tissues by quantitative PCR using 15 marker primer sets for the activation of ubiquitin–proteasome ( Atrogin‐1 and MuRF1 ), autophagy–lysosome ( LC3b , p62 and Lamp2 ), amino acid response ( Asns , Trib3 , Herpud1 , xCT , and Chop ), Nrf2‐mediated antioxidant ( HO‐1 and Gsta1 ), and amino acid transport ( Slc38a2 , Slc7a5 , and Slc7a1 ) systems. Differential activation profiles obtained in seven highly (thymus, liver, spleen, and small intestine) or mildly (stomach, kidney, and colon) atrophied tissues as well as in six non‐atrophied tissues (brain, eye, lung, heart, skeletal muscle, and testis) suggested tissue‐specific active metabolic remodeling.