TY - JOUR
T1 - Macrophage inhibitory cytokine 1 (MIC-1/GDF15) decreases food intake, body weight and improves glucose tolerance in mice on normal & obesogenic diets
AU - Macia, Laurence
AU - Tsai, Vicky Wang Wei
AU - Nguyen, Amy D.
AU - Johnen, Heiko
AU - Kuffner, Tamara
AU - Shi, Yan Chuan
AU - Lin, Shu
AU - Herzog, Herbert
AU - Brown, David A.
AU - Breit, Samuel N.
AU - Sainsbury, Amanda
PY - 2012/4/13
Y1 - 2012/4/13
N2 - Food intake and body weight are controlled by a variety of central and peripheral factors, but the exact mechanisms behind these processes are still not fully understood. Here we show that that macrophage inhibitory cytokine-1 (MIC-1/GDF15), known to have anorexigenic effects particularly in cancer, provides protection against the development of obesity. Both under a normal chow diet and an obesogenic diet, the transgenic overexpression of MIC-1/GDF15 in mice leads to decreased body weight and fat mass. This lean phenotype was associated with decreased spontaneous but not fasting-induced food intake, on a background of unaltered energy expenditure and reduced physical activity. Importantly, the overexpression of MIC-1/GDF15 improved glucose tolerance, both under normal and high fat-fed conditions. Altogether, this work shows that the molecule MIC-1/GDF15 might be beneficial for the treatment of obesity as well as perturbations in glucose homeostasis.
AB - Food intake and body weight are controlled by a variety of central and peripheral factors, but the exact mechanisms behind these processes are still not fully understood. Here we show that that macrophage inhibitory cytokine-1 (MIC-1/GDF15), known to have anorexigenic effects particularly in cancer, provides protection against the development of obesity. Both under a normal chow diet and an obesogenic diet, the transgenic overexpression of MIC-1/GDF15 in mice leads to decreased body weight and fat mass. This lean phenotype was associated with decreased spontaneous but not fasting-induced food intake, on a background of unaltered energy expenditure and reduced physical activity. Importantly, the overexpression of MIC-1/GDF15 improved glucose tolerance, both under normal and high fat-fed conditions. Altogether, this work shows that the molecule MIC-1/GDF15 might be beneficial for the treatment of obesity as well as perturbations in glucose homeostasis.
UR - http://www.scopus.com/inward/record.url?scp=84859733519&partnerID=8YFLogxK
U2 - 10.1371/journal.pone.0034868
DO - 10.1371/journal.pone.0034868
M3 - Article
C2 - 22514681
AN - SCOPUS:84859733519
SN - 1932-6203
VL - 7
JO - PLoS One
JF - PLoS One
IS - 4
M1 - e34868
ER -