TY - JOUR
T1 - Greater insulin sensitivity in calorie restricted rats occurs with unaltered circulating levels of several important myokines and cytokines
AU - Sharma, Naveen
AU - Castorena, Carlos M.
AU - Cartee, Gregory D.
N1 - Funding Information:
This research was supported by the National Institute on Aging Grants AG-010026 and AG-013283. The authors would like to thank Dr. Nathan Qi and the staff at the University of Michigan Animal Phenotyping Core for their technical assistance, and Dr. G. William Wong of Johns Hopkins School of Medicine for the anti-myonectin antibody.
PY - 2012
Y1 - 2012
N2 - Calorie restriction (CR; ∼60% of ad libitum, AL intake) has been associated with substantial alterations in body composition and insulin sensitivity. Recently, several proteins that are secreted by nontraditional endocrine tissues, including skeletal muscle and other tissues, have been discovered to modulate energy metabolism, body composition, and insulin sensitivity. The aim of this study was to characterize the influence of CR by rats on plasma levels of six of these newly recognized metabolic hormones (BDNF, FGF21, IL-1β, myonectin, myostatin, and irisin). Body composition of 9-month old male Fischer-344/Brown Norway rats (AL and CR groups) was determined by nuclear magnetic resonance. Blood sampled from the carotid artery of unanesthetized rats was used to measure concentrations of glucose and plasma proteins. As expected, CR versus AL rats had significantly altered body composition (reduced percent fat mass, increased percent lean mass) and significantly improved insulin sensitivity (based on the homeostasis model assessment-estimated insulin resistance index). Also consistent with previous reports, CR compared to AL rats had significantly greater plasma levels of adiponectin and corticosterone. However, there were no significant diet-related differences in plasma levels of BDNF, FGF21, IL-1β, myonectin, myostatin, or irisin. In conclusion, these results indicate that alterations in plasma concentration of these six secreted proteins are not essential for the CR-related improvement in insulin sensitivity in rats.
AB - Calorie restriction (CR; ∼60% of ad libitum, AL intake) has been associated with substantial alterations in body composition and insulin sensitivity. Recently, several proteins that are secreted by nontraditional endocrine tissues, including skeletal muscle and other tissues, have been discovered to modulate energy metabolism, body composition, and insulin sensitivity. The aim of this study was to characterize the influence of CR by rats on plasma levels of six of these newly recognized metabolic hormones (BDNF, FGF21, IL-1β, myonectin, myostatin, and irisin). Body composition of 9-month old male Fischer-344/Brown Norway rats (AL and CR groups) was determined by nuclear magnetic resonance. Blood sampled from the carotid artery of unanesthetized rats was used to measure concentrations of glucose and plasma proteins. As expected, CR versus AL rats had significantly altered body composition (reduced percent fat mass, increased percent lean mass) and significantly improved insulin sensitivity (based on the homeostasis model assessment-estimated insulin resistance index). Also consistent with previous reports, CR compared to AL rats had significantly greater plasma levels of adiponectin and corticosterone. However, there were no significant diet-related differences in plasma levels of BDNF, FGF21, IL-1β, myonectin, myostatin, or irisin. In conclusion, these results indicate that alterations in plasma concentration of these six secreted proteins are not essential for the CR-related improvement in insulin sensitivity in rats.
KW - Adiponectin
KW - Dietary restriction
KW - FGF21
KW - FNDC5
KW - Insulin resistance
KW - Irisin
KW - Myonectin
KW - Myostatin
UR - http://www.scopus.com/inward/record.url?scp=84867346134&partnerID=8YFLogxK
U2 - 10.1186/1743-7075-9-90
DO - 10.1186/1743-7075-9-90
M3 - Article
C2 - 23067400
AN - SCOPUS:84867346134
SN - 1743-7075
VL - 9
JO - Nutrition and Metabolism
JF - Nutrition and Metabolism
M1 - 90
ER -