TY - JOUR
T1 - Administration of melatonin and metformin prevents deleterious effects of circadian disruption and obesity in male rats
AU - Thomas, Anthony P.
AU - Hoang, Jonathan
AU - Vongbunyong, Kenny
AU - Nguyen, Andrew
AU - Rakshit, Kuntol
AU - Matveyenko, Aleksey V.
N1 - Funding Information:
This work was supported by the National Institutes of Health Grant R01DK098468 (to A.V.M.), an investigator-initiated grant from Takeda Pharmaceuticals, and the Center for Regenerative Medicine (Mayo Clinic, Rochester, MN).
Publisher Copyright:
Copyright © 2016 by the Endocrine Society.
PY - 2016/12
Y1 - 2016/12
N2 - Circadian disruption and obesity synergize to predispose to development of type 2 diabetes mellitus (T2DM), signifying that therapeutic targeting of both circadian and metabolic dysfunctions shouldbeconsidered as a potential treatment approach.Toaddress this hypothesis,westudied rats concomitantly exposed to circadian disruption and diet-induced obesity (CDO), a rat model recentlyshownto recapitulate phenotypical aspects of obeseT2DM(eg, circadian disruption, obesity, insulin resistance, and islet failure). CDO rats were subsequently treated daily (for 12 wk) by timed oralgavagewith vehicle, melatonin (aknownchronobiotic), metformin, or combination treatment of both therapeutics. Melatonin treatment alone improved circadian activity rhythms, attenuated induction of β-cell failure, and enhanced glucose tolerance. Metformin alone did not modify circadian activity but enhanced insulin sensitivity and glucose tolerance. Importantly, the combination of melatonin and metformin had synergistic actions to modify progression of metabolic dysfunction in CDO rats through improved adiposity, circadian activity, insulin sensitivity, and islet cell failure. This study suggests that management of both circadian and metabolic dysfunctions should be considered as a potential preventative and therapeutic option for treatment of obesity and T2DM.
AB - Circadian disruption and obesity synergize to predispose to development of type 2 diabetes mellitus (T2DM), signifying that therapeutic targeting of both circadian and metabolic dysfunctions shouldbeconsidered as a potential treatment approach.Toaddress this hypothesis,westudied rats concomitantly exposed to circadian disruption and diet-induced obesity (CDO), a rat model recentlyshownto recapitulate phenotypical aspects of obeseT2DM(eg, circadian disruption, obesity, insulin resistance, and islet failure). CDO rats were subsequently treated daily (for 12 wk) by timed oralgavagewith vehicle, melatonin (aknownchronobiotic), metformin, or combination treatment of both therapeutics. Melatonin treatment alone improved circadian activity rhythms, attenuated induction of β-cell failure, and enhanced glucose tolerance. Metformin alone did not modify circadian activity but enhanced insulin sensitivity and glucose tolerance. Importantly, the combination of melatonin and metformin had synergistic actions to modify progression of metabolic dysfunction in CDO rats through improved adiposity, circadian activity, insulin sensitivity, and islet cell failure. This study suggests that management of both circadian and metabolic dysfunctions should be considered as a potential preventative and therapeutic option for treatment of obesity and T2DM.
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U2 - 10.1210/en.2016-1309
DO - 10.1210/en.2016-1309
M3 - Article
C2 - 27653034
AN - SCOPUS:85001975624
SN - 0013-7227
VL - 157
SP - 4720
EP - 4731
JO - Endocrinology
JF - Endocrinology
IS - 12
ER -