Role of PPARα in the Control of Torpor through FGF21‐NPY Pathway: From Circadian Clock to Seasonal Change in Mammals
Author(s) -
Norio Ishida
Publication year - 2009
Publication title -
ppar research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.164
H-Index - 49
eISSN - 1687-4765
pISSN - 1687-4757
DOI - 10.1155/2009/412949
Subject(s) - torpor , hibernation (computing) , circadian clock , circadian rhythm , algorithm , biology , medicine , endocrinology , computer science , state (computer science) , thermoregulation
In nature, hibernating animals encounter fasting, cold temperature and short day seasonally. Torpor is a state of decreased physiological activity in an animal, usually characterized by a reduced body temperature and rate of metabolism to adapt such a severe environment. Ablation of the central clock synchronizer, the suprachiasmatic nucleus in brain, abolishes torpor, a hibernation-like state, implicating the circadian clock involved in this seasonal change. Biologists knows well the energy source of daily heterotherms/hibernators changed from glucose to lipids in winter. Here we review several lines of evidence of a master transcriptional regulator in lipid catabolism, PPAR α , in the control of torpor through FGF21-NPY pathway. This indicate the importance of circadian—and photoperiod—regulation of PPAR α to tell seasons in our body.
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