Disruption of thyroid hormone activation in type 2 deiodinase knockout mice causes obesity with glucose intolerance and liver steatosis only at thermoneutrality
Diabetes, 2011•Am Diabetes Assoc
OBJECTIVE Thyroid hormone accelerates energy expenditure; thus, hypothyroidism is
intuitively associated with obesity. However, studies failed to establish such a connection. In
brown adipose tissue (BAT), thyroid hormone activation via type 2 deiodinase (D2) is
necessary for adaptive thermogenesis, such that mice lacking D2 (D2KO) exhibit an
impaired thermogenic response to cold. Here we investigate whether the impaired
thermogenesis of D2KO mice increases their susceptibility to obesity when placed on a high …
intuitively associated with obesity. However, studies failed to establish such a connection. In
brown adipose tissue (BAT), thyroid hormone activation via type 2 deiodinase (D2) is
necessary for adaptive thermogenesis, such that mice lacking D2 (D2KO) exhibit an
impaired thermogenic response to cold. Here we investigate whether the impaired
thermogenesis of D2KO mice increases their susceptibility to obesity when placed on a high …
OBJECTIVE
Thyroid hormone accelerates energy expenditure; thus, hypothyroidism is intuitively associated with obesity. However, studies failed to establish such a connection. In brown adipose tissue (BAT), thyroid hormone activation via type 2 deiodinase (D2) is necessary for adaptive thermogenesis, such that mice lacking D2 (D2KO) exhibit an impaired thermogenic response to cold. Here we investigate whether the impaired thermogenesis of D2KO mice increases their susceptibility to obesity when placed on a high-fat diet.
RESEARCH DESIGN AND METHODS
To test this, D2KO mice were admitted to a comprehensive monitoring system acclimatized to room temperature (22°C) or thermoneutrality (30°C) and kept either on chow or high-fat diet for 60 days.
RESULTS
At 22°C, D2KO mice preferentially oxidize fat, have a similar sensitivity to diet-induced obesity, and are supertolerant to glucose. However, when thermal stress is eliminated at thermoneutrality (30°C), an opposite phenotype is encountered, one that includes obesity, glucose intolerance, and exacerbated hepatic steatosis. We suggest that a compensatory increase in BAT sympathetic activation of the D2KO mice masks metabolic repercussions that they would otherwise exhibit.
CONCLUSIONS
Thus, upon minimization of thermal stress, high-fat feeding reveals the defective capacity of D2KO mice for diet-induced thermogenesis, provoking a paradigm shift in the understanding of the role of the thyroid hormone in metabolism.
Am Diabetes Assoc