4.8 Article

Leptin mediates postprandial increases in body temperature through hypothalamus adrenal medulla-adipose tissue crosstalk

Journal

JOURNAL OF CLINICAL INVESTIGATION
Volume 130, Issue 4, Pages 2001-2016

Publisher

AMER SOC CLINICAL INVESTIGATION INC
DOI: 10.1172/JCI134699

Keywords

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Funding

  1. US Public Health Service [R01 DK116774, R01 DK11968, R01 DK113984, P30 DK045735, K99/R00 CA215315, R01 DK089098, R01 DK102648, K08AI128745, T32 DK101019, R01 NS087568, UL1TR000142, T32 DK007058]

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Meal ingestion increases body temperature in multiple species, an effect that is blunted by obesity. However, the mechanisms responsible for these phenomena remain incompletely understood. Here we show that refeeding increases plasma leptin concentrations approximately 8-fold in 48-hour-fasted lean rats, and this normalization of plasma leptin concentrations stimulates adrenomedullary catecholamine secretion. Increased adrenal medulla-derived plasma catecholamines were necessary and sufficient to increase body temperature postprandially, a process that required both fatty acids generated from adipose tissue lipolysis and p-adrenergic activation of brown adipose tissue (BAT). Diet-induced obese rats, which remained relatively hyperleptinemic while fasting, did not exhibit fasting-induced reductions in temperature. To examine the impact of feeding-induced increases in body temperature on energy balance, we compared rats fed chronically by either 2 carbohydrate-rich boluses daily or a continuous isocaloric intragastric infusion. Bolus feeding increased body temperature and reduced weight gain compared with continuous feeding, an effect abrogated by treatment with atenolol. In summary, these data demonstrate that leptin stimulates a hypothalamus-adrenal medulla-BAT axis, which is necessary and sufficient to induce lipolysis and, as a result, increase body temperature after refeeding.

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