AdipoR1 and 2 are expressed on warm sensitive neurons of the hypothalamic preoptic area and contribute to central hyperthermic effects of adiponectin

Adiponectin can act in the brain to increase energy expenditure and reduce body weight by mechanisms not entirely understood. We found that adiponectin type 1 and type 2 receptors (AdipoR1 and AdipoR2) are expressed in warm sensitive neurons of the hypothalamic preoptic area (POA) which play a criti...

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Veröffentlicht in:Brain research 2011-11, Vol.1423, p.1-9
Hauptverfasser: Klein, Izabella, Sanchez-Alavez, Manuel, Tabarean, Iustin, Schaefer, Jean, Holmberg, Kristina H, Klaus, Joe, Xia, Fengcheng, Marcondes, Maria Cecilia Garibaldi, Dubins, Jeffrey S, Morrison, Brad, Zhukov, Viktor, Sanchez-Gonzalez, Alejandro, Mitsukawa, Kayo, Hadcock, John R, Bartfai, Tamas, Conti, Bruno
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container_issue
container_start_page 1
container_title Brain research
container_volume 1423
creator Klein, Izabella
Sanchez-Alavez, Manuel
Tabarean, Iustin
Schaefer, Jean
Holmberg, Kristina H
Klaus, Joe
Xia, Fengcheng
Marcondes, Maria Cecilia Garibaldi
Dubins, Jeffrey S
Morrison, Brad
Zhukov, Viktor
Sanchez-Gonzalez, Alejandro
Mitsukawa, Kayo
Hadcock, John R
Bartfai, Tamas
Conti, Bruno
description Adiponectin can act in the brain to increase energy expenditure and reduce body weight by mechanisms not entirely understood. We found that adiponectin type 1 and type 2 receptors (AdipoR1 and AdipoR2) are expressed in warm sensitive neurons of the hypothalamic preoptic area (POA) which play a critical role in the regulation of core body temperature (CBT) and energy balance. Thus, we tested the ability of adiponectin to influence CBT in wild-type mice and in mice deficient for AdipoR1 or AdipoR2. Local injection of adiponectin into the POA induced prolonged elevation of core body temperature and decreased respiratory exchange ratio (RER) indicating that increased energy expenditure is associated with increased oxidation of fat over carbohydrates. In AdipoR1 deficient mice, the ability of adiponectin to raise CBT was significantly blunted and its ability to decrease RER was completely lost. In AdipoR2 deficient mice, adiponectin had only diminished hyperthermic effects but reduced RER similarly to wild type mice. These results indicate that adiponectin can contribute to energy homeostasis by regulating CBT by direct actions on AdipoR1 and R2 in the POA.
doi_str_mv 10.1016/j.brainres.2011.09.019
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subjects Adiponectin
Adiponectin - pharmacology
Adiponectin receptor
Analysis of Variance
Animals
body temperature
Body Temperature - drug effects
body weight
Calorimetry, Indirect
carbohydrates
energy expenditure
Energy Metabolism - drug effects
Gene Expression Regulation - drug effects
Gene Expression Regulation - genetics
Homeostasis
In Vitro Techniques
Male
Mice
Mice, Inbred C57BL
Mice, Knockout
Neurology
neurons
oxidation
Preoptic area
Preoptic Area - cytology
receptors
Receptors, Adiponectin - deficiency
Receptors, Adiponectin - metabolism
Sensory Receptor Cells - drug effects
Sensory Receptor Cells - physiology
Telemetry
Temperature
Thermosensing - drug effects
Thermosensing - physiology
Warm sensitive neuron
title AdipoR1 and 2 are expressed on warm sensitive neurons of the hypothalamic preoptic area and contribute to central hyperthermic effects of adiponectin
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