Parabrachial Interleukin-6 reduces body weight and food intake and increases thermogenesis to regulate energy metabolism
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Cell Press
Abstract
Chronic low-grade inflammation and increased
serum levels of the cytokine IL-6 accompany obesity.
For brain-produced IL-6, the mechanisms by which it
controls energy balance and its role in obesity
remain unclear. Here, we show that brain-produced
IL-6 is decreased in obese mice and rats in a neuroanatomically and sex-specific manner. Reduced IL-6
mRNA localized to lateral parabrachial nucleus
(lPBN) astrocytes, microglia, and neurons, including
paraventricular hypothalamus-innervating lPBN neurons. IL-6 microinjection into lPBN reduced food
intake and increased brown adipose tissue (BAT)
thermogenesis in male lean and obese rats by
increasing thyroid and sympathetic outflow to BAT.
Parabrachial IL-6 interacted with leptin to reduce
feeding. siRNA-mediated reduction of lPBN IL-6
leads to increased weight gain and adiposity,
reduced BAT thermogenesis, and increased food
intake. Ambient cold exposure partly normalizes
the obesity-induced suppression of lPBN IL-6. These
results indicate that lPBN-produced IL-6 regulates
feeding and metabolism and pinpoints (patho)physiological contexts interacting with lPBN IL-6
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Mishra et al. (2019). Parabrachial Interleukin-6 Reduces Body Weight and Food Intake and Increases Thermogenesis to Regulate Energy Metabolism. Cell Reports 26, 3011–3026. doi: 10.1016/j.celrep.2019.02.044
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https://doi.org/10.1016/j.celrep.2019.02.044Sponsors
This research was funded by the Swedish Research Council ( 2014-2945 to K.P.S.; 2017-00792 to I.W.A.; and 2013-7107 to Patrik Rorsman), the Novo Nordisk Foundation Excellence project grant (to K.P.S. and I.W.A.), the Ragnar Söderberg Foundation (to K.P.S.), Harald Jeanssons Stiftelse and Greta Jeanssons Stiftelse (to K.P.S.), Magnus Bergvalls Stiftelse (to K.P.S.), the Wallenberg Foundation and the Center for Molecular and Translational Medicine (to K.P.S.), postdoctoral stipendium from The Swedish Brain Foundation (to D.M.), the ERC ( BFU2015-70664-R and StG-281408 ) (to R.N.), and the NIH ( DK-21397 ) (to H.J.G.)
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© 2019 The Author(s). Open Access. This article is available under the Creative Commons CC-BY-NC-ND license and permits non-commercial use of the work as published, without adaptation or alteration provided the work is fully attributed






