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We are analyzing https://www.nature.com/articles/nrendo.2017.132.

Title:
Targeting thermogenesis in brown fat and muscle to treat obesity and metabolic disease | Nature Reviews Endocrinology
Description:
Targeting thermogenesis in brown fat and skeletal muscle to expend energy and reduce fat mass is a promising therapeutic strategy for treating obesity and related metabolic diseases. Here, Betz and Enerbäck discuss the different molecular pathways regulating thermogenesis in these organs and discuss how they can be therapeutically exploited. Brown fat is emerging as an interesting and promising target for therapeutic intervention in obesity and metabolic disease. Activation of brown fat in humans is associated with marked improvement in metabolic parameters such as levels of free fatty acids and insulin sensitivity. Skeletal muscle is another important organ for thermogenesis, with the capacity to induce energy-consuming futile cycles. In this Review, we focus on how these two major thermogenic organs — brown fat and muscle — act and cooperate to maintain normal body temperature. Moreover, in the light of disease-relevant mechanisms, we explore the molecular pathways that regulate thermogenesis in brown fat and muscle. Brown adipocytes possess a unique cellular mechanism to convert chemical energy into heat: uncoupling protein 1 (UCP1), which can short-circuit the mitochondrial proton gradient. However, recent research demonstrates the existence of several other energy-expending
Website Age:
30 years and 10 months (reg. 1994-08-11).

Matching Content Categories {📚}

  • Education
  • Health & Fitness
  • Science

Content Management System {📝}

What CMS is nature.com built with?

Custom-built

No common CMS systems were detected on Nature.com, and no known web development framework was identified.

Traffic Estimate {📈}

What is the average monthly size of nature.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


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Display Ads {🎯}


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Reseller Advertisers (38)
conversantmedia.com, rubiconproject.com, pubmatic.com, appnexus.com, openx.com, smartadserver.com, lijit.com, sharethrough.com, video.unrulymedia.com, google.com, yahoo.com, triplelift.com, onetag.com, sonobi.com, contextweb.com, 33across.com, indexexchange.com, media.net, themediagrid.com, adform.com, richaudience.com, sovrn.com, improvedigital.com, freewheel.tv, smaato.com, yieldmo.com, amxrtb.com, adyoulike.com, adpone.com, criteo.com, smilewanted.com, 152media.info, e-planning.net, smartyads.com, loopme.com, opera.com, mediafuse.com, betweendigital.com

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$63,100 per month
Estimations show Nature.com's display ad online revenue falls between $42,042 and $115,616 per month.

Keywords {🔍}

pubmed, article, google, scholar, cas, brown, tissue, adipose, central, thermogenesis, physiol, nature, fat, humans, adipocytes, cold, obesity, uncoupling, cell, human, mice, white, muscle, ucp, energy, thermogenic, clin, metab, nat, med, protein, endocrinol, biol, content, metabolic, coldinduced, mitochondrial, access, expenditure, mechanisms, adult, plos, gene, van, endocrinology, research, skeletal, temperature, kozak, sci,

Topics {✒️}

nature portfolio journals permissions reprints nature portfolio privacy policy recent research demonstrates swedish research council advertising fatty-acid-dependent ucp1 uncoupling social media regional distribution central efferent pathways skeletal-muscle-based thermogenic mechanisms author information authors east energy-expending 'futile' cycles nature+ nature 448 nature 206 nature 454 nature 387 nature 516 nature case-controlled observational study skeletal-muscle sarcoplasmic reticulum cold-induced brown adipocytes author correspondence tissue-dependent rna expression glucose-intolerant men improves central neural pathways cold-induced adaptive thermogenesis plasmic reticulum ca2+-atpase cold-acclimated rats reevaluated rhythm-generating mechanisms governing synchronized slow-amplitude modulations resist diet-induced obesity van marken lichtenbelt career development grant cold-acclimated ucp1−/− mice de quadrupedibus viviparis central core disease permissions brown adipose tissue springerlink instant access recruits beige adipocytes article betz ucp3 protein content brown fat mitochondria personal data dorsal dermal fate fatty acid synthesis

Questions {❓}

  • Role of UCP homologues in skeletal muscles and brown adipose tissue: mediators of thermogenesis or regulators of lipids as fuel substrate?
  • The 'novel' 'uncoupling' proteins UCP2 and UCP3: what do they really do?

Schema {🗺️}

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      description: Targeting thermogenesis in brown fat and skeletal muscle to expend energy and reduce fat mass is a promising therapeutic strategy for treating obesity and related metabolic diseases. Here, Betz and Enerbäck discuss the different molecular pathways regulating thermogenesis in these organs and discuss how they can be therapeutically exploited. Brown fat is emerging as an interesting and promising target for therapeutic intervention in obesity and metabolic disease. Activation of brown fat in humans is associated with marked improvement in metabolic parameters such as levels of free fatty acids and insulin sensitivity. Skeletal muscle is another important organ for thermogenesis, with the capacity to induce energy-consuming futile cycles. In this Review, we focus on how these two major thermogenic organs — brown fat and muscle — act and cooperate to maintain normal body temperature. Moreover, in the light of disease-relevant mechanisms, we explore the molecular pathways that regulate thermogenesis in brown fat and muscle. Brown adipocytes possess a unique cellular mechanism to convert chemical energy into heat: uncoupling protein 1 (UCP1), which can short-circuit the mitochondrial proton gradient. However, recent research demonstrates the existence of several other energy-expending 'futile' cycles in both adipocytes and muscle, such as creatine and calcium cycling. These mechanisms can complement or even substitute for UCP1-mediated thermogenesis. Moreover, they expand our view of cold-induced thermogenesis from a special feature of brown adipocytes to a more general physiological principle. Finally, we discuss how thermogenic mechanisms can be exploited to expend energy and hence offer new therapeutic opportunities.
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