The Chemerin-CMKLR1 Axis is Functionally Important for Central Regulation of Energy Homeostasis

2021 ◽  
Author(s):  
Rebecca Dumbell ◽  
Haesung Yun ◽  
Samantha L. Maclean ◽  
Klaus Pors ◽  
Gisela Helfer
2021 ◽  
Vol 12 ◽  
Author(s):  
Francesca Copperi ◽  
Jung Dae Kim ◽  
Sabrina Diano

Increasing evidence indicates that the melanocortin system is not only a central player in energy homeostasis, food intake and glucose level regulation, but also in the modulation of cardiovascular functions, such as blood pressure and heart rate. The melanocortins, and in particular α- and γ-MSH, have been shown to exert their cardiovascular activity both at the central nervous system level and in the periphery (e.g., in the adrenal gland), binding their receptors MC3R and MC4R and influencing the activity of the sympathetic nervous system. In addition, some studies have shown that the activation of MC3R and MC4R by their endogenous ligands is able to improve the outcome of cardiovascular diseases, such as myocardial and cerebral ischemia. In this brief review, we will discuss the current knowledge of how the melanocortin system influences essential cardiovascular functions, such as blood pressure and heart rate, and its protective role in ischemic events, with a particular focus on the central regulation of such mechanisms.


2012 ◽  
Vol 59 (5) ◽  
pp. 365-374 ◽  
Author(s):  
Hiroshi Tsuneki ◽  
Tsutomu Wada ◽  
Toshiyasu Sasaoka

Diabetes ◽  
2006 ◽  
Vol 55 (Supplement 2) ◽  
pp. S155-S160 ◽  
Author(s):  
D. Porte

2017 ◽  
Vol 45 (7) ◽  
pp. 894-903 ◽  
Author(s):  
Alexander Corr ◽  
James Smith ◽  
Paul Baldock

Although the brain is well established as a master regulator of homeostasis in peripheral tissues, central regulation of bone mass represents a novel and rapidly expanding field of study. This review examines the current understanding of central regulation of the skeleton, exploring several of the key pathways connecting brain to bone and their implications both in mice and the clinical setting. Our understanding of central bone regulation has largely progressed through examination of skeletal responses downstream of nutrient regulatory pathways in the hypothalamus. Mutations and modulation of these pathways, in cases such as leptin deficiency, induce marked bone phenotypes, which have provided vital insights into central bone regulation. These studies have identified several central neuropeptide pathways that stimulate well-defined changes in bone cell activity in response to changes in energy homeostasis. In addition, this work has highlighted the endocrine nature of the skeleton, revealing a complex cross talk that directly regulates other organ systems. Our laboratory has studied bone-active neuropeptide pathways and defined osteoblast-based actions that recapitulate central pathways linking bone, fat, and glucose homeostasis. Studies of neural control of bone have produced paradigm-shifting changes in our understanding of the skeleton and its relationship with the wider array of organ systems.


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