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Adipose Tissue Denervation Blunted the Decrease in Bone Formation Promoted by Obesity in Rats

The impact of obesity upon bone metabolism is controversial since both beneficial or harmful effects have been reported. Bone remodeling is modulated by the central nervous system through cytokines, hormones and neuromodulators. The present study aimed to evaluate the effects evoked by bilateral ret...

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Autores principales: Ormanji, Milene Subtil, Melo, Maria Victória Lazarini, Meca, Renata, Garcia, Michelle Louvaes, Anauate, Ana Carolina, Muñoz, Juan José Augusto Moyano, Oyama, Lila Missae, Nishi, Erika Emy, Bergamaschi, Cassia Toledo, Carvalho, Aluizio Barbosa, Heilberg, Ita Pfeferman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10458609/
https://www.ncbi.nlm.nih.gov/pubmed/37630764
http://dx.doi.org/10.3390/nu15163574
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author Ormanji, Milene Subtil
Melo, Maria Victória Lazarini
Meca, Renata
Garcia, Michelle Louvaes
Anauate, Ana Carolina
Muñoz, Juan José Augusto Moyano
Oyama, Lila Missae
Nishi, Erika Emy
Bergamaschi, Cassia Toledo
Carvalho, Aluizio Barbosa
Heilberg, Ita Pfeferman
author_facet Ormanji, Milene Subtil
Melo, Maria Victória Lazarini
Meca, Renata
Garcia, Michelle Louvaes
Anauate, Ana Carolina
Muñoz, Juan José Augusto Moyano
Oyama, Lila Missae
Nishi, Erika Emy
Bergamaschi, Cassia Toledo
Carvalho, Aluizio Barbosa
Heilberg, Ita Pfeferman
author_sort Ormanji, Milene Subtil
collection PubMed
description The impact of obesity upon bone metabolism is controversial since both beneficial or harmful effects have been reported. Bone remodeling is modulated by the central nervous system through cytokines, hormones and neuromodulators. The present study aimed to evaluate the effects evoked by bilateral retroperitoneal white adipose tissue (rWAT) denervation (Dnx) upon bone mineral metabolism and remodeling in an experimental model of obesity in rats. Male Wistar rats were fed during 18 weeks with high-fat diet (HFD) or standard diet (SD) as controls, and rWAT Dnx or Sham surgery was performed at the 14th week. Biochemical and hormonal parameters, bone histomorphometry, rWAT and hypothalamus protein and gene expression were analyzed. The HFD group presented decreased bone formation parameters, increased serum and bone leptin and FGF23, increased serum and hypothalamic neuropeptide Y (NPY) and decreased serum 1,25-dihydroxyvitamin D(3) and PTH. After rWAT Dnx, bone markers and histomorphometry showed restoration of bone formation, and serum and hypothalamic NPY decreased, without alteration in leptin levels. The present study shows that the denervation of rWAT improved bone formation in obese rats mediated by a preferential reduction in neurohormonal actions of NPY, emphasizing the relevance of the adipose tissue–brain–bone axis in the control of bone metabolism in obesity.
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spelling pubmed-104586092023-08-27 Adipose Tissue Denervation Blunted the Decrease in Bone Formation Promoted by Obesity in Rats Ormanji, Milene Subtil Melo, Maria Victória Lazarini Meca, Renata Garcia, Michelle Louvaes Anauate, Ana Carolina Muñoz, Juan José Augusto Moyano Oyama, Lila Missae Nishi, Erika Emy Bergamaschi, Cassia Toledo Carvalho, Aluizio Barbosa Heilberg, Ita Pfeferman Nutrients Article The impact of obesity upon bone metabolism is controversial since both beneficial or harmful effects have been reported. Bone remodeling is modulated by the central nervous system through cytokines, hormones and neuromodulators. The present study aimed to evaluate the effects evoked by bilateral retroperitoneal white adipose tissue (rWAT) denervation (Dnx) upon bone mineral metabolism and remodeling in an experimental model of obesity in rats. Male Wistar rats were fed during 18 weeks with high-fat diet (HFD) or standard diet (SD) as controls, and rWAT Dnx or Sham surgery was performed at the 14th week. Biochemical and hormonal parameters, bone histomorphometry, rWAT and hypothalamus protein and gene expression were analyzed. The HFD group presented decreased bone formation parameters, increased serum and bone leptin and FGF23, increased serum and hypothalamic neuropeptide Y (NPY) and decreased serum 1,25-dihydroxyvitamin D(3) and PTH. After rWAT Dnx, bone markers and histomorphometry showed restoration of bone formation, and serum and hypothalamic NPY decreased, without alteration in leptin levels. The present study shows that the denervation of rWAT improved bone formation in obese rats mediated by a preferential reduction in neurohormonal actions of NPY, emphasizing the relevance of the adipose tissue–brain–bone axis in the control of bone metabolism in obesity. MDPI 2023-08-14 /pmc/articles/PMC10458609/ /pubmed/37630764 http://dx.doi.org/10.3390/nu15163574 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ormanji, Milene Subtil
Melo, Maria Victória Lazarini
Meca, Renata
Garcia, Michelle Louvaes
Anauate, Ana Carolina
Muñoz, Juan José Augusto Moyano
Oyama, Lila Missae
Nishi, Erika Emy
Bergamaschi, Cassia Toledo
Carvalho, Aluizio Barbosa
Heilberg, Ita Pfeferman
Adipose Tissue Denervation Blunted the Decrease in Bone Formation Promoted by Obesity in Rats
title Adipose Tissue Denervation Blunted the Decrease in Bone Formation Promoted by Obesity in Rats
title_full Adipose Tissue Denervation Blunted the Decrease in Bone Formation Promoted by Obesity in Rats
title_fullStr Adipose Tissue Denervation Blunted the Decrease in Bone Formation Promoted by Obesity in Rats
title_full_unstemmed Adipose Tissue Denervation Blunted the Decrease in Bone Formation Promoted by Obesity in Rats
title_short Adipose Tissue Denervation Blunted the Decrease in Bone Formation Promoted by Obesity in Rats
title_sort adipose tissue denervation blunted the decrease in bone formation promoted by obesity in rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10458609/
https://www.ncbi.nlm.nih.gov/pubmed/37630764
http://dx.doi.org/10.3390/nu15163574
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