FNDC5 could be regulated by leptin in adipose tissue

Introduction Irisin activates the thermogenic function in adipose tissues. However, little is known on the association between human irisin and different cardiometabolic risk factors. We analyse the influence of morbid obesity on irisin levels and its relation with leptin and different cardiovascula...

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Published inEuropean journal of clinical investigation Vol. 44; no. 10; pp. 918 - 925
Main Authors Gutierrez-Repiso, Carolina, Garcia-Serrano, Sara, Rodriguez-Pacheco, Francisca, Garcia-Escobar, Eva, Haro-Mora, Juan J., Garcia-Arnes, Juan, Valdes, Sergio, Gonzalo, Montserrat, Soriguer, Federico, Moreno-Ruiz, Francisco J., Rodriguez-Cañete, Alberto, Martinez-Ferriz, Abelardo, Santoyo, Julio S., Perez-Valero, Vidal, Garcia-Fuentes, Eduardo
Format Journal Article
LanguageEnglish
Published England Blackwell Publishing Ltd 01.10.2014
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ISSN0014-2972
1365-2362
1365-2362
DOI10.1111/eci.12324

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Abstract Introduction Irisin activates the thermogenic function in adipose tissues. However, little is known on the association between human irisin and different cardiometabolic risk factors. We analyse the influence of morbid obesity on irisin levels and its relation with leptin and different cardiovascular risk factors. Material and methods We measured the serum irisin level and the fibronectin type III domain containing 5 (FNDC5) expression in adipose tissue from 33 morbidly obese subjects and 12 nonobese subjects. We also studied the effect of leptin on FNDC5 expression. Results Serum irisin was higher in the nonobese subjects than in morbidly obese subjects, both before (P = 0·043) and after bariatric surgery (P = 0·042). The variable that best explained the serum irisin levels in a multiple linear regression model was the waist‐to‐hip ratio (WHR) (R2 = 0·201) (Beta = −0·357, P = 0·046). Those morbidly obese subjects with android‐type obesity had lower serum irisin levels than those with gynecoid‐type obesity, both before (P = 0·027) and after bariatric surgery (P = 0·006). Only the percentage change in WHR was associated with serum irisin levels after bariatric surgery (r = −0·529, P = 0·005). FNDC5 expression levels in subcutaneous adipose tissue (SAT) were higher in the nonobese than in the morbidly obese subjects (P = 0·042). In SAT explants from nonobese subjects, leptin (20 and 150 ng/mL) produced a decrease in FNDC5 expression (P = 0·009 and P = 0·037, respectively). Conclusions We showed decreased serum irisin levels in morbidly obese subjects, related mainly to WHR. FNDC5 expression could be regulated by leptin.
AbstractList Irisin activates the thermogenic function in adipose tissues. However, little is known on the association between human irisin and different cardiometabolic risk factors. We analyse the influence of morbid obesity on irisin levels and its relation with leptin and different cardiovascular risk factors. We measured the serum irisin level and the fibronectin type III domain containing 5 (FNDC5) expression in adipose tissue from 33 morbidly obese subjects and 12 nonobese subjects. We also studied the effect of leptin on FNDC5 expression. Serum irisin was higher in the nonobese subjects than in morbidly obese subjects, both before (P = 0·043) and after bariatric surgery (P = 0·042). The variable that best explained the serum irisin levels in a multiple linear regression model was the waist-to-hip ratio (WHR) (R(2) = 0·201) (Beta = -0·357, P = 0·046). Those morbidly obese subjects with android-type obesity had lower serum irisin levels than those with gynecoid-type obesity, both before (P = 0·027) and after bariatric surgery (P = 0·006). Only the percentage change in WHR was associated with serum irisin levels after bariatric surgery (r = -0·529, P = 0·005). FNDC5 expression levels in subcutaneous adipose tissue (SAT) were higher in the nonobese than in the morbidly obese subjects (P = 0·042). In SAT explants from nonobese subjects, leptin (20 and 150 ng/mL) produced a decrease in FNDC5 expression (P = 0·009 and P = 0·037, respectively). We showed decreased serum irisin levels in morbidly obese subjects, related mainly to WHR. FNDC5 expression could be regulated by leptin.
Introduction Irisin activates the thermogenic function in adipose tissues. However, little is known on the association between human irisin and different cardiometabolic risk factors. We analyse the influence of morbid obesity on irisin levels and its relation with leptin and different cardiovascular risk factors. Material and methods We measured the serum irisin level and the fibronectin type III domain containing 5 (FNDC5) expression in adipose tissue from 33 morbidly obese subjects and 12 nonobese subjects. We also studied the effect of leptin on FNDC5 expression. Results Serum irisin was higher in the nonobese subjects than in morbidly obese subjects, both before (P = 0·043) and after bariatric surgery (P = 0·042). The variable that best explained the serum irisin levels in a multiple linear regression model was the waist‐to‐hip ratio (WHR) (R2 = 0·201) (Beta = −0·357, P = 0·046). Those morbidly obese subjects with android‐type obesity had lower serum irisin levels than those with gynecoid‐type obesity, both before (P = 0·027) and after bariatric surgery (P = 0·006). Only the percentage change in WHR was associated with serum irisin levels after bariatric surgery (r = −0·529, P = 0·005). FNDC5 expression levels in subcutaneous adipose tissue (SAT) were higher in the nonobese than in the morbidly obese subjects (P = 0·042). In SAT explants from nonobese subjects, leptin (20 and 150 ng/mL) produced a decrease in FNDC5 expression (P = 0·009 and P = 0·037, respectively). Conclusions We showed decreased serum irisin levels in morbidly obese subjects, related mainly to WHR. FNDC5 expression could be regulated by leptin.
Irisin activates the thermogenic function in adipose tissues. However, little is known on the association between human irisin and different cardiometabolic risk factors. We analyse the influence of morbid obesity on irisin levels and its relation with leptin and different cardiovascular risk factors.INTRODUCTIONIrisin activates the thermogenic function in adipose tissues. However, little is known on the association between human irisin and different cardiometabolic risk factors. We analyse the influence of morbid obesity on irisin levels and its relation with leptin and different cardiovascular risk factors.We measured the serum irisin level and the fibronectin type III domain containing 5 (FNDC5) expression in adipose tissue from 33 morbidly obese subjects and 12 nonobese subjects. We also studied the effect of leptin on FNDC5 expression.MATERIAL AND METHODSWe measured the serum irisin level and the fibronectin type III domain containing 5 (FNDC5) expression in adipose tissue from 33 morbidly obese subjects and 12 nonobese subjects. We also studied the effect of leptin on FNDC5 expression.Serum irisin was higher in the nonobese subjects than in morbidly obese subjects, both before (P = 0·043) and after bariatric surgery (P = 0·042). The variable that best explained the serum irisin levels in a multiple linear regression model was the waist-to-hip ratio (WHR) (R(2) = 0·201) (Beta = -0·357, P = 0·046). Those morbidly obese subjects with android-type obesity had lower serum irisin levels than those with gynecoid-type obesity, both before (P = 0·027) and after bariatric surgery (P = 0·006). Only the percentage change in WHR was associated with serum irisin levels after bariatric surgery (r = -0·529, P = 0·005). FNDC5 expression levels in subcutaneous adipose tissue (SAT) were higher in the nonobese than in the morbidly obese subjects (P = 0·042). In SAT explants from nonobese subjects, leptin (20 and 150 ng/mL) produced a decrease in FNDC5 expression (P = 0·009 and P = 0·037, respectively).RESULTSSerum irisin was higher in the nonobese subjects than in morbidly obese subjects, both before (P = 0·043) and after bariatric surgery (P = 0·042). The variable that best explained the serum irisin levels in a multiple linear regression model was the waist-to-hip ratio (WHR) (R(2) = 0·201) (Beta = -0·357, P = 0·046). Those morbidly obese subjects with android-type obesity had lower serum irisin levels than those with gynecoid-type obesity, both before (P = 0·027) and after bariatric surgery (P = 0·006). Only the percentage change in WHR was associated with serum irisin levels after bariatric surgery (r = -0·529, P = 0·005). FNDC5 expression levels in subcutaneous adipose tissue (SAT) were higher in the nonobese than in the morbidly obese subjects (P = 0·042). In SAT explants from nonobese subjects, leptin (20 and 150 ng/mL) produced a decrease in FNDC5 expression (P = 0·009 and P = 0·037, respectively).We showed decreased serum irisin levels in morbidly obese subjects, related mainly to WHR. FNDC5 expression could be regulated by leptin.CONCLUSIONSWe showed decreased serum irisin levels in morbidly obese subjects, related mainly to WHR. FNDC5 expression could be regulated by leptin.
Author Perez-Valero, Vidal
Garcia-Escobar, Eva
Garcia-Arnes, Juan
Rodriguez-Pacheco, Francisca
Haro-Mora, Juan J.
Martinez-Ferriz, Abelardo
Santoyo, Julio S.
Gonzalo, Montserrat
Moreno-Ruiz, Francisco J.
Rodriguez-Cañete, Alberto
Garcia-Fuentes, Eduardo
Soriguer, Federico
Gutierrez-Repiso, Carolina
Valdes, Sergio
Garcia-Serrano, Sara
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Issue 10
Keywords FNDC5
morbid obesity
Adipose tissue
PCG1-α
waist-to-hip ratio
irisin
leptin
Language English
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Snippet Introduction Irisin activates the thermogenic function in adipose tissues. However, little is known on the association between human irisin and different...
Irisin activates the thermogenic function in adipose tissues. However, little is known on the association between human irisin and different cardiometabolic...
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SubjectTerms Adipose tissue
Adult
Down-Regulation
Female
Fibronectins - metabolism
FNDC5
GTP-Binding Protein alpha Subunits - metabolism
Humans
Intra-Abdominal Fat - chemistry
irisin
leptin
Leptin - physiology
Male
morbid obesity
Obesity, Morbid - blood
PCG1-α
RNA, Messenger - metabolism
Subcutaneous Fat - chemistry
Waist-Hip Ratio
waist-to-hip ratio
Title FNDC5 could be regulated by leptin in adipose tissue
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https://onlinelibrary.wiley.com/doi/abs/10.1111%2Feci.12324
https://www.ncbi.nlm.nih.gov/pubmed/25112714
https://www.proquest.com/docview/1622062121
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