Pattern of Expression of Adiponectin Receptors in Human Liver and its Relation to Nonalcoholic Steatohepatitis

Background Adiponectin has antisteatosis–anti-inflammatory properties and its circulating levels are reduced in nonalcoholic steatohepatitis (NASH). Methods To assess the role of adiponectin in NASH, we measured expression of adiponectin gene ( APM1 ) and receptors ( AdipoR1 / AdipoR2 ) in liver and...

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Published inObesity surgery Vol. 19; no. 4; pp. 467 - 474
Main Authors Nannipieri, M., Cecchetti, F., Anselmino, M., Mancini, E., Marchetti, G., Bonotti, A., Baldi, S., Solito, B., Giannetti, M., Pinchera, A., Santini, F., Ferrannini, E.
Format Journal Article
LanguageEnglish
Published New York Springer New York 01.04.2009
Springer Nature B.V
Subjects
Online AccessGet full text
ISSN0960-8923
1708-0428
DOI10.1007/s11695-008-9701-x

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Abstract Background Adiponectin has antisteatosis–anti-inflammatory properties and its circulating levels are reduced in nonalcoholic steatohepatitis (NASH). Methods To assess the role of adiponectin in NASH, we measured expression of adiponectin gene ( APM1 ) and receptors ( AdipoR1 / AdipoR2 ) in liver and subcutaneous and visceral fat in subjects with biopsy-proven NASH or pure steatosis (PS). In 103 subjects undergoing gastric bypass or elective abdominal surgery (17 with normal liver histology (C), 52 with PS, and 34 with NASH), RNA was extracted from tissue samples, and quantification of APM1 , AdipoR1 , and AdipoR2 was carried out by real-time polymerase chain reaction. Results In NASH vs C, circulating adiponectin levels (3.6[2.4] vs 5.3[4.3] μg/ml, median[interquartile range], p  < 0.05) and adiponectin concentrations, APM1 , AdipoR1 , and AdipoR2 expression in visceral fat were all reduced ( p  ≤ 0.03). These differences disappeared when adjusting for obesity. In contrast, liver AdipoR1 (1.40 [0.46] vs 1.00 [0.32] of controls) and AdipoR2 expression (1.20 [0.41] vs 0.78 [0.43]) were increased in NASH, and group differences were statistically significant ( p  < 0.0001 for AdipoR1 and p  = 0.0001 for AdipoR2 ). Results for PS were generally intermediate between NASH and C. Liver receptor expression was reciprocally related to circulating adiponectin ( rho  = −0.42, p  < 0.003 for AdipoR1 and rho  = −0.26, p  < 0.009 for AdipoR2 ). In multivariate models adjusting for sex, age, fasting plasma glucose, and obesity, liver enzymes levels were directly related to both AdipoR1 and AdipoR2 expression in liver. Conclusion In obese patients with NASH, adiponectin receptors are underexpressed in visceral fat—as a likely correlate of obesity—but overexpressed in liver, possibly as a compensatory response to hypoadiponectinemia, and positively associated with liver damage.
AbstractList Adiponectin has antisteatosis-anti-inflammatory properties and its circulating levels are reduced in nonalcoholic steatohepatitis (NASH).BACKGROUNDAdiponectin has antisteatosis-anti-inflammatory properties and its circulating levels are reduced in nonalcoholic steatohepatitis (NASH).To assess the role of adiponectin in NASH, we measured expression of adiponectin gene (APM1) and receptors (AdipoR1/AdipoR2) in liver and subcutaneous and visceral fat in subjects with biopsy-proven NASH or pure steatosis (PS). In 103 subjects undergoing gastric bypass or elective abdominal surgery (17 with normal liver histology (C), 52 with PS, and 34 with NASH), RNA was extracted from tissue samples, and quantification of APM1, AdipoR1, and AdipoR2 was carried out by real-time polymerase chain reaction.METHODSTo assess the role of adiponectin in NASH, we measured expression of adiponectin gene (APM1) and receptors (AdipoR1/AdipoR2) in liver and subcutaneous and visceral fat in subjects with biopsy-proven NASH or pure steatosis (PS). In 103 subjects undergoing gastric bypass or elective abdominal surgery (17 with normal liver histology (C), 52 with PS, and 34 with NASH), RNA was extracted from tissue samples, and quantification of APM1, AdipoR1, and AdipoR2 was carried out by real-time polymerase chain reaction.In NASH vs C, circulating adiponectin levels (3.6[2.4] vs 5.3[4.3] microg/ml, median[interquartile range], p < 0.05) and adiponectin concentrations, APM1, AdipoR1, and AdipoR2 expression in visceral fat were all reduced (p < or = 0.03). These differences disappeared when adjusting for obesity. In contrast, liver AdipoR1 (1.40 [0.46] vs 1.00 [0.32] of controls) and AdipoR2 expression (1.20 [0.41] vs 0.78 [0.43]) were increased in NASH, and group differences were statistically significant (p < 0.0001 for AdipoR1 and p = 0.0001 for AdipoR2). Results for PS were generally intermediate between NASH and C. Liver receptor expression was reciprocally related to circulating adiponectin (rho = -0.42, p < 0.003 for AdipoR1 and rho = -0.26, p < 0.009 for AdipoR2). In multivariate models adjusting for sex, age, fasting plasma glucose, and obesity, liver enzymes levels were directly related to both AdipoR1 and AdipoR2 expression in liver.RESULTSIn NASH vs C, circulating adiponectin levels (3.6[2.4] vs 5.3[4.3] microg/ml, median[interquartile range], p < 0.05) and adiponectin concentrations, APM1, AdipoR1, and AdipoR2 expression in visceral fat were all reduced (p < or = 0.03). These differences disappeared when adjusting for obesity. In contrast, liver AdipoR1 (1.40 [0.46] vs 1.00 [0.32] of controls) and AdipoR2 expression (1.20 [0.41] vs 0.78 [0.43]) were increased in NASH, and group differences were statistically significant (p < 0.0001 for AdipoR1 and p = 0.0001 for AdipoR2). Results for PS were generally intermediate between NASH and C. Liver receptor expression was reciprocally related to circulating adiponectin (rho = -0.42, p < 0.003 for AdipoR1 and rho = -0.26, p < 0.009 for AdipoR2). In multivariate models adjusting for sex, age, fasting plasma glucose, and obesity, liver enzymes levels were directly related to both AdipoR1 and AdipoR2 expression in liver.In obese patients with NASH, adiponectin receptors are underexpressed in visceral fat-as a likely correlate of obesity-but overexpressed in liver, possibly as a compensatory response to hypoadiponectinemia, and positively associated with liver damage.CONCLUSIONIn obese patients with NASH, adiponectin receptors are underexpressed in visceral fat-as a likely correlate of obesity-but overexpressed in liver, possibly as a compensatory response to hypoadiponectinemia, and positively associated with liver damage.
Adiponectin has antisteatosis-anti-inflammatory properties and its circulating levels are reduced in nonalcoholic steatohepatitis (NASH). To assess the role of adiponectin in NASH, we measured expression of adiponectin gene (APM1) and receptors (AdipoR1/AdipoR2) in liver and subcutaneous and visceral fat in subjects with biopsy-proven NASH or pure steatosis (PS). In 103 subjects undergoing gastric bypass or elective abdominal surgery (17 with normal liver histology (C), 52 with PS, and 34 with NASH), RNA was extracted from tissue samples, and quantification of APM1, AdipoR1, and AdipoR2 was carried out by real-time polymerase chain reaction. In NASH vs C, circulating adiponectin levels (3.6[2.4] vs 5.3[4.3] μg/ml, median[interquartile range], p<0.05) and adiponectin concentrations, APM1, AdipoR1, and AdipoR2 expression in visceral fat were all reduced (p≤0.03). These differences disappeared when adjusting for obesity. In contrast, liver AdipoR1 (1.40 [0.46] vs 1.00 [0.32] of controls) and AdipoR2 expression (1.20 [0.41] vs 0.78 [0.43]) were increased in NASH, and group differences were statistically significant (p<0.0001 for AdipoR1 and p=0.0001 for AdipoR2). Results for PS were generally intermediate between NASH and C. Liver receptor expression was reciprocally related to circulating adiponectin (rho=-0.42, p<0.003 for AdipoR1 and rho=-0.26, p<0.009 for AdipoR2). In multivariate models adjusting for sex, age, fasting plasma glucose, and obesity, liver enzymes levels were directly related to both AdipoR1 and AdipoR2 expression in liver. In obese patients with NASH, adiponectin receptors are underexpressed in visceral fat--as a likely correlate of obesity--but overexpressed in liver, possibly as a compensatory response to hypoadiponectinemia, and positively associated with liver damage. [PUBLICATION ABSTRACT]
Background Adiponectin has antisteatosis–anti-inflammatory properties and its circulating levels are reduced in nonalcoholic steatohepatitis (NASH). Methods To assess the role of adiponectin in NASH, we measured expression of adiponectin gene ( APM1 ) and receptors ( AdipoR1 / AdipoR2 ) in liver and subcutaneous and visceral fat in subjects with biopsy-proven NASH or pure steatosis (PS). In 103 subjects undergoing gastric bypass or elective abdominal surgery (17 with normal liver histology (C), 52 with PS, and 34 with NASH), RNA was extracted from tissue samples, and quantification of APM1 , AdipoR1 , and AdipoR2 was carried out by real-time polymerase chain reaction. Results In NASH vs C, circulating adiponectin levels (3.6[2.4] vs 5.3[4.3] μg/ml, median[interquartile range], p  < 0.05) and adiponectin concentrations, APM1 , AdipoR1 , and AdipoR2 expression in visceral fat were all reduced ( p  ≤ 0.03). These differences disappeared when adjusting for obesity. In contrast, liver AdipoR1 (1.40 [0.46] vs 1.00 [0.32] of controls) and AdipoR2 expression (1.20 [0.41] vs 0.78 [0.43]) were increased in NASH, and group differences were statistically significant ( p  < 0.0001 for AdipoR1 and p  = 0.0001 for AdipoR2 ). Results for PS were generally intermediate between NASH and C. Liver receptor expression was reciprocally related to circulating adiponectin ( rho  = −0.42, p  < 0.003 for AdipoR1 and rho  = −0.26, p  < 0.009 for AdipoR2 ). In multivariate models adjusting for sex, age, fasting plasma glucose, and obesity, liver enzymes levels were directly related to both AdipoR1 and AdipoR2 expression in liver. Conclusion In obese patients with NASH, adiponectin receptors are underexpressed in visceral fat—as a likely correlate of obesity—but overexpressed in liver, possibly as a compensatory response to hypoadiponectinemia, and positively associated with liver damage.
Adiponectin has antisteatosis-anti-inflammatory properties and its circulating levels are reduced in nonalcoholic steatohepatitis (NASH). To assess the role of adiponectin in NASH, we measured expression of adiponectin gene (APM1) and receptors (AdipoR1/AdipoR2) in liver and subcutaneous and visceral fat in subjects with biopsy-proven NASH or pure steatosis (PS). In 103 subjects undergoing gastric bypass or elective abdominal surgery (17 with normal liver histology (C), 52 with PS, and 34 with NASH), RNA was extracted from tissue samples, and quantification of APM1, AdipoR1, and AdipoR2 was carried out by real-time polymerase chain reaction. In NASH vs C, circulating adiponectin levels (3.6[2.4] vs 5.3[4.3] microg/ml, median[interquartile range], p < 0.05) and adiponectin concentrations, APM1, AdipoR1, and AdipoR2 expression in visceral fat were all reduced (p < or = 0.03). These differences disappeared when adjusting for obesity. In contrast, liver AdipoR1 (1.40 [0.46] vs 1.00 [0.32] of controls) and AdipoR2 expression (1.20 [0.41] vs 0.78 [0.43]) were increased in NASH, and group differences were statistically significant (p < 0.0001 for AdipoR1 and p = 0.0001 for AdipoR2). Results for PS were generally intermediate between NASH and C. Liver receptor expression was reciprocally related to circulating adiponectin (rho = -0.42, p < 0.003 for AdipoR1 and rho = -0.26, p < 0.009 for AdipoR2). In multivariate models adjusting for sex, age, fasting plasma glucose, and obesity, liver enzymes levels were directly related to both AdipoR1 and AdipoR2 expression in liver. In obese patients with NASH, adiponectin receptors are underexpressed in visceral fat-as a likely correlate of obesity-but overexpressed in liver, possibly as a compensatory response to hypoadiponectinemia, and positively associated with liver damage.
Author Mancini, E.
Giannetti, M.
Pinchera, A.
Bonotti, A.
Santini, F.
Marchetti, G.
Baldi, S.
Ferrannini, E.
Nannipieri, M.
Cecchetti, F.
Anselmino, M.
Solito, B.
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/18923878$$D View this record in MEDLINE/PubMed
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Springer Science + Business Media, LLC 2009
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Keywords Obesity
Nonalcoholic steatohepatitis
Adiponectin receptors
Adiponectin
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Snippet Background Adiponectin has antisteatosis–anti-inflammatory properties and its circulating levels are reduced in nonalcoholic steatohepatitis (NASH). Methods To...
Adiponectin has antisteatosis-anti-inflammatory properties and its circulating levels are reduced in nonalcoholic steatohepatitis (NASH). To assess the role of...
Adiponectin has antisteatosis-anti-inflammatory properties and its circulating levels are reduced in nonalcoholic steatohepatitis (NASH). To assess the role of...
Adiponectin has antisteatosis-anti-inflammatory properties and its circulating levels are reduced in nonalcoholic steatohepatitis (NASH).BACKGROUNDAdiponectin...
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StartPage 467
SubjectTerms Adiponectin - metabolism
Adult
Clinical outcomes
Diabetes Mellitus, Type 2 - metabolism
Fatty Liver - metabolism
Female
Gastrointestinal surgery
Hepatitis
Humans
Intra-Abdominal Fat - metabolism
Liver
Liver - metabolism
Male
Medicine
Medicine & Public Health
Middle Aged
Obesity
Obesity - metabolism
Proteins
Receptors, Adiponectin - metabolism
Research Article
Surgery
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Title Pattern of Expression of Adiponectin Receptors in Human Liver and its Relation to Nonalcoholic Steatohepatitis
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