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Abdominal subcutaneous adipose tissue insulin resistance and lipolysis in patients with non-alcoholic steatohepatitis
被引:60
作者:
Armstrong, M. J.
[1
,2
]
Hazlehurst, J. M.
[3
]
Hull, D.
[1
,2
]
Guo, K.
[1
,2
]
Borrows, S.
[4
]
Yu, J.
[5
]
Gough, S. C.
[6
,7
]
Newsome, P. N.
[1
,2
]
Tomlinson, J. W.
[3
]
机构:
[1] Univ Birmingham, Liver Res Ctr, Birmingham B15 2TH, W Midlands, England
[2] Univ Birmingham, NIHR Liver Biomed Res Unit, Birmingham B15 2TH, W Midlands, England
[3] Univ Birmingham, Sch Clin & Expt Med, Inst Biomed Res, Ctr Endocrinol Diabet & Metab, Birmingham B15 2TH, W Midlands, England
[4] Queen Elizabeth Hosp, NIHR Wellcome Trust Clin Res Facil, Birmingham B15 2TH, W Midlands, England
[5] Univ Birmingham, Sch Sport Exercise & Rehabil Sci, Birmingham B15 2TH, W Midlands, England
[6] Oxford Ctr Diabet Endocrinol & Metab, Oxford, England
[7] NIHR Oxford Biomed Res Ctr, Oxford, England
基金:
英国医学研究理事会;
英国惠康基金;
关键词:
adipose tissue;
fatty liver;
insulin sensitivity;
lipolysis;
steatohepatitis;
FATTY LIVER-DISEASE;
DE-NOVO LIPOGENESIS;
REGIONAL ADIPOSITY;
CARDIOVASCULAR-DISEASE;
VISCERAL ADIPOSITY;
GLUCOSE-PRODUCTION;
OBESE-PATIENTS;
ASSOCIATION;
SENSITIVITY;
ACIDS;
D O I:
10.1111/dom.12272
中图分类号:
R5 [内科学];
学科分类号:
100201 [内科学];
摘要:
Background: Systemic insulin resistance (IR) is a primary feature in non-alcoholic steatohepatitis (NASH), however, there remain limited data on tissue-specific insulin sensitivity in vivo. Methods: We examined tissue-specific (adipose, muscle and liver) insulin sensitivity and inflammation in 16 European Caucasian patients with biopsy-confirmed NASH and in 15 healthy controls. All underwent a two-step hyperinsulinaemic euglycaemic clamp incorporating stable isotope measurements of carbohydrate and lipid metabolism with concomitant subcutaneous adipose tissue (SAT) microdialysis. Results: Hepatic and muscle insulin sensitivity were decreased in patients with NASH compared with controls, as demonstrated by reduced suppression of hepatic glucose production and glucose disposal (Gd) rates following insulin infusion. In addition, rates of lipolysis were higher in NASH patients with impaired insulin-mediated suppression of free fatty acid levels. At a tissue specific level, abdominal SAT in patients with NASH was severely insulin resistant, requiring >sixfold more insulin to cause 1/2-maximal suppression of glycerol release when compared with healthy controls. Furthermore, patients with NASH had significantly higher circulating levels of pro-inflammatory adipocytokines than controls. Conclusion: NASH patients have profound IR in the liver, muscle and in particular adipose tissues. This study represents the first in vivo description of dysfunctional SAT in patients with NASH.
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页码:651 / 660
页数:10
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