Apolipoprotein E-dependent inverse regulation of vertebral bone and adipose tissue mass in C57Bl/6 mice: modulation by diet-induced obesity.

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Apolipoprotein E-dependent inverse regulation of vertebral bone and adipose tissue mass in C57Bl/6 mice: modulation by diet-induced obesity. / Bartelt, Alexander; Beil, Frank Timo; Schinke, Thorsten; Röser, Kerstin; Ruether, Wolfgang; Heeren, Jörg; Niemeier, Andreas.

in: BONE, Jahrgang 47, Nr. 4, 4, 01.10.2010, S. 736-745.

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@article{58b062c65dfe45ca843e3f1cc9a91ac6,
title = "Apolipoprotein E-dependent inverse regulation of vertebral bone and adipose tissue mass in C57Bl/6 mice: modulation by diet-induced obesity.",
abstract = "The long prevailing view that obesity is generally associated with beneficial effects on the skeleton has recently been challenged. Apolipoprotein E (apoE) is known to influence both adipose tissue and bone. The goal of the current study was to examine the impact of apoE on the development of fat mass and bone mass in mice under conditions of diet-induced obesity (DIO). Four week-old male C57BL/6 (WT) and apoE-deficient (apoE(-/-)) mice received a control or a diabetogenic high-fat diet (HFD) for 16 weeks. The control-fed apoE(-/-) animals displayed less total fat mass and higher lumbar trabecular bone volume (BV/TV) than WT controls. When stressed with HFD to induce obesity, apoE(-/-) mice had a lower body weight, lower serum glucose, insulin and leptin levels and accumulated less white adipose tissue mass at all sites including bone marrow. While WT animals showed no significant change in BV/TV and bone formation rate (BFR), apoE deficiency led to a decrease of BV/TV and BFR when stressed with HFD. Bone resorption parameters were not affected by HFD in either genotype. Taken together, under normal dietary conditions, apoE-deficient mice acquire less fat mass and more bone mass than WT littermates. When stressed with HFD to develop DIO, the difference of total body fat mass becomes larger and the difference of bone mass smaller between the genotypes. We conclude that apoE is involved in an inverse regulation of bone mass and fat mass in growing mice and that this effect is modulated by diet-induced obesity.",
keywords = "Adipocytes, Adipose Tissue, Animals, Apolipoproteins E, Blood Glucose, Bone Marrow Cells, Bone Remodeling, Cell Proliferation, Diet, Dietary Fats, Epididymis, Insulin, Leptin, Lipids, Male, Mice, Mice, Inbred C57BL, Obesity, Organ Size, Spine, Subcutaneous Tissue, Viscera, Weight Gain",
author = "Alexander Bartelt and Beil, {Frank Timo} and Thorsten Schinke and Kerstin R{\"o}ser and Wolfgang Ruether and J{\"o}rg Heeren and Andreas Niemeier",
note = "Copyright {\textcopyright} 2010 Elsevier Inc. All rights reserved.",
year = "2010",
month = oct,
day = "1",
doi = "10.1016/j.bone.2010.07.002",
language = "Deutsch",
volume = "47",
pages = "736--745",
journal = "BONE",
issn = "8756-3282",
publisher = "Elsevier Inc.",
number = "4",

}

RIS

TY - JOUR

T1 - Apolipoprotein E-dependent inverse regulation of vertebral bone and adipose tissue mass in C57Bl/6 mice: modulation by diet-induced obesity.

AU - Bartelt, Alexander

AU - Beil, Frank Timo

AU - Schinke, Thorsten

AU - Röser, Kerstin

AU - Ruether, Wolfgang

AU - Heeren, Jörg

AU - Niemeier, Andreas

N1 - Copyright © 2010 Elsevier Inc. All rights reserved.

PY - 2010/10/1

Y1 - 2010/10/1

N2 - The long prevailing view that obesity is generally associated with beneficial effects on the skeleton has recently been challenged. Apolipoprotein E (apoE) is known to influence both adipose tissue and bone. The goal of the current study was to examine the impact of apoE on the development of fat mass and bone mass in mice under conditions of diet-induced obesity (DIO). Four week-old male C57BL/6 (WT) and apoE-deficient (apoE(-/-)) mice received a control or a diabetogenic high-fat diet (HFD) for 16 weeks. The control-fed apoE(-/-) animals displayed less total fat mass and higher lumbar trabecular bone volume (BV/TV) than WT controls. When stressed with HFD to induce obesity, apoE(-/-) mice had a lower body weight, lower serum glucose, insulin and leptin levels and accumulated less white adipose tissue mass at all sites including bone marrow. While WT animals showed no significant change in BV/TV and bone formation rate (BFR), apoE deficiency led to a decrease of BV/TV and BFR when stressed with HFD. Bone resorption parameters were not affected by HFD in either genotype. Taken together, under normal dietary conditions, apoE-deficient mice acquire less fat mass and more bone mass than WT littermates. When stressed with HFD to develop DIO, the difference of total body fat mass becomes larger and the difference of bone mass smaller between the genotypes. We conclude that apoE is involved in an inverse regulation of bone mass and fat mass in growing mice and that this effect is modulated by diet-induced obesity.

AB - The long prevailing view that obesity is generally associated with beneficial effects on the skeleton has recently been challenged. Apolipoprotein E (apoE) is known to influence both adipose tissue and bone. The goal of the current study was to examine the impact of apoE on the development of fat mass and bone mass in mice under conditions of diet-induced obesity (DIO). Four week-old male C57BL/6 (WT) and apoE-deficient (apoE(-/-)) mice received a control or a diabetogenic high-fat diet (HFD) for 16 weeks. The control-fed apoE(-/-) animals displayed less total fat mass and higher lumbar trabecular bone volume (BV/TV) than WT controls. When stressed with HFD to induce obesity, apoE(-/-) mice had a lower body weight, lower serum glucose, insulin and leptin levels and accumulated less white adipose tissue mass at all sites including bone marrow. While WT animals showed no significant change in BV/TV and bone formation rate (BFR), apoE deficiency led to a decrease of BV/TV and BFR when stressed with HFD. Bone resorption parameters were not affected by HFD in either genotype. Taken together, under normal dietary conditions, apoE-deficient mice acquire less fat mass and more bone mass than WT littermates. When stressed with HFD to develop DIO, the difference of total body fat mass becomes larger and the difference of bone mass smaller between the genotypes. We conclude that apoE is involved in an inverse regulation of bone mass and fat mass in growing mice and that this effect is modulated by diet-induced obesity.

KW - Adipocytes

KW - Adipose Tissue

KW - Animals

KW - Apolipoproteins E

KW - Blood Glucose

KW - Bone Marrow Cells

KW - Bone Remodeling

KW - Cell Proliferation

KW - Diet

KW - Dietary Fats

KW - Epididymis

KW - Insulin

KW - Leptin

KW - Lipids

KW - Male

KW - Mice

KW - Mice, Inbred C57BL

KW - Obesity

KW - Organ Size

KW - Spine

KW - Subcutaneous Tissue

KW - Viscera

KW - Weight Gain

U2 - 10.1016/j.bone.2010.07.002

DO - 10.1016/j.bone.2010.07.002

M3 - SCORING: Zeitschriftenaufsatz

C2 - 20633710

VL - 47

SP - 736

EP - 745

JO - BONE

JF - BONE

SN - 8756-3282

IS - 4

M1 - 4

ER -