Record Details

Twelve months of voluntary heavy alcohol consumption in male rhesus macaques suppresses intracortical bone remodeling

ScholarsArchive at Oregon State University

Field Value
Title Twelve months of voluntary heavy alcohol consumption in male rhesus macaques suppresses intracortical bone remodeling
Names Gaddini, Gino W. (creator)
Grant, Kathleen A. (creator)
Woodall, Andrew (creator)
Stull, Cara (creator)
Maddalozzo, Gianni F. (creator)
Zhang, Bo (creator)
Turner, Russell T. (creator)
Iwaniec, Urszula T. (creator)
Date Issued 2015-02 (iso8601)
Note To the best of our knowledge, one or more authors of this paper were federal employees when contributing to this work. This is the publisher’s final pdf. The published article is copyrighted by Elsevier and can be found at: http://www.journals.elsevier.com/bone.
Abstract Chronic heavy alcohol consumption is a risk factor for cortical bone fractures in males. The increase in fracture
risk may be due, in part, to reduced bone quality. Intracortical (osteonal) bone remodeling is the principle
mechanism for maintaining cortical bone quality. However, it is not clear how alcohol abuse impacts intracortical
bone remodeling. This study investigated the effects of long-duration heavy alcohol consumption on intracortical
bone remodeling in a non-human primate model. Following a 4-month induction period, male rhesus macaques
(Macaca mulatta, n = 21) were allowed to voluntarily self-administer water or alcohol (4% ethanol w/v) for
22 h/d, 7 d/wk for 12 months. Control monkeys (n = 13) received water and an isocaloric maltose-dextrin solution.
Tetracycline hydrochloride was administered orally 17 and 3 days prior to sacrifice for determination of
active mineralization sites. Animals in the alcohol group consumed 2.7 ± 0.2 g alcohol/kg/d (mean ± SE) during
the 12 months of self-administration, resulting in a mean daily blood alcohol concentration of 77 ± 9 mg/dl from
samples taken at 7 h after the start of a daily session. However, blood alcohol concentration varied widely
from day to day, with peak levels exceeding 250 mg/dl, modeling a binge-drinking pattern of alcohol consumption.
The skeletal response to alcohol was determined by densitometry, microcomputed tomography and
histomorphometry. Significant differences in tibial bone mineral content, bone mineral density, and cortical
bone architecture (cross-sectional volume, cortical volume, marrow volume, cortical thickness, and polar
moment of inertia) in the tibial diaphysis were not detected with treatment. However, cortical porosity was
lower (1.8 ± 0.5 % versus 0.6 ± 0.1 %, p = 0.021) and labeled osteon density was lower (0.41 ± 0.2/mm² versus
0.04 ± 0.01/mm², p < 0.003) in alcohol-consuming monkeys compared to controls, indicating a reduced rate of
intracortical bone remodeling. In concordance, plasma CTx was lower (2.5 ± 0.3 ng/ml versus 1.7 ± 0.1 ng/ml,
p = 0.028) in the alcohol group. These results suggest that chronic heavy alcohol consumption may negatively
impact bone health, in part, by suppressing intracortical bone remodeling.
Genre Article
Topic Haversian remodeling
Identifier Gaddini, G. W., Grant, K. A., Woodall, A., Stull, C., Maddalozzo, G. F., Zhang, B., ... & Iwaniec, U. T. (2015). Twelve months of voluntary heavy alcohol consumption in male rhesus macaques suppresses intracortical bone remodeling. Bone, 71, 227-236. doi:10.1016/j.bone.2014.10.025

© Western Waters Digital Library - GWLA member projects - Designed by the J. Willard Marriott Library - Hosted by Oregon State University Libraries and Press