Donate Help Contact The AHA Sign In Home
American Heart Association
Arteriosclerosis, Thrombosis, and Vascular Biology
Search: search_blue_button Advanced Search
Arteriosclerosis, Thrombosis, and Vascular Biology. 2003;23:1801-1807
Published online before print August 28, 2003, doi: 10.1161/01.ATV.0000092872.54026.8D
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Data Supplement
Right arrow All Versions of this Article:
23/10/1801    most recent
01.ATV.0000092872.54026.8Dv1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Request Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Levin, M.
Right arrow Articles by Björnheden, T.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Levin, M.
Right arrow Articles by Björnheden, T.
Related Collections
Right arrow Mechanism of atherosclerosis/growth factors
Right arrow Pathophysiology
Right arrow Energy metabolism
Right arrow Imaging
Right arrow Other imaging
(Arteriosclerosis, Thrombosis, and Vascular Biology. 2003;23:1801.)
© 2003 American Heart Association, Inc.


Vascular Biology

Mapping of ATP, Glucose, Glycogen, and Lactate Concentrations Within the Arterial Wall

M. Levin; O. Leppänen; M. Evaldsson; O. Wiklund; G. Bondjers; T. Björnheden

From the Wallenberg Laboratory for Cardiovascular Research (M.L, M.E., O.W., G.B, T.B), Göteborg University, Göteborg, and Ludwig Institute for Cancer Research (O.L.), Uppsala Branch, Uppsala, Sweden.

Correspondence to Max Levin, Wallenberg Laboratory, Sahlgrenska University Hospital, SE-413 45 Göteborg, Sweden. E-mail max.levin{at}wlab.gu.se

Objective— In large- and medium-sized arteries, the diffusion distances for oxygen and nutrients are long. This has been suggested to make these vessels prone to develop local energy metabolic deficiencies that could contribute to atherogenesis. To validate this hypothesis, we introduced a new method to measure energy metabolites within the arterial wall at high spatial resolution.

Methods and Results— Bioluminescence imaging was used to quantify local metabolite concentrations in cryosections of snap frozen (in vivo) and incubated pig carotid artery rings. Incubation at hypoxia resulted in increased lactate concentrations, whereas ATP, glucose, and glycogen concentrations were decreased, especially in the mid media, where concentrations of these metabolites were close to zero. In snap frozen arteries, glycogen concentrations were markedly higher in deep layers of the media than toward the lumen. ATP, glucose, and lactate were more homogenously distributed.

Conclusions— Bioluminescence imaging is a new and powerful tool to assess arterial wall energy metabolism at high spatial resolution. Our experiments demonstrate heterogeneous distributions of energy metabolites under hypoxic in vitro conditions. Furthermore, we show that glycogen concentrations are higher in deep medial layers in vivo. This might represent a local adaptation to a low-oxygen microenvironment.


Key Words: atherosclerosis • hypoxia • bioluminescence • energy metabolism • imaging




This article has been cited by other articles:


Home page
Circ. Res.Home page
S. Sukhanov, Y. Higashi, S.-Y. Shai, H. Itabe, K. Ono, S. Parthasarathy, and P. Delafontaine
Novel Effect of Oxidized Low-Density Lipoprotein: Cellular ATP Depletion via Downregulation of Glyceraldehyde-3-Phosphate Dehydrogenase
Circ. Res., July 21, 2006; 99(2): 191 - 200.
[Abstract] [Full Text] [PDF]