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DOI10.3233/BSI-130057
Synchrotron infrared imaging of advanced glycation endproducts (AGEs) in cardiac tissue from mice fed high glycemic diets
Birarda, Giovanni; Holman, Elizabeth A.; Fu, Shang; Weikel, Karen; Hu, Ping; Blankenberg, Francis G.; Holman, Hoi-Ying; Taylor, Allen
通讯作者Holman, HY
来源期刊BIOMEDICAL SPECTROSCOPY AND IMAGING
ISSN2212-8794
EISSN2212-8808
出版年2013
卷号2期号:4页码:301-315
英文摘要Recent research findings correlate an increased risk for dieases such as diabetes, macular degeneration and cardiovascular disease (CVD) with diets that rapidly raise the blood sugar levels; these diets are known as high glycemic index (GI) diets which include white breads, sodas and sweet deserts. Lower glycemia diets are usually rich in fruits, non-starchy vegetables and whole grain products. The goal of our study was to compare and contrast the effects of a low vs. high glycemic diet using the biochemical composition and microstructure of the heart. The improved spatial resolution and signal-to-noise for SR-FTIR obtained through the coupling of the bright synchrotron infrared photon source to an infrared spectral microscope enabled the molecular-level observation of diet-related changes within unfixed fresh frozen histologic sections of mouse cardiac tissue. High and low glycemic index (GI) diets were started at the age of five-months and continued for one year, with the diets only differing in their starch distribution (high GI diet = 100% amylopectin versus low GI diet = 30% amylopectin/70% amylose). Serial cryosections of cardiac tissue for SR-FTIR imaging alternated with adjacent hematoxylin and eosin (H&E) stained sections allowed not only fine-scale chemical analyses of glycogen and glycolipid accumulation along a vein as well as protein glycation hotspots co-localizing with collagen cold spots but also the tracking of morphological differences occurring in tandem with these chemical changes. As a result of the bright synchrotron infrared photon source coupling, we were able to provide significant molecular evidence for a positive correlation between protein glycation and collagen degradation in our mouse model. Our results bring a new insight not only to the effects of long-term GI dietary practices of the public but also to the molecular and chemical foundation behind the cardiovascular disease pathogenesis commonly seen in diabetic patients.
英文关键词AGE CVD diabetes fluorescence glycemia glycation infrared N center dot-(carboxymethyl) lysine PAGE pentosidine RAGE sugar
类型Article
语种英语
开放获取类型Bronze, Green Accepted
收录类别ESCI
WOS记录号WOS:000214729500005
WOS关键词END-PRODUCTS AGES ; OXIDATIVE STRESS ; CARDIOVASCULAR-DISEASE ; MACULAR DEGENERATION ; LIPID-PEROXIDATION ; CROSS-LINKING ; HEART-DISEASE ; DIABETIC-RAT ; MOUSE MODEL ; COLLAGEN
WOS类目Spectroscopy
WOS研究方向Spectroscopy
来源机构University of California, Berkeley
资源类型期刊论文
条目标识符http://119.78.100.177/qdio/handle/2XILL650/330303
作者单位[Birarda, Giovanni; Hu, Ping; Holman, Hoi-Ying] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Berkeley Synchrotron Infrared Struct Biol Program, Berkeley, CA 94720 USA; [Holman, Elizabeth A.; Blankenberg, Francis G.] Dept Radiol & Pediat, Mol Imaging Program, Stanford, CA USA; [Fu, Shang; Weikel, Karen; Taylor, Allen] Tufts Univ, Jean Mayer USDA HNRCA Tufts Univ, Lab Nutr & Vis Res, Boston, MA USA; [Weikel, Karen] Boston Univ, Boston Med Ctr, Sch Med, Boston, MA 02118 USA
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Birarda, Giovanni,Holman, Elizabeth A.,Fu, Shang,et al. Synchrotron infrared imaging of advanced glycation endproducts (AGEs) in cardiac tissue from mice fed high glycemic diets[J]. University of California, Berkeley,2013,2(4):301-315.
APA Birarda, Giovanni.,Holman, Elizabeth A..,Fu, Shang.,Weikel, Karen.,Hu, Ping.,...&Taylor, Allen.(2013).Synchrotron infrared imaging of advanced glycation endproducts (AGEs) in cardiac tissue from mice fed high glycemic diets.BIOMEDICAL SPECTROSCOPY AND IMAGING,2(4),301-315.
MLA Birarda, Giovanni,et al."Synchrotron infrared imaging of advanced glycation endproducts (AGEs) in cardiac tissue from mice fed high glycemic diets".BIOMEDICAL SPECTROSCOPY AND IMAGING 2.4(2013):301-315.
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