دورية أكاديمية

High-Resolution Magnetic Resonance Imaging Quantitatively Detects Individual Pancreatic Islets.

التفاصيل البيبلوغرافية
العنوان: High-Resolution Magnetic Resonance Imaging Quantitatively Detects Individual Pancreatic Islets.
المؤلفون: Lamprianou, Smaragda, Immonen, Riikka, Nabuurs, Christine, Gjinovci, Asllan, Vinet, Laurent, Montet, Xavier C. R., Gruetter, Rolf, Meda, Paolo
المصدر: Diabetes; Nov2011, Vol. 60 Issue 11, p2853-2860, 8p, 3 Color Photographs, 2 Graphs
مصطلحات موضوعية: LIVER cells, MAGNETIC resonance imaging, PHAGOCYTES, MITOCHONDRIA, OXIDASES, MICE
مستخلص: OBJECTIVE--We studied whether manganese-enhanced high- field magnetic resonance (MR) imaging (MEHFMRI) could quantitatively detect individual islets in situ and in vivo and evaluate changes in a model of experimental diabetes. RESEARCH DESIGN AND METHODS--Whole pancreata from untreated (n = 3), MnCl2 and glucose-injected mice (n = 6), and mice injected with either streptozotocin (STZ; n = 4) or citrate buffer (n = 4) were imaged ex vivo for unambiguous evaluation of islets. Exteriorized pancreata of MnCl2 and glucose-injected mice (n = 6) were imaged in vivo to directly visualize the gland and minimize movements. In all cases, MR images were acquired in a 14.1 Tesla scanner and correlated with the corresponding (immuno)histological sections. RESULTS--In ex vivo experiments, MEHFMRI distinguished different pancreatic tissues and evaluated the relative abundance of islets in the pancreata of normoglycemic mice. MEHFMRI also detected a significant decrease in the numerical and volume density of islets in STZ-injected mice. However, in the latter measurements the loss of β-cells was undervalued under the conditions tested. The experiments on the externalized pancreata confirmed that MEHFMRI could visualize native individual islets in living, anesthetized mice. CONCLUSIONS--Data show that MEHFMRI quantitatively visualizes individual islets in the intact mouse pancreas, both ex vivo and in vivo. [ABSTRACT FROM AUTHOR]
Copyright of Diabetes is the property of American Diabetes Association and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
قاعدة البيانات: Complementary Index
الوصف
تدمد:00121797
DOI:10.2337/db11-0726