TRADITIONAL POSTER - ismrm
TRADITIONAL POSTER - ismrm
TRADITIONAL POSTER - ismrm
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Poster Sessions<br />
2401. Increased Brain Lactate Transport and Metabolism During Hypoglycemia in Rats Fed a Ketogenic<br />
Diet<br />
Henk M. De Feyter 1 , Kevin Behar 1 , Lester R. Drewes 2 , Robin A. de Graaf 1 , Douglas L. Rothman 1<br />
1 Diagnostic Radiology, Yale University, New Haven, CT, United States; 2 Biochemistry & Molecular Biology, University of<br />
Minnesota, Duluth, MN, United States<br />
Repetitive iatrogenic hypoglycemic events lead to brain adaptations resulting in failing counterregulatory response and lack of warning symptoms<br />
(hypoglycemia unawareness) normally associated with low blood glucose levels. Increased blood-brain barrier lactate transport via upregulated<br />
monocarboxylic acid transporter 1 (MCT1) has been suggested as an adaptation induced by repetitive hypoglycemia. Increased lactate uptake and oxidation<br />
could (partially) replace glucose thereby contribute to hypoglycemia unawareness and failing counterregulatory response. We used 1 H-[ 13 C] MRS combined<br />
with [3- 13 C]-lactate infusion during hypoglycemia to investigate the role of increased lactate transport and/or metabolism in the brain of a rat model with<br />
ketogenic diet-induced upregulation of MCT1.<br />
2402. Acute Flupirtine Administration Reduces Glutamate/glutamine Ratio in Rat Hippocampus<br />
Renuka Sriram 1 , Robert J. Mather 2 , Serguei Liachenko 1<br />
1 BioImaging CoE, Pfizer Inc, Groton, CT, United States; 2 Neuroscience, Pfizer Inc, Groton, CT, United States<br />
Neurotransmitter levels of glutamate and glutamine are tightly coupled with modulation of one resulting in a corresponding opposing change in the other.<br />
Since glutamate is implicated in a variety of neurological disorders, the observation of an endogenous pool of glutamate (Glu) and glutamine (Gln) and/or its<br />
ratio can serve as a strong mechanistic biomarker and measure of efficacy. Flupirtine, a potassium channel opener, has been shown to cause decrease in Glu<br />
and a relative increase in Gln in the rat hippocampus.<br />
2403. 1H MRS Profiling at 9.4T in Prefrontal Cortex and Hippocampus of Ethanol Dependent Rats During<br />
Intoxication, Withdrawal and Protracted Abstinence<br />
Wolfgang Weber-Fahr 1 , Gabriele Ende 1 , Alexander Sartorius 1 , Rainer Spanagel 2 , Claudia Falfan-<br />
Melgoza 1 , Dirk Cleppien 1 , Wolfgang H. Sommer 2<br />
1 Neuroimaging, Central Institute of Mental Health, Mannheim, NA, Germany; 2 Dept. Psychopharmacology, Central Institute of<br />
Mental Health, Mannheim, NA, Germany<br />
Out of a group of 17 animals eight were made dependent by 7 weeks ethanol vapor exposure with peak levels up to 4 g/l blood alcohol concentration. We<br />
assessed metabolic profiles in two brain regions with functional importance for dependence, i.e. medial prefrontal cortex and hippocampus, using in vivo<br />
single-voxel 1H magnetic resonance spectroscopy at TE=10 ms on a 9.4T scanner. Animals were measured up to 5 times before during and after ethanol<br />
exposure. Reduced myoinositol and N-acetylaspartate levels as well as increased choline-containing compounds were found during intoxication. Raised<br />
glutamate levels were found during early withdrawal.<br />
2404. Brain Neurochemical Effects of Long-Term Sleep Fragmentation Investigated in Mice at 14.1T Using<br />
1H-MRS<br />
Nathalie Just 1,2 , Maxime Baud 3 , Jean-Marie Petit 3 , Pierre Magistretti 3,4 , Rolf Gruetter 1,5<br />
1 LIFMET, CIBM, EPFL, Lausanne, Switzerland; 2 Department of Radiology, UNIL, Lausanne, Switzerland; 3 Laboratoire de<br />
neuroénergétique et dynamique cellulaire, EPFL, Lausanne, Switzerland; 4 Brain and Mind Institute, Lausanne, Switzerland;<br />
5 Department of Radiology, UNIL and HUG, Lausanne and Geneva, Switzerland<br />
The present study examined the effects of sleep fragmentation (SF) in the hippocampus and the cortex of mice using proton MR spectroscopy at 14.1T.<br />
Disruptions in brain sensory processing and cognitive performance were seen during sleep fragmentation. Moreover, there is evidence that SF negatively<br />
affects memory and learning. Here, significant decreases in GABA and Lactate concentrations were detected in the hippocampus of mice following sleep<br />
fragmentation indicating decreased synaptic function in the hippocampus.<br />
2405. Regional Variations of Metabolite Concentrations in the Rat Brain Assessed with in Vivo 1 H MR<br />
Spectroscopy at 16.4T<br />
Sung-Tak Hong 1 , Dávid Zsolt Balla 1 , Gunamony Shajan 1 , Changho Choi 2 , Rolf Pohmann 1<br />
1 High-Field Magnetic Resonance Center , Max-Planck Institute for Biological Cybernetics, Tuebingen, Baden-Wuerttemberg,<br />
Germany; 2 Advanced Imaging Research Center, University of Texas Southwestern Medical Center, Dallas, TX, United States<br />
Regional differences of metabolites in the rat brain were investigated by using localized in vivo 1H MR spectroscopy at 16.4T. Three regions, thalamus,<br />
striatum and hippocampus, were investigated with an ultra-short TE STEAM sequence. The results demonstrated significant variations in all metabolites<br />
except aspartate and NAA. The remarkable variation of spectra was the substantially decreased level of the Tau methylene signal at 3.25 ppm in thalamus.<br />
The significant increase of the GABA methylene signal at 1.89 ppm was also observed in thalamus.<br />
2406. Measurement of the Effects of Different Anesthetics in the Rat Thalamus by in Vivo 1 H NMR<br />
Spectroscopy at 16.4T<br />
Sung-Tak Hong 1 , Chi-Bong Choi 2 , Rolf Pohmann 1<br />
1 High-Field Magnetic Resonance Center , Max-Planck Institute for Biological Cybernetics, Tuebingen, Baden-Wuerttemberg,<br />
Germany; 2 Department of Radiology, Kyung Hee University Medical Center, Hoekidong, Seoul, Korea, Republic of<br />
The effect of different anesthetic agents was investigated in the rat brain by using in vivo 1H NMR spectroscopy. A volume-of-interest was placed in<br />
thalamus under two different anesthesia, isoflurane and ketamine/xylazine. The significant increase of glucose was observed in a deep ketamine/xylazine<br />
anesthesia while additional metabolic variations on ascorbate, aspartate, glutathione and lactate were detected.