Anaesthesia for positron emission tomography scanning of animal brains

被引:60
作者
Alstrup, Aage Kristian Olsen [1 ,2 ]
Smith, Donald F. [3 ]
机构
[1] Aarhus Univ Hosp, Dept Nucl Med, DK-8000 Aarhus C, Denmark
[2] Aarhus Univ Hosp, PET Ctr, DK-8000 Aarhus C, Denmark
[3] Aarhus Univ, Hosp Psychiat, Ctr Psychiat Res, DK-8240 Risskov, Denmark
关键词
Anaesthesia; brain imaging; cerebral blood flow (CBF); neuroscience; neurotransmission; microPET; positron emission tomography; radiotracer; CEREBRAL-BLOOD-FLOW; IN-VIVO EVALUATION; RECEPTOR-BINDING; ACETYLCHOLINE-RECEPTORS; BIOLOGICAL EVALUATION; DOPAMINE TRANSPORTER; COMPUTED-TOMOGRAPHY; REBOXETINE ANALOGS; PARAMETRIC IMAGES; EX-VIVO;
D O I
10.1258/la.2012.011173
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Positron emission tomography (PET) provides a means of studying physiological and pharmacological processes as they occur in the living brain. Mice, rats, dogs, cats, pigs and non-human primates are often used in studies using PET. They are commonly anaesthetized with ketamine, propofol or isoflurane in order to prevent them from moving during the imaging procedure. The use of anaesthesia in PET studies suffers, however, from the drawback of possibly altering central neuromolecular mechanisms. As a result, PET findings obtained in anaesthetized animals may fail to correctly represent normal properties of the awake brain. Here, we review findings of PET studies carried out either in both awake and anaesthetized animals or in animals given at least two different anaesthetics. Such studies provide a means of estimating the extent to which anaesthesia affects the outcome of PET neuroimaging in animals. While no final conclusion can be drawn concerning the 'best' general anaesthetic for PET neuroimaging in laboratory animals, such studies provide findings that can enhance an understanding of neurobiological mechanisms in the living brain.
引用
收藏
页码:12 / 18
页数:7
相关论文
共 87 条
[1]   CEREBRAL PHARMACODYNAMICS OF ANESTHETIC AND SUBANAESTHETIC DOSES OF KETAMINE IN THE NORMOVENTILATED PIG [J].
AKESON, J ;
BJORKMAN, S ;
MESSETER, K ;
ROSEN, I ;
HELFER, M .
ACTA ANAESTHESIOLOGICA SCANDINAVICA, 1993, 37 (02) :211-218
[2]  
Alstrup AKO, 2011, SCAND J LAB ANIM SCI, V38, P195
[3]   Anesthesia in animal imaging: Differing effects of propofol versus isoflurane on dopamine 1 receptor binding in Gottingen minipig brain [J].
Alstrup, Aage Kristian Olsen ;
Jakobsen, Steen ;
Wegener, Gregers ;
Hansen, Axel Kornerup ;
Doudet, Doris J. ;
Landau, Anne M. .
NEUROIMAGE, 2010, 52 :S181-S181
[4]  
Alstrup AKO, 2009, SCAND J LAB ANIM SCI, V36, P55
[5]  
Alstrup AKO, 2012, SCAND J LAB IN PRESS
[6]   Cholinergic modulation of food and drug satiety and withdrawal [J].
Avena, Nicole M. ;
Rada, Pedro V. .
PHYSIOLOGY & BEHAVIOR, 2012, 106 (03) :332-336
[7]   Mood stabilizers target cellular plasticity and resilience cascades - Implications for the development of novel therapeutics [J].
Bachmann, RF ;
Schloesser, RJ ;
Gould, TD ;
Manji, HK .
MOLECULAR NEUROBIOLOGY, 2005, 32 (02) :173-202
[8]   New approaches to antidepressant drug discovery: beyond monoamines [J].
Berton, O ;
Nestler, EJ .
NATURE REVIEWS NEUROSCIENCE, 2006, 7 (02) :137-151
[9]   Awake nonhuman primate brain PET imaging without head restraint [J].
Carson, Richard E. ;
Sandiego, Christine ;
Mulnix, Tim ;
Jin, Xiao ;
Fowles, Krista ;
Liddie, Shervin ;
Ford, Siobhan ;
Weinzimmer, David ;
Campbell, David W. ;
Abbott, Amanda ;
Laruelle, Marc ;
Gunn, Roger N. ;
Ashburner, Sharon ;
Rabiner, Eugenii A. ;
Castner, Stacy A. ;
Williams, Graham V. .
NEUROIMAGE, 2010, 52 :S18-S18
[10]   RESTRAINT STRESS MODULATES SENSORY EVOKED-POTENTIALS [J].
CASADA, JH ;
DAFNY, N .
INTERNATIONAL JOURNAL OF NEUROSCIENCE, 1990, 53 (2-4) :265-274