Institute for Experimental and Clinical Pharmacology and Toxicology, Friedrich-Alexander-University, Erlangen-Nuremberg, Fahrstr. 17, D-91054, Erlangen, Germany.
J Neurosci Methods. 2011 Feb 15;195(2):236-40. doi: 10.1016/j.jneumeth.2010.12.010. Epub 2010 Dec 14.
Most animal experiments in neurosciences require anesthesia of the experimental animal. For fMRI experiments most neuroscientist would prefer (I) a recoverable anesthesia that would (II) allow strong BOLD responses which are (III) reproducibly obtained for the same animal in repetitive experiments. Strong BOLD responses are particularly needed if weak physiological stimuli like whisker deflection are used. A-chloralose, in contrast to isoflurane, fulfils the need for strong activation but has been traditionally considered as a terminal drug due to its negative physiological side effects. Here it is demonstrated, that new commercial α-chloralose in a careful application scheme allows for repeated fMRI studies on the same animal with similar responses after whisker stimulation. Only minor effects on the normal behavior were observed between drugs. These include a longer time to return to baseline values of food ingestion and slower tail reaction for the α-chloralose experiments.
大多数神经科学的动物实验都需要对实验动物进行麻醉。对于 fMRI 实验,大多数神经科学家更倾向于(I)使用可恢复的麻醉剂,这种麻醉剂可以(II)产生强烈的 BOLD 反应,并且(III)在重复实验中能够稳定地在同一只动物身上获得。如果使用像胡须偏转这样微弱的生理刺激,就特别需要强烈的 BOLD 反应。相比之下,氯醛糖满足了强烈激活的需求,但由于其负面的生理副作用,传统上被认为是一种终末药物。在这里,研究表明,在精心设计的应用方案下,新型商业氯醛糖可在同一只动物上进行重复的 fMRI 研究,在刺激胡须后获得类似的反应。两种药物之间仅观察到对正常行为的微小影响。这些影响包括:(i)恢复到基线值的食物摄入时间延长,(ii)氯醛糖实验中尾巴反应变慢。