Unit of Nutritional Neuroscience, Laboratory of Nutrition and Metabolic Regulation, Institute of Nutrition and Food Technology (INTA), University of Chile, Santiago, Chile.
Brain Res Bull. 2010 Jul 30;82(5-6):284-8. doi: 10.1016/j.brainresbull.2010.05.010. Epub 2010 May 25.
beta-Adrenergic receptor stimulation can significantly facilitate synaptic potentiation in the hippocampus and enhance memory processes, but its effect on neocortical plastic mechanisms is less conclusive. In the present study we determined the effect of propranolol, a beta-adrenoceptor antagonist, on long-term potentiation (LTP) induced in vivo in rat occipital cortex by tetanizing stimulation of corpus callosum and observed a dose-dependent inhibition of LTP. We further administered propranolol through mini-osmotic pumps during 3 days, and observed the performance of rats in a complex operant conditioning learning paradigm and assessed the expression of brain-derived neurotrophic factor (BDNF) in the occipital cortex. Propranolol exposure depressed both the number of reinforced responses in the operant conditioning task and BDNF expression in occipital cortex. Taken together, our results suggest that propranolol impairs memory formation by inhibiting cortical LTP induction and associated BDNF expression.
β-肾上腺素能受体刺激可显著促进海马体的突触强化,并增强记忆过程,但它对新皮层可塑性机制的影响尚不确定。在本研究中,我们确定了β-肾上腺素受体拮抗剂普萘洛尔对通过刺激胼胝体引起的大鼠枕叶皮层体内长时程增强(LTP)的影响,并观察到 LTP 呈剂量依赖性抑制。我们进一步通过迷你渗透泵在 3 天内给予普萘洛尔,并观察大鼠在复杂操作性条件学习范式中的表现,并评估脑源性神经营养因子(BDNF)在枕叶皮层中的表达。普萘洛尔暴露抑制了操作性条件任务中强化反应的数量和枕叶皮层中 BDNF 的表达。综上所述,我们的结果表明,普萘洛尔通过抑制皮质 LTP 诱导和相关的 BDNF 表达来损害记忆形成。