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树突状钙离子积聚和代谢型谷氨酸受体激活与海马CA1神经元中不依赖N-甲基-D-天冬氨酸受体的长时程增强相关。

Dendritic Ca2+ accumulations and metabotropic glutamate receptor activation associated with an N-methyl-D-aspartate receptor-independent long-term potentiation in hippocampal CA1 neurons.

作者信息

Petrozzino J J, Connor J A

机构信息

Roche Institute of Molecular Biology, Roche Research Center, Nutley, New Jersey 07110.

出版信息

Hippocampus. 1994 Oct;4(5):546-58. doi: 10.1002/hipo.450040504.

Abstract

Bathing hippocampal slices in the potassium channel blocker tetraethylammonium (TEA), while stimulating the Schaffer collaterals at a low frequency, induces Ca(2+)-dependent, N-methyl-D-aspartate (NMDA) receptor-independent long-term potentiation of synaptic transmission (LTPk) in CA1 neurons. We have combined ratio imaging of fura-2 and mag-fura-5 in hippocampal CA1 neurons with intracellular and field recordings to evaluate postsynaptic Ca2+ changes that occur in the induction of LTPk. Test stimuli were applied at 0.05 Hz to stratum radiatum in the presence of the NMDA receptor antagonists D,L-2-amino-5-phosphonovaleric acid (100 microM) or MK-801 (10 microM). During TEA exposure (15-25 mM; 10 min), cells fired prolonged action potentials both spontaneously and in response to test stimuli resulting in transient, micromolar Ca2+ accumulations in both somata and dendrites. The initial EPSP slope, measured 60 min after TEA wash-out, was potentiated to approximately 200% of control. The Ca2+ channel blocker nimodipine (10 microM) greatly reduced Ca2+ transients in both magnitude and duration and prevented LTPk induction. Pretreatment of slices with compounds that block metabotropic glutamate receptor (mGluR)-stimulated phosphoinositide hydrolysis, L-2-amino-3-phosphonopropionic acid (L-AP3, 50-200 microM) or L-aspartate-beta-hydroxamate (50-100 microM), as well as protein kinase C (PKC) inhibitors (sphingosine, 20 microM; RO-31-8220, 0.2 microM; or calphostin C, 2 microM) also blocked LTPk. Ca2+ transients were unaffected by L-AP3 or RO-31-8220. These findings suggest that Ca2+ influx through voltage-gated channels and co-activation of PKC by mGluRs are both necessary for induction of LTPk. Activation of mGluRs must also occur in NMDA receptor-dependent induction paradigms, but is possibly of lesser importance owing to the much greater gating of Ca2+ directly into the dendritic spines.

摘要

将海马体切片置于钾通道阻滞剂四乙铵(TEA)中,同时以低频刺激海马体传入通路,可诱导CA1神经元中依赖Ca(2+)、不依赖N-甲基-D-天冬氨酸(NMDA)受体的突触传递长时程增强(LTPk)。我们将海马体CA1神经元中fura-2和mag-fura-5的比率成像与细胞内记录和场记录相结合,以评估LTPk诱导过程中发生的突触后Ca2+变化。在存在NMDA受体拮抗剂D,L-2-氨基-5-磷酸戊酸(100 microM)或MK-801(10 microM)的情况下,以0.05 Hz的频率对辐射层施加测试刺激。在TEA暴露期间(15 - 25 mM;10分钟),细胞自发地以及对测试刺激产生延长的动作电位,导致胞体和树突中出现短暂的微摩尔级Ca2+积累。在TEA洗脱60分钟后测量的初始兴奋性突触后电位(EPSP)斜率增强至对照的约200%。Ca2+通道阻滞剂尼莫地平(10 microM)在幅度和持续时间上都大大降低了Ca2+瞬变,并阻止了LTPk的诱导。用阻断代谢型谷氨酸受体(mGluR)刺激的磷酸肌醇水解的化合物L-2-氨基-3-磷酸丙酸(L-AP3,50 - 200 microM)或L-天冬氨酸-β-羟肟酸(50 - 100 microM)以及蛋白激酶C(PKC)抑制剂(鞘氨醇,20 microM;RO-31-8220,0.2 microM;或钙磷蛋白C,2 microM)预处理切片也阻断了LTPk。Ca2+瞬变不受L-AP3或RO-31-8220的影响。这些发现表明,通过电压门控通道的Ca2+内流以及mGluRs对PKC的共同激活对于LTPk的诱导都是必需的。mGluRs的激活在依赖NMDA受体的诱导模式中也必定发生,但由于Ca2+直接进入树突棘的门控作用大得多,其重要性可能较小。

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