Alkon D L, Sánchez-Andrés J V, Ito E, Oka K, Yoshioka T, Collin C
Neural Systems Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892.
Proc Natl Acad Sci U S A. 1992 Dec 15;89(24):11862-6. doi: 10.1073/pnas.89.24.11862.
For a constant membrane potential, a predominantly inhibitory GABAergic synaptic response is shown to undergo long-term transformation into an excitatory response after pairing of exogenous gamma-aminobutyric acid (GABA) with postsynaptic depolarization or pairing of pre- and postsynaptic stimulation. Current- and voltage-clamp experiments suggest that this synaptic transformation is due to a shift from a net increase of conductance to a net decrease of conductance in response to GABA. GABA-induced elevation of intracellular calcium is prolonged after the same stimulus pairing and may, therefore, contribute to this synaptic transformation via Ca(2+)-activated phosphorylation pathways. This synaptic transformation, which does not follow unpaired stimulus presentations, occurs in a neuronal compartment spatially separated from the soma, which also changes during stimulus pairing.
对于恒定的膜电位,在外源性γ-氨基丁酸(GABA)与突触后去极化配对或突触前和突触后刺激配对后,主要起抑制作用的GABA能突触反应会长期转变为兴奋反应。电流钳和电压钳实验表明,这种突触转变是由于对GABA的反应从电导净增加转变为电导净减少所致。在相同的刺激配对后,GABA诱导的细胞内钙升高会延长,因此可能通过钙激活的磷酸化途径促成这种突触转变。这种不跟随未配对刺激呈现的突触转变发生在与胞体在空间上分离的神经元区域,该区域在刺激配对过程中也会发生变化。