Long-term potentiation (LTP) can be induced in the lateral and basolat-era1 amygdala by stimulating synaptic afferents in the external capsule (EC). We examined the sensitivity of amygdaloid LTP to the NMDA receptor antagonist 2-amino-5phosphonopentanoate (AP5), which is known to block LTP induction
Long-term potentiation in the avian hippocampus does not require activation of the N-methyl-D-aspartate (NMDA) receptor
✍ Scribed by Andrzej Wieraszko; Gregory F. Ball
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 642 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0887-4476
No coin nor oath required. For personal study only.
✦ Synopsis
Evoked potentials recorded from slices of pigeon hippocampus were reversibly attenuated by 2 mM kynurenic acid. High frequency stimulation (3 x 200 Hz for 1 sec, with 1 sec intervals) evoked a persistent increase in the evoked potential, lasting in a nondecremental form for at least 2 hr. This increase in the magnitude of the potential was not blocked by antagonists of the NMDA receptor (APV and MK-801). These data suggest that the synaptic facilitation observed in the pigeon hippocampus, which appears to be a form of long-term potentiation, does not depend on the activation of NMDA receptors.
📜 SIMILAR VOLUMES
## Abstract Zinc is an endogenous N‐methyl‐D‐aspartate (NMDA) receptor blocker. It is possible that zinc‐mediated modification of hippocampal CA1 long‐term potentiation (LTP) is linked to the expression of NMDA receptor subunits, which varies with postnatal development. In the present study, the ef
## Abstract Among the different steroids found in the brain, pregnenolone sulfate (3β‐hydroxy‐5‐pregnen‐20‐one‐3‐sulfate; PREGS) is known to enhance hippocampal‐associated memory. The present study employs rat hippocampal slices to investigate the ability of PREGS to modulate long‐term potentiation
The effects of short-period ( 2 min) perfusion of conditioning solution, which contains N-methyl-D-aspartate (NMDA), glycine, and spermine, on the synaptic transmission in the Schaffer collateral-commissural pathway were examined in hippocampal slices with the intracellular recording technique. Long
## Abstract The objective of this study was to test whether postnatal chronic inflammation resulted in altered reactivity to pain later in life when reexposed to the same inflammatory agent and whether this alteration correlated with brain‐region‐specific patterns of N‐methyl‐D‐aspartate (NMDA) rec