预突触量子大小增强可以抵消前性释放后抑郁症
Anu G Nair1,2,3, Nasrin Bollmohr1,4, Levin Schökle1
1Department of Molecular Life Sciences, University of Zurich, Zurich, Switzerland.
The Journal of physiology
|August 26, 2024
概括
在高频刺激后,突触传输仍然很强大,这是由于突触前前量子尺寸的增加,可能来自较大的囊泡,这平衡了囊泡耗尽. 这种机制在刺激后的几分钟内稳定了突触功效.
科学领域:
- 神经科学是一个神经科学.
- 突触性可塑性 突触性可塑性
- 细胞生理学 细胞生理学
背景情况:
- 重复的突触刺激可以通过耗尽资源来损害传播.
- 在高频刺激后稳定突触传输的机制尚不清楚.
- 强大的突触传输对于神经系统功能至关重要,尽管资源有限.
研究的目的:
- 研究高频刺激后突触传输如何稳定.
- 阐明Drosophila神经肌肉结 (NMJ) 中突触稳定的分子机制.
- 确定在分钟时间尺度上促进突触传输稳健性的因素.
主要方法:
- 德洛索菲拉NMJ的性刺激.
- 量子含量,量子大小和囊泡池大小测量.
- 对突触囊泡密度,直径和突触后反应的分析.
- 关键蛋白质 (动氨酸,H+-ATPase,谷氨酸受体) 的遗传和药理上的干扰.
主要成果:
- 性刺激降低了量子含量和囊泡池大小,但增加了量子大小.
- 动作潜能引起的传输基本保持不变,表明稳定.
- 量子尺寸的增加是由前突触驱动的,涉及更大的突触囊泡,以及平衡释放抑郁.
结论:
- 由较大的突触囊泡介导的前突触驱动的量子尺寸增加,在高频刺激后稳定突触传输.
- 这种机制通过抵消释放抑制来增强分钟时间尺度上的突触强度.
- 这些发现为持续的神经活动后的突触稳定机制提供了新的见解.
更多相关视频
09:51Recording Synaptic Plasticity in Acute Hippocampal Slices Maintained in a Small-volume Recycling-, Perfusion-, and Submersion-type Chamber System
Published on: January 1, 2018
11.6K
18:11Quantifying Synapses: an Immunocytochemistry-based Assay to Quantify Synapse Number
Published on: November 16, 2010
35.7K
相关概念视频
Integration of Synaptic Events
1.5K
Synaptic integration mainly includes the summation of graded potentials. Graded potentials, regardless of their type, cause subtle alterations in membrane voltage, resulting in either depolarization or hyperpolarization. These incremental changes, when combined or summed, can propel the neuron toward its threshold. Consider, for example, a membrane experiencing a +15 mV shift, causing it to depolarize from -70 mV to -55 mV. In this scenario, graded potentials govern the membrane's ability to...
1.5K
Chemical Synapses
8.8K
Chemical synapses are specialized sites between two neurons or between a neuron and a non-neuronal cell like a muscle, glandular or sensory cell.
Because chemical synapses depend on the release of neurotransmitter molecules from synaptic vesicles to pass on their signal, there is an approximately one millisecond delay between when the axon potential reaches the presynaptic terminal and when the neurotransmitter leads to opening of postsynaptic ion channels. Additionally, this signaling is...
Because chemical synapses depend on the release of neurotransmitter molecules from synaptic vesicles to pass on their signal, there is an approximately one millisecond delay between when the axon potential reaches the presynaptic terminal and when the neurotransmitter leads to opening of postsynaptic ion channels. Additionally, this signaling is...
8.8K
Excitatory and Inhibitory Effects of Neurotransmitters
9.9K
When an action potential reaches the presynaptic axon terminal, it releases neurotransmitters from the neuron into the synaptic cleft at a chemical synapse. The released neurotransmitter can be excitatory or inhibitory. The critical criteria commonly used to determine whether a molecule is a neurotransmitter at a chemical synapse are the molecule's presence in the presynaptic neuron. Second, its release is in response to strong presynaptic depolarization. And lastly, the presence of...
9.9K
Long-term Depression
30.7K
Long-term depression, or LTD, is one of the ways by which synaptic plasticity—changes in the strength of chemical synapses—can occur in the brain. LTD is the process of synaptic weakening that occurs over time between pre and postsynaptic neuronal connections. The synaptic weakening of LTD works in opposition to synaptic strengthening by long-term potentiation (LTP) and together are the main mechanisms that underlie learning and memory.
30.7K
Postsynaptic Potential (PSP)
2.4K
Postsynaptic potential (PSP) refers to a change in the electrical potential of a neuron when neurotransmitters released by presynaptic neurons bind to postsynaptic receptors. This potential can either be excitatory, leading to depolarization and ultimately action potential generation, or inhibitory, leading to hyperpolarization and suppression of the postsynaptic neuron.
There are two types of receptors: ionotropic and metabotropic.
The ionotropic receptor is the membrane protein that has an...
There are two types of receptors: ionotropic and metabotropic.
The ionotropic receptor is the membrane protein that has an...
2.4K
Long-term Potentiation
55.0K
Long-term potentiation, or LTP, is one of the ways by which synaptic plasticity—changes in the strength of chemical synapses—can occur in the brain. LTP is the process of synaptic strengthening that occurs over time between pre- and postsynaptic neuronal connections. The synaptic strengthening of LTP works in opposition to the synaptic weakening of long-term depression (LTD) and together are the main mechanisms that underlie learning and memory.
55.0K
