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ATP release from affinity-purified rat cholinergic nerve terminals.
Journal of Neurochemistry
|February 1, 1987
Summary
Cholinergic nerve terminals release adenosine triphosphate (ATP) and nucleosides dependent on calcium. Extracellular adenosine inhibits acetylcholine release, suggesting a regulatory role for purines.
Area of Science:
- Neuroscience
- Neurochemistry
- Cell Biology
Background:
- Cholinergic nerve terminals play a crucial role in neurotransmission.
- The release and metabolism of purines, such as adenosine triphosphate (ATP), at nerve terminals are not fully understood.
- Investigating purinergic signaling is important for understanding neuronal function and dysfunction.
Purpose of the Study:
- To investigate the release and metabolism of ATP and its derivatives from purified cholinergic nerve terminals.
- To explore the role of extracellular purines in regulating acetylcholine release.
- To characterize the uptake mechanism for adenosine in cholinergic terminals.
Main Methods:
- Affinity purification of cholinergic nerve terminals from rat caudate nucleus.
- Stimulation of terminals with KCl and veratridine to induce release.
- Measurement of released acetylcholine and ATP, and characterization of adenosine uptake and metabolism.
Main Results:
- ATP was released in a calcium-dependent manner upon stimulation, with a molar ratio of acetylcholine to ATP similar to that in vesicles.
- Extracellular ATP was rapidly metabolized to adenosine and inosine by ectonucleotidases.
- Cholinergic terminals possess a high-affinity adenosine uptake system, and adenosine was found to inhibit acetylcholine release via A1 receptors.
Conclusions:
- Cholinergic nerve terminals release ATP, which is subsequently metabolized to adenosine.
- Extracellular adenosine acts as an inhibitory modulator of acetylcholine release.
- Purinergic signaling plays a significant role in regulating cholinergic neurotransmission.