Ribeiro J A
Laboratory of Pharmacology, Gulbenkian Institute of Science, Oeiras, Portugal.
Pharmacol Toxicol. 1995 Nov;77(5):299-305. doi: 10.1111/j.1600-0773.1995.tb01031.x.
Neurotransmitter release and the role of adenosine in its regulation has been investigated for more than twenty years, and it is now widely accepted that adenosine tonically inhibits the release of excitatory neurotransmitters. This effect of adenosine is operated by an A1 adenosine receptor. Since activation of this receptor could inhibit Ca2+ conductance, increase K+ conductance, inhibit adenylate cyclase or phospholipase C, it is not clear if there is only one mechanism or several mechanisms operated by adenosine to inhibit neurotransmitter release, and in that case, what is the relative importance of each mechanism. The mechanism by which adenosine inhibits evoked synchronous transmitter release might be different from that used by the nucleoside to inhibit spontaneous asynchronous release. In some systems adenosine triphosphate per se acts like adenosine and inhibits neurotransmitter release. However, in most cases the inhibitory effect of this adenine nucleotide depends upon its hydrolysis into adenosine by a cascade of ectoenzymes, the last step being mediated by ecto-5'-nucleotidase.
神经递质释放以及腺苷在其调节中的作用已被研究了二十多年,目前人们普遍认为腺苷持续抑制兴奋性神经递质的释放。腺苷的这种作用是通过A1腺苷受体发挥的。由于该受体的激活可抑制Ca2+电导、增加K+电导、抑制腺苷酸环化酶或磷脂酶C,因此尚不清楚腺苷抑制神经递质释放是只有一种机制还是多种机制,若存在多种机制,每种机制的相对重要性又如何。腺苷抑制诱发的同步递质释放的机制可能与该核苷抑制自发异步释放的机制不同。在某些系统中,三磷酸腺苷本身的作用类似于腺苷,并抑制神经递质释放。然而,在大多数情况下,这种腺嘌呤核苷酸的抑制作用取决于其通过一系列胞外酶水解为腺苷,最后一步由胞外5'-核苷酸酶介导。