Brundege J M, Dunwiddie T V
Department of Pharmacology, University of Colorado Health Science Center, Denver 80262, USA.
Neuroreport. 1998 Sep 14;9(13):3007-11. doi: 10.1097/00001756-199809140-00016.
The mechanisms that regulate adenosine release in the brain are not well understood. The present study investigated the hypothesis that individual neurons can generate and release sufficient adenosine to regulate their synaptic inputs. We utilized the whole-cell recording technique to apply enzyme inhibitors and nucleotides directly into the cytoplasm of single rat hippocampal CA1 pyramidal neurons. Cytoplasmic delivery of adenosine induced the release of sufficient adenosine to inhibit excitatory synaptic inputs. However, intracellular delivery of nucleotides and enzyme inhibitors failed to increase adenosine receptor-mediated inhibition. These data suggest that while pyramidal neurons in the hippocampus are capable of releasing large amounts of adenosine into the extracellular space, they do not readily form adenosine from endogenous sources.
大脑中调节腺苷释放的机制尚未完全明确。本研究探讨了一个假说,即单个神经元能够产生并释放足够的腺苷来调节其突触输入。我们利用全细胞记录技术,将酶抑制剂和核苷酸直接应用于单个大鼠海马CA1锥体神经元的细胞质中。向细胞质中递送腺苷可诱导释放足够的腺苷以抑制兴奋性突触输入。然而,向细胞内递送核苷酸和酶抑制剂未能增强腺苷受体介导的抑制作用。这些数据表明,虽然海马体中的锥体神经元能够向细胞外空间释放大量腺苷,但它们不易从内源性来源形成腺苷。