Premium
Gap junctional communication and pharmacological heterogeneity in astrocytes cultured from the rat striatum
Author(s) -
Venance Laurent,
Prémont Joël,
Glowinski Jacques,
Giaume Christian
Publication year - 1998
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1111/j.1469-7793.1998.429bk.x
Subject(s) - carbachol , gap junction , muscarinic acetylcholine receptor , endocrinology , chemistry , striatum , medicine , calcium , methoxamine , biophysics , biology , receptor , microbiology and biotechnology , biochemistry , agonist , dopamine , intracellular
1 Indo‐1 and fluo‐3 imaging techniques were used to investigate the role of gap junctions in the changes in cytosolic calcium concentrations ([Ca 2+ ] i ) induced by several receptor agonists. Subpopulations of confluent cultured astrocytes from the rat striatum were superfused with submaximal concentrations of endothelin‐1 (Et1) and the α1‐adrenergic and muscarinic receptor agonists, methoxamine and carbachol, respectively. 2 Combined binding and autoradiographic studies indicated that all striatal astrocytes possess binding sites for Et1. In contrast, α1‐adrenergic and muscarinic binding sites were found to be heterogeneously distributed. In agreement with these findings, Et1 induced fast calcium responses in all cells while only subsets of striatal astrocytes responded to the application of either methoxamine or carbachol. 3 Halothane, heptanol and octanol, which are commonly used as gap junction inhibitors, drastically reduced the amplitude of Et1‐induced calcium responses. In contrast, 18‐α‐glycyrrhetinic acid (αGA) used at a concentration known to block gap junction permeability in astrocytes had no significant effect on the amplitude of these calcium responses. 4 As demonstrated by quantitative and topological analysis, Et1 application similarly increased [Ca 2+ ] i levels in all astrocytes in both the absence and presence of αGA. 5 In control conditions, subpopulations of cells responding to methoxamine or carbachol exhibited two main types of calcium responses which differed in their shape and kinetic characteristics. In the presence of αGA the number of cells responding to these receptor agonists was significantly reduced. Indeed, responses characterized by their long latency, slow rise time and weak amplitude disappeared in the presence of αGA while responses with short latency and fast rise time were preserved. 6 These results indicate that permeable gap junction channels tend to attenuate the pharmacological and functional heterogeneity of populations of astrocytes, while their inhibition restricts calcium responses in astrocytes expressing high densities of transmitter receptors coupled to phospholipase C.