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J Physiol Volume 572, Number 3, 677-689, May 1, 2006 DOI: 10.1113/jphysiol.2005.103820
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Pharmacological comparison of swelling-activated excitatory amino acid release and Cl currents in cultured rat astrocytes

Iskandar F. Abdullaev1, Alena Rudkouskaya2, Gary P. Schools1, Harold K. Kimelberg1 and Alexander A. Mongin2

1 Ordway Research Institute, Albany, NY 12208, USA
2 Center for Neuropharmacology and Neuroscience, Albany Medical College, Albany, NY 12208, USA

Ubiquitously expressed volume-regulated anion channels (VRACs) are chloride channels which are permeable to a variety of small organic anions, including the excitatory amino acids (EAAs) glutamate and aspartate. Broad spectrum anion channel blockers strongly reduce EAA release in cerebral ischaemia and other pathological states associated with prominent astrocytic swelling. However, it is uncertain whether VRAC serves as a major pathway for EAA release from swollen cells. In the present study, we measured swelling-activated release of EAAs as D-[3H]aspartate efflux, and VRAC-mediated Cl currents by whole-cell patch clamp in cultured rat astrocytes. We compared the pharmacological profiles of the swelling-activated EAA release pathway and Cl currents. The expression of candidate Cl channels was confirmed by RT-PCR. The maxi Cl channel (p-VDAC) blocker Gd3+, the ClC-2 inhibitor Cd2+, and the MDR-1 blocker verapamil did not affect EAA release or VRAC currents. An antagonist of calcium-sensitive Cl channels (CaCC), niflumic acid, had little effect on EAA release and only partially inhibited swelling-activated Cl currents. The phorbol ester PDBu, which blocks ClC-3-mediated Cl currents, had no effect on VRAC currents and up-regulated EAA release. In contrast, DCPIB, which selectively inhibits VRACs, potently suppressed both EAA release and VRAC currents. Two other relatively selective VRAC inhibitors, tamoxifen and phloretin, also blocked the VRAC currents and strongly reduced EAA release. Taken together, our data suggest that (i) astrocytic volume-dependent EAA release is largely mediated by the VRAC, and (ii) the ClC-2, ClC-3, ClC-4, ClC-5, VDAC, CaCC, MDR-1 and CFTR gene products do not contribute to EAA permeability.

(Received 17 December 2005; accepted after revision 2 March 2006; first published online 9 March 2006)
Corresponding author A. A. Mongin: Center for Neuropharmacology and Neuroscience, Albany Medical College, 47 New Scotland Ave. (MC-136), Albany, NY 12208, USA. Email: mongina{at}mail.amc.edu




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