Title

Arachidonic acid reversibly enhances N-type calcium current at an extracellular site

UMMS Affiliation

Program in Cellular and Molecular Physiology

Date

4-5-2001

Document Type

Article

Subjects

Animals; Animals, Newborn; Arachidonic Acid; Calcium Channel Agonists; Cell Membrane; Cells, Cultured; Guanosine Diphosphate; Kinetics; Membrane Potentials; Neurons; Pyrroles; Rats; Rats, Sprague-Dawley; Serum Albumin, Bovine; Superior Cervical Ganglion; Tetrodotoxin; Thionucleotides; omega-Conotoxin GVIA

Disciplines

Life Sciences | Medicine and Health Sciences

Abstract

We examined the effects of arachidonic acid (AA) on whole cell Ca(2+) channel activity in rat superior cervical ganglion neurons. Our companion paper (Liu L, Barrett CF, and Rittenhouse AR. Am J Physiol Cell Physiol 280: C1293-C1305, 2001) demonstrates that AA induces several effects, including enhancement of current amplitude at negative voltages, and increased activation kinetics. This study examines the mechanisms underlying these effects. First, enhancement is rapidly reversible by bath application of BSA. Second, enhancement appears to occur extracellularly, since intracellular albumin was without effect on enhancement, and bath-applied arachidonoyl coenzyme A, an amphiphilic AA analog that cannot cross the cell membrane, mimicked enhancement. In addition, enhancement is voltage dependent, in that currents were enhanced to the greatest degree at -10 mV, whereas virtually no enhancement occurred positive of +30 mV. We also demonstrate that AA-induced increases in activation kinetics are correlated with enhancement of current amplitude. An observed increase in the voltage sensitivity may underlie these effects. Finally, the majority of enhancement is mediated through N-type current, thus providing the first demonstration that this current type can be enhanced by AA.

Rights and Permissions

Citation: Am J Physiol Cell Physiol. 2001 May;280(5):C1306-18.

Related Resources

Link to article in PubMed

Journal Title

American journal of physiology. Cell physiology

PubMed ID

11287344