<scp>N</scp>‐arachidonoyl glycine suppresses <scp><scp>Na<sup>+</sup></scp></scp>/<scp><scp>Ca<sup>2+</sup></scp></scp> exchanger‐mediated <scp><scp>Ca<sup>2+</sup></scp></scp> entry into endothelial cells and activates <scp>BK<sub>Ca</sub></scp> channels independently of <scp>GPCR</scp>s
British journal of pharmacology