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<p>to enter the cell. This in turn depolarizes the cell and opens voltage-gated calcium channels, flooding the cell with positive calcium ions and leading to <a href="page.php?w=neurotransmitter">neurotransmitter</a> release. ENaC can be blocked by the drug <a href="page.php?w=amiloride">amiloride</a> in many mammals, particularly rats. The sensitivity of the low-salt taste to amiloride in humans is much less pronounced, leading to speculation that there may be additional low-salt receptors besides ENaC to be discovered.</p>

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