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The study investigated the impact of dietary bicarbonate (KHCO3) on potassium secretion machinery in mice. It was found that high KHCO3 diets increased urinary K+ excretion and trans-tubular K+ gradient more than high KCl diets, upregulating key potassium-secretory transporters ENaC and ROMK in principal cells, and BK, pendrin, and KCC3a in pendrin-positive IC cells. The mechanism prevents hyperkalemia and alkalosis with alkaline-ash-rich diets but may lead to potassium wasting and hypokalemia in alkalosis.
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