{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,28]],"date-time":"2026-10-28T22:58:39Z","timestamp":1793228319358,"version":"4.5.0"},"reference-count":46,"publisher":"American Physiological Society","issue":"3","funder":[{"name":"NIH","award":["DK 54983"],"award-info":[{"award-number":["DK 54983"]}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["American Journal of Physiology-Renal Physiology"],"published-print":{"date-parts":[[2019,3,1]]},"abstract":"<jats:p>The aim of this mini review is to provide an overview regarding the role of inwardly rectifying potassium channel 4.1 (Kir4.1)\/Kir5.1 in regulating renal K<jats:sup>+<\/jats:sup>excretion. Deletion of Kir4.1 in the kidney inhibited thiazide-sensitive NaCl cotransporter (NCC) activity in the distal convoluted tubule (DCT) and slightly suppressed Na-K-2Cl cotransporter (NKCC2) function in the thick ascending limb (TAL). Moreover, increased dietary K<jats:sup>+<\/jats:sup>intake inhibited, whereas decreased dietary K<jats:sup>+<\/jats:sup>intake stimulated, the basolateral potassium channel (a Kir4.1\/Kir5.1 heterotetramer) in the DCT. The alteration of basolateral potassium conductance is essential for the effect of dietary K<jats:sup>+<\/jats:sup>intake on NCC because deletion of Kir4.1 in the DCT abolished the effect of dietary K<jats:sup>+<\/jats:sup>intake on NCC. Since potassium intake-mediated regulation of NCC plays a key role in regulating renal K<jats:sup>+<\/jats:sup>excretion and potassium homeostasis, the deletion of Kir4.1 caused severe hypokalemia and metabolic alkalosis under control conditions and even during increased dietary K<jats:sup>+<\/jats:sup>intake. Finally, recent studies have suggested that the angiotensin II type 2 receptor (AT2R) and bradykinin-B2 receptor (BK2R) are involved in mediating the effect of high dietary K<jats:sup>+<\/jats:sup>intake on Kir4.1\/Kir5.1 in the DCT.<\/jats:p>","DOI":"10.1152\/ajprenal.00412.2018","type":"journal-article","created":{"date-parts":[[2019,1,9]],"date-time":"2019-01-09T12:48:43Z","timestamp":1547038123000},"page":"F582-F586","source":"Crossref","is-referenced-by-count":65,"title":["Kir4.1\/Kir5.1 in the DCT plays a role in the regulation of renal K<sup>+<\/sup>excretion"],"prefix":"10.1152","volume":"316","author":[{"given":"Xiao-Tong","family":"Su","sequence":"first","affiliation":[{"name":"Department of Pharmacology, New York Medical College, Valhalla, New York"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-2915-265X","authenticated-orcid":false,"given":"David H.","family":"Ellison","sequence":"additional","affiliation":[{"name":"Division 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