Role of Angiotensin II Type 1a Receptor (AT1aR) of Renal Tubules in Regulating Inwardly Rectifying Potassium Channels 4.2 (Kir4.2), Kir4.1, and Epithelial Na

amiloride angiotensin II genotype knockout mice perfusion

Journal

Hypertension (Dallas, Tex. : 1979)
ISSN: 1524-4563
Titre abrégé: Hypertension
Pays: United States
ID NLM: 7906255

Informations de publication

Date de publication:
01 Nov 2023
Historique:
medline: 1 11 2023
pubmed: 1 11 2023
entrez: 1 11 2023
Statut: aheadofprint

Résumé

Kir4.2 and Kir4.1 play a role in regulating membrane transport in the proximal tubule (PT) and in the distal-convoluted-tubule (DCT), respectively. We generated kidney-tubule-specific-AT1aR-knockout (Ks-AT1aR-KO) mice to examine whether renal AT1aR regulates Kir4.2 and Kir4.1. Ks-AT1aR-KO mice had a lower systolic blood pressure than AT1aR determines the baseline membrane potential of PT by controlling Kir4.2 expression/activity but AT1aR is not required for determining the baseline membrane potential of the DCT and Kir4.1/Kir5.1 activity/expression. However, AT1aR is required for angiotensin II-induced hyperpolarization of basolateral membrane of PT and DCT. Deletion of AT1aR had no effect on baseline renal outer medullary potassium channel activity but increased ENaC activity in the CCD.

Sections du résumé

BACKGROUND BACKGROUND
Kir4.2 and Kir4.1 play a role in regulating membrane transport in the proximal tubule (PT) and in the distal-convoluted-tubule (DCT), respectively.
METHODS METHODS
We generated kidney-tubule-specific-AT1aR-knockout (Ks-AT1aR-KO) mice to examine whether renal AT1aR regulates Kir4.2 and Kir4.1.
RESULTS RESULTS
Ks-AT1aR-KO mice had a lower systolic blood pressure than
CONCLUSIONS CONCLUSIONS
AT1aR determines the baseline membrane potential of PT by controlling Kir4.2 expression/activity but AT1aR is not required for determining the baseline membrane potential of the DCT and Kir4.1/Kir5.1 activity/expression. However, AT1aR is required for angiotensin II-induced hyperpolarization of basolateral membrane of PT and DCT. Deletion of AT1aR had no effect on baseline renal outer medullary potassium channel activity but increased ENaC activity in the CCD.

Identifiants

pubmed: 37909221
doi: 10.1161/HYPERTENSIONAHA.123.21389
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Xin-Peng Duan (XP)

Department of Physiology, Xuzhou Medical University, China (X.-P.D.).
Department of Pharmacology, New York Medical College, Valhalla (X.-P.D., Y.X., J.-Y.Z., D.-H.L., W.-H.W.).

Yu Xiao (Y)

Department of Physiology, Qiqihar Medical College, Heilongjiang, China (Y.X.).
Department of Pharmacology, New York Medical College, Valhalla (X.-P.D., Y.X., J.-Y.Z., D.-H.L., W.-H.W.).

Xiao-Tong Su (XT)

Department of Medicine, Oregon Health & Science University, Portland (X.-T.S., S.G., J.E., C.-L.Y., J.M., D.H.E.).

Jun-Ya Zheng (JY)

Department of Pharmacology, New York Medical College, Valhalla (X.-P.D., Y.X., J.-Y.Z., D.-H.L., W.-H.W.).

Susan Gurley (S)

Department of Medicine, Oregon Health & Science University, Portland (X.-T.S., S.G., J.E., C.-L.Y., J.M., D.H.E.).

Jacqueline Emathinger (J)

Department of Medicine, Oregon Health & Science University, Portland (X.-T.S., S.G., J.E., C.-L.Y., J.M., D.H.E.).

Chao-Ling Yang (CL)

Department of Medicine, Oregon Health & Science University, Portland (X.-T.S., S.G., J.E., C.-L.Y., J.M., D.H.E.).

James McCormick (J)

Department of Medicine, Oregon Health & Science University, Portland (X.-T.S., S.G., J.E., C.-L.Y., J.M., D.H.E.).

David H Ellison (DH)

Department of Medicine, Oregon Health & Science University, Portland (X.-T.S., S.G., J.E., C.-L.Y., J.M., D.H.E.).

Dao-Hong Lin (DH)

Department of Pharmacology, New York Medical College, Valhalla (X.-P.D., Y.X., J.-Y.Z., D.-H.L., W.-H.W.).

Wen-Hui Wang (WH)

Department of Pharmacology, New York Medical College, Valhalla (X.-P.D., Y.X., J.-Y.Z., D.-H.L., W.-H.W.).

Classifications MeSH