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Effects of Atrial Natriuretic Peptide on Bicarbonate Transport in Long- and Short-Looped Medullary Thick Ascending Limbs of Rats

Atrial natriuretic peptide (ANP) is known to influence NaCl transport in the medullary thick ascending limbs (MAL), where the largest NaCl reabsorption occurs among distal nephron segments in response to arginine vasopressin (AVP). In the present study, we investigated the effect of ANP on bicarbona...

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Detalles Bibliográficos
Autores principales: Nonoguchi, Hiroshi, Izumi, Yuichiro, Nakayama, Yushi, Matsuzaki, Takanobu, Yasuoka, Yukiko, Inoue, Takeaki, Inoue, Hideki, Mouri, Tomohiko, Kawahara, Katsumasa, Saito, Hideyuki, Tomita, Kimio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3871552/
https://www.ncbi.nlm.nih.gov/pubmed/24376658
http://dx.doi.org/10.1371/journal.pone.0083146
Descripción
Sumario:Atrial natriuretic peptide (ANP) is known to influence NaCl transport in the medullary thick ascending limbs (MAL), where the largest NaCl reabsorption occurs among distal nephron segments in response to arginine vasopressin (AVP). In the present study, we investigated the effect of ANP on bicarbonate (HCO(3) (−)) transport in the MAL using an isolated tubule perfusion technique. The HCO(3) (−) concentration was measured using free-flow ultramicro-fluorometer. We first observed basal HCO(3) (−) reabsorption in both long- and short-looped MALs (lMALs, and sMALs, respectively). AVP inhibited HCO(3) (−) reabsorption in both lMALs and sMALs, whereas ANP did not change HCO(3) (−) transport. However, in the presence of AVP, ANP restored the HCO(3) (−) reabsorption inhibited by AVP both in lMAL and sMAL. The effects of ANP on HCO(3) (−) transport was mimicked by cyclic GMP. The mRNA expression level of the vasopressin V2 receptor in lMALs was significantly higher than in sMALs, whereas expression of the V1a receptor was unchanged. In summary, AVP inhibits HCO(3) (−) transport, and ANP counteracts the action of AVP on HCO(3) (−) transport both in lMALs and sMALs.