In the ileum of the brushtail possum, Trichosurus vulpecula, fluid secretion appears to be driven by electrogenic HCO secretion. Consistent with this, the cystic fibrosis transmembrane conductance regulator is expressed in the apical membrane of the ileal epithelial cells and the pancreatic or secretory variant of the NaHCO cotransporter in the basolateral membrane. This suggests that in the possum ileum, electrogenic HCO secretion is driven by basolateral NaHCO cotransporter (NBC) activity. To determine if the NBC contributes to HCO secretion in the possum ileum, intracellular pH (pHi) measurements in isolated villi were used to demonstrate NBC activity in the ileal epithelial cells and investigate the effect of cAMP-dependent secretagogues. In CO/HCO-free solutions, recovery of the epithelial cells from an acid load was Na-dependent and ≈80% inhibited by ethyl-isopropyl-amiloride (EIPA, 10 µmol L), indicative of the presence of an Na/H exchanger, most likely NHE1. However, in the presence of CO/HCO, EIPA only inhibited ≈ 50% of the recovery, the remainder was inhibited by 4,4'-diisothiocyano-2,2'-stilbenedisulfonic acid (DIDS, 500 µmol L), indicative of NBC activity. Under steady-state conditions, NHE1 inhibition by EIPA had little effect on pHi in the presence or absence of secretagogues, but NBC inhibition with DIDS resulted in a rapid acidification of the cells, which was increased fivefold by secretagogues. These data demonstrate the functional activity of an NaHCO cotransporter in the ileal epithelial cells. Furthermore, the stimulation of NBC activity by secretagogues is consistent with the involvement of an NaHCO cotransporter in electrogenic HCO secretion.
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http://dx.doi.org/10.1007/s00360-017-1063-z | DOI Listing |
Am J Physiol Cell Physiol
May 2023
Department of Anesthesiology, Vanderbilt University School of Medicine, Nashville, Tennessee, United States.
A primary function of intercalated cells in the distal tubule of the kidney is to maintain pH homeostasis. For example, type B intercalated cells secrete bicarbonate largely through the action of the apical Cl/HCO exchanger, pendrin, which helps correct metabolic alkalosis. Since both the K-Cl cotransporter, KCC3a and pendrin colocalize to the apical region of type B and non-A, non-B intercalated cells and since both are upregulated in models of metabolic alkalosis, such as with dietary NaHCO loading, we raised the possibility that apical KCC3a facilitates pendrin-mediated bicarbonate secretion, such as through apical Cl recycling.
View Article and Find Full Text PDFJ Physiol
August 2020
Key Laboratory of Molecular Biophysics of Ministry of Education, School of Life Science & Technology, Huazhong University of Science & Technology, Wuhan, Hubei, 430074, China.
Key Points: The roles of the Na /HCO cotransporters NBCn1 and NBCn2 as well as their activators IRBIT and L-IRBIT in the regulation of the mTAL transport of NH , HCO , and NaCl are investigated. Dietary challenges of NH Cl, NaHCO or NaCl all increase the abundance of NBCn1 and NBCn2 in the outer medulla. The three challenges generally produce parallel increases in the abundance of IRBIT and L-IRBIT in the outer medulla.
View Article and Find Full Text PDFDiabetol Metab Syndr
January 2020
2Department of Endocrinology, Metabolism, Rheumatology and Nephrology, Faculty of Medicine, Oita University, 1-1 Idai-ga-oka, Hasama-machi, Yufu, Oita 879-5593 Japan.
Hypertension
November 2019
Department of Molecular Pharmacology and Physiology, University of South Florida College of Medicine, Tampa (S.J., X.W., J.W., G.Z., J.Z., L.W., R.L.).
Sodium bicarbonate has long been used to treat chronic kidney disease. It has been demonstrated to slow the decline in glomerular filtration rate in chronic kidney disease patient; however, the mechanisms are not completely understood. We hypothesized that NaHCO dilates afferent arterioles (Af-Art) by stimulating nitric oxide (NO) release mediated by the Na/HCO cotransporter (NBC) contributing to the elevation in glomerular filtration rate.
View Article and Find Full Text PDFAm J Physiol Renal Physiol
August 2018
Department of Nephrology, Hiroshima University Hospital, Hiroshima , Japan.
Recently, in addition to epithelial sodium channel alpha-subunit (αENaC), the thiazide-sensitive sodium-chloride cotransporter (NCC) and pendrin, also known as sodium-independent chloride/iodide transporter, were reported to be activated by aldosterone. Here, we investigated whether chloride (Cl) is responsible for hypertension, inflammation, and renal damage in aldosterone-infused rats. Following left nephrectomy, 8-wk-old male Sprague-Dawley rats were allocated into four groups: 1) drinking 1.
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