Mechanism of regulation of rabbit intestinal villus cell brush border membrane Na/H exchange by nitric oxide
Abstract
In the mammalian small intestine, coupled NaCl absorption occurs via the dual operation of Na/H and Cl/HCO(3) exchange on the villus cell brush border membrane (BBM). Although constitutive nitric oxide (cNO) has been demonstrated to alter gastrointestinal tract functions, how cNO may specifically alter these two transporters to regulate coupled NaCl absorption is unknown. In villus cells, inhibition of cNO synthase (cNOS) with l-N(G)-nitroarginine methylester (l-NAME) stimulated Na/H exchange whereas Cl/HCO(3) exchange was unaffected. In villus cell BBM vesicles (BBMV) prepared from rabbits treated with l-NAME, Na/H exchange was also stimulated. d-NAME, an inactive analog of l-NAME, and N(6)-(1-imonoethyl)-l-lysine dihydrochloride, a more selective inhibitor of inducible NO synthase, did not affect Na/H exchange. Kinetic studies demonstrated that the mechanism of stimulation is secondary to an increase in the maximal rate of uptake of Na, without an alteration in the affinity of the transporter for Na. Northern blot studies demonstrated an increase in the message for the BBM Na/H exchanger NHE3, and Western blot studies showed that the immunoreactive protein levels of NHE3 was increased when cNOS was inhibited. Thus these results indicate that cNO under nominal physiological states most likely maintains an inhibitory tone on small intestinal coupled NaCl absorption by specifically inhibiting BBM Na/H expression.
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Intracellular cNO differentially regulates NHE3 and SGLT1 in vitro in IEC-18 cells and in vivo in rabbit small intestine.
“Furthermore, intracellular cNO was shown to differentially regulate NHE3 and SGLT1 in vitro in IEC-18 cells [23,24,25] and in vivo in rabbit small intestine [25,55,56], which implies functional compensation between the two primary Na absorptive pathways.”
From Regulation of Enterocyte Brush Border Membrane Primary Na-Absorptive Transporters in Human Intestinal Organoid-Derived Monolayers (2024) · cites this paper as [56]
The differential regulation of NHE3 and SGLT1 by cNO implies functional compensation between the two primary Na absorptive pathways.
“Furthermore, intracellular cNO was shown to differentially regulate NHE3 and SGLT1 in vitro in IEC-18 cells [23,24,25] and in vivo in rabbit small intestine [25,55,56], which implies functional compensation between the two primary Na absorptive pathways.”
From Regulation of Enterocyte Brush Border Membrane Primary Na-Absorptive Transporters in Human Intestinal Organoid-Derived Monolayers (2024) · cites this paper as [56]
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Palaniappan, B., Manoharan, P., Arthur, S., Singh, S., Murughiyan, U., & Sundaram, U. (2019) · Physiological Reports · doi:10.14814/phy2.14086 · Cited by 3 · see citing works
Self-citationHaynes, J., Palaniappan, B., Crutchley, J. M., & Sundaram, U. (2024) · Cells · doi:10.3390/cells13191623 · Cited by 2 · see citing works
“Furthermore, intracellular cNO was shown to differentially regulate NHE3 and SGLT1 in vitro in IEC-18 cells [23–25] and in vivo in rabbit small intestine [25,55,56], which implies functional compensation between the two primary Na absorptive pathways.”
BackgroundSelf-citation
- Authors
- Coon, S., Shao, G., Wisel, S., Vulaupalli, R., & Sundaram, U.
- Affiliations
- West Virginia University (US)
- Venue
- American Journal of Physiology-Gastrointestinal and Liver Physiology
- Publisher
- American Physiological Society
- Published
- 2007-02
- Volume
- 292
- Issue
- 2
- Pages
- G475-G481
- ISSN
- 0193-1857 (ISSN-L)
- 1522-1547
- OpenAlex
- W2104291647
- Cited by
- 11
- References
- 0
- Citations by year
- 2024: 1 · 2022: 1 · 2020: 1 · 2019: 1 · 2018: 1 · 2014: 2 · 2012: 1
- FWCI
- 0.26
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- American Journal of Physiology-Gastrointestinal and Liver Physiology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (5r29dk045062-06)
- National Institute of Diabetes and Digestive and Kidney Diseases (DK-45062, R01DK058034, DK 58034)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion Transport and Channel Regulation
- Health Sciences › Medicine › Physiology › Nitric Oxide and Endothelin Effects
- Health Sciences › Medicine › Gastroenterology › Gastrointestinal motility and disorders
- Keywords
- nitric oxide, Na+/H+ exchange, NHE3, brush border membrane, Cl-/HCO3- exchange, nitric oxide synthase inhibition, L-NAME, inducible nitric oxide synthase, small intestine, rabbits
- MeSH terms
- Sodium-Hydrogen Exchanger 3, Ammonium Chloride, Animals, Cell Membrane, Enteritis, Enzyme Inhibitors, Epithelial Cells, Hydrogen-Ion Concentration, Intestinal Mucosa, Kinetics, Lysine, Microvilli, Nitric Oxide, Rabbits, Sodium, Gene Expression, Sodium-Hydrogen Exchangers, Nitric Oxide Synthase, NG-Nitroarginine Methyl Ester, Chloride-Bicarbonate Antiporters, Nitric Oxide Synthase Type II
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