Upregulation of endothelium-derived hyperpolarizing factor compensates for the loss of nitric oxide in mesenteric arteries of dahl salt-sensitive hypertensive rats

Kenichi Goto, Yasuo Kansui, Hideyuki Oniki, Toshio Ohtsubo, Kiyoshi Matsumura, Takanari Kitazono

Research output: Contribution to journalArticle

17 Citations (Scopus)

Abstract

This study was designed to determine whether a high-salt diet would alter endothelial function and, if so, the relative contributions of endothelium-derived hyperpolarizing factor (EDHF) and nitric oxide (NO) to any changes in vasomotor responses. Male Dahl salt-sensitive (DS) rats were given either a high-salt diet (8% NaCl, DS-H) or a low-salt diet (0.4% NaCl, DS-L) for 6 weeks. Membrane potentials and contractile responses were recorded from the isolated superior mesenteric arteries. After salt loading, DS-H developed hypertension, while DS-L remained normotensive. No difference was found in acetylcholine (ACh)-induced, endothelium-dependent relaxation between the groups. However, after treatment with indomethacin and NO synthase inhibitor, EDHF-like relaxation was significantly greater in DS-H than in DS-L. In contrast, NO-mediated relaxation was significantly smaller in DS-Hthan in DS-L. Iberiotoxin (IbTx), a specific blocker of large-conductance calcium-dependent potassium (BKCa) channels, attenuated EDHF-like relaxation in DS-H but not in DS-L. IbTx marginally inhibited EDHF-mediated hyperpolarization only in DS-H. Endothelium-independent relaxation in response to sodium nitroprusside or levcromakalim was similar in both groups. In conclusion, EDHF-like relaxation is upregulated through the activation of BKCa channels in the mesenteric arteries of DS-H. As the overall relaxation in response to ACh did not differ between the groups, the upregulation of EDHF appears to compensate for the loss of NO in the mesenteric arteries of DS-H.

Original languageEnglish
Pages (from-to)849-854
Number of pages6
JournalHypertension Research
Volume35
Issue number8
DOIs
Publication statusPublished - Aug 1 2012

Fingerprint

Inbred Dahl Rats
Mesenteric Arteries
Endothelium
Nitric Oxide
Up-Regulation
Salts
Acetylcholine
Cromakalim
Diet
Sodium-Restricted Diet
Calcium-Activated Potassium Channels
Superior Mesenteric Artery

All Science Journal Classification (ASJC) codes

  • Internal Medicine
  • Physiology
  • Cardiology and Cardiovascular Medicine

Cite this

Upregulation of endothelium-derived hyperpolarizing factor compensates for the loss of nitric oxide in mesenteric arteries of dahl salt-sensitive hypertensive rats. / Goto, Kenichi; Kansui, Yasuo; Oniki, Hideyuki; Ohtsubo, Toshio; Matsumura, Kiyoshi; Kitazono, Takanari.

In: Hypertension Research, Vol. 35, No. 8, 01.08.2012, p. 849-854.

Research output: Contribution to journalArticle

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