Vascular dysfunction produced by hyperhomocysteinemia is more severe in the presence of low folate

J. David Symons, John C Rutledge, U. Simonsen, Roshny A. Pattathu

Research output: Contribution to journalArticle

25 Citations (Scopus)

Abstract

Earlier we reported that dietary folate depletion causes hyperhomocysteinemia (HHcy) and arterial dysfunction in rats (Symons JD, Mullick AE, Ensunsa JL, Ma AA, and Rutledge JC. Arterioscler Thromb Vasc Biol 22: 772-780, 2002). Both HHcy and low folate (LF) are risk factors for cardiovascular disease. Therefore, the dysfunction we observed could have resulted from HHcy, LF, and/or their combination (HHcy + LF). We tested the hypothesis that HHcy-induced vascular dysfunction is more severe in the presence of LF. Four groups of rats consumed diets for ∼10 wk that produced plasma homocysteine (μM) and liver folate (μg folate/g liver) concentrations, respectively, of 7 ± 1 and 15 ± 1 (Control; Con; n = 16), 17 ± 2 and 15 ± 2 (HHcy; n = 17), 10 ± 1 and 8 ± 1 (LF; n = 14), and 21 ± 2 and 8 ± 1 (HHcy + LF; n = 18). We observed that maximal ACh-evoked vasorelaxation was greatest in aortas and mesenteric arteries from Con rats vs. all groups. While the extent of dysfunction was similar between LF and HHcy animals, it was less severe compared with arteries from HHcy + LF rats. Maximal ACh-evoked vasorelaxation in coronary arteries was not different between Con and LF rats, but both were greater than HHcy + LF animals. In segments of aortas, 1) ACh-evoked vasorelaxation was similar among groups after incubation with the nonenzymatic intracellular O2 - scavenger Tiron, 2) vascular O2 - estimated using dihydroethidium staining was greatest in HHcy + LF vs. all groups, and 3) tension development in response to nitric oxide (NO) synthase inhibition was greatest in Con vs. all other groups. We conclude that HHcy + LF evokes greater dysfunction than either HHcy alone (aortas, mesentery) or LF alone (aortas, mesentery, coronary), likely by producing more O2 - within the vasculature and thereby reducing NO bioavailability.

Original languageEnglish (US)
JournalAmerican Journal of Physiology - Heart and Circulatory Physiology
Volume290
Issue number1
DOIs
StatePublished - Jan 2006

Fingerprint

Hyperhomocysteinemia
Folic Acid
Blood Vessels
Aorta
Vasodilation
Mesentery
1,2-Dihydroxybenzene-3,5-Disulfonic Acid Disodium Salt
Mesenteric Arteries
Liver
Homocysteine

Keywords

  • Coronary function
  • Endothelium
  • Mesenteric artery function
  • Nitric oxide bioavailability
  • Superoxide anion
  • Vascular smooth muscle

ASJC Scopus subject areas

  • Physiology

Cite this

Vascular dysfunction produced by hyperhomocysteinemia is more severe in the presence of low folate. / Symons, J. David; Rutledge, John C; Simonsen, U.; Pattathu, Roshny A.

In: American Journal of Physiology - Heart and Circulatory Physiology, Vol. 290, No. 1, 01.2006.

Research output: Contribution to journalArticle

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