Thiocyanate supplementation decreases atherosclerotic plaque in mice expressing human myeloperoxidase

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Thiocyanate supplementation decreases atherosclerotic plaque in mice expressing human myeloperoxidase. / Morgan, P E; Laura, R P; Maki, R A; Reynolds, W F; Davies, Michael Jonathan.

In: Free Radical Research, Vol. 49, No. 6, 27.03.2015, p. 743-9.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Morgan, PE, Laura, RP, Maki, RA, Reynolds, WF & Davies, MJ 2015, 'Thiocyanate supplementation decreases atherosclerotic plaque in mice expressing human myeloperoxidase', Free Radical Research, vol. 49, no. 6, pp. 743-9. https://doi.org/10.3109/10715762.2015.1019347

APA

Morgan, P. E., Laura, R. P., Maki, R. A., Reynolds, W. F., & Davies, M. J. (2015). Thiocyanate supplementation decreases atherosclerotic plaque in mice expressing human myeloperoxidase. Free Radical Research, 49(6), 743-9. https://doi.org/10.3109/10715762.2015.1019347

Vancouver

Morgan PE, Laura RP, Maki RA, Reynolds WF, Davies MJ. Thiocyanate supplementation decreases atherosclerotic plaque in mice expressing human myeloperoxidase. Free Radical Research. 2015 Mar 27;49(6):743-9. https://doi.org/10.3109/10715762.2015.1019347

Author

Morgan, P E ; Laura, R P ; Maki, R A ; Reynolds, W F ; Davies, Michael Jonathan. / Thiocyanate supplementation decreases atherosclerotic plaque in mice expressing human myeloperoxidase. In: Free Radical Research. 2015 ; Vol. 49, No. 6. pp. 743-9.

Bibtex

@article{c7fc7053e8d94354b522c8d5f1a034e6,
title = "Thiocyanate supplementation decreases atherosclerotic plaque in mice expressing human myeloperoxidase",
abstract = "Elevated levels of the heme enzyme myeloperoxidase (MPO) are associated with adverse cardiovascular outcomes. MPO predominantly catalyzes formation of the oxidants hypochlorous acid (HOCl) from Cl(-), and hypothiocyanous acid (HOSCN) from SCN(-), with these anions acting as competitive substrates. HOSCN is a less powerful and more specific oxidant than HOCl, and selectively targets thiols; such damage is largely reversible, unlike much HOCl-induced damage. We hypothesized that increased plasma SCN(-), and hence HOSCN formation instead of HOCl, may decrease artery wall damage. This was examined using high-fat fed atherosclerosis-prone LDLR(-/-) mice transgenic for human MPO, with and without SCN(-) (10 mM) added to drinking water. Serum samples, collected fortnightly, were analyzed for cholesterol, triglycerides, thiols, MPO, and SCN(-); study-long exposure was calculated by area under the curve (AUC). Mean serum SCN(-) concentrations were elevated in the supplemented mice (200-320 μM) relative to controls (< 120 μM). Normalized aortic root plaque areas at sacrifice were 26% lower in the SCN(-)-supplemented mice compared with controls (P = 0.0417), but plaque morphology was not appreciably altered. Serum MPO levels steadily increased in mice on the high-fat diet, however, comparison of SCN(-)-supplemented versus control mice showed no significant changes in MPO protein, cholesterol, or triglyceride levels; thiol levels were decreased in supplemented mice at one time-point. Plaque areas increased with higher cholesterol AUC (r = 0.4742; P = 0.0468), and decreased with increasing SCN(-) AUC (r = - 0.5693; P = 0.0134). These data suggest that increased serum SCN(-) levels, which can be achieved in humans by dietary manipulation, may decrease atherosclerosis burden.",
author = "Morgan, {P E} and Laura, {R P} and Maki, {R A} and Reynolds, {W F} and Davies, {Michael Jonathan}",
year = "2015",
month = mar,
day = "27",
doi = "10.3109/10715762.2015.1019347",
language = "English",
volume = "49",
pages = "743--9",
journal = "Free Radical Research",
issn = "1071-5762",
publisher = "Taylor & Francis",
number = "6",

}

RIS

TY - JOUR

T1 - Thiocyanate supplementation decreases atherosclerotic plaque in mice expressing human myeloperoxidase

AU - Morgan, P E

AU - Laura, R P

AU - Maki, R A

AU - Reynolds, W F

AU - Davies, Michael Jonathan

PY - 2015/3/27

Y1 - 2015/3/27

N2 - Elevated levels of the heme enzyme myeloperoxidase (MPO) are associated with adverse cardiovascular outcomes. MPO predominantly catalyzes formation of the oxidants hypochlorous acid (HOCl) from Cl(-), and hypothiocyanous acid (HOSCN) from SCN(-), with these anions acting as competitive substrates. HOSCN is a less powerful and more specific oxidant than HOCl, and selectively targets thiols; such damage is largely reversible, unlike much HOCl-induced damage. We hypothesized that increased plasma SCN(-), and hence HOSCN formation instead of HOCl, may decrease artery wall damage. This was examined using high-fat fed atherosclerosis-prone LDLR(-/-) mice transgenic for human MPO, with and without SCN(-) (10 mM) added to drinking water. Serum samples, collected fortnightly, were analyzed for cholesterol, triglycerides, thiols, MPO, and SCN(-); study-long exposure was calculated by area under the curve (AUC). Mean serum SCN(-) concentrations were elevated in the supplemented mice (200-320 μM) relative to controls (< 120 μM). Normalized aortic root plaque areas at sacrifice were 26% lower in the SCN(-)-supplemented mice compared with controls (P = 0.0417), but plaque morphology was not appreciably altered. Serum MPO levels steadily increased in mice on the high-fat diet, however, comparison of SCN(-)-supplemented versus control mice showed no significant changes in MPO protein, cholesterol, or triglyceride levels; thiol levels were decreased in supplemented mice at one time-point. Plaque areas increased with higher cholesterol AUC (r = 0.4742; P = 0.0468), and decreased with increasing SCN(-) AUC (r = - 0.5693; P = 0.0134). These data suggest that increased serum SCN(-) levels, which can be achieved in humans by dietary manipulation, may decrease atherosclerosis burden.

AB - Elevated levels of the heme enzyme myeloperoxidase (MPO) are associated with adverse cardiovascular outcomes. MPO predominantly catalyzes formation of the oxidants hypochlorous acid (HOCl) from Cl(-), and hypothiocyanous acid (HOSCN) from SCN(-), with these anions acting as competitive substrates. HOSCN is a less powerful and more specific oxidant than HOCl, and selectively targets thiols; such damage is largely reversible, unlike much HOCl-induced damage. We hypothesized that increased plasma SCN(-), and hence HOSCN formation instead of HOCl, may decrease artery wall damage. This was examined using high-fat fed atherosclerosis-prone LDLR(-/-) mice transgenic for human MPO, with and without SCN(-) (10 mM) added to drinking water. Serum samples, collected fortnightly, were analyzed for cholesterol, triglycerides, thiols, MPO, and SCN(-); study-long exposure was calculated by area under the curve (AUC). Mean serum SCN(-) concentrations were elevated in the supplemented mice (200-320 μM) relative to controls (< 120 μM). Normalized aortic root plaque areas at sacrifice were 26% lower in the SCN(-)-supplemented mice compared with controls (P = 0.0417), but plaque morphology was not appreciably altered. Serum MPO levels steadily increased in mice on the high-fat diet, however, comparison of SCN(-)-supplemented versus control mice showed no significant changes in MPO protein, cholesterol, or triglyceride levels; thiol levels were decreased in supplemented mice at one time-point. Plaque areas increased with higher cholesterol AUC (r = 0.4742; P = 0.0468), and decreased with increasing SCN(-) AUC (r = - 0.5693; P = 0.0134). These data suggest that increased serum SCN(-) levels, which can be achieved in humans by dietary manipulation, may decrease atherosclerosis burden.

U2 - 10.3109/10715762.2015.1019347

DO - 10.3109/10715762.2015.1019347

M3 - Journal article

C2 - 25812586

VL - 49

SP - 743

EP - 749

JO - Free Radical Research

JF - Free Radical Research

SN - 1071-5762

IS - 6

ER -

ID: 138272069