TY - JOUR
T1 - Endothelium-dependent relaxation of rabbit atherosclerotic aorta was not restored by control of hyperlipidemia
T2 - the possible role of peroxynitrite (ONOO-)
AU - Hayashi, Toshio
AU - Yamada, Kazuyoshi
AU - Esaki, Teiji
AU - Kano, Hatsuyo
AU - Asai, Yukako
AU - Kumar Thakur, Navin
AU - Jayachandran, Muthuvel
AU - Sumi, Daigo
AU - Iguchi, Akihisa
N1 - Funding Information:
This study was supported in part by Grant-in-Aid No. 09470166 of the Japanese ministry of Education. We thank Michiko Doi and Norie Kametsuta for their excellent technical assistance.
PY - 1999/9/9
Y1 - 1999/9/9
N2 - We determined the role of ONOO- in nitric oxide (NO) mediated vascular response in atherosclerosis and regression following removal of dietary cholesterol. The effect of ONOO- on NO-mediated vascular responses was examined in vitro. Basal and stimulated NO release was estimated by an NO-selective electrode as well as vascular response and the plasma NO metabolites. An immunohistochemical study was also carried out. Responses were compared in normal controls, atherosclerotic rabbits fed 1% cholesterol diet for 6 or 9 weeks (atherosclerotic group) and animals fed a normal diet for 6-36 weeks after the high cholesterol diet for 6 or 9 weeks (regression group). ONOO- impaired the basal and acetylcholine-stimulated NO release, but did not affect endothelium-independent relaxation. After 15 weeks on a normal diet, the acetylcholine-stimulated and basal NO-mediated relaxation, which was diminished in the aorta induced by 6 weeks high cholesterol diet, became restored. However, the vascular response in the 9 weeks high cholesterol diet group did not return to normal after 36 weeks on a normal diet. iNOS was observed in atherosclerotic plaques in atherosclerotic and regression groups along with ONOO- in the 9 weeks high cholesterol diet group, but not in the 6 weeks group. Conclusively, ONOO- can play a role in impairment of NO-mediated vascular response during the regression of dietary cholesterol-induced atherosclerosis, not in the initiation of atherosclerosis. Copyright (C) 1999 Elsevier Science Ireland Ltd.
AB - We determined the role of ONOO- in nitric oxide (NO) mediated vascular response in atherosclerosis and regression following removal of dietary cholesterol. The effect of ONOO- on NO-mediated vascular responses was examined in vitro. Basal and stimulated NO release was estimated by an NO-selective electrode as well as vascular response and the plasma NO metabolites. An immunohistochemical study was also carried out. Responses were compared in normal controls, atherosclerotic rabbits fed 1% cholesterol diet for 6 or 9 weeks (atherosclerotic group) and animals fed a normal diet for 6-36 weeks after the high cholesterol diet for 6 or 9 weeks (regression group). ONOO- impaired the basal and acetylcholine-stimulated NO release, but did not affect endothelium-independent relaxation. After 15 weeks on a normal diet, the acetylcholine-stimulated and basal NO-mediated relaxation, which was diminished in the aorta induced by 6 weeks high cholesterol diet, became restored. However, the vascular response in the 9 weeks high cholesterol diet group did not return to normal after 36 weeks on a normal diet. iNOS was observed in atherosclerotic plaques in atherosclerotic and regression groups along with ONOO- in the 9 weeks high cholesterol diet group, but not in the 6 weeks group. Conclusively, ONOO- can play a role in impairment of NO-mediated vascular response during the regression of dietary cholesterol-induced atherosclerosis, not in the initiation of atherosclerosis. Copyright (C) 1999 Elsevier Science Ireland Ltd.
KW - (ONOO), peroxynitrite
KW - Arteriosclerosis
KW - Hypercholesterolemia
KW - Immunohistochemistry
KW - NO, nitric oxide
KW - NOS, nitric oxide synthase
KW - Nitric oxide
KW - Peroxynitrite
KW - Regression
KW - e-NOS, endothelial nitric oxide synthase
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U2 - 10.1016/S0021-9150(99)00205-1
DO - 10.1016/S0021-9150(99)00205-1
M3 - Article
C2 - 10559521
AN - SCOPUS:0032739620
SN - 0021-9150
VL - 147
SP - 349
EP - 363
JO - Atherosclerosis
JF - Atherosclerosis
IS - 2
ER -