Endothelial dysfunction and vascular disease

The endothelium can evoke relaxations (dilatations) of the underlying vascular smooth muscle, by releasing vasodilator substances. The best characterized endothelium-derived relaxing factor (EDRF) is nitric oxide (NO). The endothelial cells also evoke hyperpolarization of the cell membrane of vascul...

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Vydané v:Acta Physiologica Ročník 196; číslo 2; s. 193 - 222
Hlavní autori: Vanhoutte, P.M, Shimokawa, H, Tang, E.H.C, Feletou, M
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: Oxford, UK Oxford, UK : Blackwell Publishing Ltd 01.06.2009
Blackwell Publishing Ltd
Wiley-Blackwell
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ISSN:1748-1708, 1748-1716, 1748-1716
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Abstract The endothelium can evoke relaxations (dilatations) of the underlying vascular smooth muscle, by releasing vasodilator substances. The best characterized endothelium-derived relaxing factor (EDRF) is nitric oxide (NO). The endothelial cells also evoke hyperpolarization of the cell membrane of vascular smooth muscle (endothelium-dependent hyperpolarizations, EDHF-mediated responses). Endothelium-dependent relaxations involve both pertussis toxin-sensitive Gi (e.g. responses to serotonin and thrombin) and pertussis toxin-insensitive Gq (e.g. adenosine diphosphate and bradykinin) coupling proteins. The release of NO by the endothelial cell can be up-regulated (e.g. by oestrogens, exercise and dietary factors) and down-regulated (e.g. oxidative stress, smoking and oxidized low-density lipoproteins). It is reduced in the course of vascular disease (e.g. diabetes and hypertension). Arteries covered with regenerated endothelium (e.g. following angioplasty) selectively loose the pertussis toxin-sensitive pathway for NO release which favours vasospasm, thrombosis, penetration of macrophages, cellular growth and the inflammatory reaction leading to atherosclerosis. In addition to the release of NO (and causing endothelium-dependent hyperpolarizations), endothelial cells also can evoke contraction (constriction) of the underlying vascular smooth muscle cells by releasing endothelium-derived contracting factor (EDCF). Most endothelium-dependent acute increases in contractile force are due to the formation of vasoconstrictor prostanoids (endoperoxides and prostacyclin) which activate TP receptors of the vascular smooth muscle cells. EDCF-mediated responses are exacerbated when the production of NO is impaired (e.g. by oxidative stress, ageing, spontaneous hypertension and diabetes). They contribute to the blunting of endothelium-dependent vasodilatations in aged subjects and essential hypertensive patients.
AbstractList The endothelium can evoke relaxations (dilatations) of the underlying vascular smooth muscle, by releasing vasodilator substances. The best characterized endothelium-derived relaxing factor (EDRF) is nitric oxide (NO). The endothelial cells also evoke hyperpolarization of the cell membrane of vascular smooth muscle (endothelium-dependent hyperpolarizations, EDHF-mediated responses). Endothelium-dependent relaxations involve both pertussis toxin-sensitive Gi (e.g. responses to serotonin and thrombin) and pertussis toxin-insensitive Gq (e.g. adenosine diphosphate and bradykinin) coupling proteins. The release of NO by the endothelial cell can be up-regulated (e.g. by oestrogens, exercise and dietary factors) and down-regulated (e.g. oxidative stress, smoking and oxidized low-density lipoproteins). It is reduced in the course of vascular disease (e.g. diabetes and hypertension). Arteries covered with regenerated endothelium (e.g. following angioplasty) selectively loose the pertussis toxin-sensitive pathway for NO release which favours vasospasm, thrombosis, penetration of macrophages, cellular growth and the inflammatory reaction leading to atherosclerosis. In addition to the release of NO (and causing endothelium-dependent hyperpolarizations), endothelial cells also can evoke contraction (constriction) of the underlying vascular smooth muscle cells by releasing endothelium-derived contracting factor (EDCF). Most endothelium-dependent acute increases in contractile force are due to the formation of vasoconstrictor prostanoids (endoperoxides and prostacyclin) which activate TP receptors of the vascular smooth muscle cells. EDCF-mediated responses are exacerbated when the production of NO is impaired (e.g. by oxidative stress, ageing, spontaneous hypertension and diabetes). They contribute to the blunting of endothelium-dependent vasodilatations in aged subjects and essential hypertensive patients.
The endothelium can evoke relaxations (dilatations) of the underlying vascular smooth muscle, by releasing vasodilator substances. The best characterized endothelium-derived relaxing factor (EDRF) is nitric oxide (NO). The endothelial cells also evoke hyperpolarization of the cell membrane of vascular smooth muscle (endothelium-dependent hyperpolarizations, EDHF-mediated responses). Endothelium-dependent relaxations involve both pertussis toxin-sensitive G(i) (e.g. responses to serotonin and thrombin) and pertussis toxin-insensitive G(q) (e.g. adenosine diphosphate and bradykinin) coupling proteins. The release of NO by the endothelial cell can be up-regulated (e.g. by oestrogens, exercise and dietary factors) and down-regulated (e.g. oxidative stress, smoking and oxidized low-density lipoproteins). It is reduced in the course of vascular disease (e.g. diabetes and hypertension). Arteries covered with regenerated endothelium (e.g. following angioplasty) selectively loose the pertussis toxin-sensitive pathway for NO release which favours vasospasm, thrombosis, penetration of macrophages, cellular growth and the inflammatory reaction leading to atherosclerosis. In addition to the release of NO (and causing endothelium-dependent hyperpolarizations), endothelial cells also can evoke contraction (constriction) of the underlying vascular smooth muscle cells by releasing endothelium-derived contracting factor (EDCF). Most endothelium-dependent acute increases in contractile force are due to the formation of vasoconstrictor prostanoids (endoperoxides and prostacyclin) which activate TP receptors of the vascular smooth muscle cells. EDCF-mediated responses are exacerbated when the production of NO is impaired (e.g. by oxidative stress, ageing, spontaneous hypertension and diabetes). They contribute to the blunting of endothelium-dependent vasodilatations in aged subjects and essential hypertensive patients.
The endothelium can evoke relaxations (dilatations) of the underlying vascular smooth muscle, by releasing vasodilator substances. The best characterized endothelium‐derived relaxing factor (EDRF) is nitric oxide (NO). The endothelial cells also evoke hyperpolarization of the cell membrane of vascular smooth muscle (endothelium‐dependent hyperpolarizations, EDHF‐mediated responses). Endothelium‐dependent relaxations involve both pertussis toxin‐sensitive G i (e.g. responses to serotonin and thrombin) and pertussis toxin‐insensitive G q (e.g. adenosine diphosphate and bradykinin) coupling proteins. The release of NO by the endothelial cell can be up‐regulated (e.g. by oestrogens, exercise and dietary factors) and down‐regulated (e.g. oxidative stress, smoking and oxidized low‐density lipoproteins). It is reduced in the course of vascular disease (e.g. diabetes and hypertension). Arteries covered with regenerated endothelium (e.g. following angioplasty) selectively loose the pertussis toxin‐sensitive pathway for NO release which favours vasospasm, thrombosis, penetration of macrophages, cellular growth and the inflammatory reaction leading to atherosclerosis. In addition to the release of NO (and causing endothelium‐dependent hyperpolarizations), endothelial cells also can evoke contraction (constriction) of the underlying vascular smooth muscle cells by releasing endothelium‐derived contracting factor (EDCF). Most endothelium‐dependent acute increases in contractile force are due to the formation of vasoconstrictor prostanoids (endoperoxides and prostacyclin) which activate TP receptors of the vascular smooth muscle cells. EDCF‐mediated responses are exacerbated when the production of NO is impaired (e.g. by oxidative stress, ageing, spontaneous hypertension and diabetes). They contribute to the blunting of endothelium‐dependent vasodilatations in aged subjects and essential hypertensive patients.
The endothelium can evoke relaxations (dilatations) of the underlying vascular smooth muscle, by releasing vasodilator substances. The best characterized endothelium-derived relaxing factor (EDRF) is nitric oxide (NO). The endothelial cells also evoke hyperpolarization of the cell membrane of vascular smooth muscle (endothelium-dependent hyperpolarizations, EDHF-mediated responses). Endothelium-dependent relaxations involve both pertussis toxin-sensitive G(i) (e.g. responses to serotonin and thrombin) and pertussis toxin-insensitive G(q) (e.g. adenosine diphosphate and bradykinin) coupling proteins. The release of NO by the endothelial cell can be up-regulated (e.g. by oestrogens, exercise and dietary factors) and down-regulated (e.g. oxidative stress, smoking and oxidized low-density lipoproteins). It is reduced in the course of vascular disease (e.g. diabetes and hypertension). Arteries covered with regenerated endothelium (e.g. following angioplasty) selectively loose the pertussis toxin-sensitive pathway for NO release which favours vasospasm, thrombosis, penetration of macrophages, cellular growth and the inflammatory reaction leading to atherosclerosis. In addition to the release of NO (and causing endothelium-dependent hyperpolarizations), endothelial cells also can evoke contraction (constriction) of the underlying vascular smooth muscle cells by releasing endothelium-derived contracting factor (EDCF). Most endothelium-dependent acute increases in contractile force are due to the formation of vasoconstrictor prostanoids (endoperoxides and prostacyclin) which activate TP receptors of the vascular smooth muscle cells. EDCF-mediated responses are exacerbated when the production of NO is impaired (e.g. by oxidative stress, ageing, spontaneous hypertension and diabetes). They contribute to the blunting of endothelium-dependent vasodilatations in aged subjects and essential hypertensive patients.The endothelium can evoke relaxations (dilatations) of the underlying vascular smooth muscle, by releasing vasodilator substances. The best characterized endothelium-derived relaxing factor (EDRF) is nitric oxide (NO). The endothelial cells also evoke hyperpolarization of the cell membrane of vascular smooth muscle (endothelium-dependent hyperpolarizations, EDHF-mediated responses). Endothelium-dependent relaxations involve both pertussis toxin-sensitive G(i) (e.g. responses to serotonin and thrombin) and pertussis toxin-insensitive G(q) (e.g. adenosine diphosphate and bradykinin) coupling proteins. The release of NO by the endothelial cell can be up-regulated (e.g. by oestrogens, exercise and dietary factors) and down-regulated (e.g. oxidative stress, smoking and oxidized low-density lipoproteins). It is reduced in the course of vascular disease (e.g. diabetes and hypertension). Arteries covered with regenerated endothelium (e.g. following angioplasty) selectively loose the pertussis toxin-sensitive pathway for NO release which favours vasospasm, thrombosis, penetration of macrophages, cellular growth and the inflammatory reaction leading to atherosclerosis. In addition to the release of NO (and causing endothelium-dependent hyperpolarizations), endothelial cells also can evoke contraction (constriction) of the underlying vascular smooth muscle cells by releasing endothelium-derived contracting factor (EDCF). Most endothelium-dependent acute increases in contractile force are due to the formation of vasoconstrictor prostanoids (endoperoxides and prostacyclin) which activate TP receptors of the vascular smooth muscle cells. EDCF-mediated responses are exacerbated when the production of NO is impaired (e.g. by oxidative stress, ageing, spontaneous hypertension and diabetes). They contribute to the blunting of endothelium-dependent vasodilatations in aged subjects and essential hypertensive patients.
Author Tang, E. H. C.
Shimokawa, H.
Vanhoutte, P. M.
Feletou, M.
Author_xml – sequence: 1
  fullname: Vanhoutte, P.M
– sequence: 2
  fullname: Shimokawa, H
– sequence: 3
  fullname: Tang, E.H.C
– sequence: 4
  fullname: Feletou, M
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Issue 2
Keywords Endocrinopathy
Hypertension
Prostaglandin-endoperoxide synthase
Enzyme
Diabetes mellitus
Cardiovascular disease
cyclooxygenase
Vascular disease
Vertebrata
Mammalia
prostanoids
Nitric oxide
Prostanoid
Endothelial dysfunction
Oxidoreductases
G-proteins
diabetes
G protein
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2003; 278
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1996; 78
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2007; 12
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1988a; 333
1997a; 29
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1994; 12
1999; 34
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1996; 28
1993; 72
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1997; 62
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2006; 13
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2006
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2002; 23
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2006; 148
1989; 13
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2007; 49
2003; 67
2007; 101
1997; 42
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1986; 78
1993; 22
2007; 100
1993; 21
2006; 36
2000; 86
2008b; 32
2000; 130
2006; 296
2000; 131
2006; 291
2006; 290
2007; 73
1998; 83
2007; 74
2007; 76
1987a; 9
2007a; 293
1993a; 87
1993; 122
2005a; 46
2008a; 155
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1991; 87
2006; 27
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1991; 83
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2003; 46
1988; 332
2007; 7
1989a; 256
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2007; 3
1989; 38
1998; 98
2003; 40
2003; 41
1985; 10
1998; 97
2003; 42
2007; 68
1988
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1986; 237
2007; 447
1989; 65
2005; 352
1988; 19
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2005; 112
2006; 55
2002b; 7
1993; 44
2002; 136
1997
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2002; 137
2002; 4
1991
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1996; 14
1989b; 13
1995; 8
2003; 33
1989; 408
2003; 108
2006; 41
2003; 107
2007; 556
1986; 126
1997; 33
2006; 46
2006; 44
2000; 106
2006; 47
1997; 35
2006; 48
2003; 24
2000; 81
1989c; 64
2000; 101
1988; 319
1994; 94
1994; 93
2005; 11
2003; 21
1995; 75
2006; 71
2004; 122
1987; 148
1989; 80
1995; 76
1986; 250
1994; 23
2003; 13
1982; 222
1992; 19
2003; 17
2001; 89
2003; 477
1998; 43
2003; 112
2005; 23
2001; 85
1998; 44
2003; 10
1988b; 244
1990; 85
1993b; 21
1991; 261
1983; 221
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2006; 69
1997; 100
2003; 481
1997; 18
1999; 99
1988; 255
1998; 125
1988; 42
2005; 38
1987b; 9
1989; 79
2008; 154
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1983; 335
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1997; 811
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2006; 99
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2006; 6
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1995; 80
2000; 35
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1997; 122
2004; 13
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1998; 31
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Snippet The endothelium can evoke relaxations (dilatations) of the underlying vascular smooth muscle, by releasing vasodilator substances. The best characterized...
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SubjectTerms Animals
Biological and medical sciences
cyclooxygenase
diabetes
Endothelium, Vascular - metabolism
Endothelium, Vascular - physiology
Endothelium, Vascular - physiopathology
Fundamental and applied biological sciences. Psychology
G-proteins
Humans
hypertension
Models, Biological
nitric oxide
prostaglandin synthase
prostaglandins
prostanoids
Vascular Diseases - metabolism
Vascular Diseases - physiopathology
Vasoconstriction - physiology
Vasodilation - physiology
Vertebrates: anatomy and physiology, studies on body, several organs or systems
Title Endothelial dysfunction and vascular disease
URI https://api.istex.fr/ark:/67375/WNG-0FD3VSLM-2/fulltext.pdf
https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fj.1748-1716.2009.01964.x
https://www.ncbi.nlm.nih.gov/pubmed/19220204
https://www.proquest.com/docview/46254679
https://www.proquest.com/docview/733100800
Volume 196
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