2005
DOI: 10.1097/00000441-200505000-00002
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Angiotensin-Converting Enzyme Inhibitors and Angiotensin II Receptor Blockers Effectively and Directly Potentiate Superoxide Scavenging by Polymorphonuclear Leukocytes from Patients with Type 2 Diabetes Mellitus

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Cited by 12 publications
(8 citation statements)
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“…Experimental studies in both animals and humans have demonstrated that the ACE inhibitors and ARBs possess antioxidant effects 41,42 through their action on the AT 1 R and AT 2 R. ROS have been implicated in the development and progression of atherosclerosis, diabetic nephropathy, endothelial cell dysfunction, and microvascular permeability. Superoxide anion is the most potent member of ROS and is inactivated by superoxide dismutase, and both ACE inhibitors and ARBs have been shown to stimulate superoxide dismutase 43 . It is, therefore, quite possible that the beneficial effects of ACE inhibitors and ARBs on CV remodeling, LVH regression, HF, CV mortality, renal disease progression, and stroke prevention could be due in part to their antioxidant effects.…”
Section: Antioxidant Effectsmentioning
confidence: 99%
See 1 more Smart Citation
“…Experimental studies in both animals and humans have demonstrated that the ACE inhibitors and ARBs possess antioxidant effects 41,42 through their action on the AT 1 R and AT 2 R. ROS have been implicated in the development and progression of atherosclerosis, diabetic nephropathy, endothelial cell dysfunction, and microvascular permeability. Superoxide anion is the most potent member of ROS and is inactivated by superoxide dismutase, and both ACE inhibitors and ARBs have been shown to stimulate superoxide dismutase 43 . It is, therefore, quite possible that the beneficial effects of ACE inhibitors and ARBs on CV remodeling, LVH regression, HF, CV mortality, renal disease progression, and stroke prevention could be due in part to their antioxidant effects.…”
Section: Antioxidant Effectsmentioning
confidence: 99%
“…Superoxide anion is the most potent member of ROS and is inactivated by superoxide dismutase, and both ACE inhibitors and ARBs have been shown to stimulate superoxide dismutase. 43 It is, therefore, quite possible that the beneficial effects of ACE inhibitors and ARBs on CV remodeling, LVH regression, HF, CV mortality, renal disease progression, and stroke prevention could be due in part to their antioxidant effects.…”
Section: Antioxidant Effectsmentioning
confidence: 99%
“…Whether the renoprotective effects of RAS inhibitors can be fully accounted for by BP reductions or whether other mechanisms are involved has not been clearly established. The most debated point is the role and real clinical relevance of ancillary mechanisms, such as the antinflammatory and antiproliferative effects exerted by RAS‐active drugs, largely documented in cell and animal models 28,29 but not confirmed so far by large clinical trials.…”
Section: Prevention and Treatment Of Ckd In Type 2 Diabetesmentioning
confidence: 99%
“…Whether the renoprotective effects of RAS inhibitors can be fully accounted for by BP reductions or whether other mechanisms are involved has not been clearly established. The most debated point is the role and real clinical relevance of ancillary mechanisms, such as the antinflammatory and antiproliferative effects exerted by RAS-active drugs, largely documented in cell and animal models 28,29 but not confirmed so far by large clinical trials. The evidence for a better effect of ACE inhibitors and ARBs in preventing macrovascular complications as compared with other drug classes is not strong, mainly for cerebrovascular disease, where calcium channel blockers, for any given BP level, seem to confer some advantage.…”
Section: Prevention and Treatment Of Ckd In Type 2 Diabetes Hypertensionmentioning
confidence: 99%
“…The conditions for which the ARBs have shown benefit and their use is recommended by the JNC-7, 35 except for stroke, are listed in Table 5. Other beneficial effects of some of the ARBs include their; (a) antiatherogenic, 57,58 (b) antioxidant, 59 (c) antidiabetic, 60 (d) antiplatelet 61 and (e) atrial antifibrillatory effects. 62,63 All these effects of ARBs could contribute to their stroke protective effects independent of BP control.…”
Section: Treatment Indications Of Arbsmentioning
confidence: 99%