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December 1, 2007Journal of Cardiovascular Pharmacology

Peroxynitrite is Involved in the Dysfunction of Vasorelaxation in SHR/NDmcr-cp Rats, Spontaneously Hypertensive Obese Rats

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Key result

Telmisartan, but not amlodipine or moxonidine, ameliorated the impairment of endothelium-dependent relaxation and decreased oxidative stress markers in SHR-cp rats.

Why the study?

Does treatment with antihypertensive drugs (amlodipine, moxonidine, or telmisartan) improve endothelium-dependent relaxation in spontaneously hypertensive obese rats?

Population

SHR/NDmcr-cp rats

Design

Preclinical

Authors

SKSatomi KagotaVascular MedicineYTYukari TadaMukogawa Women's UniversityYKYōko KubotaNational Cancer Center

Discussion

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Member takes

Overview

Telmisartan may improve endothelial function via oxidative stress reduction in obese hypertensive rats; leaves open human translation.

Structured PICO

Does treatment with antihypertensive drugs (amlodipine, moxonidine, or telmisartan) improve endothelium-dependent relaxation in spontaneously hypertensive obese rats?

P
Population
SHR/NDmcr-cp rats, an animal model displaying typical symptoms and features of metabolic syndrome.
I
Intervention
Treatment with antihypertensive drugs: amlodipine (calcium channel blocker), moxonidine (alpha 2 and imidazoline receptor agonist), or telmisartan (angiotensin II type 1 receptor antagonist)
O
Outcome
Endothelium-dependent relaxation in response to acetylcholine in thoracic aortassurrogate

Telmisartan improves endothelial dysfunction in a rat model of metabolic syndrome by reducing oxidative stress and peroxynitrite formation, an effect not seen with amlodipine or moxonidine despite similar blood pressure lowering.

Cite This Study

Kagota et al. (2007) studied Metabolic syndrome and hypertension. Telmisartan, amlodipine, and moxonidine vs. Untreated/each other was evaluated on Endothelium-dependent relaxation in response to acetylcholine and protein expression of endothelium NO synthase. Telmisartan, but not amlodipine or moxonidine, ameliorated the impairment of endothelium-dependent relaxation and decreased oxidative stress markers in SHR-cp rats.

synapsesocial.com/papers/6a64d3bf9aeeefc9b8ef47ffhttps://doi.org/10.1097/fjc.0b013e3181583d80
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Also Consider

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