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May 1, 1994Hypertension113 citationsOpen Access

Dose-dependent effects of perindopril on blood pressure and small-artery structure.

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NTNiels K. ThyboNKNiels KorsgaardSES Eriksen

Key Result

Perindopril caused a dose-dependent reduction in blood pressure and media-lumen ratio during treatment, with an inverse relation between dose and persistent effect after withdrawal.

Key Points

  • The aim is to determine the impact of perindopril on blood pressure and small-artery structure during treatment and after withdrawal.
  • Young spontaneously hypertensive rats (SHR) treated from age 4 to 24 weeks with perindopril at 0.4, 0.8, or 1.5 mg/kg/day.
  • Control groups included untreated SHR and Wistar-Kyoto rats.
  • Small arteries were analyzed morphologically and functionally after treatment cessation.
  • Perindopril led to a dose-dependent reduction in blood pressure during treatment.
  • The media-lumen ratio and media area of small arteries decreased, while lumen diameter increased, in a dose-dependent manner.
  • Blood pressure normalization in SHR was recorded, but not accompanied by full structural normalization compared to Wistar-Kyoto rats.

Structured PICO

Does perindopril dose-dependently reduce blood pressure and improve small-artery structure in spontaneously hypertensive rats?

P
Population
Spontaneously hypertensive rats treated from age 4 to 24 weeks with perindopril and followed until 36 weeks of age to assess blood pressure and small-artery structure.
I
Intervention
Perindopril at three doses (0.4, 0.8, or 1.5 mg/kg per day) administered from age 4 to 24 weeks.
C
Comparator
Untreated spontaneously hypertensive rats (SHR) and Wistar-Kyoto rats.
O
Outcome
Blood pressure and small-artery structure (media-lumen ratio, media area, lumen diameter) during treatment and recovery of blood pressure after treatment withdrawal.surrogate

In spontaneously hypertensive rats, perindopril dose-dependently reduces blood pressure and improves small-artery structure, with persistent effects after treatment withdrawal.

Abstract

Long-term treatment of young spontaneously hypertensive rats (SHR) with angiotensin-converting enzyme (ACE) inhibitors has a persistent effect on blood pressure when treatment is withdrawn. The aim of the present study was to determine whether this effect could be mediated by the effect of treatment on resistance-artery structure. We determined the dose dependence of ACE-inhibitor therapy on blood pressure and small-artery structure during treatment and on the recovery of blood pressure when treatment was withdrawn. SHR (40 per group) were treated from age 4 to 24 weeks with one of three doses of perindopril (0.4, 0.8, or 1.5 mg/kg per day). Control groups were untreated SHR and Wistar-Kyoto rats. At 24 weeks, treatment was stopped and small arteries were taken from half of the rats from the mesenteric, femoral, cerebral, and coronary vascular beds for morphological and functional measurements. The blood pressure of the other half of the rats was followed until 36 weeks of age. During treatment, perindopril caused a dose-dependent reduction in blood pressure and in the media-lumen ratio and media area of the small arteries, whereas there was a dose-dependent increase in lumen diameter. The effect of treatment on the structure of arteries from the different vascular beds was homogeneous. Compared with values from Wistar-Kyoto rats, blood pressure normalization in SHR was not associated with full normalization of structure. After withdrawal of treatment, there was an inverse relation between perindopril dose and the persistent effect.(ABSTRACT TRUNCATED AT 250 WORDS)

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Cite This Study

Thybo et al. (1994) studied Hypertension (spontaneously hypertensive rats). Perindopril vs. Untreated SHR and Wistar-Kyoto rats was evaluated on Blood pressure and small-artery structure (media-lumen ratio, media area, lumen diameter). Perindopril caused a dose-dependent reduction in blood pressure and media-lumen ratio during treatment, with an inverse relation between dose and persistent effect after withdrawal.

synapsesocial.com/papers/6a6c50d447a1bfb288f37ed0https://doi.org/10.1161/01.hyp.23.5.659
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