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May 1, 1982Proceedings of the National Academy of Sciences265 citationsOpen Access

Regression of left ventricular hypertrophy and prevention of left ventricular dysfunction by captopril in the spontaneously hypertensive rat.

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JPJ M PfefferMPMichael A. PfefferIMI. Mirsky

Key Result

Chronic therapy with captopril reduced left ventricular hypertrophy in spontaneously hypertensive rats (3.01 vs 4.37 mg/g; P<0.02) and prevented the deterioration of cardiac performance.

Structured PICO

Does captopril reduce left ventricular hypertrophy and improve cardiac performance in spontaneously hypertensive rats?

P
Population
14-month-old female spontaneously hypertensive rats (SHR) and normotensive American Wistar rats (NWR)
I
Intervention
Captopril (2 g/liter of drinking water) for 10 months
C
Comparator
Untreated SHR and NWR
O
Outcome
Left ventricular hypertrophy (mg/g of body weight) and cardiac performance (aortic blood flows, stroke volume, ejection-fraction index)surrogate

Chronic captopril therapy produces marked regression of cardiac hypertrophy and prevents deterioration of cardiac performance in a rat model of long-standing hypertension.

Main Result

Absolute Event Rate: 3.01% vs 4.37%

p-value: p=<0.02

Abstract

To determine whether chronic antihypertensive therapy prevents the progression of cardiac hypertrophy and the deterioration in cardiac performance observed in spontaneously hypertensive rats (SHR) with long-term hypertension, 14-month-old female SHR and normotensive American Wistar rats (NWR) were treated for 10 months with an inhibitor of angiotensin I-converting enzyme, captopril (2 g/liter of drinking water). Captopril reduced the marked left ventricular hypertrophy of 24-month-old SHR (untreated, 4.37 +/- 0.2 mg/g of body weight; treated, 3.01 +/- 0.1 mg/g; P less than 0.02) to levels observed in 6-month-old SHR. Treatment prevented the reductions in baseline and maximal aortic blood flows that occurred in SHR between ages 12 and 24 months yet had no effect on the blood flows of NWR. The diminished maximal stroke volume of untreated SHR was ejected from a significantly increased left ventricular end-diastolic volume, so that the ejection-fraction index was markedly reduced (24-month-old untreated NWR, 84 +/- 3%; untreated SHR, 56 +/- 5%; P less than 0.001). Therapy restores this index in SHR to normal (77 +/- 4%). The relationship between ejection-fraction index, and afterload was also normal in treated SHR. Thus, chronic therapy with captopril produced a marked regression of cardiac hypertrophy and prevented the deterioration of cardiac performance in SHR with long-standing hypertension.

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Cite This Study

Pfeffer et al. (1982) studied Hypertension and cardiac hypertrophy. Captopril vs. Untreated SHR and NWR was evaluated on Left ventricular hypertrophy (mg/g of body weight) (p=<0.02). Chronic therapy with captopril reduced left ventricular hypertrophy in spontaneously hypertensive rats (3.01 vs 4.37 mg/g; P<0.02) and prevented the deterioration of cardiac performance.

synapsesocial.com/papers/6a093458071d6da4469612d3https://doi.org/10.1073/pnas.79.10.3310
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