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Pharmacological strategies for improving diastolic dysfunction in the setting of chronic pulmonary hypertension.

Publication ,  Journal Article
Chen, EP; Craig, DM; Bittner, HB; Davis, RD; Van Trigt, P
Published in: Circulation
April 28, 1998

BACKGROUND: Right ventricular (RV) hypertrophy is an adaptive process that occurs in the setting of chronic pulmonary hypertension (CPH) and can lead to alterations in normal RV diastolic properties. This study was designed to investigate the effects of NO and milrinone on RV diastolic dysfunction in the setting of CPH and RV hypertrophy by use of a canine model of monocrotaline pyrrole (MCTP)-induced CPH. METHODS AND RESULTS: Sixteen mongrel dogs (22 to 24 kg) were used. Animals underwent percutaneous pulmonary artery (PA) catheterization to measure pulmonary hemodynamics before and 8 weeks after injection of 3 mg/kg MCTP (n=8) or placebo (control, n=8). Eight weeks after injection, all hearts were instrumented with a PA flow probe, sonomicrometric dimension transducers, and micromanometers. Data were collected at baseline and after both NO and milrinone administration. Diastolic properties were quantified by use of the end-diastolic pressure-volume relationship and the time constant of ventricular isovolumic relaxation. Eight weeks after injection, significant increases in the PA pressure and pulmonary vascular resistance were observed in MCTP dogs. Significant worsening of RV diastolic function occurred in association with significant increases in the ratio of RV dry weight to LV+septal dry weight. NO and milrinone administration both led to significant improvements in RV diastolic properties. CONCLUSIONS: In the setting of MCTP-induced CPH, significant worsening of RV diastolic function was observed in association with significant increases in the ratio of RV dry weight to LV+septal dry weight, suggesting that these changes are partially due to RV hypertrophy. The significant improvement in RV diastolic properties after both NO and milrinone administration suggests that these agents may be effective forms of pharmacological therapy for improving RV diastolic dysfunction in the setting of CPH.

Duke Scholars

Published In

Circulation

DOI

ISSN

0009-7322

Publication Date

April 28, 1998

Volume

97

Issue

16

Start / End Page

1606 / 1612

Location

United States

Related Subject Headings

  • Pyridones
  • Nitric Oxide
  • Milrinone
  • Hypertension, Pulmonary
  • Heart Ventricles
  • Dogs
  • Diastole
  • Chronic Disease
  • Cardiovascular System & Hematology
  • Cardiotonic Agents
 

Citation

APA
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ICMJE
MLA
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Chen, E. P., Craig, D. M., Bittner, H. B., Davis, R. D., & Van Trigt, P. (1998). Pharmacological strategies for improving diastolic dysfunction in the setting of chronic pulmonary hypertension. Circulation, 97(16), 1606–1612. https://doi.org/10.1161/01.cir.97.16.1606
Chen, E. P., D. M. Craig, H. B. Bittner, R. D. Davis, and P. Van Trigt. “Pharmacological strategies for improving diastolic dysfunction in the setting of chronic pulmonary hypertension.Circulation 97, no. 16 (April 28, 1998): 1606–12. https://doi.org/10.1161/01.cir.97.16.1606.
Chen EP, Craig DM, Bittner HB, Davis RD, Van Trigt P. Pharmacological strategies for improving diastolic dysfunction in the setting of chronic pulmonary hypertension. Circulation. 1998 Apr 28;97(16):1606–12.
Chen, E. P., et al. “Pharmacological strategies for improving diastolic dysfunction in the setting of chronic pulmonary hypertension.Circulation, vol. 97, no. 16, Apr. 1998, pp. 1606–12. Pubmed, doi:10.1161/01.cir.97.16.1606.
Chen EP, Craig DM, Bittner HB, Davis RD, Van Trigt P. Pharmacological strategies for improving diastolic dysfunction in the setting of chronic pulmonary hypertension. Circulation. 1998 Apr 28;97(16):1606–1612.

Published In

Circulation

DOI

ISSN

0009-7322

Publication Date

April 28, 1998

Volume

97

Issue

16

Start / End Page

1606 / 1612

Location

United States

Related Subject Headings

  • Pyridones
  • Nitric Oxide
  • Milrinone
  • Hypertension, Pulmonary
  • Heart Ventricles
  • Dogs
  • Diastole
  • Chronic Disease
  • Cardiovascular System & Hematology
  • Cardiotonic Agents