17β-Estradiol mediates superior adaptation of right ventricular function to acute strenuous exercise in female rats with severe pulmonary hypertension

Tim Lahm, Andrea L. Frump, Marjorie E. Albrecht, Amanda J. Fisher, Todd G. Cook, Thomas J. Jones, Bakhtiyor Yakubov, Jordan Whitson, Robyn K. Fuchs, Aiping Liu, Naomi C. Chesler, M. Beth Brown

Research output: Contribution to journalArticle

21 Citations (Scopus)

Abstract

17β-Estradiol (E2) exerts protective effects on right ventricular (RV) function in pulmonary arterial hypertension (PAH). Since acute exercise-induced increases in afterload may lead to RV dysfunction in PAH, we sought to determine whether E2 allows for superior RV adaptation after an acute exercise challenge. We studied echocardiographic, hemodynamic, structural, and biochemical markers of RV function in male and female rats with sugen/hypoxia (SuHx)-induced pulmonary hypertension, as well as in ovariectomized (OVX) SuHx females, with or without concomitant E2 repletion (75 g·kg–1·day–1) immediately after 45 min of treadmill running at 75% of individually determined maximal aerobic capacity (75% aerobic capacity reserve). Compared with males, intact female rats exhibited higher stroke volume and cardiac indexes, a strong trend for better RV compliance, and less pronounced increases in indexed total pulmonary resistance. OVX abrogated favorable RV adaptations, whereas E2 repletion after OVX markedly improved RV function. E2’s effects on pulmonary vascular remodeling were complex and less robust than its RV effects. Postexercise hemodynamics in females with endogenous or exogenous E2 were similar to hemodynamics in nonexercised controls, whereas OVX rats exhibited more severely altered postexercise hemodynamics. E2 mediated inhibitory effects on RV fibrosis and attenuated increases in RV collagen I/III ratio. Proapoptotic signaling, endothelial nitric oxide synthase phosphorylation, and autophagic flux markers were affected by E2 depletion and/or repletion. Markers of impaired autophagic flux correlated with endpoints of RV structure and function. Endogenous and exogenous E2 exerts protective effects on RV function measured immediately after an acute exercise challenge. Harnessing E2’s mechanisms may lead to novel RV-directed therapies.

Original languageEnglish (US)
Pages (from-to)L375-L388
JournalAmerican Journal of Physiology - Lung Cellular and Molecular Physiology
Volume311
Issue number2
DOIs
StatePublished - Aug 1 2016

Fingerprint

Right Ventricular Function
Pulmonary Hypertension
Estradiol
Exercise
Hemodynamics
Right Ventricular Dysfunction
Lung
Nitric Oxide Synthase Type III
Running
Stroke Volume
Compliance
Fibrosis
Collagen
Biomarkers
Phosphorylation

Keywords

  • Apoptosis
  • Autophagy
  • Endothelial nitric oxide synthase
  • Fibrosis
  • Sugen/hypoxia

ASJC Scopus subject areas

  • Physiology
  • Medicine(all)
  • Pulmonary and Respiratory Medicine
  • Cell Biology
  • Physiology (medical)

Cite this

17β-Estradiol mediates superior adaptation of right ventricular function to acute strenuous exercise in female rats with severe pulmonary hypertension. / Lahm, Tim; Frump, Andrea L.; Albrecht, Marjorie E.; Fisher, Amanda J.; Cook, Todd G.; Jones, Thomas J.; Yakubov, Bakhtiyor; Whitson, Jordan; Fuchs, Robyn K.; Liu, Aiping; Chesler, Naomi C.; Brown, M. Beth.

In: American Journal of Physiology - Lung Cellular and Molecular Physiology, Vol. 311, No. 2, 01.08.2016, p. L375-L388.

Research output: Contribution to journalArticle

Lahm, Tim ; Frump, Andrea L. ; Albrecht, Marjorie E. ; Fisher, Amanda J. ; Cook, Todd G. ; Jones, Thomas J. ; Yakubov, Bakhtiyor ; Whitson, Jordan ; Fuchs, Robyn K. ; Liu, Aiping ; Chesler, Naomi C. ; Brown, M. Beth. / 17β-Estradiol mediates superior adaptation of right ventricular function to acute strenuous exercise in female rats with severe pulmonary hypertension. In: American Journal of Physiology - Lung Cellular and Molecular Physiology. 2016 ; Vol. 311, No. 2. pp. L375-L388.
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