HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Sildenafil improves microvascular O2 delivery-to-utilization matching and accelerates exercise O2 uptake kinetics in chronic heart failure.

Abstract
Nitric oxide (NO) can temporally and spatially match microvascular oxygen (O(2)) delivery (Qo(2mv)) to O(2) uptake (Vo(2)) in the skeletal muscle, a crucial adjustment-to-exercise tolerance that is impaired in chronic heart failure (CHF). To investigate the effects of NO bioavailability induced by sildenafil intake on muscle Qo(2mv)-to-O(2) utilization matching and Vo(2) kinetics, 10 males with CHF (ejection fraction = 27 ± 6%) undertook constant work-rate exercise (70-80% peak). Breath-by-breath Vo(2), fractional O(2)extraction in the vastus lateralis {∼deoxygenated hemoglobin + myoglobin ([deoxy-Hb + Mb]) by near-infrared spectroscopy}, and cardiac output (CO) were evaluated after sildenafil (50 mg) or placebo. Sildenafil increased exercise tolerance compared with placebo by ∼20%, an effect that was related to faster on- and off-exercise Vo(2) kinetics (P < 0.05). Active treatment, however, failed to accelerate CO dynamics (P > 0.05). On-exercise [deoxy-Hb + Mb] kinetics were slowed by sildenafil (∼25%), and a subsequent response "overshoot" (n = 8) was significantly lessened or even abolished. In contrast, [deoxy-Hb + Mb] recovery was faster with sildenafil (∼15%). Improvements in muscle oxygenation with sildenafil were related to faster on-exercise Vo(2) kinetics, blunted oscillations in ventilation (n = 9), and greater exercise capacity (P < 0.05). Sildenafil intake enhanced intramuscular Qo(2mv)-to-Vo(2) matching with beneficial effects on Vo(2) kinetics and exercise tolerance in CHF. The lack of effect on CO suggests that improvement in blood flow to and within skeletal muscles underlies these effects.
AuthorsPriscila A Sperandio, Mayron F Oliveira, Miguel K Rodrigues, Danilo C Berton, Erika Treptow, Luiz E Nery, Dirceu R Almeida, J Alberto Neder
JournalAmerican journal of physiology. Heart and circulatory physiology (Am J Physiol Heart Circ Physiol) Vol. 303 Issue 12 Pg. H1474-80 (Dec 15 2012) ISSN: 1522-1539 [Electronic] United States
PMID23023868 (Publication Type: Clinical Trial, Journal Article)
Chemical References
  • Piperazines
  • Purines
  • Sulfones
  • Vasodilator Agents
  • Nitric Oxide
  • Sildenafil Citrate
  • Cyclic Nucleotide Phosphodiesterases, Type 5
  • Oxygen
Topics
  • Aged
  • Cardiac Output (drug effects, physiology)
  • Chronic Disease
  • Cyclic Nucleotide Phosphodiesterases, Type 5 (metabolism)
  • Exercise (physiology)
  • Exercise Tolerance (drug effects, physiology)
  • Heart Failure (metabolism, physiopathology)
  • Humans
  • Male
  • Microcirculation (drug effects, physiology)
  • Middle Aged
  • Muscle, Skeletal (blood supply, metabolism)
  • Nitric Oxide (metabolism)
  • Oxygen (metabolism)
  • Oxygen Consumption (drug effects, physiology)
  • Piperazines (pharmacology)
  • Prospective Studies
  • Purines (pharmacology)
  • Regional Blood Flow (physiology)
  • Signal Transduction (drug effects, physiology)
  • Sildenafil Citrate
  • Sulfones (pharmacology)
  • Vasodilator Agents (pharmacology)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: