Literature DB >> 17023203

Chronic oral ascorbic acid therapy worsens skeletal muscle metabolism in patients with chronic heart failure.

Angus K Nightingale1, Jenifer G Crilley, Nicholas C Pegge, Ernie A Boehm, Catherine Mumford, Doris J Taylor, Peter Styles, Kieran Clarke, Michael P Frenneaux.   

Abstract

BACKGROUND: Chronic heart failure (CHF) is associated with abnormalities of skeletal muscle metabolism. This may be due to impaired oxygen delivery as a result of endothelial dysfunction. AIMS: We postulated that ascorbic acid would improve oxygen delivery to exercising muscle and improve skeletal muscle metabolism.
METHODS: We studied skeletal muscle metabolism using (31)P magnetic resonance spectroscopy in 39 CHF patients. Endothelial function was assessed by changes in pulse wave velocity. Subjects were randomised to receive 4 g ascorbic acid daily for 4 weeks in a placebo-controlled double-blind study.
RESULTS: Ascorbic acid significantly increased phosphocreatine utilization during exercise. In addition, glycolytic ATP synthesis increased in the ascorbic acid group (change in rate of ATP synthesis at 1 min -0.21+/-0.76 with placebo, 2.06+/-0.60 following ascorbic acid; p<0.05). Phosphocreatine and ADP recovery after exercise were not changed. The fall in pulse wave velocity during reactive hyperaemia was increased by ascorbic acid from -6.3+/-2.6% to -12.1+/-2.0% (p<0.05).
CONCLUSIONS: These findings suggest that ascorbic acid increased both phosphocreatine utilization and glycolytic ATP synthesis during exercise in patients with CHF implying worsened skeletal muscle metabolism despite improvements in endothelial function.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 17023203     DOI: 10.1016/j.ejheart.2006.06.006

Source DB:  PubMed          Journal:  Eur J Heart Fail        ISSN: 1388-9842            Impact factor:   15.534


  7 in total

Review 1.  Effects of vitamin C supplementation on blood pressure: a meta-analysis of randomized controlled trials.

Authors:  Stephen P Juraschek; Eliseo Guallar; Lawrence J Appel; Edgar R Miller
Journal:  Am J Clin Nutr       Date:  2012-04-04       Impact factor: 7.045

2.  Influence of Nrf2 activators on subcellular skeletal muscle protein and DNA synthesis rates after 6 weeks of milk protein feeding in older adults.

Authors:  Adam R Konopka; Jaime L Laurin; Robert V Musci; Christopher A Wolff; Justin J Reid; Laurie M Biela; Qian Zhang; Fredrick F Peelor; Christopher L Melby; Karyn L Hamilton; Benjamin F Miller
Journal:  Geroscience       Date:  2017-03-10       Impact factor: 7.713

3.  Evaluation of skeletal muscle during calf exercise by 31-phosphorus magnetic resonance spectroscopy in patients on statin medications.

Authors:  Jim S Wu; Catherine Buettner; Howard Smithline; Long H Ngo; Robert L Greenman
Journal:  Muscle Nerve       Date:  2011-01       Impact factor: 3.217

4.  Mitochondrial ROS Drive Sudden Cardiac Death and Chronic Proteome Remodeling in Heart Failure.

Authors:  Swati Dey; Deeptankar DeMazumder; Agnieszka Sidor; D Brian Foster; Brian O'Rourke
Journal:  Circ Res       Date:  2018-06-13       Impact factor: 17.367

Review 5.  Mitochondrial dysfunction and oxidative stress in heart disease.

Authors:  Jessica N Peoples; Anita Saraf; Nasab Ghazal; Tyler T Pham; Jennifer Q Kwong
Journal:  Exp Mol Med       Date:  2019-12-19       Impact factor: 8.718

Review 6.  The Comparative Effects of Different Types of Oral Vitamin Supplements on Arterial Stiffness: A Network Meta-Analysis.

Authors:  Alicia Saz-Lara; Iván Cavero-Redondo; Vicente Martínez-Vizcaíno; Isabel Antonia Martínez-Ortega; Blanca Notario-Pacheco; Carlos Pascual-Morena
Journal:  Nutrients       Date:  2022-02-27       Impact factor: 5.717

Review 7.  Molecular mechanisms of sacubitril/valsartan in cardiac remodeling.

Authors:  Nor Hidayah Mustafa; Juriyati Jalil; Satirah Zainalabidin; Mohammed S M Saleh; Ahmad Yusof Asmadi; Yusof Kamisah
Journal:  Front Pharmacol       Date:  2022-08-08       Impact factor: 5.988

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.