Literature DB >> 10416043

Coenzyme Q10 improves the tolerance of the senescent myocardium to aerobic and ischemic stress: studies in rats and in human atrial tissue.

F L Rosenfeldt1, S Pepe, R Ou, J A Mariani, M A Rowland, P Nagley, A W Linnane.   

Abstract

The inferior recovery of cardiac function after interventional cardiac procedures in elderly patients compared to younger patients suggests that the aged myocardium is more sensitive to stress. We report two studies that demonstrate an age-related deficit in myocardial performance after aerobic and ischemic stress and the capacity of CoQ10 treatment to correct age-specific diminished recovery of function. In Study 1 the functional recovery of young (4 mo) and senescent (35 mo) isolated working rat hearts after aerobic stress produced by rapid electrical pacing was examined. After pacing, the senescent hearts, compared to young, showed reduced recovery of pre-stress work performance. CoQ10 pretreatment (daily intraperitoneal injections of 4 mg/kg CoQ10 for 6 weeks) in senescent hearts improved their recovery to match that of young hearts. Study 2 tested whether the capacity of human atrial trabeculae (obtained during surgery) to recover contractile function, following ischemic stress in vitro (60 min), is decreased with age and whether this decrease can be reversed by CoQ10. Trabeculae from older individuals (> or = 70 yr) showed reduced recovery of developed force after simulated ischemia compared to younger counterparts (< 70 yr). Notably, this age-associated effect was prevented in trabeculae pretreated in vitro (30 min at 24 degrees C) with CoQ10 (400 MicroM). We measured significantly lower CoQ10 content in trabeculae from > or = 70 yr patients. In vitro pretreatment raised trabecular CoQ10 content to similar levels in all groups. We conclude that, compared to younger counterparts, the senescent myocardium of rats and humans has a reduced capacity to tolerate ischemic or aerobic stress and recover pre-stress contractile performance, however, this reduction is attenuated by CoQ10 pretreatment.

Entities:  

Mesh:

Substances:

Year:  1999        PMID: 10416043     DOI: 10.1002/biof.5520090226

Source DB:  PubMed          Journal:  Biofactors        ISSN: 0951-6433            Impact factor:   6.113


  6 in total

1.  Coenzyme q10 and statin-induced mitochondrial dysfunction.

Authors:  Richard Deichmann; Carl Lavie; Samuel Andrews
Journal:  Ochsner J       Date:  2010

2.  Dysfunctional survival-signaling and stress-intolerance in aged murine and human myocardium.

Authors:  Jason N Peart; Salvatore Pepe; Melissa E Reichelt; Nikkie Beckett; Louise See Hoe; Victoria Ozberk; Ingrid R Niesman; Hemal H Patel; John P Headrick
Journal:  Exp Gerontol       Date:  2013-12-04       Impact factor: 4.032

3.  Effect of co-enzyme Q10 and alpha-lipoic acid on response of rabbit urinary bladder to repetitive stimulation and in vitro ischemia.

Authors:  Wei-Yu Lin; Alexandra Rehfuss; Catherine Schuler; Robert M Levin
Journal:  Urology       Date:  2008-02-20       Impact factor: 2.649

4.  Influence of diagnostic categories, age, and gender on antioxidative defense and lipid peroxidation in skeletal muscle of patients with neuromuscular diseases.

Authors:  Hans-Joerg Stuerenburg; Birgit Stangneth; Alfried Kohlschütter; Barbara Finckh
Journal:  J Am Aging Assoc       Date:  2003-01

Review 5.  Bioenergetic and antioxidant properties of coenzyme Q10: recent developments.

Authors:  Gian Paolo Littarru; Luca Tiano
Journal:  Mol Biotechnol       Date:  2007-09       Impact factor: 2.695

6.  Mitochondria and the aging heart.

Authors:  Ketul R Chaudhary; Haitham El-Sikhry; John M Seubert
Journal:  J Geriatr Cardiol       Date:  2011-09       Impact factor: 3.327

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.