Literature DB >> 10569188

Effects of L-carnitine and its acetyl and propionyl esters on ATP and PCr levels of isolated rat hearts perfused without fatty acids and investigated by means of 31P-NMR spectroscopy.

H Löster1, T Keller, J Grommisch, W Gründer.   

Abstract

31P-NMR in vivo spectroscopy is a non-invasive and non-hazardous technique which investigates chemical composition and metabolism of living objects, for example by determining phosphocreatine (PCr) and ATP concentrations. In the present study we investigated the influence of L-carnitine, acetyl-L-carnitine and propionyl-L-carnitine on the energetic state of the Langendorff rat heart subjected to an ischemic period of 20 min followed by a reperfusion period of 60 min. To avoid an overlapping of the effects of fatty acids and glucose, the hearts were perfused with a Tyrode solution containing no fatty acids. Ischemia causes a rapid decrease in the PCr signal, followed by a decrease in the ATP signal after a prolonged period of ischemia. At the same time, a drastic increase in the Pi signal was observed. A partial recovery of the ATP and PCr signals was observed in the reperfusion period. With L-carnitine a markedly improved recovery of the high energy phosphates (e.g. increased PCr/P ratios) was found. With acetyl-L-carnitine this effect was enhanced in the first postischemic phase. It was followed, however, by a more rapid decrease in the PCr/Pi ratio in the late reperfusion period. The effect of propionyl-L-carnitine was not significantly improved in the first minutes of the reperfusion period, but during the whole reperfusion phase a stabilization of the PCr/Pi ratio was observed. Intracellular pH can be calculated from determination of the Pi-chemical shift. This shows that L-carnitine and its derivatives have a protective effect against intracellular pH decrease during ischemia. L-carnitine improves the energetic state of the heart, which leads to increased ischemia tolerance. Hearts under L-carnitine were able to tolerate up to four ischemia-reperfusion periods in succession, whereas the controls were not able to do so. These NMR results confirm the hypothesis that L-carnitine and its esters have a protective effect in the reperfusion period of the ischemic rat heart. This could be of importance for the treatment of ischemic cardiac diseases.

Entities:  

Mesh:

Substances:

Year:  1999        PMID: 10569188     DOI: 10.1023/a:1006966817286

Source DB:  PubMed          Journal:  Mol Cell Biochem        ISSN: 0300-8177            Impact factor:   3.396


  76 in total

1.  Modulation of adenine nucleotide translocase activity during myocardial ischemia.

Authors:  A L Shug; R Subramanian
Journal:  Z Kardiol       Date:  1987

2.  Effect of propionyl-L-carnitine on mechanical function of isolated rabbit heart.

Authors:  R Ferrari; E Pasini; E Condorelli; A Boraso; R Lisciani; A Marzo; O Visiou
Journal:  Cardiovasc Drugs Ther       Date:  1991-02       Impact factor: 3.727

3.  Reversible inhibition of adenine nucleotide translocation by long chain acyl-CoA esters in bovine heart mitochondria and inverted submitochondrial particles. Comparison with atractylate and bongkrekic acid.

Authors:  B H Chua; E Shrago
Journal:  J Biol Chem       Date:  1977-10-10       Impact factor: 5.157

4.  Intracellular high-energy phosphate transfer in normal and hypertrophied myocardium.

Authors:  J A Bittl; J S Ingwall
Journal:  Circulation       Date:  1987-01       Impact factor: 29.690

5.  Stunned myocardium after rapid correction of acidosis. Increased oxygen cost of contractility and the role of the Na(+)-H+ exchange system.

Authors:  K Hata; T Takasago; A Saeki; T Nishioka; Y Goto
Journal:  Circ Res       Date:  1994-05       Impact factor: 17.367

6.  Effects of ischemia on rat myocardial function and metabolism in diabetes.

Authors:  D Feuvray; J A Idell-Wenger; J R Neely
Journal:  Circ Res       Date:  1979-03       Impact factor: 17.367

7.  Effect of ischemia on NMR detection of phosphorylated metabolites in the intact rat heart.

Authors:  F M Jeffrey; C J Storey; R L Nunnally; C R Malloy
Journal:  Biochemistry       Date:  1989-06-27       Impact factor: 3.162

Review 8.  Paradoxical role of lipid metabolism in heart function and dysfunction.

Authors:  N S Dhalla; V Elimban; H Rupp
Journal:  Mol Cell Biochem       Date:  1992-10-21       Impact factor: 3.396

9.  Anaplerotic effect of propionyl carnitine in rat heart mitochondria.

Authors:  V Tassani; F Cattapan; L Magnanimi; A Peschechera
Journal:  Biochem Biophys Res Commun       Date:  1994-03-15       Impact factor: 3.575

10.  Effects of L-propionylcarnitine on mechanical recovery during reflow in intact hearts.

Authors:  A J Liedtke; L DeMaison; S H Nellis
Journal:  Am J Physiol       Date:  1988-07
View more
  5 in total

Review 1.  The use of levo-carnitine in children with renal disease: a review and a call for future studies.

Authors:  Brook Belay; Nora Esteban-Cruciani; Christine A Walsh; Frederick J Kaskel
Journal:  Pediatr Nephrol       Date:  2005-12-23       Impact factor: 3.714

2.  L-carnitine reduces malondialdehyde concentrations in isolated rat hearts in dependence on perfusion conditions.

Authors:  H Löster; U Böhm
Journal:  Mol Cell Biochem       Date:  2001-01       Impact factor: 3.396

3.  The protective effect of L-carnitine on ischemia-reperfusion heart.

Authors:  Jiang Xie; Qiutang Zeng; Le Wang
Journal:  J Huazhong Univ Sci Technolog Med Sci       Date:  2006

Review 4.  Critical update for the clinical use of L-carnitine analogs in cardiometabolic disorders.

Authors:  Carmen Mingorance; Rosalía Rodríguez-Rodríguez; María Luisa Justo; María Alvarez de Sotomayor; María Dolores Herrera
Journal:  Vasc Health Risk Manag       Date:  2011-03-28

5.  Neuroprotective effects of L-carnitine against oxygen-glucose deprivation in rat primary cortical neurons.

Authors:  Yu Jin Kim; Soo Yoon Kim; Dong Kyung Sung; Yun Sil Chang; Won Soon Park
Journal:  Korean J Pediatr       Date:  2012-07-17
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.