Effects of an increase in intracellular free [Mg2+] after myocardial stunning on sarcoplasmic reticulum Ca2+ transport
- PMID: 1884459
- DOI: 10.1161/01.cir.84.3.1378
Effects of an increase in intracellular free [Mg2+] after myocardial stunning on sarcoplasmic reticulum Ca2+ transport
Abstract
Background: Myocardial stunning has been associated with a greater than twofold increase in intracellular free [Mg2+] from 0.6 to 1.5 mM. The effect of this increase in free [Mg2+] on the function of the sarcoplasmic reticulum (SR) Ca2+ pump was assessed in SR isolated from Langendorff perfused, isovolumic rabbit hearts after 15 minutes of global ischemia.
Methods and results: Our results indicate that myocardial stunning results in a shift in the Ca2+ sensitivity of oxalate-supported, Ca2+ transport over the entire range of free [Ca2+] associated with the cardiac cycle. Using 0.6 mM free Mg2+ as control, maximal rates of Ca2+ transport occurred at 1 microM free Ca2+ (control, 519 +/- 32; stunned, 337 +/- 37 nmol Ca2+.min-1.mg-1). At 0.56 microM free Ca2+, SR Ca2+ transport was reduced from a control of 351 +/- 49 to 263 +/- 12 nmol Ca2+.min-1.mg-1 at 0.6 mM free [Mg2+]. Moreover, an increase in the free [Mg2+] from 0.6 to 1.5 mM results in a greater shift in the Ca2+ activation curve with no change in the level of maximal activation. Ca2+ transport at 0.56 microM free Ca2+ was shifted in the stunned SR from 263 +/- 12 to 138 +/- 29 nmol Ca2+.min-1.mg-1 at 0.6 and 1.5 mM free Mg2+, respectively.
Conclusions: These results indicate that an increase in free [Mg2+] after stunning in combination with the inherent defect in the SR Ca2+ ATPase may reduce the ability of the cell to regulate Ca2+ to a greater extent than previously observed. This impairment in Ca2+ regulatory function may contribute directly to the increase in diastolic tone and indirectly to the reduced systolic function characteristic of the stunned myocardium.
Similar articles
-
Effect of increased free [Mg2+]i with myocardial stunning on sarcoplasmic reticulum Ca(2+)-ATPase activity.Am J Physiol. 1991 Jul;261(1 Pt 2):H229-35. doi: 10.1152/ajpheart.1991.261.1.H229. Am J Physiol. 1991. PMID: 1830458
-
Alterations in cardiac sarcoplasmic reticulum calcium transport in the postischemic "stunned" myocardium.Circ Res. 1989 Aug;65(2):526-30. doi: 10.1161/01.res.65.2.526. Circ Res. 1989. PMID: 2752555
-
Magnesium permeability of sarcoplasmic reticulum. Mg2+ is not countertransported during ATP-dependent Ca2+ uptake by sarcoplasmic reticulum.J Biol Chem. 1985 Sep 25;260(21):11697-705. J Biol Chem. 1985. PMID: 3930482
-
Role of sarcoplasmic reticulum in the contractile dysfunction during myocardial ischaemia and reperfusion.Physiol Res. 1997;46(5):333-9. Physiol Res. 1997. PMID: 9728477 Review.
-
Mitochondrial Bioenergetics During Ischemia and Reperfusion.Adv Exp Med Biol. 2017;982:141-167. doi: 10.1007/978-3-319-55330-6_8. Adv Exp Med Biol. 2017. PMID: 28551786 Review.
Cited by
-
The effect of Mg2+ on cardiac muscle function: Is CaATP the substrate for priming myofibril cross-bridge formation and Ca2+ reuptake by the sarcoplasmic reticulum?Biochem J. 2001 Mar 15;354(Pt 3):539-51. doi: 10.1042/0264-6021:3540539. Biochem J. 2001. PMID: 11237858 Free PMC article.
-
The effect of Mg2+ on Ca2+ binding to cardiac troponin C in hypertrophic cardiomyopathy associated TNNC1 variants.FEBS J. 2022 Dec;289(23):7446-7465. doi: 10.1111/febs.16578. Epub 2022 Aug 2. FEBS J. 2022. PMID: 35838319 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Research Materials
Miscellaneous