» Articles » PMID: 22140052

Reduced Mitochondrial Ca2+ Loading and Improved Functional Recovery After Ischemia-reperfusion Injury in Old Vs. Young Guinea Pig Hearts

Overview
Authors
Affiliations
Soon will be listed here.
Abstract

Oxidative damage and impaired cytosolic Ca(2+) concentration ([Ca(2+)](cyto)) handling are associated with mitochondrial [Ca(2+)] ([Ca(2+)](mito)) overload and depressed functional recovery after cardiac ischemia-reperfusion (I/R) injury. We hypothesized that hearts from old guinea pigs would demonstrate impaired [Ca(2+)](mito) handling, poor functional recovery, and a more oxidized state after I/R injury compared with hearts from young guinea pigs. Hearts from young (∼4 wk) and old (>52 wk) guinea pigs were isolated and perfused with Krebs-Ringer solution (2.1 mM Ca(2+) concentration at 37°C). Left ventricular pressure (LVP, mmHg) was measured with a balloon, and NADH, [Ca(2+)](mito) (nM), and [Ca(2+)](cyto) (nM) were measured by fluorescence with a fiber optic probe placed against the left ventricular free wall. After baseline (BL) measurements, hearts were subjected to 30 min global ischemia and 120 min reperfusion (REP). In old vs. young hearts we found: 1) percent infarct size was lower (27 ± 9 vs. 57 ± 2); 2) developed LVP (systolic-diastolic) was higher at 10 min (57 ± 11 vs. 29 ± 2) and 60 min (55 ± 10 vs. 32 ± 2) REP; 3) diastolic LVP was lower at 10 and 60 min REP (6 ± 3 vs. 29 ± 4 and 3 ± 3 vs. 21 ± 4 mmHg); 4) mean [Ca(2+)](cyto) was higher during ischemia (837 ± 39 vs. 541 ± 39), but [Ca(2+)](mito) was lower (545 ± 62 vs. 975 ± 38); 5) [Ca(2+)](mito) was lower at 10 and 60 min REP (129 ± 2 vs. 293 ± 23 and 122 ± 2 vs. 234 ± 15); 6) reduced inotropic responses to dopamine and digoxin; and 7) NADH was elevated during ischemia in both groups and lower than BL during REP. Contrary to our stated hypotheses, old hearts showed reduced [Ca(2+)](mito), decreased infarction, and improved basal mechanical function after I/R injury compared with young hearts; no differences were noted in redox state due to age. In this model, aging-associated protection may be linked to limited [Ca(2+)](mito) loading after I/R injury despite higher [Ca(2+)](cyto) load during ischemia in old vs. young hearts.

Citing Articles

Age-Dependent Changes in Calcium Regulation after Myocardial Ischemia-Reperfusion Injury.

Bencurova M, Lysikova T, Leskova Majdova K, Kaplan P, Racay P, Lehotsky J Biomedicines. 2023; 11(4).

PMID: 37189811 PMC: 10136092. DOI: 10.3390/biomedicines11041193.


Hypothermia Prevents Cardiac Dysfunction during Acute Ischemia Reperfusion by Maintaining Mitochondrial Bioenergetics and by Promoting Hexokinase II Binding to Mitochondria.

Sun J, Mishra J, Yang M, Stowe D, Heisner J, An J Oxid Med Cell Longev. 2022; 2022:4476448.

PMID: 35873800 PMC: 9301761. DOI: 10.1155/2022/4476448.


Aging Attenuates Cardiac Contractility and Affects Therapeutic Consequences for Myocardial Infarction.

Dong M, Yang Z, Fang H, Xiang J, Xu C, Zhou Y Aging Dis. 2020; 11(2):365-376.

PMID: 32257547 PMC: 7069457. DOI: 10.14336/AD.2019.0522.


Developmental increase in β-MHC enhances sarcomere length-dependent activation in the myocardium.

Reda S, Gollapudi S, Chandra M J Gen Physiol. 2019; 151(5):635-644.

PMID: 30602626 PMC: 6504293. DOI: 10.1085/jgp.201812183.


Endogenous and Agonist-induced Opening of Mitochondrial Big Versus Small Ca2+-sensitive K+ Channels on Cardiac Cell and Mitochondrial Protection.

Stowe D, Yang M, Heisner J, Camara A J Cardiovasc Pharmacol. 2017; 70(5):314-328.

PMID: 28777255 PMC: 5726766. DOI: 10.1097/FJC.0000000000000524.


References
1.
Riess M, Camara A, Novalija E, Chen Q, Rhodes S, Stowe D . Anesthetic preconditioning attenuates mitochondrial Ca2+ overload during ischemia in Guinea pig intact hearts: reversal by 5-hydroxydecanoic acid. Anesth Analg. 2002; 95(6):1540-6, table of contents. DOI: 10.1097/00000539-200212000-00013. View

2.
Rhodes S, Ropella K, Camara A, Chen Q, Riess M, Stowe D . How inotropic drugs alter dynamic and static indices of cyclic myoplasmic [Ca2+] to contractility relationships in intact hearts. J Cardiovasc Pharmacol. 2003; 42(4):539-53. DOI: 10.1097/00005344-200310000-00013. View

3.
Fitzsimons D, Patel J, Moss R . Aging-dependent depression in the kinetics of force development in rat skinned myocardium. Am J Physiol. 1999; 276(5):H1511-9. DOI: 10.1152/ajpheart.1999.276.5.H1511. View

4.
Stowe D, Varadarajan S, An J, Smart S . Reduced cytosolic Ca(2+) loading and improved cardiac function after cardioplegic cold storage of guinea pig isolated hearts. Circulation. 2000; 102(10):1172-7. DOI: 10.1161/01.cir.102.10.1172. View

5.
Lakatta E, Levy D . Arterial and cardiac aging: major shareholders in cardiovascular disease enterprises: Part II: the aging heart in health: links to heart disease. Circulation. 2003; 107(2):346-54. DOI: 10.1161/01.cir.0000048893.62841.f7. View