Dynamics of interstitial calcium in rat myocardial ischemia reperfusion injury in vivo

Shao-hong Huang, Jiang-ping Song, Jie Qin, Jian Rong, Zhong-kai Wu

Current Medical Science ›› 2014, Vol. 34 ›› Issue (1) : 37-41.

Current Medical Science ›› 2014, Vol. 34 ›› Issue (1) : 37-41. DOI: 10.1007/s11596-014-1229-9
Article

Dynamics of interstitial calcium in rat myocardial ischemia reperfusion injury in vivo

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Abstract

Intracellular calcium overload is a key factor for myocardial ischemia reperfusion injury (IR). However, there was no report for interstitial calcium concentration dynamics. We investigated the interstitial calcium dynamics in rat myocardial IR model in vivo. A microdialysis system was involved, and the time delay of the system and recovery time was introduced and tested with a fluids switching method. Twelve SD rats were divided into IR or control group. Myocardial IR was induced by ligating (20 min) then releasing (60 min) the suture underlying left anterior descending branch. Mycrodialyisis probe was implanted into the left ventricular myocardium perfusion area for occlusion. Dialysate samples were collected every 10 min. Dialysate calcium concentration was detected with an atomic absorption spectrophotometer. Recovery time for the microdialysis system was 20 min, and recovery rate was 16%. Dialysate calcium concentration showed no changes during ischemia, descended immediately after reperfusion, reached the lowest level (67% of baseline value) 20 min after reperfusion, then escalated slowly. Recovery time was an important parameter for mycrodialysis technique, and it should not be neglected and needed to be tested. Our data suggest that interstitial calcium concentration in rats with myocardial IR in vivo kept steady in ischemia, descended rapidly at the initial reperfusion, then rebounded slowly. In conclusion, we introduced the concept of recovery time for microdialysis and provided a simple testing method.

Keywords

myocardium / ischemia / reperfusion / calcium / microdialysis

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Shao-hong Huang, Jiang-ping Song, Jie Qin, Jian Rong, Zhong-kai Wu. Dynamics of interstitial calcium in rat myocardial ischemia reperfusion injury in vivo. Current Medical Science, 2014, 34(1): 37‒41 https://doi.org/10.1007/s11596-014-1229-9

References

[1]
GiorgiC, RomagnoliA, PintonP, et al.. Ca2+ signaling, mitochondria and cell death. Curr Mol Med, 2008, 8(2): 119-130
CrossRef Google scholar
[2]
JavadovS, KarmazynM. Mitochondrial permeability transition pore opening as an endpoint to initiate cell death and as a putative target for cardioprotection. Cell Physiol Biochem, 2007, 20(1–4): 1-22
CrossRef Google scholar
[3]
MurphyE, SteenbergenC. Ion transport and energetics during cell death and protection. Physiology (Bethesda), 2008, 23: 115-123
CrossRef Google scholar
[4]
LeeMS, WuYS, YangDY, et al.. Significantly decreased extracellular magnesium in brains of gerbils subjected to cerebral ischemia. Clin Chim Acta, 2002, 318(1–2): 121-125
CrossRef Google scholar
[5]
LinMC, HuangYL, LiuHW, et al.. On-line microdialysis-graphite furnace atomic absorption spectrometry in the determination of brain magnesium levels in gerbils subjected to cerebral ischemia/reperfusion. J Am Coll Nutr, 2004, 23(5): 561S-565S
CrossRef Google scholar
[6]
ObataT. Adenosine production and its interaction with protection of ischemic and reperfusion injury of the myocardium. Life Sci, 2002, 71(18): 2083-2103
CrossRef Google scholar
[7]
MiuraT, KawamuraS, TatsunoH, et al.. Ischemic preconditioning attenuates cardiac sympathetic nerve injury via ATP-sensitive potassium channels during myocardial ischemia. Circulation, 2001, 104(9): 1053-1058
CrossRef Google scholar
[8]
KennergrenC, MantovaniV, StrindbergL, et al.. Myocardial interstitial glucose and lactate before, during, and after cardioplegic heart arrest. Am J Physiol Endocrinol Metab, 2003, 284(4): E788-E794
[9]
MultaniMM, IkonomidisJS, KimPY, et al.. Dynamic and differential changes in myocardial and plasma endothelin in patients undergoing cardiopulmonary bypass. J Thorac Cardiovasc Surg, 2005, 129(3): 584-590
CrossRef Google scholar
[10]
PokelaM, DahlbackaS, BiancariF, et al.. pH-stat versus alpha-stat perfusion strategy during experimental hypothermic circulatory arrest: a microdialysis study. Ann Thorac Surg, 2003, 76(4): 1215-1226
CrossRef Google scholar
[11]
MurphyE, SteenbergenC. Mechanisms underlying acute protection from cardiac ischemia-reperfusion injury. Physiol Rev, 2008, 88(2): 581-609
CrossRef Google scholar
[12]
InserteJ, BarbaI, HernandoV, et al.. Effect of acidic reperfusion on prolongation of intracellular acidosis and myocardial salvage. Cardiovasc Res, 2008, 77(4): 782-790
CrossRef Google scholar
[13]
FujitaM, AsanumaH, HirataA, et al.. Prolonged transient acidosis during early reperfusion contributes to the cardioprotective effects of postconditioning. Am J Physiol Heart Circ Physiol, 2007, 292(4): H2004-H2008
CrossRef Google scholar
[14]
GoldsteinDA. WalkerHK, HallWD, HurstJW. Serum Calcium. Clinical Methods: The History, Physical, and Laboratory Examinations, 1990, Stoneham (MA), Butterworth Publishers, 677-679
[15]
ShineKI, SerenaSD, LangerGA. Kinetic localization of contractile calcium in rabbit myocardium. Am J Physiol, 1971, 221(5): 1408-1417
[16]
LangerGA. The intrinsic control of myocardial contraction—ionic factors. N Engl J Med, 1971, 285(19): 1065-1071
CrossRef Google scholar
[17]
LangerGA. Coupling calcium in mammalian ventricle: its source and factors regulating its quantity. Cardiovasc Res, 197171-75
[18]
SharmaAD, SaffitzJE, LeeBI, et al.. Alpha adrenergic-mediated accumulation of calcium in reperfused myocardium. J Clin Invest, 1983, 72(3): 802-818
CrossRef Google scholar
[19]
KnopfH, TheisingR, MoonCH, et al.. Continuous determination of extracellular space and changes of K+, Na+, Ca2+, and H+ during global ischaemia in isolated rat hearts. J Mol Cell Cardiol, 1990, 22(11): 1259-1272
CrossRef Google scholar
[20]
SchumacherCA, BaartscheerA, CoronelR, et al.. Energy-dependent transport of calcium to the extracellular space during acute ischemia of the rat heart. J Mol Cell Cardiol, 1998, 30(8): 1631-1642
CrossRef Google scholar

This project was supported by grants from the National Natural Science Foundation of China (No. 81371714) and the Natural Science Foundation of Guangdong Province (No. S2012010008151).

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