Abstract
In this study, we provide new evidence that orientin from bamboo leaves (Phyllostachys nigra) protect H9c2 cardiomyocytes against ischemia/reperfusion (I/R) injury through the
mitochondrial apoptotic pathway. A previous work has identified that orientin could
protect myocardium against ischemia/reperfusion injury. Mitochondria are both critical
determinants of cardioprotection and crucial targets of cardioprotective signaling.
Their role during reperfusion is conspicuously critical because the conditions promote
apoptosis through the mitochondrial pathway and necrosis though irreversible damage
to mitochondria, which is in association with mitochondrial permeability transition
(MPT). After myocardial ischemia, opening of the mPTP is a critical determinant of
cell death. The relationship of orientin and mPTP in mediating reperfusion-induced
cardiomyocytes injury is still elusive. Here, our results indicate that the protective
effect of orientin in H9c2 cells subjected to I/R injury is associated with depression
of the mPTP opening, resultant mitochondrial dysfunction, and apoptosis. Further investigation
of cellular mechanisms revealed that these effects were associated with inhibition
of reactive oxygen species (ROS) generation, repolarization of mitochondrial membrane
potential (Δψ
m), suppression of mitochondrial cytochrome c release, enhancement of the Bcl-2 level, and inhibition of Bax and Smac/DIABLO levels.
Furthermore, these beneficial effects of orientin were blocked by the phosphatidylinositol
3-kinase (PI3K) inhibitor wortmannin, and orientin could enhance Akt phosphorylation.
In summary, we demonstrate that orientin protects H9c2 cardiomytocytes against I/R-induced
apoptosis by modulating the mPTP opening, and this role of orientin may involve the
PI3K/Akt signaling pathway.
Key words
orientin - mitochondrial permeability transition - cardiomyocytes - ischemia/reperfusion
(I/R) - apoptosis
References
- 1
Zhang Y, Wu X Q, Yu Z Y.
Comparison study on total flavonoid content and anti-free radical activity of the
leaves of bamboo, Phyllostachys nigra, and Ginkgo biloba.
Zhongguo Zhong Yao Za Zhi.
2002;
27
254-257
- 2
Dietrych-Szostak D, Oleszek W.
Effect of processing on the flavonoid content in buckwheat (Fagopyrum esculentum Möench) grain.
J Agric Food Chem.
1999;
47
4384-4387
- 3
Suzuki K, Sawa Y, Kaneda Y, Ichikawa H, Shirakura R, Matsuda H.
In vivo gene transfection with heat shock protein 70 enhances myocardial tolerance to ischemia-reperfusion
injury in rat.
J Clin Invest.
1997;
99
1645-1650
- 4
Sun Y, Deng T, Lu N, Yan M, Zheng X.
B-type natriuretic peptide protect cardiomyocytes at reperfusion via mitochondrial
calcium uniporter.
Biomed Pharmacother.
2010;
64
170-176
- 5
Halestrap A P, Clarke S J, Javadov S A.
Mitochondrial permeability transition pore opening during myocardial reperfusion–a
target for cardioprotection.
Cardiovasc Res.
2004;
61
372-385
- 6
Lemasters J J, Nieminen A L, Qian T, Trost L C, Elmore S P, Nishimura Y, Crowe R A,
Cascio W E, Bradham C A, Brenner D A, Herman B.
The mitochondrial permeability transition in cell death: a common mechanism in necrosis,
apoptosis and autophagy.
Biochim Biophys Acta.
1998;
1366
177-196
- 7
Sun Y, Zhang Y, Yan M, Wu Y, Zheng X.
B-type natriuretic peptide-induced cardioprotection against reperfusion is associated
with attenuation of mitochondrial permeability transition.
Biol Pharm Bull.
2009;
32
1545-1551
- 8
Redegeld F A, Moison R M, Koster A S, Noordhoek J.
Depletion of ATP but not of GSH affects viability of rat hepatocytes.
Eur J Pharmacol.
1992;
228
229-236
- 9
Green D R, Reed J C.
Mitochondria and apoptosis.
Science.
1998;
281
1309-1312
- 10
Kang P M, Haunstetter A, Aoki H, Usheva A, Izumo S.
Morphological and molecular characterization of adult cardiomyocyte apoptosis during
hypoxia and reoxygenation.
Circ Res.
2000;
87
118-125
- 11
Baines C P.
The mitochondrial permeability transition pore and ischemia-reperfusion injury.
Basic Res Cardiol.
2009;
104
181-188
- 12
Gustafsson A B, Gottlieb R A.
Heart mitochondria: gates of life and death.
Cardiovasc Res.
2008;
77
334-343
- 13
Kominsky D J, Bickel R J, Tyler K L.
Reovirus-induced apoptosis requires mitochondrial release of Smac/DIABLO and involves
reduction of cellular inhibitor of apoptosis protein levels.
J Virol.
2002;
76
11414-11424
- 14
Abas L, Bogoyevitch M A, Guppy M.
Mitochondrial ATP production is necessary for activation of the extracellular-signal-regulated
kinases during ischaemia/reperfusion in rat myocyte-derived H9c2 cells.
Biochem J.
2000;
349
119-126
- 15
Akao M, Teshima Y, Marban E.
Antiapoptotic effect of nicorandil mediated by mitochondrial ATP-sensitive potassium
channels in cultured cardiac myocytes.
J Am Coll Cardiol.
2002;
40
803-810
- 16
Deng T, Zhang L, Ge Y, Lu M, Zheng X.
Redistribution of intracellular calcium and its effect on apoptosis in macrophages:
Induction by oxidized LDL.
Biomed Pharmacother.
2008;
63
267-274
- 17
Braunwald E, Kloner R A.
Myocardial reperfusion: a double-edged sword?.
J Clin Invest.
1985;
76
1713-1719
- 18
Ambrosio G, Zweier J L, Duilio C, Kuppusamy P, Santoro G, Elia P P, Tritto I, Cirillo P,
Condorelli M, Chiariello M, Flaherty J T.
Evidence that mitochondrial respiration is a source of potentially toxic oxygen free
radicals in intact rabbit hearts subjected to ischemia and reflow.
J Biol Chem.
1993;
268
18532-18541
- 19
Kim J S, Ohshima S, Pediaditakis P, Lemasters J J.
Nitric oxide protects rat hepatocytes against reperfusion injury mediated by the mitochondrial
permeability transition.
Hepatology.
2004;
39
1533-1543
- 20
Robin E, Guzy R D, Loor G, Iwase H, Waypa G B, Marks J D, Hoek T L, Schumacker P T.
Oxidant stress during simulated ischemia primes cardiomyocytes for cell death during
reperfusion.
J Biol Chem.
2007;
282
19133-19143
- 21
Borutaite V, Brown G C.
Mitochondria in apoptosis of ischemic heart.
FEBS Lett.
2003;
541
1-5
- 22
Suleiman M S, Halestrap A P, Griffiths E J.
Mitochondria: a target for myocardial protection.
Pharmacol Ther.
2001;
89
29-46
- 23
Crompton M.
The mitochondrial permeability transition pore and its role in cell death.
Biochem J.
1999;
341
233-249
- 24
Fu X C, Wang M W, Li S P, Wang H L.
Anti-apoptotic effect and mechanism of orientin on ischaemic/reperfused myocardium.
J Asian Nat Prod Res.
2006;
8
265-272
- 25
Kroemer G, Dallaporta B, Resche-Rigon M.
The mitochondrial death/life regulator in apoptosis and necrosis.
Annu Rev Physiol.
1998;
60
619-642
- 26
Hausenloy D J, Yellon D M.
New directions for protecting the heart against ischaemia-reperfusion injury: targeting
the Reperfusion Injury Salvage Kinase (RISK)-pathway.
Cardiovasc Res.
2004;
61
448-460
- 27
Zhu M, Feng J, Lucchinetti E, Fischer G, Xu L, Pedrazzini T, Schaub M C, Zaugg M.
Ischemic postconditioning protects remodeled myocardium via the PI3K-PKB/Akt reperfusion
injury salvage kinase pathway.
Cardiovasc Res.
2006;
72
152-162
- 28
Armstrong S C.
Protein kinase activation and myocardial ischemia/reperfusion injury.
Cardiovasc Res.
2004;
61
427-436
- 29
Miyamoto S, Rubio M, Sussman M A.
Nuclear and mitochondrial signalling Akts in cardiomyocytes.
Cardiovasc Res.
2009;
82
272-285
- 30
Venkatapuram S, Wang C, Krolikowski J G, Weihrauch D, Kersten J R, Warltier D C, Pratt Jr P F,
Pagel P S.
Inhibition of apoptotic protein p 53 lowers the threshold of isoflurane-induced cardioprotection
during early reperfusion in rabbits.
Anesth Analg.
2006;
103
1400-1405
Prof. Xiaoxiang Zheng
Department of Biomedical Engineering
Key Laboratory of Biomedical Engineering, MOE
Zhejiang University (Yuquan Campus)
Zheda Road 38
310027 Hangzhou
P. R. China
Phone: +86 5 71 87 95 38 60
Fax: +86 5 71 87 95 16 76
Email: zxx@bme.zju.edu.cn