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Effect of Diazoxide Preconditioning on Cultured Rat Myocardium Microvascular Endothelial Cells against Apoptosis and Relation of PI3K/Akt Pathway

Yıl 2014, , 83 - 87, 07.08.2014
https://doi.org/10.5152/balkanmedj.2013.8458

Öz

Background: Anti-apoptotic mechanism for cell protection on reperfusion may provide a new method to reduce reperfusion injury. Aims: The aim of the present study is to explore the effect of mitochondrial ATP sensitive potassium channel (Mito-KATP) opener diazoxide (DZ) preconditioning on hypoxia/ reoxygen (H/R) injury of rat myocardium microvascular endothelial cells (MMECs) against apoptosis and relation of PI3K/Akt pathway. Study Design: Animal experimentation. Methods: The rat MMECs were cultivated, and H/R model was made to imitate ischemia-reperfusion injury. The cells were seeds in 96-wellplates (100μL/hole) or in 6cm diameter dishes (2 mL/dish) with the density of 1×106/mL and randomly divided into 4 groups (n=6 each): control group (Group N), hypoxia-regoxygen group (Group H/R), Diazoxide preconditioning+H/R group (Group DZ) and Diazoxide preconditioning +mitochondrial KATP blocker 5-hydroxydecanoate (5-HD) + H/R group (Group DZ+5-HD). The cells were exposed to 2h hypoxia followed by 2h reoxygenation. Diazoxide 100μmol/L and diazoxide 100μmol/L+ 5-HD100μmol/L were added to the culture medium 2h before hypoxia in DZ and DZ+5-HD groups respectively. Each group was observed the proliferation in MTT, apoptotic rate in Annexin V-FITC/PI double standard, cell structure of Hoechst staining, and the levels of PI3K, Akt and p53 mRNA by RT-qPCR. Results: Compared with Group N, apoptotic rate of Group H/R increased (p<0.01) and the vitality decreased significantly (p<0.05), and the expression of PI3K, Akt and p53 mRNA elevated in Group H/R (p<0.05). Compared with Group H/R, apoptotic rate and p53 mRNA level of Group DZ depressed significantly (p<0.01, p<0.05), while the vitality, PI3K and Akt mRNA levels increased (p<0.05). Compared with Group DZ, apoptotic rate and p53 mRNA level of Group DZ+5-HD increased significantly (p<0.01, p<0.05), but the vitality, PI3K and Akt mRNA levels decreased (p<0.05). Conclusion: Under the condition of H/R, mito-KATP opened by DZ may depend on PI3K/Akt pathway to regulate expression level of the downstream p53 mRNA to inhibit apoptosis and improve viability of MMECs at the same time. (Balkan Med J 2014;31:83-87).

Kaynakça

  • Kamada K, Dayton CB, Yamaguchi T, Korthuis RJ, et al., Antecedent ethanol ingestion prevents postischemic microvascular dysfunction. Pathophysiology 2004;10:131-7. [CrossRef]
  • Kakkar AK, Lefer DJ. Leukocyte and endothelial adhesion molecule studies in knockout mice. Curr Opin Pharmacol 2004;4:154-8. [CrossRef]
  • Abe E, Fujiki M, Nagai Y, Shiqi K, Kubo T, Ishii K, et al., The phosphatidylinositol-3 kinase/Akt pathway mediates geranylgeranylacetoneinduced neuroprotection against cerebral infarction in rats. Brain Res 2010;1330:151-7. [CrossRef]
  • Bodiga S, Zhang R, Jacobs DE, Larsen BT, Tampo A, Manthati VL, et al., Protective actions of epoxyeicosatrienoic acid:dual targeting of cardiovascular PI3K and KATP channels. J Mol Cell Cardiol 2009;46:978-88. [CrossRef]
  • Zdychová J, Komers R. Emerging role of Akt kinase/protein kinase B signaling in pathophysiology of diabetes and its complications. Physiol Res 2005;54:1-16. 6.
  • Yoon K, Jung EJ, Lee SY. TRAF6-mediated regulation of the PI3 kinase (PI3K)-Akt-GSK3beta cascade is required for TNF-induced cell survival. Biochem Biophys Res Commun 2008;371:118-21.
  • Brader S, Eccles SA. Phosphoinositide 3-kinase signalling pathways in tumor progression, invasion and angiogenesis. Tumori 2004;90:2-8.
  • Tapuria N, Kumar Y, Habib MM, Abu Amara M, Seifalian AM, Davidson BR. Remote ischemic preconditioning: a novel protective method from ischemia reperfusion injury--a review. J Surg Res 2008;150: 304[CrossRef]
  • Milano G, von Segesser LK, Morel S, Joncic A, Bianciardi P, Vassalli G, et al., Phosphorylation of phosphatidylinositol-3-kinase-protein kinase B and extracellular signal-regulated kinases 1/2 mediate reoxygenationinduced cardioprotection during hypoxia. Exp Biol Med (Maywood) 2010;235:401-10. [CrossRef]
  • Hirsch E, Ciraolo E, Ghigo A, Costa C. Taming the PI3K team to hold inflammation and cancer at bay. Pharmacol Ther 2008;118:192-205. [CrossRef]
  • Manning BD, Cantley LC. United at last:the tuberous sclerosis complex gene products connect the phosphoinositide 3-kinase/Akt pathway to mammalian target of rapamycin (mTOR) signalling. Biochem Soc Trans 2003;31:573-8. [CrossRef]
  • Dong Z, Zeitlin BD, Song W, Sun Q, Karl E, Spencer DM, et al. Level of endothelial cell apoptosis required for a significant decrease in microvessel density. Exp Cell Res 2007;313:3645-57. [CrossRef]
  • Yang Y, Shi W, Cui N, Wu Z, Jiang C. Oxidative stress inhibits vascular K(ATP) channels by S-glutathionylation. J Biol Chem 2010;285:38641-8. [CrossRef]
  • Gier B, Krippeit-Drews P, Sheiko T, Aguilar-Bryan L, Bryan J, Düfer M, et al. Suppression of KATP channel activity protects murine pancreatic beta cells against oxidative stress. J Clin Invest 2009;119:3246-56.
  • Okorokov AL, Orlova EV. Structural biology of the p53 tumour suppressor. Curr Opin Struct Biol 2009;19: 197-202. [CrossRef]
  • Naito AT, Okada S, Minamino T, Iwanaga K, Liu ML, Sumida T, et al. Promotion of CHIP-mediated p53 degradation protects the heart from ischemic injury. Circ Res 2010;106:1692-702. [CrossRef]
  • Kimata M, Matoba S, Iwai-Kanai E, Nakamura H, Hoshino A, Nakaoka M, et al. p53 and TIGAR regulate cardiac myocyte energy homeostasis under hypoxic stress. Am J Physiol Heart Circ Physiol 2010;299: H1908-16. [CrossRef]
  • Han JS, Wang HS, Yan DM, Wang ZW, Han HG, Zhu HY, et al. Myocardial ischemic and diazoxide preconditioning both increase PGC-1alpha and reduce mitochondrial damage. Acta Cardiol 2010;65:639-44.
  • Kabir AM, Clark JE, Tanno M, Cao X, Hothersall JS, Dashnyam S, et al. Cardioprotection initiated by reactive oxygen species is dependent on activation of PKCepsilon. Am J Physiol Heart Circ Physiol 2006;291:H1893-9. [CrossRef]
  • Costa AD, Quinlan CL, Andrukhiv A, West IC, Jaburek M, Garlid KD. The direct physiological effects of mitoK(ATP) opening on heart mitochondria. Am J Physiol Heart Circ Physiol 2006;290:H406-15. [CrossRef]

Effect of Diazoxide Preconditioning on Cultured Rat Myocardium Microvascular Endothelial Cells against Apoptosis and Relation of PI3K/Akt Pathway

Yıl 2014, , 83 - 87, 07.08.2014
https://doi.org/10.5152/balkanmedj.2013.8458

Öz

Kaynakça

  • Kamada K, Dayton CB, Yamaguchi T, Korthuis RJ, et al., Antecedent ethanol ingestion prevents postischemic microvascular dysfunction. Pathophysiology 2004;10:131-7. [CrossRef]
  • Kakkar AK, Lefer DJ. Leukocyte and endothelial adhesion molecule studies in knockout mice. Curr Opin Pharmacol 2004;4:154-8. [CrossRef]
  • Abe E, Fujiki M, Nagai Y, Shiqi K, Kubo T, Ishii K, et al., The phosphatidylinositol-3 kinase/Akt pathway mediates geranylgeranylacetoneinduced neuroprotection against cerebral infarction in rats. Brain Res 2010;1330:151-7. [CrossRef]
  • Bodiga S, Zhang R, Jacobs DE, Larsen BT, Tampo A, Manthati VL, et al., Protective actions of epoxyeicosatrienoic acid:dual targeting of cardiovascular PI3K and KATP channels. J Mol Cell Cardiol 2009;46:978-88. [CrossRef]
  • Zdychová J, Komers R. Emerging role of Akt kinase/protein kinase B signaling in pathophysiology of diabetes and its complications. Physiol Res 2005;54:1-16. 6.
  • Yoon K, Jung EJ, Lee SY. TRAF6-mediated regulation of the PI3 kinase (PI3K)-Akt-GSK3beta cascade is required for TNF-induced cell survival. Biochem Biophys Res Commun 2008;371:118-21.
  • Brader S, Eccles SA. Phosphoinositide 3-kinase signalling pathways in tumor progression, invasion and angiogenesis. Tumori 2004;90:2-8.
  • Tapuria N, Kumar Y, Habib MM, Abu Amara M, Seifalian AM, Davidson BR. Remote ischemic preconditioning: a novel protective method from ischemia reperfusion injury--a review. J Surg Res 2008;150: 304[CrossRef]
  • Milano G, von Segesser LK, Morel S, Joncic A, Bianciardi P, Vassalli G, et al., Phosphorylation of phosphatidylinositol-3-kinase-protein kinase B and extracellular signal-regulated kinases 1/2 mediate reoxygenationinduced cardioprotection during hypoxia. Exp Biol Med (Maywood) 2010;235:401-10. [CrossRef]
  • Hirsch E, Ciraolo E, Ghigo A, Costa C. Taming the PI3K team to hold inflammation and cancer at bay. Pharmacol Ther 2008;118:192-205. [CrossRef]
  • Manning BD, Cantley LC. United at last:the tuberous sclerosis complex gene products connect the phosphoinositide 3-kinase/Akt pathway to mammalian target of rapamycin (mTOR) signalling. Biochem Soc Trans 2003;31:573-8. [CrossRef]
  • Dong Z, Zeitlin BD, Song W, Sun Q, Karl E, Spencer DM, et al. Level of endothelial cell apoptosis required for a significant decrease in microvessel density. Exp Cell Res 2007;313:3645-57. [CrossRef]
  • Yang Y, Shi W, Cui N, Wu Z, Jiang C. Oxidative stress inhibits vascular K(ATP) channels by S-glutathionylation. J Biol Chem 2010;285:38641-8. [CrossRef]
  • Gier B, Krippeit-Drews P, Sheiko T, Aguilar-Bryan L, Bryan J, Düfer M, et al. Suppression of KATP channel activity protects murine pancreatic beta cells against oxidative stress. J Clin Invest 2009;119:3246-56.
  • Okorokov AL, Orlova EV. Structural biology of the p53 tumour suppressor. Curr Opin Struct Biol 2009;19: 197-202. [CrossRef]
  • Naito AT, Okada S, Minamino T, Iwanaga K, Liu ML, Sumida T, et al. Promotion of CHIP-mediated p53 degradation protects the heart from ischemic injury. Circ Res 2010;106:1692-702. [CrossRef]
  • Kimata M, Matoba S, Iwai-Kanai E, Nakamura H, Hoshino A, Nakaoka M, et al. p53 and TIGAR regulate cardiac myocyte energy homeostasis under hypoxic stress. Am J Physiol Heart Circ Physiol 2010;299: H1908-16. [CrossRef]
  • Han JS, Wang HS, Yan DM, Wang ZW, Han HG, Zhu HY, et al. Myocardial ischemic and diazoxide preconditioning both increase PGC-1alpha and reduce mitochondrial damage. Acta Cardiol 2010;65:639-44.
  • Kabir AM, Clark JE, Tanno M, Cao X, Hothersall JS, Dashnyam S, et al. Cardioprotection initiated by reactive oxygen species is dependent on activation of PKCepsilon. Am J Physiol Heart Circ Physiol 2006;291:H1893-9. [CrossRef]
  • Costa AD, Quinlan CL, Andrukhiv A, West IC, Jaburek M, Garlid KD. The direct physiological effects of mitoK(ATP) opening on heart mitochondria. Am J Physiol Heart Circ Physiol 2006;290:H406-15. [CrossRef]
Toplam 20 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Sağlık Kurumları Yönetimi
Bölüm Makaleler
Yazarlar

Cao Su Bu kişi benim

Tao Xia Bu kişi benim

Shen Ren Bu kişi benim

She Qing Bu kişi benim

Ding Jing Bu kişi benim

Huang Lian Bu kişi benim

Qin Bin Bu kişi benim

Zhou Yuan Bu kişi benim

Zhu Xiang Bu kişi benim

Yayımlanma Tarihi 7 Ağustos 2014
Yayımlandığı Sayı Yıl 2014

Kaynak Göster

APA Su, C., Xia, T., Ren, S., Qing, S., vd. (2014). Effect of Diazoxide Preconditioning on Cultured Rat Myocardium Microvascular Endothelial Cells against Apoptosis and Relation of PI3K/Akt Pathway. Balkan Medical Journal, 2014(1), 83-87. https://doi.org/10.5152/balkanmedj.2013.8458
AMA Su C, Xia T, Ren S, Qing S, Jing D, Lian H, Bin Q, Yuan Z, Xiang Z. Effect of Diazoxide Preconditioning on Cultured Rat Myocardium Microvascular Endothelial Cells against Apoptosis and Relation of PI3K/Akt Pathway. Balkan Medical Journal. Ocak 2014;2014(1):83-87. doi:10.5152/balkanmedj.2013.8458
Chicago Su, Cao, Tao Xia, Shen Ren, She Qing, Ding Jing, Huang Lian, Qin Bin, Zhou Yuan, ve Zhu Xiang. “Effect of Diazoxide Preconditioning on Cultured Rat Myocardium Microvascular Endothelial Cells Against Apoptosis and Relation of PI3K/Akt Pathway”. Balkan Medical Journal 2014, sy. 1 (Ocak 2014): 83-87. https://doi.org/10.5152/balkanmedj.2013.8458.
EndNote Su C, Xia T, Ren S, Qing S, Jing D, Lian H, Bin Q, Yuan Z, Xiang Z (01 Ocak 2014) Effect of Diazoxide Preconditioning on Cultured Rat Myocardium Microvascular Endothelial Cells against Apoptosis and Relation of PI3K/Akt Pathway. Balkan Medical Journal 2014 1 83–87.
IEEE C. Su, T. Xia, S. Ren, S. Qing, D. Jing, H. Lian, Q. Bin, Z. Yuan, ve Z. Xiang, “Effect of Diazoxide Preconditioning on Cultured Rat Myocardium Microvascular Endothelial Cells against Apoptosis and Relation of PI3K/Akt Pathway”, Balkan Medical Journal, c. 2014, sy. 1, ss. 83–87, 2014, doi: 10.5152/balkanmedj.2013.8458.
ISNAD Su, Cao vd. “Effect of Diazoxide Preconditioning on Cultured Rat Myocardium Microvascular Endothelial Cells Against Apoptosis and Relation of PI3K/Akt Pathway”. Balkan Medical Journal 2014/1 (Ocak 2014), 83-87. https://doi.org/10.5152/balkanmedj.2013.8458.
JAMA Su C, Xia T, Ren S, Qing S, Jing D, Lian H, Bin Q, Yuan Z, Xiang Z. Effect of Diazoxide Preconditioning on Cultured Rat Myocardium Microvascular Endothelial Cells against Apoptosis and Relation of PI3K/Akt Pathway. Balkan Medical Journal. 2014;2014:83–87.
MLA Su, Cao vd. “Effect of Diazoxide Preconditioning on Cultured Rat Myocardium Microvascular Endothelial Cells Against Apoptosis and Relation of PI3K/Akt Pathway”. Balkan Medical Journal, c. 2014, sy. 1, 2014, ss. 83-87, doi:10.5152/balkanmedj.2013.8458.
Vancouver Su C, Xia T, Ren S, Qing S, Jing D, Lian H, Bin Q, Yuan Z, Xiang Z. Effect of Diazoxide Preconditioning on Cultured Rat Myocardium Microvascular Endothelial Cells against Apoptosis and Relation of PI3K/Akt Pathway. Balkan Medical Journal. 2014;2014(1):83-7.