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Urinary trypsin inhibitors afford cardioprotective effects through activation of PI3K-Akt and ERK signal transduction and inhibition of p38 MAPK and JNK.
Cardiology. 2009; 114(4):264-70.C

Abstract

BACKGROUND

We determined the effect of urinary trypsin inhibitors (UTI) in regional myocardial ischemia/reperfusion (I/R) injury and its underlying mechanisms involving the role of prosurvival kinases such as phosphatidylinositol-3-OH kinases (PI3K)-Akt and extracellular signal-regulated kinases (ERK 1/2) and apoptotic kinases such as p38 and JNK.

METHODS

The rats were anesthetized and subjected to an I/R insult consisting of 30-min left anterior descending coronary artery (LAD) occlusion followed by reperfusion. Infarct size was measured after 120 min of reperfusion. UTI was given alone or along with wortmannin (inhibitor of PI3K) or PD098059 (inhibitor of ERK1/2) before LAD occlusion. The phosphorylation of Akt, ERK1/2, p38 and JNK was determined by immunoblotting after 5 min of reperfusion. UTI was administered 10 min before LAD occlusion, and wortmannin and PD098059 were administered 20 min before LAD occlusion.

RESULTS

UTI significantly reduced the infarct size compared with the control. Wortmannin or PD098059 alone did not affect the infarct size, but they abolished the UTI-induced cardioprotective effect. UTI significantly reduced the phosphorylation of p38 and JNK, while it enhanced that of Akt and ERK1/2.

CONCLUSIONS

UTI has a protective effect against regional myocardial I/R injury through activation of survival kinases PI3K-Akt and ERK1/2 and attenuation of p38 and JNK.

Authors+Show Affiliations

Department of Anesthesiology and Pain Medicine, Chonnam National University Medical School, Gwangju, South Korea.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

19684396

Citation

Kim, Seok J., et al. "Urinary Trypsin Inhibitors Afford Cardioprotective Effects Through Activation of PI3K-Akt and ERK Signal Transduction and Inhibition of P38 MAPK and JNK." Cardiology, vol. 114, no. 4, 2009, pp. 264-70.
Kim SJ, Yoo KY, Jeong CW, et al. Urinary trypsin inhibitors afford cardioprotective effects through activation of PI3K-Akt and ERK signal transduction and inhibition of p38 MAPK and JNK. Cardiology. 2009;114(4):264-70.
Kim, S. J., Yoo, K. Y., Jeong, C. W., Kim, W. M., Lee, H. K., Bae, H. B., Kwak, S. H., Li, M., & Lee, J. (2009). Urinary trypsin inhibitors afford cardioprotective effects through activation of PI3K-Akt and ERK signal transduction and inhibition of p38 MAPK and JNK. Cardiology, 114(4), 264-70. https://doi.org/10.1159/000234321
Kim SJ, et al. Urinary Trypsin Inhibitors Afford Cardioprotective Effects Through Activation of PI3K-Akt and ERK Signal Transduction and Inhibition of P38 MAPK and JNK. Cardiology. 2009;114(4):264-70. PubMed PMID: 19684396.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Urinary trypsin inhibitors afford cardioprotective effects through activation of PI3K-Akt and ERK signal transduction and inhibition of p38 MAPK and JNK. AU - Kim,Seok J, AU - Yoo,Kyung Y, AU - Jeong,Cheol W, AU - Kim,Woong M, AU - Lee,Hyung K, AU - Bae,Hong B, AU - Kwak,Sang H, AU - Li,Mei, AU - Lee,JongUn, Y1 - 2009/08/13/ PY - 2009/01/25/received PY - 2009/05/08/accepted PY - 2009/8/18/entrez PY - 2009/8/18/pubmed PY - 2010/1/16/medline SP - 264 EP - 70 JF - Cardiology JO - Cardiology VL - 114 IS - 4 N2 - BACKGROUND: We determined the effect of urinary trypsin inhibitors (UTI) in regional myocardial ischemia/reperfusion (I/R) injury and its underlying mechanisms involving the role of prosurvival kinases such as phosphatidylinositol-3-OH kinases (PI3K)-Akt and extracellular signal-regulated kinases (ERK 1/2) and apoptotic kinases such as p38 and JNK. METHODS: The rats were anesthetized and subjected to an I/R insult consisting of 30-min left anterior descending coronary artery (LAD) occlusion followed by reperfusion. Infarct size was measured after 120 min of reperfusion. UTI was given alone or along with wortmannin (inhibitor of PI3K) or PD098059 (inhibitor of ERK1/2) before LAD occlusion. The phosphorylation of Akt, ERK1/2, p38 and JNK was determined by immunoblotting after 5 min of reperfusion. UTI was administered 10 min before LAD occlusion, and wortmannin and PD098059 were administered 20 min before LAD occlusion. RESULTS: UTI significantly reduced the infarct size compared with the control. Wortmannin or PD098059 alone did not affect the infarct size, but they abolished the UTI-induced cardioprotective effect. UTI significantly reduced the phosphorylation of p38 and JNK, while it enhanced that of Akt and ERK1/2. CONCLUSIONS: UTI has a protective effect against regional myocardial I/R injury through activation of survival kinases PI3K-Akt and ERK1/2 and attenuation of p38 and JNK. SN - 1421-9751 UR - https://www.unboundmedicine.com/medline/citation/19684396/Urinary_trypsin_inhibitors_afford_cardioprotective_effects_through_activation_of_PI3K_Akt_and_ERK_signal_transduction_and_inhibition_of_p38_MAPK_and_JNK_ L2 - https://www.karger.com?DOI=10.1159/000234321 DB - PRIME DP - Unbound Medicine ER -