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Isolation and study of insulin activated nitric oxide synthase inhibitory protein in acute myocardial infarction subjects

Citation

Ray, U and Khan, GA and Chakraborty, K and Basuroy, S and Patra, SC and Girish, G and Bhattacharya, G and Sinha, AK, Isolation and study of insulin activated nitric oxide synthase inhibitory protein in acute myocardial infarction subjects, Journal of Thrombosis and Thrombolysis, 33, (3) pp. 218-229. ISSN 0929-5305 (2012) [Refereed Article]

DOI: doi:10.1007/s11239-011-0672-8

Abstract

Insulin inhibits platelet aggregation through nitric oxide synthesis by stimulating platelet insulin activated nitric oxide synthase. Impaired platelet insulin activated nitric oxide synthase in acute myocardial infarction (AMI) patients had been reported and thus our aim was to identify and isolate the factors impairing insulin activated nitric oxide in acute myocardial infarction patients' plasma and study its effect on platelets aggregation in vitro. The insulin activated nitric oxide synthase inhibitor was identified as a protein and was purified from the plasma of AMI subjects using DEAE cellulose and Sephadex G-50 column, molecular weight determined by SDS-PAGE, nitric oxide quantified by methaemoglobin method, inhibitor protein quantified in plasma by immunoblot and ELISA, platelet aggregation studies done using an aggregometer, thromboxane- A2 in the platelets determined by radioimmunoassay, 125I-insulin radioligand binding studies done using normal subject platelets. The purified nitric oxide synthase inhibitor protein was ,66 kDa, concentration in AMI subjects' plasma varied from 114 to 9,090 lM and was undetected in normal subjects' plasma. The inhibitor protein competes with insulin for insulin receptor binding sites. The Incubation of the normal subject PRP with 5.0 lM inhibitor for 30 min followed by 0.4 lM ADP addition caused platelet aggregation in vitro, 130 lM aspirin or 400 lU insulin/ml addition was able to abrogate 0.4 lM ADP induced platelet aggregation even in the presence of 5.0 lM inhibitor. A potent inhibitory protein against insulin activated nitric oxide synthase in platelets appears in circulation of AMI subjects impairing nitric oxide production, potentiating ADP induced platelet aggregation and increasing the thromboxane-A2 level in platelets.

Item Details

Item Type:Refereed Article
Research Division:Medical and Health Sciences
Research Group:Cardiorespiratory Medicine and Haematology
Research Field:Cardiology (incl. Cardiovascular Diseases)
Objective Division:Health
Objective Group:Clinical Health (Organs, Diseases and Abnormal Conditions)
Objective Field:Cardiovascular System and Diseases
Author:Ray, U (Associate Professor Udayan Ray)
ID Code:119612
Year Published:2012
Web of Science® Times Cited:2
Deposited By:Medicine (Discipline)
Deposited On:2017-08-03
Last Modified:2017-08-03
Downloads:0

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