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dc.contributor.authorTaliyan, Rajeev-
dc.date.accessioned2023-12-13T06:46:33Z-
dc.date.available2023-12-13T06:46:33Z-
dc.date.issued2012-
dc.identifier.urihttps://doi.org/10.4103%2F0253-7613.91870-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/13391-
dc.description.abstractIschemic preconditioning (IPC) has been demonstrated to make myocardium transiently more resistant to deleterious effect of prolonged ischemia. The opening of the mitochondrial permeability transition pore (mPTP) at the time of myocardial reperfusion is a critical determinant of cell death. L-thyroxine pre-treatment increases the tolerance of the heart to ischemia and produces cardioprotection similar to ischemic precondition. This study has been designed to investigate the mechanism involved in L-thyroxine-induced cardiomyocyte protection against ischemia-reperfusion (I/R) injury in rats.en_US
dc.language.isoenen_US
dc.publisherMednow Pubicationsen_US
dc.subjectPharmacyen_US
dc.subjectIschemic preconditioning (IPC)en_US
dc.subjectMitochondrial permeability transition pore (mPTP)en_US
dc.titleEvaluation of thyroid hormone induced pharmacological preconditioning on cardiomyocyte protection against ischemic-reperfusion injuryen_US
dc.typeArticleen_US
Appears in Collections:Department of Pharmacy

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