## Abstract The aim of this study was to investigate intestinal ischemia‐reperfusion and its local and systemic hemorheological relations in the rat. Ten anaesthetized female CD outbred rats were equally divided into 2 experimental groups. (1) Ischemia‐reperfusion (I/R): the superior mesenterial ar
Altered expression and localization of N-myristoyltransferase in experimentally induced rat model of ischemia-reperfusion
✍ Scribed by Raju V.S. Rajala; Rakesh Kakkar; Rani Kanthan; Jasim M. Radhi; Xintao Wang; Rui Wang; Raju S.S. Datla; Rajendra K. Sharma
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 400 KB
- Volume
- 86
- Category
- Article
- ISSN
- 0730-2312
No coin nor oath required. For personal study only.
✦ Synopsis
N-myristoyltransferase (NMT) catalyzes the attachment of myristate onto the amino-terminal glycine residue of select polypeptides. In the present study, we investigated the expression and activity of NMT in rat heart after ischemia and reperfusion. Western blot analysis of rat heart samples indicated a prominent immunoreactive band of 66 kDa probed with human NMT antibody. Both the expression and activity of NMT were increased by ischemia-reperfusion. Immunohistochemical studies showed cytosolic localization of NMT in normal rat heart and predominant nuclear localization after ischemia followed by reperfusion. The pre-ischemic perfusion and post-ischemic reperfusion of hearts with a cell-permeable calpain inhibitor (N-Ac-Leu-Leu-methioninal) suppressed the increase in calpain expression and reversed the localization of NMT from nucleus to cytoplasm. This is the first study demonstrating the expression and alteration of NMT localization in cardiac ischemia and pertaining to a possible role of co-translational modification of proteins in cardiac functions and injury.
📜 SIMILAR VOLUMES
## Background: The neurotransmitter glutamate is involved in fast excitatory synaptic transmission in the mammalian brain. glutamate released from presynaptic terminals must be removed rapidly from the synaptic cleft by high affinity, sodium-dependent glutamate transporters to keep the extracellula
We investigated the role of anticoagulant in the ischemia/reperfusion injury of the liver, using activated protein C (APC), active human urinary thrombomodulin (UTM), and factor Xa blocked at the active site (DEGR-Xa). Liver ischemia was induced in male Wistar rats by occlusion of the portal vein wi