“
“Please cite this paper as: Di Filippo, Monopoli, Ongini, Perretti and D’Amico (2010). The Cardio-Protective Properties of Ncx-6550, a Nitric Oxide Donating Pravastatin, in the Mouse. Microcirculation17(6), 417–426. Objective:  Determine the cardio-protective properties of a nitric oxide-releasing pravastatin (Ncx-6550), in comparison to pravastatin. Methods:  A mouse model of myocardial

infarct was used assessing tissue damage both at 2 and 24 hour post-reperfusion, administering compounds both prophylactically and therapeutically. Results:  Ncx-6550 induced a significant dose-dependent (2.24–22.4 μmol/kg i.p.) cardioprotection in the two hour reperfusion protocol. In vehicle-treated mice, infarct size (expressed as fraction of area at risk; Inhibitor Library high throughput IS/AR) was 41.2 ± 1%, and it was reduced to 22.2 ± 0.9% and 32.6 ± 0.9% following 22.4 and 6.72 μmol/kg Ncx-6550 (p < 0.05). 22.4 μmol/kg Ncx-6550 also increased cardiac levels of the enzyme heme oxygenase-1. Treatment of mice with pravastatin induced significant reduction of myocardial injury only at 22.4 μmol/kg (IS/AR value: 33.7 ± 0.9%). In a 24 hour

reperfusion protocol, Ncx-6550 and pravastatin were tested only at 22.4 μmol/kg i.p. being given either one hour prior to ischemia (prophylactic protocol) Acalabrutinib in vivo or one hour into reperfusion (therapeutic protocol). With either treatment scheme, Ncx-6550 produced higher cardioprotection compared to pravastatin, as reflected also by a reduction in the incidence of lethality as well as in circulating troponin I and interleukin-1β levels. Conclusions:  These results indicate Ncx-6550 as a novel therapeutic agent with a potential for the treatment of

myocardial infarct. “
“Three‐dimensional images of microvascular trees, within their surrounding tissue, are obtainable by micro‐computed tomography (micro‐CT) imaging of intact small animals or tissue specimens. With a resolution down to a few micrometers, these images can be used to measure the interbranch segment diameters, branching angles, volume of tissue perfused, and study the vascular anatomic relationships Exoribonuclease to organ microstructures such as glomeruli in kidney, hepatic lobules in liver, and so on. Such data can be used to model intravascular flow, endothelial shear stress, and altered branching geometry such as that which may occur in localized angiogenesis and around tissue infarction and tumors. Endothelial permeability can also be evaluated using cryostatic micro‐CT methods, and special contrast agents can be used to convey permeability and vascular lumen volumes. In this chapter, we provide background information of micro‐CT image systems, sample preparation methods such as ex vivo casting methods, in situ contrast agent injection techniques, special considerations pertaining to in vivo studies, and the use of probes (such as microspheres in “simulated embolization” experiments).