PubMed Health⌕ Search

Biomedical subjects

D Chesler

Publications and source records attributed to D Chesler.

5 recordsLinked to original sources

Mechanisms of cytokine-mediated inhibition of viral replication.

In this report, the role of nitric oxide synthase (NOS) and IL-12 administration in inhibition of vesicular stomatitis virus (VSV) from infected neuroblastoma cells was examined. We previously have shown that cytokine treatment of cells results in the induction of NOS-1, and this is associated with a 2 log inhibition of VSV production. We performed these studies to examine the mechanism by which viral replication is suppressed. Neuroblastoma cells (NB41A3) were treated with either IL-12 or medium and subsequently infected with VSV. Viral protein and mRNA were isolated from these cells, and their levels were measured by Western or Northern blots, respectively. mRNA levels were decreased modestly, but viral proteins were decreased substantially in cells pretreated with IL-12, suggesting that the inhibitory effect of NO is working at the translational level. Cytokine treatment of cells was not associated with oxidative stress. The viral proteins also were nitrosylated. These data suggest that the mechanism of NO inhibition of viral replication occurs through translational interference and posttranslational modifications of viral components.

Blotting, Northern↗

Pitfalls in MR measurement of tissue blood flow with intravascular tracers: which mean transit time?

Measuring tissue blood flow with NMR imaging of intravascular tracers is more difficult than measurements of tissue blood volume. One major obstacle to the application of the Central Volume Principle is the direct measurement of the mean transit time. In this note, we demonstrate that mean transit time (MTT), which relates tissue blood volume to blood flow via the Central Volume Principle, is not the first moment of the concentration-time curve for MR or CT imaging of purely intravascular tracers. However, while first moment methods cannot be used by themselves to determine absolute flow, we show that transit curves may provide a useful relative measure of flow, for example, by considering ratios of the first moments.

Blood Flow Velocity↗

MR velocity imaging by phase display.

The ability of the nuclear magnetic resonance signal to encode information about macroscopic motion has been recognized since the works of Hahn and Carr and Purcell. In the medical imaging setting this ability has led to a variety of ingenious magnetic resonance flow imaging schemes that ultimately may become competitive with X-ray angiography in sensitivity and specificity while remaining radically noninvasive. This work demonstrates that conventional spin-echo Fourier transform image acquisitions naturally encode a component of flow velocity that lies within the image plane. By displacing just the real part of the complex image data (phase display), the velocity distribution within the subject is revealed in image form. This method of flow imaging requires neither special pulse sequences nor image reconstruction and format software for its implementation. Further, images that intersect a flow channel longitudinally, demonstrating in-plane flow, yield an unusually large quantity of physiologic information per image. Phantom and in vivo flow images are presented. Also described is a phantom based on a rotating disk that enables calibration of the velocity/phase-shift constant for an untested pulse sequence.

Data Display↗