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Biomedical subjects

J Frahm

Publications and source records attributed to J Frahm.

At least 145 records · Page 8Linked to original sources

Localized proton NMR spectroscopy in different regions of the human brain in vivo. Relaxation times and concentrations of cerebral metabolites.

High-resolution proton NMR spectra of normal human brain in vivo have been obtained from selected 27- and 64-ml volumes-of-interest (VOI) localized in the insular area, the occipital area, the thalamus, and the cerebellum of normal volunteers. Localization was achieved by stimulated echo (STEAM) sequences using a conventional 1.5-T whole-body MRI system (Siemens Magnetom). The proton NMR spectra show resonances from lipids, lactate, acetate, N-acetylaspartate (NAA), gamma-aminobutyrate, glutamine, glutamate, aspartate, creatine and phosphocreatine, choline-containing compounds, taurine, and inositols. While T1 relaxation times of most of these metabolites were about 1100-1700 ms without significant regional differences, their T2 relaxation times varied between 100 and 500 ms. The longest T2 values of about (500 +/- 50) ms were observed for the methyl protons of NAA in the white matter of the occipital lobe compared to (320 +/- 30) ms in the other parts of the brain. No significant regional T2 differences were found for choline and creatine methyl resonances. The relative concentrations of NAA in gray and white matter were found to be 35% higher than those in the thalamus and cerebellum. Assuming a concentration of 10 mM for total creatine the resulting NAA concentrations of 13-18 mM are by a factor of 2-3 higher than previously reported using analytical techniques. Cerebral lactate reached a maximum concentration of about 1.0 mM.

Brain↗

The influence of flow and motion in MRI of diffusion using a modified CE-FAST sequence.

Severe motion and flow artifacts are a problem in MRI of diffusion in vivo due to the application of strong magnetic field gradients. Here it is shown that image artifacts can be removed by using a modified fast-scan MRI sequence (CE-FAST) in conjunction with averaging of diffusion-weighted images. In phantom studies slow (coherent) flow (less than 1 mm s-1) in the presence of strong diffusion gradients is shown to cause signal losses in diffusion-weighted images that depend on the relative orientations of the flow direction and the diffusion gradient. On the other hand, pulsatile motions of macroscopic dimensions (e.g., 1 mm, 1 Hz, in-plane) lead to smearing and ghosting of signal intensities along the phase-encoding direction of the images. In both phantoms and rabbit brains in vivo motion artifacts were found to be reducible by averaging 8-16 images. Unfortunately, the resulting image contrast no longer represents a "true" diffusion contrast but is affected by additional signal losses due to motion averaging. All experiments were performed on a 40-cm-bore 2.35-T Bruker Medspec system.

Animals↗

Localized NMR spectroscopy in vivo. Progress and problems.

Metabolites in brain and muscle of normal human volunteers have been studied by localized 1H and 31P NMR spectroscopy in vivo. Localization was achieved by means of stimulated echo (STEAM) sequences for both water-suppressed 1H NMR (TE = 20 ms) and 31P NMR (TE = 3 ms). Volumes-of-interest and measuring times selected for brain spectroscopy were 8 mL and 6.5 min for 1H NMR and 125 mL and 13 min for 31P NMR, respectively. General problems relating to spatial localization, spectral resolution, and quantitation of in vivo NMR data are discussed with respect to the nucleus and organs under investigation. They are correlated to studies of tissue extracts obtained at field strengths of 2.35 T (Bruker Biospec) and 7.0 T (Bruker MSL 300). Human studies were performed at 2.0 T on a whole-body research system (Siemens Magnetom).

Brain↗

Noninvasive differentiation of tumors with use of localized H-1 MR spectroscopy in vivo: initial experience in patients with cerebral tumors.

A recently developed method for image-selected localized hydrogen-1 magnetic resonance (MR) spectroscopy was assessed in the differential diagnosis of nine primary and secondary cerebral tumors, including four gliomas, two meningiomas, one neurilemoma, one arachnoid cyst, and one metastasis of breast cancer. Well-resolved H-1 MR spectra of these tumors were obtained in vivo with a conventional 1.5-T whole-body MR imaging system. All tumor spectra were remarkably different from spectra from normal brain tissue. Spectra obtained from different tumors exhibited reproducible differences, while histologically similar tumors yielded characteristic spectra with only minor differences. The observed spectral alterations reflect variations in concentrations and relaxation times of the H-1 MR sensitive pool of free (mobile) metabolites within the tissues. In most cases, the concentrations of N-acetyl-aspartate and creatine/phosphocreatine are reduced below detectability, whereas choline-containing compounds are generally enhanced. The spectral differences between the tumors are mainly due to the differing concentrations of lipids, lactic acid, and carbohydrates. Localized H-1 MR spectroscopy may become an important clinical tool for the differentiation of tumors as well as for therapeutic control.

Adult↗

Direct FLASH MR imaging of magnetic field inhomogeneities by gradient compensation.

MR images based on gradient echoes are sensitive to artifacts caused by inhomogeneities of the static magnetic field. This paper describes the effects of local gradients in rapid FLASH MR images and presents a way of directly imaging affected areas. The idea is to compensate for signal losses due to mutual cancellation of dephased magnetizations by deliberate "misadjustments" of the refocusing part of the slice selection gradient. In contrast to conventional field imaging techniques no three-dimensional data acquisition or subsequent Fourier analysis is required to obtain images at a particular gradient strength. Conventional as well as inhomogeneity compensated FLASH images have been obtained on phantoms and human heads using a 2.35-T 40-cm magnet and a 1.5-T whole-body system, respectively.

Head↗

Rapid line scan NMR angiography.

This paper describes a new technique for NMR angiography based on rapid line scan projection imaging and presaturation of stationary spins. The resulting line scan angiograms are free from both misregistration artifacts common to subtraction methods and motion artifacts encountered in Fourier imaging. Moreover, line scan angiograms may be recorded within seconds and offer arbitrary fields of view as well as gradient zooming without problems due to aliasing. Three-dimensional information is obtained by rotation of the read gradient axis generating multiple view angles. Experimental line scan angiograms of the forearms of healthy volunteers have been recorded using a Bruker 2.35-T 40-cm magnet.

Angiography↗

Suppression of nuclear ADP-ribosyltransferase activity in Ehrlich ascites tumor cells by 5-azacytidine and its analogs.

The exposure of freshly isolated, activity growing Ehrlich ascites tumor cells to the antileukemic agent 5-azacytidine and its analogs, 5-azacytosine (but not 6-azacytosine), 5-aza-2'-deoxycytidine and, in particular, 5-fluorocytidine in the serum-free medium caused a time- and dose-dependent suppression of the nuclear ADP-ribosyltransferase activity. The azacytidine suppression was apparently dependent on the cellular activity of DNA synthesis but not related to the nuclear activity of DNA methylation, indicating the 5-azacytidine incorporation into DNA, but not drug-induced hypomethylation of DNA, being responsible for the 5-azacytidine-suppression of chromatin-bound ADP-ribosyltransferase.

Animals↗

Flow suppression in rapid FLASH NMR images.

Rapid FLASH (fast low angle shot) NMR images are very sensitive to flow phenomena. In particular, a steady reflow of unsaturated spins from outside the imaging plane results in high image intensities which depend on the flip angle, the repetition time, and the flow velocity. Here we describe a technique that suppresses these signals by saturating remote spins prior to entering the imaging plane, e.g., by intercalating the FLASH sequence with slice-selective 1-2-1 pulse packages. Experiments have been carried out on phantoms and human extremities. Flow artifacts in the phase-encoding direction of the images are strongly reduced. Vascular structures may be easily delineated using difference images obtained with and without flow suppression.

Arm↗

Rapid FLASH NMR imaging.

Nuclear magnetic resonance (NMR) spectroscopy and imaging provide new tools for non-invasive investigations of living systems. Recent developments in rapid NMR imaging now offer considerable improvements for both scientific applications and medical diagnosis. Using fast imaging sequences cross-sectional images may be recorded within seconds and, therefore, become free from motional artifacts due to breathing or peristalsis. New functional imaging experiments include dynamic studies of the application of paramagnetic contrast agents or ECG-synchronized recordings of cardiac NMR movies. Superior anatomical information is achieved by three-dimensional NMR imaging with measuring times of minutes rather than hours.

Arm↗

Suppression of nuclear ADP-ribosyltransferase activity in regenerating rat liver by 5-azacytidine and its relevance to the nuclear methylating activities.

A single administration of 5-azacytidine (5-ACR) to partially hepatectomized rats 24 h following operation resulted in a dose-dependent reduction of nuclear ADP-ribosyltransferase (ADPRT) activity in the liver, when assayed after the nuclei were isolated 22 h after injection. No such a suppression by 5-ACR was observed in the liver of intact rats. Cytidine, a known agent which prevents the incorporation of 5-ACR into DNA, abolished the suppression of ADPRT, when it was given in combination with 5-ACR. The 5-ACR suppressed nuclei from regenerating liver showed no decreased DNA methylating activity, as estimated from the rate of radiolabel transfer from [methyl-3H]SAM to the bulk DNA. The methylation of nuclear RNA and protein was markedly reduced. These results suggest that the incorporation of 5-ACR into nucleic acids inactivates chromatin-bound ADPRT without inhibition of DNA methylation.

Animals↗

Nuclear magnetic resonance imaging of mummified corpses.

Clinical applications of nuclear magnetic resonance (NMR) imaging have demonstrated its great potential for noninvasive examinations of soft tissues. Here preliminary experiments are reported on mummified human tissue by means of NMR cross-sectional and transmission imaging. For this purpose the natural viscosity of the tissues has been lowered by rehydration with an aqueous solution of 20% acetone.

Acetone↗

Rapid NMR imaging of dynamic processes using the FLASH technique.

FLASH (Fast Low-Angle SHot) imaging is a new method for rapid NMR imaging which has been demonstrated to provide abdominal images without artifacts due to respiratory or peristaltic motions. The sequence typically employs 15 degrees radiofrequency excitation pulses and acquires a free induction decay signal in the form of a gradient echo. Here FLASH images are recorded in the presence of dynamic processes with time constants even smaller than the measuring time of about 2 s for an image with a 128 X 128-pixel resolution. Experiments are carried out on flow phantoms and on rabbits yielding heart images without gating of the cardiac motion.

Animals↗

Multipurpose NMR imaging using stimulated echoes.

STEAM (stimulated-echo acquisition mode) imaging techniques recently introduced by the authors are demonstrated to provide a versatile tool for improving the parametric specificity in NMR imaging. Stimulated echoes can be excited by a sequence of at least three rf pulses with flip angles of 90 degrees or less. The main characteristics of the STEAM method are based on the great functional flexibility of an imaging sequence comprising three rf pulses unequal to 180 degrees and three intervals prior to acquisition of the data. Major advantages are the easy access to contiguous multiplanar images, to CHESS (chemical-shift-selective) images, and to T1 information. Moreover, the rf power deposition is considerably reduced as compared to spin-echo NMR imaging sequences. Here first in vivo results on human extremities are presented including contiguous multislice images, multiple CHESS images, and spin-lattice relaxation time images calculated from a series of simultaneously recorded T1-weighted STEAM images.

Biophysical Phenomena↗

Dynamic digital subtraction imaging using fast low-angle shot MR movie sequence.

High-quality magnetic resonance (MR) images can be recorded within seconds with the use of fast low-angle shot (FLASH) MR imaging. This technique also gives new access to the time evolution of both periodic functions, such as cardiac motion, and nonperiodic physiologic processes, such as flow within internal organs. The time course and regional distribution of dynamic processes detectable by FLASH MR movies are often demonstrated best within series of difference images obtained by digital subtraction of the original data, especially after the use of MR contrast agents. In addition, quantitative information is provided by the analysis of time-intensity profiles for selected regions of interest. Dynamic digital subtraction MR imaging was evaluated in rabbit brain and kidney using a 2.3-T, 40-cm-bore magnet. The time resolution was 1.5 seconds for brain studies and 28 seconds for kidney studies. The total examination times were 1.5 and 30 minutes, respectively.

Angiography↗

MR imaging using stimulated echoes (STEAM).

The introduction of STEAM (stimulated echo acquisition mode) magnetic resonance (MR) sequences provides access to a variety of MR parameters. T1-weighted and calculated T1 proton MR images of the head of healthy volunteers and a patient with an astrocytoma are presented. MR examinations were performed with a 2.0-T whole-body system. The STEAM T1 method can be used to characterize multiexponential relaxation behavior, to evaluate T1 relaxation times, and to improve the T1 contrast within MR images. Both the measuring time and the spatial resolution are the same as for a conventional image.

Astrocytoma↗