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Biomedical subjects

J Bernarding

Publications and source records attributed to J Bernarding.

24 records · Page 2Linked to original sources
PubMed1998

Magnetic resonance imaging studies with cluster algorithm for characterization of brain edema after controlled cortical impact injury (CCII).

Objective of this study was the characterization of traumatic brain injury induced by a "Controlled Cortical Impact" with magnetic resonance imaging techniques. The impact was applied to the intact dura of the left hemisphere in Sprague-Dawley rats. The pneumatic impactor was accelerated to a velocity of 7 m/s contusing the left temporo-parietal hemisphere to a depth of 2 mm. Posttraumatic hemispheric swelling and water content were determined gravimetrically, Evans Blue extravasation photometrically, and volume of ischemia by TTC-staining and planimetry. Magnetic resonance imaging was performed by a Bruker biospec 24/40, 90 min, 24 and 72 h post trauma using a T2w RARE sequence, a T1w sequence, before and after application of contrast agent, and a set of diffusion weighted images for calculation of ADC-maps. Data analysis was performed using a cluster algorithm enabling to interpret corresponding image pairs simultaneously. T2w imaging indicates the maximum edema about 24 h post trauma. Blood-brain barrier damage, detected by T1w imaging, is more predominant in the early posttraumatic phase. The cluster algorithm detects different edema components: from the necrotic core to the perifocal vasogenic rim. MRI in combination with the cluster algorithm will hopefully be a valuable tool in testing neuroprotective agents.

Animals↗
PubMed1996

Non-invasive functional mapping of the human motor cortex using near-infrared spectroscopy.

We applied non-invasive multisite near-infrared spectroscopy (NIRS) to assess oxygenation changes during performance of a sequential finger opposition task in five healthy human adults. Oxygenation response was localized anatomically using three-dimensional high-resolution magnetic resonance imaging (3D MRI). NIRS measurements showed a localized increase in [oxy-Hb] and a decrease in [deoxy-Hb] in all subjects. The largest response was obtained when the measurement position was over the primary motor and sensory cortex hand area. Interestingly, changes in [deoxy-Hb] seemed to be more localized than changes in [oxy-Hb]. We conclude that this simple, non-invasive and flexible optical bedside method may be used for functional brain mapping.

Adult↗
PubMed1995

Differentiation of normal and pathologic brain structures in MRI using exact T1 and T2 values followed by a multidimensional cluster analysis.

A new method to differentiate and classify normal and pathologic brain tissue in Magnetic Resonance Imaging (MRI) is introduced. With a special pulse sequence, exact T1 and T2 values are simultaneously acquired, where the T2 values may show a biexponential decay behavior. The automatic segmentation of the tissue is based on a histogram analysis of the multidimensional parameters. The tissue-characterizing parameters are stored in a database, which serves as an objective classification of different tissues. A pilot study with 15 healthy volunteers and 100 patients showed a good differentiation between normal tissue like white and gray matter, cerebrospinal fluid, muscle, and fat, thereby revealing a biexponential decay behavior of fat. Pathologic tissue-like edema and meningioma could be classified with high accuracy, while glioblastoma or astrocytoma were difficult to classify because of their non-homogeneous structures.

Adipose Tissue↗
PubMed1988

Analysis of the electron transfer from Pheo- to QA in PS II membrane fragments from spinach by time resolved 325 nm absorption changes in the picosecond domain.

Absorption changes at 325 nm (delta A325) induced by 15 ps laser flashes (lambda = 650 nm) in PS II membrane fragments were measured with picosecond time-resolution. In samples with the reaction centers (RCs) kept in the open state (P I QA) the signals are characterized by a very fast rise (not resolvable by our equipment) followed by only small changes within our time window of 1.6 ns. In the closed state (PI QA-) of the reaction center the signal decays with an average half-life time of about 250 ps. It is shown that under our excitation conditions (E = 2 x 10(14) photons/cm2 per pulse) subtraction of the absorption changes in closed RCs (delta A closed 325) from those in open RCs (delta A open 325) leads to a difference signal which is dominated by the reduction kinetics of QA. From the rise kinetics of this signal and by comparison with data in the literature it is inferred that QA becomes reduced by direct electron transfer from Pheo- with a time constant of about 350 +/- 100 ps.

Cell-Free System↗