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Biomedical subjects

S Eddy

Publications and source records attributed to S Eddy.

6 recordsLinked to original sources

Myasthenia gravis: another autoimmune disease associated with hepatitis C virus infection.

We report on a male Egyptian patient who developed myasthenia gravis with typical symptoms, beneficial response to pyridostigmine, and the presence of anti-acetylcholine receptor antibodies and anti-striated muscle antibodies during the course of a chronic hepatitis C infection complicated by liver cirrhosis. As also reported for the herpes simplex and for the HIV virus, hepatitis C may lead to myasthenia gravis via a mechanism of cross-reactivity between viral epitopes and the acetylcholine receptor.

Autoantibodies↗

Biomechanical properties of threaded inserts for lumbar interbody spinal fusion.

STUDY DESIGN: Calf and human cadaveric spines were used to determine motion segment stiffness and laxity after implantation of threaded inserts (the Ray Threaded Fusion Cage, Surgical Dynamics, Inc., Concord, CA), comparing direction of placement, number of implants, shape of the device, and integrity of anterior spine structures. Stiffness and laxity of spines with inserts were compared with those with bone grafts, with and without posterior fixation plates. OBJECTIVES: To determine the mechanical stabilizing properties of a threaded insert used for lumbar and lumbosacral fusion and the factors affecting stability. SUMMARY OF BACKGROUND DATA: Limited biomechanical information has shown that implantation of these devices adds stiffness to the lumbar spine, but little information is available concerning stiffness in loading directions other than flexion and extension, the effect on stiffness of position and number of implants, and the effect of this device on motion segment laxity. METHODS: Mechanical properties were determined by testing lumbar vertebral motion segments in flexion, extension, lateral bending, and torsion combined with axial compressive loading. Stiffness (slope of the load/deflection curve) and neutral zone angle or laxity (angular displacement of the vertebra from no load to 1.0 Nm moment) were determined. Initial tests were performed on calf lumbar vertebrae to determine the effects of placement and number of inserts. Comparisons of bone grafts and inserts with and without supplemental plates were made using human lumbar spines. Cylindrical- and conical-shaped inserts, when placed from anterior, were tested in calf spines. The load-bearing capacity of the insert supported in calf vertebral body bone was determined. RESULTS: There was no significant effect of placement of inserts in different orientations (lateral, posterolateral, or posterior) on stiffness, except in torsion where posterior placement damaged facets or lamina, reducing stiffness. Placement of two inserts from posterior decreased flexion and lateral bending laxity compared with the intact motion segment. Compared with intact, bone grafts produced more stiffness only in lateral bending and had no effect on laxity. Supplemental posterior plates fixed by pedicle screws across the fusion segment increased flexion and lateral bending stiffness and reduced laxity in flexion, extension, and lateral bending. Conical-shaped inserts placed from anterior into cylindrical holes distracted soft tissue structures, decreasing laxity. Cutting the anterior structures increased laxity by relieving some tissue tension caused by distraction. The mean maximum compressive load that could be supported by the insert was 2998 N (standard deviation = 980 N). Structural failure occurred in the supporting bone. CONCLUSIONS: Threaded inserts increase vertebral motion segment stiffness and decrease laxity by distracting intervertebral structures. They are not sensitive to placement, except if vertebral structures are injured during insertion and produce constructs with more consistent mechanical properties than bone grafts.

Animals↗

Bio-/haemocompatibility: implications and outcomes for sensors?

Sensors are a sample contacting technology, and when exposed to biological matrices tend to suffer from the problem of poor biocompatibility and surface fouling. The effects are evidenced by time dependent signal drift (particularly for those devices which are implanted intravascularly). Practical methods to reduce such effects require an understanding of the interface between the electrode and its environment prior to assessment of the potential areas for improvement. Current procedures employed to overcome the observed losses in electrode sensitivity (following exposure to whole blood) include surface modification of the outer diffusion limiting membrane (via variation in film porosity) or even biomimicry of the fluid cell membrane. At amperometric electrodes incorporation of additional inner perm-selective membranes has achieved a reduction in electrode passivation from undesirable surface active compounds as has the use of low polarisation potentials. Other studies have attempted to induce an aqueous barrier between the matrix and the electrode tip which physically prevents passage of cellular components from the sensor surface. Careful choice of the system and materials will ultimately lead to biocompatible non-fouling devices capable of functioning in an array of bio-environments suitable for clinical monitoring of the critically ill patient.

Biocompatible Materials↗

Autogenous translational operator recognized by bacteriophage T4 DNA polymerase.

The synthesis of the DNA polymerase of bacteriophage T4 is autogenously regulated. This protein (gp43), the product of gene 43, binds to a segment of its mRNA that overlaps its ribosome binding site, and thereby blocks translation. We have determined the Kd of the gp43-operator interaction to be 1.0 x 10(-9) M. The minimum operator sequence to which gp43 binds consists of 36 nucleotides that include a hairpin (containing a 5 base-pair helix and an 8 nucleotide loop) and a single-stranded segment that contains the Shine-Dalgarno sequence of the ribosome binding site. In the distantly related bacteriophage RB69 there is a remarkable conservation of this hairpin and loop sequence at the ribosome binding site of its DNA polymerase gene. We have constructed phage operator mutants that overproduce gp43 in vivo, yet are unchanged for in vivo replication rates and phage yield. We present data that show that the replicative and autoregulatory functions are mutually exclusive activities of this polymerase, and suggest a model for gp43 synthesis that links autoregulation to replicative demand.

Amino Acid Sequence↗