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Biomedical subjects

O Müller

Publications and source records attributed to O Müller.

At least 163 records · Page 9Linked to original sources
PubMed1976

[Total hip replacement with isoelastic prosthesis in animals (author's transl)].

Uncemented fixation and low-fraction materials are the basis of this experiment. Plastics with an elasticity similar to the bone ("isoelasticity") show very propitious material qualities. The direct cementless incorporation of test bodies must be checked. In 63 sheep isoelastic total hip joints were implanted. After 2 till 51 weeks the animals were sacrificed and 44 specimen of hips and organs were explored macroscopically, radiologically, spherimetrically and histologically. The result was: 1. Plastic hip prosthesis are incorporated in the bone, but the boundary layer is built by a collagenous fiber tissue. 2. Loosening brings resoption of the bone and expansion of the structural changed soft tissue. 3. The transformation of the femoral cortex to osteoporosis is considered possibly as the consequence of an insufficient biological transfer of the weight. 4. Fractures of the femoral prosthesis-stem could not be observed. 5. The radiology allows at the pelvis prosthesis a concret statement concerning stability, on the femoral part a probable one. 6. The abrasion is minimal, the tissue reaction to abrasion products is unessential. 7. Small abrasion particles are carried of by the lymph tract and stored in the first regional gland. A more distant spreading is not demonstrable.

Animals↗
PubMed1976

Interferon in treatment of dendritic keratitis in humans: a preliminary report.

Seventy-three patients with herpetic epithelial keratitis were randomly divided into three groups and were treated by local applications of human leukocyte interferon, thermocautery plus human leukocyte interferon, or thermocautery plus mock human leukocyte interferon to obtain information on whether therapy with human leukocyte interferon can serve as a substitute for mechanical debridement of the involved epithelium or can improve the results when given as additional therapy. Fifty-five patients (75%) yielded herpes simplex virus before treatment, and only the results in these patients with keratitis of proved viral etiology were included in the analysis. These results indicated that mechanical debridement cannot be replaced with local application of human leukocyte interferon (3-4 X 10(4) units per day). When given in addition to thermocautery, human leukocyte interferon may have been of some value in a number of patients. However, the results were not statistically significant. A more potent dosage of human leukocyte interferon might provide better results.

Administration, Topical↗
PubMed1976

[An enzymic assay for the determination of vitamin B12 (author's transl)].

A procedure which extends the very sensitive propanediol-dehydratase reaction for 5'-deoxy-5'-adenosylcobalamine determination to cyanocobalamine and hydroxocobalamine is described. In this procedure, the cobalamines are adenosylated by vitamin B12 coenzyme synthetase and the resulting 5'-deoxy-5'-adenosylcobalamine can be determined by the propanediol-dehydratase reaction. Aldehyde, the product of the latter, can be registered by the alcohol dehydrogenase reaction.

Adenosine↗
PubMed1975

The fate of injected human IgG in the mouse liver: Uptake, immunological inactivation, and lysosomal reactions.

1. Human IgG is stored in the form of remarkable droplets in the cytoplasm of mouse hepatocytes following intravenous injection. 2. The earliest protein uptake occurs within 1 minute after injection and droplets can be found up to 32 hours thereafter; 64 hours p.i. the foreign protein is no longer visible in hepatocytes. 3. Electron microscopy reveals that the uptake occurs by a process of "macropinocytosis". The resulting protein droplets fuse with primary lysosomes and are transformed into phagolysosomes. 4. At the same time as the phagolysosomes are formed the IgG-droplets loose their immunological activity--as early as 2 hours after injection.

Acid Phosphatase↗
PubMed1975

[The circadian structure of the parotid gland. morphologic and morphometric investigations (author's transl)].

Male Wistar rats were standardized on a "light-dark" cycle. Daily light exposure was maintained from 07.00 to 19.00, while food and water were freely provided to each animal. During one 24-hour period, subgroups of five animals were sacrificed at four-hour intervals. The parotid glands were quickly removed from each animal, after which individual gland volume and weight were determined. Tissue samples were then fixed in glutaraldehyde and osmium and embedded in epon. Other samples were fixed in Carnoy and embedded in paraffin. A stereologic model of the rat parotid gland was constructed by morphometric methods. It could be demonstrated that the volume and weight of the glandular components changed during a 24-hour period. The maximum and minimum for each component were found to vary significantly; in most instances, the maximum occured during the evening at the onset of the eating cycle, whereas the minimum occurred in the morning with the completion of eating. The most dramatic differences were seen within the glandular acinar cells (Fig. 1 and 2). During a normal 24-hour period or physiological secretory cycle, the following volume changes were found: secretory granules, 160%; nuclei, 30%; nucleoli, 80%; golgi-areas, 60%; rough endoplasmic reticulum, 10%. The present study indicates that the parotid gland has a time-dependent structure which reflects the rhythmic activity of the gland in production, storage and extrusion of secretory material.

Animals↗