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Biomedical subjects

G Heder

Publications and source records attributed to G Heder.

50 records · Page 3Linked to original sources

The chick embryo choriallantoic membrane as a bioassay for angiogenesis factors: reactions induced by carrier materials.

A variety of filter materials, sponges, and gels were placed on the chick chorioallantoic membrane (CAM), the reactions of it investigated and compared with those induced by natural egg materials (white eggshell membrane, coagulated albumen and yolk). Independently of the kind and nature of the naterials the CAM reacted nearly regularly underneath these diverse materials with a proliferation of ectodermal cells, fibroblasts, and blood vessels forming a highly capillarized granulation tissue. The area of the CAM surrounding the foreign materials frequently displayed an increase of small blood vessels macroscopically discernible and showing a radial arrangement (spoke-wheel-appearance according to FOLKMAN 1974). It is concluded that this type of vascular reaction cannot be considered as a characteristic feature for the action of a special tumour angiogenesis factor, since it can be induced by a variety of stimuli leading to an inflammatory reaction in the CAM. For the detection of special angiogenetic activities an objective quantification of the vessel reactions is necessary under consideration of the reactions induced by the mere presence of such foreign materials.

Allantois↗

Mouse brain extract with "fibroblast growth factor"-activity.

Crude tissue extracts prepared by homogenization and ammonium sulfate precipitation of mouse brains as described by Gospodarowicz et al. (1975) for brains and hypophyses of cattle have also been found to contain fibroblast growth factor-activity. In the presence as well as in the absence of calf serum in the medium the survival and proliferation of primary mouse embryo fibroblasts in culture were promoted as documented by dose-dependent increase of cell number and protein content during an incubation period of 48 hours. In the case of serum-free incubation also a significant rise of thymidine incorporation induced within 24 hours by the extract was noted. In contrast, the proliferation of primary chicken embryo fibroblasts or transformed mouse cells of the line "L" was not stimulated. Some possibilities for a practical use of such extracts are discussed.

Animals↗

[Insulin catabolism by transformed, cultivated mouse fibroblasts (L-cells)].

Cultivated, transformed mouse fibroblasts (L-cells) are endowed with enzyme systems for insulin breakdown that are comparable to those of many other types of non-dedifferentiated insulin target cells (time and substrate dependence, Km value). It cannot yet be decided, however, which of the potential enzyme systems (thiolproteindisulfide-oxidoreductase (TPO) [E.C. 1.8.4.2] or proteinase) is prevalent in insulin breakdown in intact L-cells. Despite the lack of typical target symptoms for insulin, the cultivated L-cell could provide an appropriate experimental model for the insulin metabolism.

Animals↗

Occurrence and potential importance of angiotensin-converting enzyme in semen of boars.

The activities of angiotensin-converting enzyme (ACE) and leucinaminopeptidase (LAP) are positively correlated with corresponding concentrations of sperm cells in semen of boars kept under normal conditions. The spermatozoa bound ACE activity, in general, does not reflect differences in the quality of semen (bull and boars). On the other hand, the ACE activity directly bound on the sperm cells is significantly elevated, if 'exogenic noxes' (by feeding or keeping) influence the fertility of boars in a drastic manner. These results are discussed with regard to the differential diagnostic importance for estimating the semen quality and to the causal relations between increased enzyme binding and injury of sperm cells.

Animals↗

Angiotensin-converting enzyme and other peptidolytic enzymes in human semen and relations to its spermatologic parameters.

Angiotensin-converting enzyme (ACE) and other enzymes of the renin-angiotensin system (RAS) occur in human semen in high activities. In contrast to bull ejaculates, not all zinc-dependent metallopeptidases are found to be in close correlation to the microscopically determined semen parameters; such a relationship was established only partly for the ACE. On the other hand, the RAS-dependent spermatozoa-bound enzymes, inclusive ACE, uniformly show negative correlations to the spermatologic parameters of human semen. These results, for the first time, point to different functions of the sperm-cell-bound (testicular) and of the seminal plasma (pulmonary) ACE activities.

Amino Acid Sequence↗

Investigations on the influence of bradykinin upon the motility of ram spermatozoa.

The influence of bradykinin, a component of the kallikrein-kinin system, on the motility of ram spermatozoa was examined in vitro (photometric motility evaluation, penetration test in cervical mucus of sheep, estimation of the percentage of forward-moving spermatozoa in the thermal resistance test). Whereas the motility was found to be influenced by bradykinin the acrosomal status remained undisturbed by it. With fresh as well as with frozen semen, the drug mainly increased the motility of samples with a low initial motility. With frozen semen, the penetration test revealed greater motility rises at 22 degrees C than at 38 degrees C. The importance of the results in relation to the angiotensin-converting enzyme (kininase) as well as the motility evaluation capabilities of the methods used are discussed. There was, however, no positive drug effect after adding the drug in the course of cryopreservation prior to freezing semen in straws although bradykinin solutions frozen in liquid nitrogen maintained their effectiveness.

Animals↗

The enzymatic degradation of bradykinin in semen of various species.

The degradation of bradykinin in semen and on washed sperm cells of various species (human, pig, cattle, sheep) is mainly controlled by two peptidases, the angiotensin-converting enzyme (ACE/kininase II; E.C. 3.4.15.1) and neutral metalloendopeptidase (NEP; E.C. 3.4.24.11). In addition, minor activities of kininase I (carboxypeptidase N/CPN; E.C. 3.4.17.3) were measured exclusively in human samples. Samples of the investigated species varied considerably in their ratios of the activities of bradykinin degrading peptidases. This should be considered in any approach aimed at maintaining the promoting effect of bradykinin on sperm motility by use of enzyme inhibitors.

Amino Acid Sequence↗

[The usefulness of ruthenium red in dye exclusion test on cultured cells (author's transl)].

QUESTION: The reliability of statements and the reproducibility of results derived from experiments on cell cultures are dependent on the use of practicable methods for most objective assay of the state of the cells. The experiments were to clarify the following questions: 1. Is it possible to assay vital and nonvital cells by use of the dye exclusion test (FET)? 2. Are intact cells also stained by FET? 3. Will there be a possibility to make FET more sensitive to obtain more reliable statements?

Cell Line↗

Occurrence and potential importance of selected peptidases in bull ejaculates.

The zinc containing peptidases angiotensin-converting enzyme (ACE), neutral metalloendopeptidase (NEP), and leucine aminopeptidase (LAP) occur in bull ejaculates in high activities. These enzyme activities are in close correlation with some routineously determined semen parameters. These ejaculat parameters are used for quality classification and selection of ejaculates and are according to long term experience in good correlation to the male fertility. Semen quality related correlations could not be found for the dipeptidyl aminopeptidase (DPIV) and the aminopeptidase A (APA). Origin and possible function of the zinc containing peptidases in the semen are examined and discussed.

Animals↗