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Biomedical subjects

J Ellinger

Publications and source records attributed to J Ellinger.

26 records · Page 2Linked to original sources
PubMedDate not supplied

Platelet interactions with heparin binding growth factor and fibronectin.

A fibronectin (Fn)/heparin/heparin binding growth factor (HBGF)/heparin (FHHH) complex can be affixed to vascular grafts. This study examines the effect of HBGF, Fn, and FHHH on platelet adhesion and aggregation. Expanded polytetrafluoroethylene (PTFE) grafts (5 cm X 4 mm) were treated with Fn (n = 9), FHHH (n = 9), or neither (n = 10) and interposed into canine aortoiliac systems, using each dog as its own control. Autogenous radiolabeled (111In oxine-650 muCi) platelets were injected IV prior to re-establishment of circulation. Blood flow was determined by electromagnetic flowmetry and perfusion maintained for 30 min. Grafts were removed with native aorta and ipsilateral iliac arteries (IIA). Specimens, excluding anastomoses, were sectioned for gamma counting and computerized planimetry. Results showed that FHHH and Fn treated grafts contained significantly more radioactivity than control segments, when normalized to their IIA. FHHH treated grafts contained 27 +/- 16 times more radioactivity per mm2 than IIA, Fn treated prostheses 12 +/- 8 times more, and untreated PTFE 4 +/- 3 times more. FHHH was significantly more radioactive than Fn alone (p less than or equal to 0.03). Platelet aggregation in response to either Fn or HBGF was studied in vitro. Aggregation was not activated by either Fn (1-100 micrograms/100 microliters) or HBGF (25-2,500 ng/100 microliters). These data suggest that Fn and HBGF promote platelet adhesion but not aggregation.

Animals↗
PubMedDate not supplied

Biomaterial-induced macrophage activation and monokine release.

This study quantifies macrophage acid phosphatase release as a marker of cell activation when cultured with or without biomaterials. Peritoneal macrophages were harvested from six New Zealand White rabbits and cultured in minimum essential media with 10% equine serum. After cell identification by morphology, nonspecific esterase, and RAM 11 immunoperoxidase, cells were passaged twice, and second-passage macrophages were seeded in 96-well plates (5,000 cells/well) and grown to confluence. After collection of day zero media, circular disks of polyglactin 910 and two types of commercially available polyethylene terephthalate with different construction and sterilization characteristics were placed on the cell monolayer. Controls without biomaterials were also established. Media was collected and pooled for each group and time point beginning on day 2 and continuing every other day for 22 days. Conditioned media were quantitatively assayed for acid phosphatase colorimetrically at 402 nm using p-nitrophenylphosphate as the substrate. Acid phosphatase activity increased progressively at late time points for each group but no difference was noted between groups at any time point. These data show that the activation of cultured macrophages with time is not altered differentially by the presence of biomaterials. The previously demonstrated monokine release following biomaterial exposure is therefore a specific event and not simply part of the generalized activation phenomenon.

Acid Phosphatase↗
PubMedDate not supplied

Kinetics of collagen deposition within bioresorbable and nonresorbable vascular prostheses.

This study compares the kinetics of collagen deposition within the prosthesis/tissue complexes formed following implantation of either polyglactin 910 (PG910), polydioxanone (PDS), or Dacron prostheses into rabbit infrarenal aortas. The grafts were explanted in triplicate at 1, 3, and 12 months, and then processed for spectrophotometric hydroxyproline quantitation. A 2 mm longitudinal strip from each sample was processed for histologic evaluation by light and electron microscopy. Results showed more extensive collagen deposition within the prosthesis/tissue complexes of both PG910 and PDS continuing throughout 3 months, as compared to less collagen deposition in Dacron grafts at all time points. Differences between PG910 and Dacron, and between PDS and Dacron at each time point were statistically significant. When correlated with previous related studies done in our laboratory, data showed that in resorbable grafts the rate of collagen deposition parallels the kinetics of cellular proliferation, tissue thickening, and graft resorption.

Animals↗
PubMedDate not supplied

Prostacyclin production by blood-contacting surfaces of endothelialized vascular prostheses.

This study examines prostacyclin production by blood-contacting surfaces within woven vascular prostheses of polydioxanone (PDS), polyglactin 910 (PG910), or Dacron interposed into rabbit infrarenal aortas. Grafts and normal aortic segments were explanted after 1, 3, and 6 months for pulsatile perfusion with Medium-199 for 60 minutes. Aliquots were removed serially for 6-keto-PGF1 alpha assay. After 30 minutes sodium arachidonate (10 micrograms/ml) was added. Specimens were studied by light microscopy, SEM and TEM. Patency in all three groups exceeded 90%. All three showed re-endothelialization at one month. Normal aorta produced low basal 6-keto-PGF1 alpha with a marked evanescent post arachidonate increase. Dacron did not differ from normal aorta. PG910 and PDS both produced significantly less 6-keto-PGF1 alpha post arachidonate at one month but both increased to normal by three months.

6-Ketoprostaglandin F1 alpha↗
PubMedDate not supplied

The validity of canine platelet aggregometry in predicting vascular graft patency.

Several laboratories have found canine platelet aggregometry predictive of thrombotic potential in vascular grafts. Adenosine diphosphate (ADP) is a frequently used agonist, often at unspecified or differing concentrations. This study was designed to evaluate the predictive value of ADP-induced platelet aggregometry and the validity of the methodology. Platelet aggregometry in response to 2 x 10(-5) M ADP was assayed in 70 dogs. Twenty-six percent were aggregators, 51% were non-aggregators, and 20% were indeterminant. All dogs were then treated with aspirin and dipyridamole. Vascular prostheses were implanted bilaterally (aorto-iliac) and anti-platelet therapy continued for two weeks. Dose-response to ADP was studied at three concentrations in 20 dogs. At 2 x 10(-5) 1/20 aggregated, at 4 x 10(-5) 3/19 aggregated and at 2 x 10(-4) 15/20 aggregated. Time between samples and study was evaluated in 11 dogs, with 2/11 changing from non-aggregator to aggregator at two or three hours. Daily reproducibility was studied in 70 dogs, 14 of which changed aggregation status between days. Patency was 58/68 (85%) for non-aggregators, 23/34 (68%) for aggregators (p = 0.038). Platelet aggregometry has significant predictive value for graft patency but methodology must be specified and standardized.

Adenosine Diphosphate↗