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1.
Cancers (Basel) ; 14(19)2022 Sep 26.
Article in English | MEDLINE | ID: mdl-36230596

ABSTRACT

Percutaneous transhepatic biliary drainage (PTBD) is a decompression procedure for malignant proximal biliary obstruction. In this research, over a six-year period, 89 patients underwent PTBD procedure for jaundice caused by malignant disease to restart chemotherapy or for palliative intent. Clinical outcomes after PTBD procedure in the two groups of patients, according to the adequate bilirubin decline (ABD) needed for subsequent chemotherapy, are presented in this paper. Survival and logistic regression were plotted and compared using Kaplan−Meier survival multivariate analysis with a long-range test. Results were processed by MEDCALC software. In the series, 58.4% (52/89) of patients were in good performance status (ECOG 0/1), and PTBD was performed with the intention to (re)start chemotherapy. The normalization of the bilirubin level was seen in 23.0% (12/52), but only 15.4% (8/52) received chemotherapy. The median survival time after PTBD was 9 weeks. In patients with ABD that received chemotherapy, the median survival time was 64 weeks, with 30-day mortality of 27.7%, and 6.4% of death within 7 days. The best outcome was in patients with good performance status (ECOG 0−1), low bilirubin (<120 µmol/L) and LDH (<300 µmol/L) levels and elevated leukocytes at the time of the procedures. PTBD is considered in ABD patients who are candidates for chemotherapy.

2.
Animals (Basel) ; 12(10)2022 May 18.
Article in English | MEDLINE | ID: mdl-35625147

ABSTRACT

The study was conducted on a commercial pig farm located in Serbia. Thirty Duroc or Landrace breed boars were randomly selected for this study. The experimental group was fed a compound feed with added organic selenium and Oxynat 3D. The antioxidant status parameters of boar seminal plasma were evaluated using a biochemical analyzer and commercial Randox kits. The sperm chromatin structure assay (SCSA) using flow cytometry (FC) provided information about spermatozoa's DNA status. Additionally, the total number of motile spermatozoa and spermatozoa kinematic parameters were measured using the computer-assisted sperm analysis (CASA) system. The aim of this study was to improve the parameters of semen by combining two preparations that have a potential antioxidant effect, but also to establish the level of various antioxidant enzymes in native sperm. There was no statistically significant difference in total antioxidant capacity and glutathione peroxidase activity in the seminal plasma obtained from the experimental and control groups of boars. Regarding the superoxide dismutase activity, the research results showed a difference in the control group compared to the experimental one. Moreover, spermatozoa DNA fragmentation and the total number of motile spermatozoa showed statistically significant lower and higher values, respectively, in experimental compared to the control groups. The combination of these two preparations shows significantly enhanced vital parameters of semen. To the best of our knowledge, this study is the first in which the ejaculate parameters were examined after the application of a combination of these two antioxidant supplements.

3.
Microsc Microanal ; 25(5): 1257-1262, 2019 10.
Article in English | MEDLINE | ID: mdl-31530326

ABSTRACT

This study aimed to compare three methods of cell death assessment [trypan blue exclusion (TBE), propidium iodide viability assay (PIVA), and transmission electron microscopy] to evaluate fresh and frozen-thawed chicken primordial germ cells (PGCs). For this study, chicken PGCs were collected from ROSS 908 and Oravka breed hens, cryopreserved-thawed according to the protocol, and submitted for different cell death assessments. We observed significant differences between TBE and PIVA techniques in the detectable proportion of dead cells in fresh (14.14 ± 1.27 versus 7.16 ± 1.02%, respectively) and frozen-thawed (44.00 ± 2.11 versus 33.33 ± 1.67%, respectively) samples of the Oravka breed. Moreover, significant differences (p < 0.05) between TBE and PIVA techniques in the detectable proportion of dead cells in fresh (9.20 ± 0.60 versus 5.37 ± 0.51%) samples of ROSS 908 breed were recorded. Differences may be due to methodological, sensitivity, and toxicity features of each technique tested, where TB stains cell cytoplasm of dead cells and PI penetrates and intercalates into DNA of dead cells. Therefore, we suggest using a more precise and sensitive PIVA for viability evaluation of PGCs. Further research is needed to apply various fluorochromes for more detailed cell viability evaluation.


Subject(s)
Cell Survival/radiation effects , Cryopreservation/methods , Germ Cells/physiology , Germ Cells/radiation effects , Microscopy, Fluorescence/methods , Microscopy/methods , Staining and Labeling/methods , Animals , Chickens , Microscopy, Electron, Transmission/methods , Sensitivity and Specificity
4.
Folia Biol (Krakow) ; 53(3-4): 129-32, 2005.
Article in English | MEDLINE | ID: mdl-19058533

ABSTRACT

The stability of transgene transmission, milk production and milk content of recombinant human protein C (rhPC) in transgenic rabbits of the F3 generation was determined. Transgenic rabbits carrying the 4.2kb mouse whey acid protein promoter and 9.4kb genomic human protein C were produced after mating transgenic (F2 generation) and non-transgenic rabbits. PCR analysis of F3 samples showed that the transgene was transmitted. Milk production, obtained at the 10th, 15th, 20th and 30th day of the first lactation by the weight-suckle-weight method showed no significant difference between transgenic and non-transgenic does. Concerning rhPC secretion, Western blotting detected a light chain (21 kDa) of rhPC in the milk and an ELISA test confirmed rhPC at the level of 0.109-0.301 microg/ml. A milk sample from a non-transgenic rabbit was hPC negative. In conclusion, the stability of hPC transgene transmission and production of rhPC protein C was confirmed in generation F3 of transgenic rabbits, with similar efficiency as in F1 and F2 generations, without reduction of milk production.


Subject(s)
Milk/chemistry , Protein C/metabolism , Rabbits/genetics , Rabbits/metabolism , Recombinant Proteins/metabolism , Animals , Animals, Genetically Modified , Female , Humans , Protein C/genetics , Recombinant Proteins/chemistry , Recombinant Proteins/genetics , Reproduction
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