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1.
Folia Histochem Cytobiol ; 48(2): 202-7, 2010 Jan.
Article in English | MEDLINE | ID: mdl-20675275

ABSTRACT

Oxidative stress markers and apoptosis were estimated during elective surgical heart revascularization. Eight patients with good ejection fraction underwent coronary artery bypass grafting (CABG) with the use of warm blood cardioplegia. Two right atrium auricle biopsy specimens were collected before and after the operation. Specimens underwent immunocytochemical analysis of mitochondrial manganese superoxide dismutase (MnSOD) expression and apoptosis estimation by the TUNEL method. Ultrastructure analysis under electron microscope was made. Satisfactory results of the operation were obtained. After CABG the MnSOD expression increase in sections of auricles was observed through the increase of stain intensity and the percentage of cells with positive stain (from 30 to 80%). The apoptotic cells percentage remained at approximately the same level. Under the electron microscope insignificant pathological changes were observed. On this basis one may assume that in the case of cardiosurgical procedures with short aorta cross-clamping time and low operation risk level the application of cardioplegia sufficiently prevents reactive oxygen forms (ROF) cytotoxic activity although it does not inhibit the expression of oxidative stress (OS) markers. In our opinion the method of examining right atrium sections is safe and provides results comparable with other publications. It may also be a voice in the discussion on new methods of heart protection during cardiac surgery procedures.


Subject(s)
Apoptosis/physiology , Atrial Appendage , Biomarkers/metabolism , Heart Arrest, Induced/methods , Heart Atria , Myocardial Revascularization/methods , Myocytes, Cardiac/metabolism , Oxidative Stress , Aged , Aged, 80 and over , Atrial Appendage/cytology , Atrial Appendage/metabolism , Atrial Appendage/surgery , Cardioplegic Solutions/metabolism , Coronary Artery Bypass/methods , Female , Heart Atria/cytology , Heart Atria/metabolism , Heart Atria/surgery , Humans , In Situ Nick-End Labeling , Male , Middle Aged , Myocytes, Cardiac/ultrastructure , Superoxide Dismutase/metabolism
2.
Folia Histochem Cytobiol ; 48(2): 222-9, 2010 Jan.
Article in English | MEDLINE | ID: mdl-20675278

ABSTRACT

Polyphenols are present in several edible plants and for many years induce high interest mainly due to their antioxidative and anti-inflammatory influence. At present, numerous studies are conducted on antineoplastic effects of the compounds. One of most effective biopolyphenols involves the flavonol quercetin. Our studies aimed at evaluation of antiproliferative and pro-apoptotic effects of quercetin alone and in combinations with daunorubicin on cells of human pancreatic carcinoma lines. The experiments were conducted on two cell lines, sensitive to daunorubicin EPP85-181P line, and its resistant variant EPP85-181RDB. Effect of studied substances on cell proliferation was detected using sulphorhodamine B (SRB) protein staining method. Apoptotic damage was estimated using comet and TUNEL techniques. Our data demonstrated that quercetin exerted cytotoxic action on cells of the both neoplastic cell lines in concentration-dependent manner. In the case of EPP85-181RDB cell line, quercetin seemed to sensitize resistant cells to daunorubicin. In parallel, the effect of both substances on the sensitive cell line was synergistic. Results of the studies confirmed that quercetin may probably break resistance of neoplastic cells to chemotherapy. On the other side, studied flavonol augmented action of cytostatic drug in case of sensitive tumour cells what suggest, that it might allow to decrease dosage of cytostatic drugs and reduce negative side effects of the treatment.


Subject(s)
Antioxidants , Apoptosis/drug effects , Cell Line, Tumor/drug effects , Cell Proliferation/drug effects , Pancreatic Neoplasms/drug therapy , Quercetin , Antineoplastic Agents/pharmacology , Antineoplastic Agents/therapeutic use , Antioxidants/pharmacology , Antioxidants/therapeutic use , DNA Damage , Daunorubicin/pharmacology , Daunorubicin/therapeutic use , Drug Therapy, Combination , Humans , In Situ Nick-End Labeling , Pancreatic Neoplasms/physiopathology , Quercetin/pharmacology , Quercetin/therapeutic use
3.
Acta Pharmacol Sin ; 30(2): 184-92, 2009 Feb.
Article in English | MEDLINE | ID: mdl-19194452

ABSTRACT

AIM: The cytotoxicity of marcaine was estimated in combination with a calcium channel blocker. In addition, the influence of marcaine and marcaine plus lekoptin on a model system using the H9C2 cardiac cell line was investigated. METHODS: Cells were incubated for five hours with marcaine, lekoptin, or with both drugs simultaneously. Apoptotic cells were detected using the TUNEL assay and the alkaline comet assay. Mitochondrial cell function after drug uptake was examined using the MTT assay. The concentration of MDA (malondialdehyde) -- the final product of fatty-acid peroxidation, was quantified spectrophotometrically. The expression of glutathione S-transferase pi (GST-pi) was detected by immunofluorescence (IF) and Western blotting (WB) and inducible nitric oxide synthase (iNOS) was assessed by immunocytochemical staining (ABC). RESULTS: Incubation with marcaine resulted in the highest number of apoptotic cells. After incubation with both marcaine and lekoptin, moderate damage to cells (54.2%+/-1.775% of DNA destruction) was observed. The highest levels of iNOS and GST-pi expression were observed in cells treated with marcaine and marcaine plus lekoptin. The characteristic nuclear GST-pi expression was observed in cells treated with both drugs. CONCLUSION: Lekoptin stimulated cells to proliferate. Marcaine caused membrane damage and ultimately cell death.


Subject(s)
Bupivacaine/pharmacology , Calcium Channel Blockers/pharmacology , Myoblasts/drug effects , Myoblasts/metabolism , Verapamil/pharmacology , Anesthetics, Local/pharmacology , Animals , Apoptosis/physiology , Cell Line , Ki-67 Antigen/metabolism , Lipid Peroxidation , Myoblasts/cytology , Myocardium/cytology , Nitric Oxide Synthase Type II/metabolism , Oxidation-Reduction , Rats
4.
Histol Histopathol ; 23(5): 531-8, 2008 05.
Article in English | MEDLINE | ID: mdl-18283637

ABSTRACT

Decreased expression of p16 may result from hypermethylation of the promoter or from deletion of the gene. It can lead to intensified proliferation of neoplastic cells and to cytostatic drug resistance. The study was aimed at the examination of prognostic value of p16 expression in relation to Ki67 and caspase-3 in ovarian cancers using immunohistochemistry. The immunohistochemical studies were performed on 73 paraffin-embedded samples of ovarian cancers from 43 patients and samples from 6 healthy ovaries. We have used monoclonal antibodies against p16. ABC method and DAB were used for antigens visualisation. The intensity of the immunohistochemical reactions was appraised using the semi-quantitative IRS scale. In healthy ovaries we have shown strong reaction in the nuclei of surface epithelium. In the case of studied ovarian cancers, the reaction of a nuclear and cytoplasmic localization was obtained. The mean overall immunoreactivity score of nuclear p16 expression amounted to 5.30+/-3.44 SD in primary laparotomy material and 6.61+/-4.34 SD in secondary cytoreduction material. Statistical analysis demonstrated that lower p16 expression was typical of the younger patients and the patients who died. Kaplan-Meier's analysis proved that lower expression of p16 was characteristic of cases with shorter overall survival. In the present study we have demonstrated that lowered p16 expression represented an unfavourable prognostic index in ovarian cancer. Lowered p16 expression was also typical for chemotherapy-resistant ceases (cases of lower caspase-3 and higher Ki67 at secondary cytoreduction expression).


Subject(s)
Adenocarcinoma/metabolism , Cyclin-Dependent Kinase Inhibitor p16/metabolism , Ovarian Neoplasms/metabolism , Ovary/metabolism , Adenocarcinoma/mortality , Adenocarcinoma/secondary , Adenocarcinoma/therapy , Biomarkers, Tumor/metabolism , Caspase 9/metabolism , Cell Nucleus/metabolism , Cell Nucleus/pathology , Combined Modality Therapy , Cytoplasm/metabolism , Cytoplasm/pathology , Female , Fluorescent Antibody Technique, Indirect , Humans , Immunoenzyme Techniques , Ki-67 Antigen/metabolism , Middle Aged , Neoplasm Recurrence, Local , Neoplasm Staging , Ovarian Neoplasms/mortality , Ovarian Neoplasms/pathology , Ovarian Neoplasms/therapy , Ovary/pathology , Retrospective Studies , Survival Rate
5.
Folia Histochem Cytobiol ; 45(1): 21-5, 2007.
Article in English | MEDLINE | ID: mdl-17378241

ABSTRACT

Langerhans cell histiocytoses (LCH) represent rare diseases of unclear etiology and pathogenesis. Most of the cases include children, 1 to 15 years of age, and various organs are involved (bones, skin, liver, lymph nodes, bone marrow and other). The diagnosis of LCH used to be established by biopsy of the inflamed tissue and demonstration of expression of markers specific for Langerhans cells: CD1a and langerin. The diagnosis can be ultimately confirmed by demonstration of Birbeck's granules in the electron microscopy. The present study was aimed at immunocytochemical demonstration, in the examined LCH material (skin, bones, lymph nodes), of the specific antigen expression and at comparing it with the presence of Birbeck's granules. In the examined 11 cases co-expression of CD1a with langerin and with the presence of Birbeck's granules was noted. Also in all examined biopsies the expression of S-100 protein on inflammatory cells was found. The results corroborate the usefulness of immunocytochemical studies on CD 1 a and langerin expression in diagnosis of LCH.


Subject(s)
Antigens, CD1/metabolism , Antigens, CD/metabolism , Histiocytosis, Langerhans-Cell/diagnosis , Immunohistochemistry , Langerhans Cells/immunology , Lectins, C-Type/metabolism , Mannose-Binding Lectins/metabolism , Adolescent , Antigens, CD1/immunology , Child, Preschool , Cytoplasmic Granules/ultrastructure , Female , Histiocytosis, Langerhans-Cell/pathology , Humans , Infant , Infant, Newborn , Langerhans Cells/ultrastructure , Male
6.
Folia Histochem Cytobiol ; 44(3): 195-200, 2006.
Article in English | MEDLINE | ID: mdl-16977800

ABSTRACT

The induction of exercise-induced apoptosis in not actively involved in exercise organs, such as kidney could be a result of oxidative stress. Metallothionein (MT) exerts a protective effect in the cell against oxidative stress and apoptosis. We have previously demonstrated an increased incidence of apoptosis in distal tubular cells and collecting ducts in rat kidney after acute exercise. The present study was designed to test the hypothesis that MT may play a protective role in rat renal tubules against exercise-induced apoptosis after the acute exercise and regular training. Male Wistar rats were divided into control, acute exercised and 8-wk regularly trained groups. The kidneys were removed after a rest period of 6 h and 96 h. The ultrastructure of renal tubular cells was examined by electron microscopy. Apoptosis was detected in paraffin sections by the TUNEL technique. Expression of MT was examined by immunohistochemistry. The level of lipid peroxidation (thiobarbituric acid reactive substances - TBARS) was assayed in renal tissue homogenates. After acute exercise, the occurrence of apoptosis was restricted to distal tubules and collecting ducts of rat kidney, whereas the proximal tubules remained unaffected. The 8-wk training did not result in increased apoptosis in tubular cell. MT expression was confined exclusively to proximal tubules in all groups. However, it was significantly increased in acutely exercised animals, as compared to control and trained rats. After the 8-wk training, MT expression remained unaltered as compared to the control group. TBARS levels were significantly increased after acute exercise, while after regular training they remained unchanged. A significant correlation between TBARS level and MT expression was demonstrated. The findings could suggest a protective role of MT against oxidative stress and apoptosis in proximal tubular cells.


Subject(s)
Kidney Tubules/metabolism , Metallothionein/metabolism , Physical Conditioning, Animal/physiology , Physical Endurance/physiology , Animals , Apoptosis/physiology , Fatigue/metabolism , Kidney Tubules/cytology , Kidney Tubules/ultrastructure , Lipid Peroxidation , Male , Rats , Rats, Wistar , Thiobarbituric Acid Reactive Substances/analysis
7.
Folia Morphol (Warsz) ; 63(1): 107-10, 2004 Feb.
Article in English | MEDLINE | ID: mdl-15039913

ABSTRACT

Tumour growth and expansion are the result of proliferative activity and the capacity to eliminate cells by apoptosis and/or necrosis. The present study was aimed at comparing the apoptosis and proliferation intensity in cells of adenocarcinomas of the large intestine with the expression of metallothionein (MT), the grade of the tumour and the depth to which the tumour infiltrated the intestinal wall. The TUNEL technique and immunocytochemical reactions (expression of caspase-3, Ki-67, MT) were used to detect apoptosis. The results demonstrated augmented levels of all the variables examined, positively correlated with grade of malignancy, G, and with the depth of intestinal wall infiltration by the tumour cells. The testing of apoptosis, proliferation and MT expression may prove useful in the appraisal of the growth and progression of primary adenocarcinomas in the large intestine.


Subject(s)
Adenocarcinoma/pathology , Apoptosis , Intestinal Neoplasms/pathology , Metallothionein/metabolism , Adenocarcinoma/metabolism , Caspase 3 , Caspases/metabolism , Cell Division , Humans , Immunohistochemistry , In Situ Nick-End Labeling , Intestinal Neoplasms/metabolism , Ki-67 Antigen/metabolism , Neoplasm Invasiveness/pathology
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