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1.
J Biomed Phys Eng ; 11(3): 315-324, 2021 Jun.
Article in English | MEDLINE | ID: mdl-34189120

ABSTRACT

BACKGROUND: The paper points out the importance of quantifying the extent and nature of organ and tissue injury within the assessment of severity of damage to health caused by effect of blunt or combined force. OBJECTIVE: This study aims to determine the value of mechanical violence that caused the injury using the Fortis system based on the detected range of injured soft tissue and the localization of the sites affected by said violence. MATERIAL AND METHODS: In this experimental study the authors carried out measurements and calculations in 10 pedestrians, who died of polytrauma in an accident. The morphometric Ellipse v.2.0.7.1.software was used for the purpose (Vidito Kosice, Slovak Republic). RESULTS: The internal organ injuries were successfully evaluated in a planographic manner on serial sections with the following calculation of total extent of tissue damage (TETD). It turned out that if TETD is more than 40%, it will be possible to evaluate an injury as severe or life-threatening. CONCLUSION: The above classification and localization of pedestrian injuries facilitate calculations in simulation programs to determine how the movement of a pedestrian´s body during and after the collision occurred based on the unrepeatability of movement parameters; besides, contacts with a vehicle help determine the input data to calculate the collision. Based on the submitted case reports and performed measurements and calculations, the presented method of the extent classification of soft tissue damage is evaluated to be useful to standardize the injury parameters and assess polytrauma as a result of disproportionate force.

2.
J Med Life ; 14(5): 636-644, 2021.
Article in English | MEDLINE | ID: mdl-35027965

ABSTRACT

This study presents (1) a case of an injury to an unbelted passenger and (2) the possibilities of proving the occurrence of injuries to traffic accident participants. We demonstrate the case of an injury to a passenger who failed to fasten her seat belt, and question whether her injuries would have been equally serious if she had fastened her seat belt. Theoretical bases and methods for the interdisciplinary procedure of medical examiners using the PC Fortis program and technical analysts of traffic accidents using the PC Crash program are presented. Furthermore, individual practical steps are documented, the result showing that the injuries to the passenger would have occurred, but, to a minimum extent, i.e., 6.9% of the original injuries, which would have not exceeded the legal limit for damage to health.


Subject(s)
Seat Belts , Wounds and Injuries , Accidents, Traffic , Female , Humans , Wounds and Injuries/epidemiology , Wounds and Injuries/etiology
3.
Dis Markers ; 2017: 9185934, 2017.
Article in English | MEDLINE | ID: mdl-29158612

ABSTRACT

The progression of thoracic aortic aneurysm depends on regulation of aortic wall homeostasis and on changes in the structural components of the extracellular matrix, which are affected by multiple molecular signalling pathways. We decided to correlate the diameter of ascending thoracic aneurysm with gene expression of inflammation markers (IL-6, CRP), cytokine receptors (IL-6R, TNFR1, and TNFR2), and extracellular matrix components (Emilin-1, MMP9, and TIMP) for detection of the degree of pathological process of TAA formation. The experimental group was divided into three groups according to the diameter of the aortic aneurysm. Whole blood and tissue samples were properly collected and used for nucleic acid, chromatin, and protein isolation. The mRNA levels were detected by qRT-PCR. For the detection of protein levels a Cytokine Array IV assay kit was used in combination with a biochip analyzer. In aortic tissue, significant positive correlations were found between increased mRNA levels of inflammatory cytokines (CRP and IL-6) on both mRNA levels in tissue and protein from the blood with maximum in stage 3. Changes of gene expression of selected genes can be used for the experimental study of the inflammatory receptor inhibitors during trials targeted on slowing down the progress of aortic wall aneurysm.


Subject(s)
Aortic Aneurysm, Thoracic/metabolism , Cytokines/metabolism , Extracellular Matrix Proteins/metabolism , Receptors, Cytokine/metabolism , Adult , Aorta, Thoracic/metabolism , Aorta, Thoracic/pathology , Aortic Aneurysm, Thoracic/blood , Aortic Aneurysm, Thoracic/pathology , Biomarkers/blood , Biomarkers/metabolism , Case-Control Studies , Cytokines/blood , Cytokines/genetics , Extracellular Matrix Proteins/genetics , Female , Humans , Male , Middle Aged , Polymorphism, Genetic , RNA, Messenger/genetics , RNA, Messenger/metabolism , Receptors, Cytokine/genetics
4.
Anticancer Res ; 36(6): 2719-28, 2016 Jun.
Article in English | MEDLINE | ID: mdl-27272781

ABSTRACT

BACKGROUND/AIM: Chemopreventive activity of a new probiotic strain Lactobacillus plantarum LS/07 (PRO) and prebiotic oligofructose-enriched inulin (PRE) in rat mammary carcinogenesis induced by procarcinogen 7,12-dimethylbenz[a]anthracene has been reported before. This study evaluated the anticancer and immunomodulatory efficacy of PRO, PRE, PRO+PRE (PRO/PRE) and combination with melatonin (PRO+PRE+MEL) in a rat model, when breast cancer was induced by a direct-acting carcinogen N-nitroso-N-methylurea (NMU). MATERIALS AND METHODS: Daily administration of PRO (at a dose of 8.4×10(8) colony-forming units (c.f.u.)/rat), PRE (in the diet, 20 g/kg) and MEL (in tap water, 20 mg/l) started 14 days before the first NMU dose and lasted for 16 weeks. RESULTS: Although tumor growth was not altered, a marked decrease in the ratio of high-/low-grade carcinomas and in tumoral Ki-67 expression was found after PRO+PRE treatment; melatonin augmented these effects. PRO+PRE+MEL combination enhanced CD4(+) and CD8(+) T-cell tumor infiltration induced by PRO/PRE and increased CD25(+)FoxP3(+) regulatory T-cells in tumors. CONCLUSION: In mammary carcinogenesis, Lactobacillus plantarum LS/07 and inulin exert prodifferentiating, antiproliferative and immunomodulatory activities, which are significantly amplified by melatonin co-administration.


Subject(s)
Antineoplastic Agents/pharmacology , Immunologic Factors/pharmacology , Inulin/pharmacology , Lactobacillus plantarum , Mammary Neoplasms, Experimental/drug therapy , Melatonin/pharmacology , Probiotics/pharmacology , Animals , Female , Interleukin-6/physiology , Methylnitrosourea , Rats , Rats, Sprague-Dawley , Transforming Growth Factor beta1/physiology
5.
Anticancer Res ; 34(9): 4969-75, 2014 Sep.
Article in English | MEDLINE | ID: mdl-25202079

ABSTRACT

AIM: The purpose of the present study was to evaluate the chemopreventive efficacy of a new probiotic bacterial strain, Lactobacillus plantarum LS/07 (PRO), prebiotic oligofructose-enriched inulin (PRE) and PRO-PRE combination in a rat model of breast cancer. MATERIALS AND METHODS: Mammary carcinogenesis was induced by 7,12-dimethylbenz[a]anthracene (DMBA). Daily oral administration of PRO (at a dose of 8.4×10(8) c.f.u./rat) and PRE (in the diet, 20 g/kg) started two weeks before the first DMBA dose and lasted until the end of the experiment (16 weeks). RESULTS: Administration of PRO, PRE and PRO-PRE combination significantly suppressed the tumor frequency, increased Cd4(+) T-cells in tumor tissue and reduced serum tumor necrosis factor-α concentration. In PRO and PRO-PRE groups, the decline of Cd8(+) T-cells in blood and their increase in tumor tissue was observed. CONCLUSION: Long-term administration of Lactobacillus plantarum LS/07 with and without inulin is effective against breast cancer, at least partially, through immunomodulatory mechanisms.


Subject(s)
Dietary Fiber/administration & dosage , Lactobacillus plantarum/physiology , Mammary Neoplasms, Experimental/prevention & control , Probiotics/administration & dosage , 9,10-Dimethyl-1,2-benzanthracene/adverse effects , Animals , Cell Transformation, Neoplastic/chemically induced , Cytokines/biosynthesis , Diet , Disease Models, Animal , Female , Inulin/administration & dosage , Mammary Neoplasms, Experimental/immunology , Mammary Neoplasms, Experimental/metabolism , Mammary Neoplasms, Experimental/pathology , Neoplasm Invasiveness , Neoplasm Staging , Rats , T-Lymphocyte Subsets/immunology , T-Lymphocyte Subsets/metabolism
6.
J Surg Res ; 178(1): 188-95, 2012 Nov.
Article in English | MEDLINE | ID: mdl-22480834

ABSTRACT

BACKGROUND: Mesenchymal stromal cells (MSCs) in the pancreatic microenvironment can improve diabetes mellitus (DM). The aim of the present study was to determine whether different pancreatic microenvironments influence the improvement of hyperglycemia and insulin deficiency. METHODS: MSCs isolated from rat bone marrow were transplanted directly into different pancreatic microenvironments in male DM rats. DM was induced in the rats by streptozotocin injection. The rats were divided into 5 groups: normal control rats, DM control rats, and 3 experimental groups (DM rats plus MSCs injected into the head of the pancreas, the tail of the pancreas, or the whole pancreas). The body weight and blood glucose of the rats were monitored during the experiment after transplantation of the MSCs. Histopathologic and immunohistochemical analyses were used to detect the presence and number of islets and insulin production in the pancreatic tissue of the rats after MSC transplantation. RESULTS: At 28 days after MSC transplantation, we observed a statistically significant decrease in the blood glucose level and an increase in weight in DM rats compared with DM control rats (P < 0.0001 and P < 0.03, respectively). A comparison of each of the DM rat groups treated with MSCs showed no significant differences in the blood glucose levels or body weight. CONCLUSION: Our results suggest that transplantation of MSCs could improve DM in the pancreatic microenvironment in an animal model with streptozotocin-induced DM. The different pancreatic areas into which the MSCs were implanted had no significant influence on the improvement in hyperglycemia and insulin deficiency.


Subject(s)
Cellular Microenvironment/physiology , Diabetes Mellitus, Experimental/therapy , Hyperglycemia/therapy , Mesenchymal Stem Cell Transplantation/methods , Mesenchymal Stem Cells/cytology , Pancreas/metabolism , Animals , Blood Glucose/metabolism , Body Weight/physiology , Bone Marrow Transplantation/methods , Cells, Cultured , Diabetes Mellitus, Experimental/metabolism , Diabetes Mellitus, Experimental/pathology , Hyperglycemia/metabolism , Hyperglycemia/pathology , Insulin/deficiency , Insulin/metabolism , Islets of Langerhans/metabolism , Male , Mesenchymal Stem Cells/metabolism , Pancreas/cytology , Rats , Rats, Wistar , Transplantation, Homologous
7.
Eur J Cancer Prev ; 21(2): 163-70, 2012 Mar.
Article in English | MEDLINE | ID: mdl-22044852

ABSTRACT

The neurohormone melatonin is primarily involved in the regulation of circadian rhythms, but also acts as an antioxidant and anticarcinogenic agent, especially in breast cancer. Resveratrol (3,5,4'-trihydroxy-trans-stilbene) is a widely known polyphenolic agent from red wine, which has been shown to exert antioxidant, anti-inflammatory and anticarcinogenic effects. The objective of this study was therefore to investigate the effects of melatonin in combination with resveratrol in a rat model of experimental mammary carcinogenesis. Female Sprague-Dawley rats aged 31 days were used in the experiment. Mammary carcinogenesis was induced by N-methyl-N-nitrosourea (NMU), which was administered in two intraperitoneal doses (50 mg/kg of body weight). Chemoprevention with resveratrol and melatonin started 2 weeks before the first dose of NMU and lasted until the end of the experiment. The basic parameters evaluated were: tumour incidence, latency period, tumour frequency per group and tumour volume. In addition, oestrogen receptors ERα and ERß, melatonin receptor MT1, proliferating cell nuclear antigen and vascular endothelial growth factor were determined by immunohistochemical staining. The combination of resveratrol and melatonin reduced tumour incidence by approximately 17% and significantly decreased the quantity of invasive and in-situ carcinomas. Food intake declined in the second and seventh weeks after the administration of carcinogen. Resveratrol in combination with melatonin returned food intake to the level of intact controls. Resveratrol in combination with melatonin has some protective effects on NMU-induced rodent breast cancer. Further studies are necessary to confirm these effects of this promising combination.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Carcinoma/prevention & control , Chemoprevention/methods , Mammary Neoplasms, Experimental/prevention & control , Melatonin/administration & dosage , Stilbenes/administration & dosage , Algorithms , Animals , Carcinogens , Carcinoma/blood , Carcinoma/chemically induced , Carcinoma/pathology , Drug Evaluation, Preclinical , Estrogen Receptor alpha/metabolism , Female , Mammary Neoplasms, Experimental/blood , Mammary Neoplasms, Experimental/chemically induced , Mammary Neoplasms, Experimental/pathology , Melatonin/blood , Methylnitrosourea , Proliferating Cell Nuclear Antigen/metabolism , Rats , Rats, Sprague-Dawley , Resveratrol , Vascular Endothelial Growth Factor A/metabolism
8.
Photomed Laser Surg ; 29(9): 613-8, 2011 Sep.
Article in English | MEDLINE | ID: mdl-21456943

ABSTRACT

OBJECTIVE: The aim of the present study was to evaluate whether LLLT at 830 nm is able to positively modulate trachea incisional wound healing in Sprague-Dawley rats. BACKGROUND DATA: Tracheotomy may be associated with numerous complications. Development of excess granulation tissue represents a late complication that may lead to airway occlusion. Low-level laser therapy (LLLT) has been shown to have stimulatory effects on wound healing of different tissues. Therefore, it may be suggested that LLLT could be able to positively modulate trachea wound healing as well. MATERIALS AND METHODS: Using general anesthesia, a median incision was performed from the second to the fifth tracheal cartilage ring in 24 rats. Animals were then randomly divided into sham-irradiated control and laser-treated groups. LLLT (power density: 450 mW/cm(2); total daily dose: 60 J/cm(2); irradiated area ∼1 cm(2)) treatment was performed daily during the first week after surgery. Samples for histological evaluation were removed 7 and 28 days after surgical procedure. Histological sections were stained with hematoxylin-eosin and van Gieson. RESULTS: Results from our investigation showed that LLLT was able to reduce granulation tissue formation and simultaneously increase new cartilage development at both evaluated time intervals. CONCLUSIONS: From this point of view, LLLT at 830 nm may be a valuable tool in trachea wound healing modulation. Nevertheless, further detailed research is needed to find optimal therapeutic parameters and to test these findings on other animal models.


Subject(s)
Low-Level Light Therapy , Trachea/injuries , Tracheotomy , Wound Healing/radiation effects , Wounds, Penetrating/radiotherapy , Animals , Granulation Tissue/pathology , Granulation Tissue/radiation effects , Male , Rats , Rats, Sprague-Dawley , Tracheotomy/adverse effects , Wounds, Penetrating/etiology , Wounds, Penetrating/pathology
9.
Exp Dermatol ; 20(9): 703-8, 2011 Sep.
Article in English | MEDLINE | ID: mdl-21507066

ABSTRACT

Oestrogen deprivation is one of the major factors responsible for many age-related processes, including poor wound healing in women. Previously, it has been shown that oestrogens have a modulatory effect in different wound-healing models. Therefore, in this study, the effect of selective oestrogen receptor (ER) agonists (PPT - ER-α agonist, DPN - ER-ß agonist) on excisional and incisional wound-healing models was compared in ovariectomised rats in vivo as well as on human dermal fibroblasts (HDF) and human umbilical endothelial cells (HUVEC) in vitro. In the in vivo study, 4 months after either ovariectomy or sham ovariectomy, Sprague-Dawley rats were randomly divided into four groups and subjected to two incisional and excisional wounds: (i) control - sham operated, vehicle-treated; (ii) ovariectomised, vehicle-treated; (iii) ovariectomised, PPT treated; (iv) ovariectomised, DPN treated. In the in vitro study, HDFs and HUVECs were used. After treatment with ER agonists, cells were processed for immunocytochemistry and gelatin zymography. Our study shows that stimulation of ER-α leads to the differentiation of fibroblasts into myofibroblasts both in vivo and in vitro. On the other hand, the formation of extracellular matrix was more prominent, and wound tensile strength (TS) was increased when ER-ß was stimulated. In contrast, stimulation of ER-α led to a more prominent increase in the expression of MMP-2 and decrease in wound TS. New information is presented in this investigation concerning oestrogen replacement therapy (ERT) in different wound-healing models. This study demonstrates that the ERT should be both wound and receptor-type specific.


Subject(s)
Estrogen Receptor alpha/agonists , Estrogen Receptor beta/agonists , Extracellular Matrix/drug effects , Fibroblasts/drug effects , Skin/drug effects , Skin/injuries , Animals , Cell Differentiation/drug effects , Cells, Cultured , Female , Fibroblasts/cytology , Human Umbilical Vein Endothelial Cells , Humans , In Vitro Techniques , Myofibroblasts/cytology , Myofibroblasts/drug effects , Nitriles/pharmacology , Ovariectomy , Phenols/pharmacology , Pyrazoles/pharmacology , Rats , Rats, Sprague-Dawley , Selective Estrogen Receptor Modulators/pharmacology , Skin/physiopathology , Tensile Strength/drug effects , Wound Healing/drug effects
10.
Lasers Med Sci ; 25(5): 761-6, 2010 Sep.
Article in English | MEDLINE | ID: mdl-20496092

ABSTRACT

The optimal parameters for low-level laser therapy (LLLT) for wound healing are still open to discussion. Hence, our study was aimed at comparing the effects of different power densities of LLLT at 670 nm in rats. Four round full-thickness skin wounds were placed on the backs of 16 rats which were divided into two groups (non-steroid and steroid-treated). Three wounds were stimulated daily with a diode laser (daily dose 5 J/cm(2)) at different power densities (5, 15 and 40 mW/cm(2), respectively), and the fourth wound served as a control. Six days after surgery all animals were killed and samples removed for histological evaluation. Significant acceleration of fibroblast proliferation and new vessel formation was observed in wounds treated at the selected power densities. No significant differences were found in corticosteroid-treated rats. In conclusion, LLLT with the methodology used improved wound healing in non-steroid rats, but was not effective after corticosteroid-treatment.


Subject(s)
Lasers, Semiconductor/therapeutic use , Low-Level Light Therapy/methods , Skin/injuries , Skin/radiation effects , Wound Healing/radiation effects , Adrenal Cortex Hormones/pharmacology , Animals , Rats , Rats, Sprague-Dawley , Skin/drug effects , Skin/pathology , Wound Healing/drug effects
11.
J Surg Res ; 147(1): 117-22, 2008 Jun 01.
Article in English | MEDLINE | ID: mdl-18222474

ABSTRACT

BACKGROUND: The most effective method of increasing the level of estrogen in the wounds of post-menopausal women undergoing routine surgical procedures is by long-term preoperative administration. However, in the case of acute surgery or trauma, the most effective method of increasing the level of estrogen is administration immediately pre- or postsurgery. This study, therefore, was aimed at assessing the effect of postsurgical administration of estradiol benzoate on wound healing in ovariectomized (OVX) Sprague Dawley rats. MATERIALS AND METHODS: Three months prior to the wound healing experiment, 16 rats were anesthetized and underwent ovariectomy, while the other eight rats were sham operated. Two parallel full thickness skin incisions and two round full thickness skin excisions were performed on the dorsum of each rat. Dose of 10 microg/d of estradiol benzoate was administered to eight OVX rats for 6 d postoperatively, whereas the other animals received a placebo. After 6 d, all animals were sacrificed and samples removed for biomechanical and histological evaluation. RESULTS: The mean wound tensile strength of OVX estrogen treated rats (9.54 +/- 3.24 g/mm(2)) was significantly lower compared with vehicle-treated OVX animals (14.57 +/- 4.12 g/mm(2)) as well as with control rats subjected to sham-OVX surgery (11.71 +/- 3.33 g/mm(2)). Nevertheless, the histological evaluation in OVX estrogen treated rats showed a significantly increased process of neo-angiogenesis associated with slightly decreased collagen deposition. CONCLUSION: Our results indicate that the question of the clinical significance of this type of hormone replacement therapy remains open and requires further research.


Subject(s)
Estradiol/analogs & derivatives , Estrogen Replacement Therapy , Wound Healing/drug effects , Animals , Estradiol/pharmacology , Female , Ovariectomy , Progesterone/blood , Rats , Rats, Sprague-Dawley , Skin/pathology , Tensile Strength
12.
Phytomedicine ; 14(2-3): 172-8, 2007 Feb.
Article in English | MEDLINE | ID: mdl-17095201

ABSTRACT

Histomorphological changes in murine fibrosarcoma after photodynamic therapy (PDT) based on the natural photosensitizer hypericin were evaluated. C3H/DiSn mice were inoculated with fibrosarcoma G5:1:13 cells. When the tumour reached a volume of 40-80 mm(3) the mice were intraperitoneally injected with hypericin, either in a single dose (5 mg/kg; 1 or 6 h before laser irradiation) or two fractionated doses (2.5 mg/kg; 6 and 1 h before irradiation with laser light; 532 nm, 70 mW/cm(2), 168 J/cm(2)). All groups of PDT-treated animals with single and fractionated hypericin dosing presented primary vascular reactions including vascular dilatation, congestion, thrombosis and oedema. Two hours after PDT there were necrotic changes with small, rather focal appearance. One day after therapy the necrotic areas were enhanced, often affecting a complete superficial layer of tumour tissue. Necrotic areas were accompanied with inflammation and haemorrhages.


Subject(s)
Antineoplastic Agents, Phytogenic/pharmacology , Hypericum , Perylene/analogs & derivatives , Photochemotherapy , Photosensitizing Agents/pharmacology , Phytotherapy , Animals , Anthracenes , Antineoplastic Agents, Phytogenic/administration & dosage , Antineoplastic Agents, Phytogenic/therapeutic use , Cell Line, Tumor/drug effects , Disease Models, Animal , Fibrosarcoma/drug therapy , Fibrosarcoma/pathology , Humans , Injections, Intraperitoneal , Male , Mice , Mice, Inbred C3H , Perylene/administration & dosage , Perylene/pharmacology , Perylene/therapeutic use , Photosensitizing Agents/administration & dosage , Photosensitizing Agents/therapeutic use , Plant Extracts/administration & dosage , Plant Extracts/pharmacology , Plant Extracts/therapeutic use , Radiation Dosage
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