Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 8 de 8
Filter
Add more filters










Database
Language
Publication year range
1.
Animals (Basel) ; 14(13)2024 Jun 29.
Article in English | MEDLINE | ID: mdl-38998038

ABSTRACT

The aim of the study was to point out the importance of recognizing non-accidental injuries (NAI) and to highlight the importance of reporting such cases, as well as prosecuting the perpetrators, in order to detect potentially existing violence or prevent future violence in society. A total of 338 dogs and 54 cats were submitted for necropsy. Out of 338 dogs examined, 175 (51.8%) died due to non-natural cause of death, 122 from natural causes (36.1%), and 35 (10.3%) due to accidental injuries, and in 6 cases (1.8%) the cause and manner of death were undetermined due to advanced post-mortal changes. Out of 54 examined cats, 21 died due to non-natural causes (38.9%) and the same number of cats died due to natural causes. The prevalence of accidental injuries resulting in death were 20.4% (n = 11) and in 1.8% (n = 1) the manner of death remained indeterminate. The high number of animals confirmed to have died from unnatural causes in this study highlights the need for greater involvement from the police, prosecution, and society as a whole to reduce the number of violent animal deaths in the future.

2.
Acta Vet Hung ; 2022 Jun 16.
Article in English | MEDLINE | ID: mdl-35895555

ABSTRACT

The aim of this study is to describe new diagnostic and surgical orbital approaches using video endoscopy in canines. Four different endoscopic approaches were investigated in this study of video endoscopy in cadavers: dorsal transorbital ligament approach via incision of the orbital ligament (DTOLA), dorsal subpalpebral transconjunctival approach (DSTA), ventral subpalpebral transconjunctival approach (VSTA), and transoral orbital approach (TOA). Two additional approaches, the ventral transpalpebral approach (VTA) and dorsal caudal transmuscular approach (DCTA) along with the DTOLA and DSTA were used in clinical patients. The most technically demanding approach was DTOLA; however, it provided the best visualisation of different anterior and posterior orbital structures. Visualisation of primarily the dorsal orbital wall, dorsal portion of the eye globe, and dorsal extraconal space also was achieved by DSTA. The VSTA enabled good visualisation of the ventral orbital floor and the ventral extraconal and intraconal space. In contrast, the TOA provided relatively poor visualisation of orbital structures, limited to the ventral orbital quadrant. Meanwhile, the VTA provided visualisation similar to the VSTA, while DCTA visualisation was limited to the dorsal and caudal orbital space. Orbital endoscopy is an effective and minimally invasive procedure that can be used for diagnostic and surgical orbital procedures.

3.
Eur J Pharmacol ; 882: 173281, 2020 Sep 05.
Article in English | MEDLINE | ID: mdl-32562800

ABSTRACT

Voltage-gated potassium (Kv) channels are the largest superfamily of potassium (K) channels. A variety of Kv channels are expressed in the vascular smooth muscle cells (SMC). Studies have shown that gestational diabetes mellitus (GDM) and pregnancy-induced hypertension (PIH) cause various changes in the human umbilical vein (HUV). Recently, we have shown that 4-AP, a nonspecific Kv1-4 channel inhibitor, significantly decreases vasorelaxation induced by K channel opener pinacidil in vascular SMCs of the HUVs from normal pregnancies, but not in GDM and PIH. The goal of this study was to provide more detailed insight in the Kv channel subtypes involved in pinacidil-induced vasodilation of HUVs, as well as to investigate potential alterations of their function and expression during GDM and PIH. Margatoxin, a specific blocker of Kv1.2 and Kv1.3 channels, significantly antagonized pinacidil-induced vasorelaxation in normal pregnancy, while in HUVs from GDM and PIH that was not the case, indicating damage of Kv1.2 and Kv1.3 channel function. Immunohistochemistry and Western blot revealed similar expression of Kv1.2 channels in all groups. The expression of Kv1.3 subunit was significantly decreased in PIH, while it remained unchanged in GDM compared to normal pregnancy. Phrixotoxin, specific blocker of Kv4.2 and Kv4.3 channels, did not antagonize response to pinacidil in any of the groups. The major novel findings show that margatoxin antagonized pinacidil-induced relaxation in normal pregnancy, but not in GDM and PIH. Decreased expression of Kv1.3 channels in HUV during PIH may be important pathophysiological mechanism contributing to an increased risk of adverse pregnancy outcomes.


Subject(s)
Hypertension, Pregnancy-Induced/metabolism , Kv1.3 Potassium Channel/metabolism , Muscle, Smooth, Vascular/metabolism , Umbilical Veins/metabolism , Adult , Antihypertensive Agents/pharmacology , Diabetes, Gestational/metabolism , Female , Humans , Kv1.2 Potassium Channel/metabolism , Pinacidil/pharmacology , Pregnancy , Young Adult
4.
Biomolecules ; 9(12)2019 12 17.
Article in English | MEDLINE | ID: mdl-31861240

ABSTRACT

Since cisplatin therapy is usually accompanied with numerous toxicities, including neurotoxicity, that involve tissue oxidative damage, the aim of this study was to evaluate the possible protective effect of N-acetylcysteine (NAC) on the anxiogenic response to cisplatin (CIS). Thirty-two male Wistar albino rats divided into four groups (control, cisplatin, NAC, and CIS + NAC). All treatments were delivered intraperitoneally. On day one, the control and cisplatin groups received saline while the NAC and CIS + NAC groups were administered with NAC (500 mg/kg). On the fifth day, the control group received saline while the CIS group was treated with cisplatin (7.5 mg/kg), the NAC group again received NAC (500 mg/kg), and the CIS + NAC group was simultaneously treated with cisplatin and NAC (7.5 and 500 mg/kg, respectively). Behavioral testing, performed on the tenth day in the open field (OF) and elevated plus maze (EPM) tests, revealed the anxiogenic effect of cisplatin that was significantly attenuated by NAC. The hippocampal sections evaluation showed increased oxidative stress (increased lipid peroxidation and decline in antioxidant enzymes activity) and proapoptotic action (predominantly by diminished antiapoptotic gene expression) following a single dose of cisplatin. NAC supplementation along with cisplatin administration reversed the prooxidative and proapoptotic effects of cisplatin. In conclusion, the results obtained in this study confirmed that antioxidant supplementation with NAC may attenuate the cisplatin-induced anxiety. The mechanism of anxiolytic effect achieved by NAC may include the decline in oxidative damage that down regulates increased apoptosis and reverses the anxiogenic action of cisplatin.


Subject(s)
Acetylcysteine/pharmacology , Anti-Anxiety Agents/pharmacology , Anxiety/chemically induced , Anxiety/drug therapy , Cisplatin/adverse effects , Protective Agents/pharmacology , Acetylcysteine/administration & dosage , Acetylcysteine/chemistry , Animals , Anti-Anxiety Agents/administration & dosage , Anti-Anxiety Agents/chemistry , Antineoplastic Agents/administration & dosage , Antioxidants/administration & dosage , Behavior, Animal/drug effects , Cisplatin/administration & dosage , Male , Oxidative Stress/drug effects , Protective Agents/administration & dosage , Protective Agents/chemistry , Rats , Rats, Wistar
5.
Exp Mol Pathol ; 111: 104323, 2019 12.
Article in English | MEDLINE | ID: mdl-31669131

ABSTRACT

Gestational diabetes mellitus (GDM) and pregnancy-induced hypertension (PIH) can jeopardize mother and/or fetus. Vascular ATP-sensitive potassium (KATP) channels most likely participate in the processes of diabetes and hypertension. The aim of this research was to examine whether GDM and PIH cause changes in the expression and function of KATP channels in vascular smooth muscle of human umbilical vein (HUV). Western blot and immunohistochemistry detected significantly decreased expression of Kir6.1 subunit of KATP channels in GDM and PIH, while the expression of SUR2B was unchanged. In GDM, a K+ channel opener, pinacidil caused reduced relaxation of the endothelium-denuded HUVs compared to normal pregnancy. However, its effects in HUVs from PIH subjects were similar to normal pregnancy. In all groups KATP channel blocker glibenclamide antagonized the relaxation of HUV induced by pinacidil without change in the maximal relaxations indicating additional KATP channel-independent mechanisms of pinacidil action. Iberiotoxin, a selective antagonist of large-conductance calcium-activated potassium channels, inhibited the relaxant effect of pinacidil in PIH, but not in normal pregnancy and GDM. Experiments performed in K+-rich solution confirmed the existence of K+-independent effects of pinacidil, which also appear to be impaired in GDM and PIH. Thus, the expression of KATP channels is decreased in GDM and PIH. In GDM, vasorelaxant response of HUV to pinacidil is reduced, while in PIH it remains unchanged. It is very likely that KATP channels modulation and more detailed insight in KATP channel-independent actions of pinacidil may be precious in the therapy of pathological pregnancies.


Subject(s)
Adenosine Triphosphate/metabolism , Diabetes, Gestational/physiopathology , Hypertension, Pregnancy-Induced/physiopathology , KATP Channels/metabolism , Muscle, Smooth, Vascular/metabolism , Umbilical Veins/metabolism , Adult , Female , Humans , Muscle, Smooth, Vascular/pathology , Pregnancy , Umbilical Veins/pathology
6.
Parasit Vectors ; 12(1): 270, 2019 May 28.
Article in English | MEDLINE | ID: mdl-31138280

ABSTRACT

BACKGROUND: Canine generalized demodicosis is a common parasitic disease caused by the proliferation of Demodex mites. The introduction of isoxazoline class treatments in veterinary dermatology has resulted in apparently effective treatment of generalized demodicosis. The objective of this study was to evaluate the effectiveness of fluralaner for the treatment of canine generalized demodicosis using real-time PCR for the detection and quantification of Demodex DNA. METHODS: Twenty privately owned dogs with clinical symptoms of generalized demodicosis and deep skin scrapings positive for Demodex canis mites were enrolled in the study. Following diagnosis (day 0) each dog was treated with fluralaner at the recommended commercial dose for tick and flea treatment (25-56 mg/kg) based on body weight. Clinical and mite count assessments, and hair sampling for molecular analyses were performed on days 0, 28, 56, 84 and 112. Demodex DNA was detected and quantified using real-time PCR. RESULTS: A single oral dose of fluralaner reduced Demodex mite counts in skin scrapings by an average of 98.9% in all dogs by day 28. No mites were recovered from skin scrapings from any treated dog by day 56, at which time the dog was considered to be clinically cured, with total hair regrowth. There were significant differences among examined dogs in qPCR cycle threshold (Ct) values on days 0, 28, 56, 84 and 112. Demodex DNA levels decreased (increasing Ct values) throughout the study. Mite DNA was present on day 112, possibly from dead mites, at values significantly lower than in samples taken on days 0, 28 and 56. Based on qPCR testing of diluted samples, the Demodex mite population was reduced by approximately 1000-fold on day 112. CONCLUSIONS: Oral administration of fluralaner at the recommended dose to dogs with generalized demodicosis is highly effective for reducing Demodex mite populations and resolving clinical signs of generalized demodicosis. The presence of mite DNA may indicate that treatment did not kill all Demodex mites.


Subject(s)
Acaricides/therapeutic use , Dog Diseases/drug therapy , Isoxazoles/therapeutic use , Mite Infestations/veterinary , Mites/drug effects , Administration, Oral , Animals , Arthropod Proteins/analysis , Dog Diseases/parasitology , Dogs , Female , Male , Mite Infestations/drug therapy , Real-Time Polymerase Chain Reaction , Skin/parasitology , Treatment Outcome
7.
Neurosci Lett ; 660: 17-21, 2017 Nov 01.
Article in English | MEDLINE | ID: mdl-28893591

ABSTRACT

Various studies reported beneficial effects of dehydroepiandrosterone (DHEA) and its sulphate (DHEAS), the neurosteroids involved in various brain functions, on synaptic plasticity, neuronal survival, memory, learning and behavior. This study aimed to investigate the behavioral profile of acute DHEA treatment by using active avoidance (AA) task, primarily predictive of the effects on the retrieval-based learning, and by applying forced swim test (FST), for assessment of antidepressant-like potential. Adult male Wistar rats received intraperitoneal injections of either DHEA (2, 10, 20mg/kg) or solvent, 30min prior to testing. DHEA, in a manner resembling an inverted U shape, influenced the retrieval imposed to rats in AA paradigm. The significant improvement of the performance in the retention session was observed following 10mg/kg DHEA treatment and it was not due to the changes in the motor activity, as indicated by unaltered locomotor parameters (inter-trial crossing). Moreover, 10mg/kg of DHEA significantly decreased the duration of immobility in FST, demonstrating antidepressant-like effects. The capability of bicuculline (2mg/kg) to antagonize the effects of DHEA has been evaluated simultaneously. The retrieval-facilitating as well as antidepressant-like effects of 10mg/kg DHEA were counteracted by bicuculline, a competitive antagonist of GABAA receptors, suggesting involvement of GABAergic system. These results support administration of DHEA as potential therapeutic strategy for treating depression and related cognitive impairments, but emphasized the importance of adequate dosing, as DHEA levels that are too high or too low may not be beneficial.


Subject(s)
Antidepressive Agents/administration & dosage , Avoidance Learning/drug effects , Dehydroepiandrosterone/administration & dosage , Depression/drug therapy , Mental Recall/drug effects , Animals , Behavior, Animal/drug effects , Male , Motor Activity/drug effects , Rats, Wistar , Retention, Psychology/drug effects
8.
Neuro Endocrinol Lett ; 37(5): 383-388, 2016 Oct.
Article in English | MEDLINE | ID: mdl-28231683

ABSTRACT

OBJECTIVES: The aim of this study was the estimation of effects induced by chronic administration of supraphysiological dose of TE and prolonged exercise in male rats on anxiety levels (alterations in exploratory activity patterns in EPM). MATERIAL AND METHODS: Two sedentary (control - C and testosterone-enanthate - T) and two exercise (exercise - E and testosterone-enanthate plus exercise - T+E) groups (n=32) underwent adequate protocols - the swimming protocol (1 h/day) and TE (20 mg/kg/w, s.c.) for six weeks. Testing was performed in EPM. RESULTS: Anxiolytic effects of exercise were manifested as increased exploratory activity in EPM - increase in cumulative duration in open arms, the number of rearings and head-dippings, and TEA. Supraphysiological dose of TE decreased the number of rearings and head-dippings, cumulative duration in open arms and TEA compared to the control group, while this effect of TE was more pronounced compared to the exercise group. The applied dose of TE attenuated beneficial effects of exercise by means of all estimated parameters. CONSLUSIONS: Our results confirmed the beneficial effect of exercise on anxiety levels observed in EPM by means of parameters considering the alterations in exploratory activity. Supraphysiological dose of TE resulted in anxiogenic-like behavior in EPM. The effect of TE was so pronounced that the beneficial effect of exercise was reversed to the control values (or even below them). Based on the results of this trial, we propose that use of the TEA (a new parameter for overall exploratory activity) can improve the evaluation of EPM test results.


Subject(s)
Anti-Anxiety Agents/adverse effects , Behavior, Animal/drug effects , Exploratory Behavior/drug effects , Testosterone/analogs & derivatives , Testosterone/adverse effects , Animals , Male , Maze Learning/drug effects , Models, Animal , Physical Conditioning, Animal , Rats, Wistar , Swimming/physiology , Testosterone/administration & dosage , Testosterone/pharmacology
SELECTION OF CITATIONS
SEARCH DETAIL
...