Nymannmccracken9450
Unlike dogs, feline abdominal studies are rare. Note that anatomical estudies in felines are scarce and almost unique using feline cadaver by means of sectional anatomy and computed tomography (CT) or magnetic resonance imaging (MRI).
In this study, a non-pathological vascularization model of feline abdomen was conducted on three adult cats was using anatomical and diagnostic imaging techniques.
A live pet cat and two cat cadavers were used in this study. Cat cadavers were injected with colored latex to show well-differentiated vascular structures and serial sections of cat abdomen were then provided. Computed tomography was performed by injecting an iodinated contrast medium through the cephalic vein of a live cat immediately before scanning. compound 78c The CT images showed the arterial and venous vascular formations hyper-attenuated with two tomographic windows. The correlation between anatomical sections and their CTs was studied to identify vascular and and visceral structures.
Hyper-attenuated vascular structures with the contrast medium were identified and marked along their path in the series of Dicom images with the Amira program. In this approach, sequentially and semiautomatically, vascular volumetric reconstruction was obtained without visceral formations. With the OsiriX program, volumetric reconstruction was automatic and maintained the fidelity of all visceral and vascular formations.
We conclude that these improved prototypes could be used in veterinary clinics as normal vascular models and as a basis for obtaining future 3D models of vascular anomalies such as portosystemic shunts.
We conclude that these improved prototypes could be used in veterinary clinics as normal vascular models and as a basis for obtaining future 3D models of vascular anomalies such as portosystemic shunts.
is considered as a main cause of community-acquired diarrhea in humans, however, sources of the multi-drug resistant (MDR) strains and their link with the disease are not well known.
This study aimed to investigate the frequency, serogroup diversity, and antimicrobial susceptibility patterns of
strains in poultry meat and stool samples of patients with community acquired diarrhea in Tehran.
We compared the frequency of non-typhoidal
serogroups, the similarities of their resistance patterns to 10 antimicrobial compounds, the prevalence of extended spectrum β-lactamase (ESBL) and ampicillinase C (AmpC) genetic determinants, and class 1 and 2 integrons in 100 chicken meat and 400 stool samples of symptomatic patients in Tehran during June 2018 to March 2019.
was isolated from 75% and 5.5% of the chicken meats and human stool samples, respectively. The chicken meat isolates mainly belonged to serogroup C (88%, 66/75), while the human stool isolates were mainly related to serogroup D (59.1%, 13/22). The MDR phenotype and the most common rates of resistance to antibiotics, including tetracycline, trimethoprim/sulfamethoxazole (TS) and azithromycin, were detected in 4.5% and 45.3%, 59% and 13.6%, 43% and 9.1%, 42% and 9.1% of the human stool and chicken meat samples, respectively. Carriage of
,
, and
genes in the meat isolate with ESBL resistance phenotype and
,
, and
among the 7 meat strains with AmpC resistance phenotype was not confirmed using polymerase chain reaction (PCR). High prevalence of class 1 and 2 integrons was characterized and showed a correlation with resistance to TS and chloramphenicol.
These findings showed a lack of association between chicken meats and human isolates due to discrepancy between the characterized serogroups and resistance phenotypes.
These findings showed a lack of association between chicken meats and human isolates due to discrepancy between the characterized serogroups and resistance phenotypes.
Trastuzumab is an antibody drug used to treat human epidermal growth factor receptor 2 (HER2) overexpressing human metastatic breast cancer. Antibody-dependent cellular cytotoxicity (ADCC) is considered to be the major mechanism of cytotoxicity of the drug. However, its ability to induce an ADCC response in canine peripheral blood mononuclear cells (PBMCs) is not well established.
We aimed to evaluate the ability of trastuzumab in enhancing the cytotoxicity of PBMCs against canine tumor cells.
We used canine tumor cell lines isolated from metastatic mammary gland tumors (CHMm and CIPm) and thyroid adenocarcinoma (CTAC). The binding of trastuzumab to the cells was confirmed using flow cytometry analysis. Peripheral blood mononuclear cells obtained from healthy beagles and lymphokine-activated killer (LAK) cells, generated by interleukin-2 (IL-2) stimulation of PBMCs, were used as effector cells. Standard lactate dehydrogenase (LDH) release assay was used to measure the cytotoxicity of the LAK cells againe potential antitumor activity of trastuzumab in canines.
Pulsed wave (PW) Doppler echocardiography provides a convenient and noninvasive tool for measuring cardiac output (CO) alternations after the administration of sedative drugs, but this is not a usual method for camelids.
The aim of the present study was to investigate the changes of the left and right ventricular outflow tracts (LVOT and RVOT), CO, and systolic time intervals following the intravenous (IV) injection of medetomidine (M) and xylazine (X) using PW Doppler echocardiography.
Twenty apparently healthy immature male one-humped camels (
) were selected and divided into four groups (five animals per group). Medetomidine and X were injected to the left jugular vein at two different doses of 10 and 20 μg/kg, and 0.2 and 0.4 mg/kg, respectively. Effects on echocardiographic parameters were assessed at 4 intervals before, 3, 60, and 120 min after drug administrations.
Velocity time integrity (VTI), maximum/mean flow velocity (Vmax and Vmean) and maximum/mean pressure gradient (PGmax and PGmean) decreased in aortic and pulmonic valves. Left ventricular ejection time (LVET) and LVET + pre ejection period (PEP) decreased and PEP and PEP/LVET increased in all groups except the low dose X group, 3 min after drug administration (P<0.05). The least values of VTI, velocity (V), PG and CO were observed after 60 min in the low dose X group (P<0.05).
A relationship was found between the intensity and the duration of changes in cardiac parameters and both types and dosages of the injected drugs. We concluded that X and M have transient depressor effects on the ventricular outflow tract and CO of healthy camels.
A relationship was found between the intensity and the duration of changes in cardiac parameters and both types and dosages of the injected drugs. We concluded that X and M have transient depressor effects on the ventricular outflow tract and CO of healthy camels.
