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1.
Braz. j. med. biol. res ; 53(1): e9136, Jan. 2020. tab, graf
Article in English | LILACS | ID: biblio-1055487

ABSTRACT

The aim of this study was to investigate the influence of enhanced external counterpulsation (EECP) on the cardiac function of beagle dogs after prolonged ventricular fibrillation. Twenty-four adult male beagles were randomly divided into control and EECP groups. Ventricular fibrillation was induced in the animals for 12 min, followed by 2 min of cardiopulmonary resuscitation. They then received EECP therapy for 4 h (EECP group) or not (control group). The hemodynamics was monitored using the PiCCO2 system. Blood gas and hemorheology were assessed at baseline and at 1, 2, and 4 h after return of spontaneous circulation (ROSC). The myocardial blood flow (MBF) was quantified by 18F-flurpiridaz PET myocardial perfusion imaging at baseline and 4 h after ROSC. Survival time of the animals was recorded within 24 h. Ventricular fibrillation was successfully induced in all animals, and they achieved ROSC after cardiopulmonary resuscitation. Survival time of the control group was shorter than that of the EECP group [median of 8 h (min 8 h, max 21 h) vs median of 24 h (min 16 h, max 24 h) (Kaplan Meyer plot analysis, P=0.0152). EECP improved blood gas analysis findings and increased the coronary perfusion pressure and MBF value. EECP also improved the cardiac function of Beagles after ROSC in multiple aspects, significantly increased blood flow velocity, and decreased plasma viscosity, erythrocyte aggregation index, and hematocrit levels. EECP improved the hemodynamics of beagle dogs and increased MBF, subsequently improving cardiac function and ultimately improving the survival time of animals after ROSC.


Subject(s)
Animals , Male , Dogs , Counterpulsation/methods , Cardiopulmonary Resuscitation/methods , Hemodynamics/physiology , Case-Control Studies , Disease Models, Animal , Kaplan-Meier Estimate
2.
Clinics ; 68(9): 1231-1238, set. 2013. tab, graf
Article in English | LILACS | ID: lil-687768

ABSTRACT

OBJECTIVE: The role of Ulinastatin in neuronal injury after cardiopulmonary resuscitation has not been elucidated. We aim to evaluate the effects of Ulinastatin on inflammation, oxidation, and neuronal injury in the cerebral cortex after cardiopulmonary resuscitation. METHODS: Ventricular fibrillation was induced in 76 adult male Wistar rats for 6 min, after which cardiopulmonary resuscitation was initiated. After spontaneous circulation returned, the rats were split into two groups: the Ulinastatin 100,000 unit/kg group or the PBS-treated control group. Blood and cerebral cortex samples were obtained and compared at 2, 4, and 8 h after return of spontaneous circulation. The protein levels of tumor necrosis factor alpha (TNF-α) and interleukin 6 (IL-6) were assayed using an enzyme-linked immunosorbent assay, and mRNA levels were quantified via real-time polymerase chain reaction. Myeloperoxidase and Malondialdehyde were measured by spectrophotometry. The translocation of nuclear factor-κB p65 was assayed by Western blot. The viable and apoptotic neurons were detected by Nissl and terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL). RESULTS: Ulinastatin treatment decreased plasma levels of TNF-α and IL-6, expression of mRNA, and Myeloperoxidase and Malondialdehyde in the cerebral cortex. In addition, Ulinastatin attenuated the translocation of nuclear factor-κB p65 at 2, 4, and 8 hours after the return of spontaneous circulation. Ulinastatin increased the number of living neurons and decreased TUNEL-positive neuron numbers in the cortex at 72 h after the return of spontaneous circulation. CONCLUSIONS: Ulinastatin preserved neuronal survival and inhibited neuron apoptosis after the return of spontaneous circulation in Wistar rats via attenuation of the oxidative stress response and translocation of nuclear factor-κB p65 in the cortex. In addition, Ulinastatin decreased the production of TNF-α, ...


Subject(s)
Animals , Male , Rats , Apoptosis/drug effects , Cardiopulmonary Resuscitation/adverse effects , Cerebral Cortex/drug effects , Glycoproteins/pharmacology , Trypsin Inhibitors/pharmacology , Ventricular Fibrillation/metabolism , Blotting, Western , Cerebral Cortex/metabolism , Encephalitis/drug therapy , Glycoproteins/therapeutic use , /blood , Malondialdehyde/metabolism , Neurons/drug effects , Neurons/physiology , Oxidative Stress/drug effects , Peroxidase/metabolism , Rats, Wistar , Real-Time Polymerase Chain Reaction , Reproducibility of Results , Time Factors , Treatment Outcome , Trypsin Inhibitors/therapeutic use , Tumor Necrosis Factor-alpha/blood
3.
Journal of Huazhong University of Science and Technology (Medical Sciences) ; (6): 204-209, 2011.
Article in Chinese | WPRIM | ID: wpr-298638

ABSTRACT

To assess a novel cell manipulation technique of tissue engineering with respect to its ability to augment superparamagnetic iron oxide particles (SPIO) labeled mesenchymal stem cells (MSCs) density at a localized cartilage defect site in an in vitro phantom by applying magnetic force.Meanwhile,non-invasive imaging techniques were use to track SPIO-labeled MSCs by magnetic resonance imaging (MRI).Human bone marrow MSCs were cultured and labeled with SPIO.Fresh degenerated human osteochondral fragments were obtained during total knee arthroplasty and a cartilage defect was created at the center.Then,the osteochondral fragments were attached to the sidewalls of culture flasks filled with phosphate-buffered saline (PBS) to mimic the human joint cavity.The SPIO-labeled MSCs were injected into the culture flasks in the presence of a 0.57 Tesla (T) magnetic force.Before and 90 min after cell targeting,the specimens underwent T2-weighted turbo spin-echo (SET2WI) sequence of 3.0 T MRI.MRI results were compared with histological findings.Macroscopic observation showed that SPIO-labeled MSCs were steered to the target region of cartilage defect.MRI revealed significantchanges in signal intensity (P<0.01).HE staining exibited that a great number of MSCs formed a three-dimensional (3D) cell "sheet" structure at the chondral defect site.It was concluded that 0.57 T magnetic force permits spatial delivery of magnetically labeled MSCs to the target region in vitro.High-field MRI can serve as an very sensitive non-invasive technique for the visualization of SPIO-labeled MSCs.

4.
Journal of Southern Medical University ; (12): 2553-2555, 2010.
Article in Chinese | WPRIM | ID: wpr-267737

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the effect of minimally invasive percutaneous plate osteosynthesis (MIPPO) for treatment of proximal humerus fractures with PHILOS plate.</p><p><b>METHODS</b>From January 2008 to July 2009, 22 cases of proximal humerus fractures were treated with MIPPO with PHILOS plate. According to Neer classification, 7 cases had two-part fractures, 12 had three-part fractures, and 3 had four-part fractures.</p><p><b>RESULTS</b>All the 22 cases were followed up ranging from 6 to 12 months with an average of 10 months. The functional results of the shoulder, according to Neer scores, were classified as excellent in 9 cases, good in 10 cases and fair in 3 cases, with an average score was 86.4%.</p><p><b>CONCLUSION</b>PHILOS using MIPPO shows good results for treating proximal humerus fractures.</p>


Subject(s)
Adult , Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged , Bone Plates , Fracture Fixation, Internal , Methods , Internal Fixators , Minimally Invasive Surgical Procedures , Methods , Shoulder Fractures , General Surgery , Treatment Outcome
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