Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 15 de 15
Filter
Add more filters











Publication year range
1.
Hipertens Riesgo Vasc ; 41(3): 145-153, 2024.
Article in English | MEDLINE | ID: mdl-38871574

ABSTRACT

BACKGROUND: The COVID-19 pandemic has highlighted the vulnerability of particular patient groups to SARS-CoV-2 infection, including those with cardiovascular diseases, hypertension, and intestinal dysbiosis. COVID-19 affects the gut, suggesting diet and vitamin D3 supplementation may affect disease progression. AIMS: To evaluate levels of Ang II and Ang-(1-7), cytokine profile, and gut microbiota status in patients hospitalized for mild COVID-19 with a history of cardiovascular disease and treated with daily doses of vitamin D3. METHODS: We recruited 50 adult patients. We screened 50 adult patients and accessed pathophysiology study 22, randomized to daily oral doses of 10,000IU vitamin D3 (n=11) or placebo (n=11). Plasma levels of Ang II and Ang-(1-7) were determined by radioimmunoassay, TMA and TMAO were measured by liquid chromatography and interleukins (ILs) 6, 8, 10 and TNF-α by ELISA. RESULTS: The Ang-(1-7)/Ang II ratio, as an indirect measure of ACE2 enzymatic activity, increased in the vitamin D3 group (24±5pg/mL vs. 4.66±2pg/mL, p<0.01). Also, in the vitamin D3-treated, there was a significant decline in inflammatory ILs and an increase in protective markers, such as a substantial reduction in TMAO (5±2µmoles/dL vs. 60±10µmoles/dL, p<0.01). In addition, treated patients experienced less severity of infection, required less intensive care, had fewer days of hospitalization, and a reduced mortality rate. Additionally, improvements in markers of cardiovascular function were seen in the vitamin D3 group, including a tendency for reductions in blood pressure in hypertensive patients. CONCLUSIONS: Vitamin D3 supplementation in patients with COVID-19 and specific conditions is associated with a more favourable prognosis, suggesting therapeutic potential in patients with comorbidities such as cardiovascular disease and gut dysbiosis.


Subject(s)
COVID-19 , Cardiovascular Diseases , Cholecalciferol , Dietary Supplements , Dysbiosis , Gastrointestinal Microbiome , Peptide Fragments , Humans , Cholecalciferol/administration & dosage , Male , Female , Cardiovascular Diseases/prevention & control , Cardiovascular Diseases/etiology , Cardiovascular Diseases/epidemiology , Middle Aged , COVID-19/complications , Peptide Fragments/blood , Aged , Angiotensin I/blood , Angiotensin II/blood , COVID-19 Drug Treatment , Vitamins/administration & dosage , Methylamines/blood , Cytokines/blood , Angiotensin-Converting Enzyme 2/metabolism , SARS-CoV-2 , Double-Blind Method
2.
Vaccine X ; 11: 100187, 2022 Aug.
Article in English | MEDLINE | ID: mdl-35755140

ABSTRACT

Background: In December 2020, Sputnik V was incorporated to the National COVID-19 Immunization Plan in Argentina. Studies had shown 98% of antibody response rate. To date, data on immunogenicity and antibody persistence in Argentina are scarce.The objective was to assess humoral immune response after two doses of Sputnik V in Health Care Workers (HCWs) at the Ricardo Gutierrez Children's Hospital (RGCH). Methods: A prospective, cohort study in HCWs immunized with two doses of Sputnik V between February and March 2021. The following variables were assessed: age, gender, risk factors for severe COVID-19 or mortality, immunosuppressive therapy and history of SARS-CoV-2. Blood samples were drawn on the day of the first dose, 28 days and 180 days after the second. Anti-Spike IgG was measured using an ELISA assay. Differences in immune response were evaluated according to study variables. Comparison analyses between groups with or without history of infection were performed, with T-test and ANOVA or Mann-Whitney tests. For each subject, we compared baseline values with 28 days and 180 days after the second vaccine.STATA version 14 and R Sofware were used for data analyses. Results: We included 528 individuals, mean age 41.5 years, 82.9% female, 14.4% (76/528) reported previous SARS-CoV-2 infection.All subjects developed antibodies post-vaccination. At day 28, concentrations were significantly higher in previously infected than naïve subjects (p < 0.001) with no differences according to age, gender and comorbidities.At day 180, 17% (95% CI 13.17-21.53) of naïve subjects were negative. Antibody concentrations decreased significantly in all subjects except in those who reported SARS-CoV-2 infection after vaccination (n = 31). This last group had significantly higher antibody concentrations. Conclusion: This study assessed immune response to a new COVID-19 vaccine in real life in a cohort of subjects. Antibody concentrations varied according to history of SARS-COV-2 infection and decreased over time.

3.
Inflamm Res ; 57(1): 39-43, 2008 Jan.
Article in English | MEDLINE | ID: mdl-18209964

ABSTRACT

OBJECTIVE AND DESIGN: This study was carried out in order to investigate the potential cytoprotective effects of ozonized sunflower oil (OSO) in the damage of rat gastric mucosa induced by indomethacin and also to elucidate the role of reactive oxygen species (ROS), lipid peroxidation and some constituents of antioxidant defense such as superoxide dismutase (SOD) and catalase (CAT) in these effects. MATERIAL AND METHODS: The gastric damage was induced by indomethacin (20 mg/kg) as solution in 0.5% sodium bicarbonate and given intragastrically. Three hours later OSO (4, 12 and 24 mg/kg) and cimetidine 25 mg/kg were administered also by oral route. Four hours thereafter the rats were killed and the stomachs were removed for biochemical analysis and histological study. RESULTS: The gastric ulcer index was reduced by OSO and cimetidine. OSO also reduced TBARS concentration, but it increased SOD activity in gastric mucosa homogenates. In contrast, CAT activity was not significantly modified the treatment. Histological study confirmed the cytoprotective effects of OSO in rat gastric mucosa damaged by indomethacin. CONCLUSION: It was concluded that cytoprotective effects of OSO in rat gastric mucosa are mediated at least partially by upregulation of the antioxidant system and mainly SOD.


Subject(s)
Gastric Mucosa/drug effects , Indomethacin/toxicity , Oxidative Stress , Plant Oils/pharmacology , Animals , Gastric Mucosa/metabolism , Gastric Mucosa/pathology , Lipid Peroxidation/drug effects , Male , Ozone/chemistry , Rats , Rats, Sprague-Dawley , Sunflower Oil , Superoxide Dismutase/metabolism
4.
Liver Int ; 24(1): 55-62, 2004 Feb.
Article in English | MEDLINE | ID: mdl-15102001

ABSTRACT

BACKGROUND: Many studies indicate that oxygen free-radical formation after reoxygenation of liver may initiate the cascade of hepatocellular injury. It has been demonstrated that controlled ozone administration may promote an oxidative preconditioning or adaptation to oxidative stress, preventing the damage induced by reactive oxygen species and protecting against liver ischaemia-reperfusion (I/R) injury. AIMS: In the present study, the effects of ozone oxidative preconditioning (OzoneOP) on nitric oxide (NO) generation and the cellular redox balance have been studied. METHODS: Six groups of rats were classified as follows: (1). sham-operated; (2). sham-operated+l-NAME (N(omega)-nitro-l-arginine methyl ester); (3). I/R (ischaemia 90 min-reperfusion 90 min); (4). OzoneOP+I/R; (5). OzoneOP+l-NAME+I/R; and (6). l-NAME+I/R. The following parameters were measured: plasma transaminases (aspartate aminotransferase, alanine aminotransferase) as an index of hepatocellular injury; in homogenates of hepatic tissue: nitrate/nitrite as an index of NO production; superoxide dismutase (SOD), catalase (CAT) and glutathione levels as markers of endogenous antioxidant system; and finally malondialdehyde+4-hydroxyalkenals (MDA+4-HDA) and total hydroperoxides (TH) as indicators of oxidative stress. RESULTS: A correspondence between liver damage and the increase of NO, CAT, TH, glutathione and MDA+4-HDA concentrations were observed just as a decrease of SOD activity. OzoneOP prevented and attenuated hepatic damage in I/R and OzoneOP+l-NAME+I/R, respectively, in close relation with the above-mentioned parameters. CONCLUSIONS: These results show that OzoneOP protected against liver I/R injury through mechanisms that promote a regulation of endogenous NO concentrations and maintenance of cellular redox balance. Ozone treatment may have important clinical implications, particularly in view of the increasing hepatic transplantation programs.


Subject(s)
Nitric Oxide/biosynthesis , Oxidants, Photochemical/administration & dosage , Ozone/administration & dosage , Reperfusion Injury/prevention & control , Adaptation, Physiological/drug effects , Animals , Liver/blood supply , Liver/drug effects , Male , Models, Animal , Oxidation-Reduction/drug effects , Oxidative Stress/drug effects , Rats , Rats, Wistar , Reactive Oxygen Species/metabolism , Reperfusion Injury/metabolism
5.
Mycoses ; 45(8): 329-32, 2002 Oct.
Article in English | MEDLINE | ID: mdl-12572723

ABSTRACT

Ozonized sunflower oil, Oleozon, has a remarkable gerrmicidal action. In the present study, the efficacy of Oleozon in the treatment of tinea pedis was demonstrated in a controlled randomized phase III assay, comparing topical Oleozon with ketoconazole cream 2% (Nizoral) in 200 patients (100 in each group). The treatment administered was twice per day for a period of 6 weeks. The efficacy was evaluated clinically (disappearance of all lesions, with or without negative mycological results) and mycologically (negative culture results). A complete clinical and mycological cure was obtained in 75 and 81% for Oleozon and ketoconazole, respectively, with no significant differences between both groups. No side-effects or bacterial super-infections were observed. Patients were evaluated 6 months after the end of the treatment and no recurrence was observed in the Oleozon group. Oleozon can be an effective alternative low-cost antimycotic drug.


Subject(s)
Antifungal Agents/therapeutic use , Ketoconazole/therapeutic use , Plant Oils/therapeutic use , Tinea Pedis/drug therapy , Adolescent , Adult , Candida albicans/drug effects , Epidermophyton/drug effects , Female , Humans , Ketoconazole/administration & dosage , Male , Ozone/metabolism , Plant Oils/administration & dosage , Sunflower Oil , Tinea Pedis/microbiology , Treatment Outcome , Trichophyton/drug effects
6.
Pharmacol Res ; 44(5): 391-6, 2001 Nov.
Article in English | MEDLINE | ID: mdl-11712870

ABSTRACT

Ozone has been used as a therapeutical agent and beneficial effects have been observed. However so far only a few biochemical and pharmacodynamic mechanisms have been elucidated. We demonstrate that controlled ozone administration may promote an oxidative preconditioning or adaptation to oxidative stress, preventing the damage induced by reactive oxygen species (ROS). Taking into account that diabetes is a disorder associated with oxidative stress, we postulate that ozone treatment in our experimental conditions might protect antioxidant systems and maintain, at a physiological level, other markers of endothelial cell damage associated with diabetic complications. Five groups of rats were classified as follows: (1) control group treated only with physiological saline solution; (2) positive control group using streptozotocin (STZ) as a diabetes inductor; (3) ozone group, receiving 10 treatments (1.1 mg kg(-1)), one per day after STZ-induced diabetes; (4) oxygen group (26 mg kg(-1)), one per day, as in group 3 but using oxygen only; (5) control ozone group, as group 3, but without STZ. The ozone treatment improved glycemic control and prevented oxidative stress, the increase of aldose reductase, fructolysine content and advanced oxidation protein products. Nitrite and nitrate levels were maintained without changes with regard to non-diabetic control. The results of this study show that repeated administration of ozone in non-toxic doses might play a role in the control of diabetes and its complications.


Subject(s)
Diabetes Mellitus, Experimental/metabolism , Endothelium, Vascular/metabolism , Endothelium, Vascular/pathology , Oxidants, Photochemical/pharmacology , Oxidative Stress/drug effects , Ozone/therapeutic use , Animals , Biomarkers/analysis , Body Weight/drug effects , Diabetes Mellitus, Experimental/blood , Diabetes Mellitus, Experimental/drug therapy , Diabetes Mellitus, Experimental/physiopathology , Endothelium, Vascular/drug effects , Glycosylation/drug effects , Lipid Peroxidation/drug effects , Male , Nitrates/metabolism , Nitric Oxide/biosynthesis , Nitrites/metabolism , Oxidants, Photochemical/therapeutic use , Oxidation-Reduction/drug effects , Ozone/administration & dosage , Proteins/metabolism , Rats , Rats, Sprague-Dawley
7.
J Appl Toxicol ; 21(4): 297-301, 2001.
Article in English | MEDLINE | ID: mdl-11481663

ABSTRACT

The rectal insufflation of a judicious dose of ozone, selected from that used in clinical practice, is able to promote oxidative preconditioning or oxidative stress tolerance preventing the hepatocellular damage mediated by free radicals. In order to evaluate the effects of ozone oxidative preconditioning on carbon tetrachloride-mediated hepatotoxicity, the following experimental protocol was designed: group 1 (negative control, sunflower oil i.p.); group 2 (CCl(4) in sunflower oil, 1 ml kg(-1) i.p.); group 3 (15 ozone-oxygen pretreatments at a dose of 1 mg kg(-1) via rectal insufflation + CCl(4) as in group 2); group 4 (ozone control group, 15 ozone-oxygen pretreatments + sunflower oil i.p.). Ozone pretreatment prevented glycogen depletion (as demonstrated by biochemical and histopathological findings) and avoided lactate overproduction associated with the hepatotoxic effects of CCl(4). The administration of CCl(4) increased lipid peroxidation (as measured by thiobarbituric acid-reactive substances) and uric acid levels and inhibited superoxide dismutase activity. All these deleterious effects induced by CCl(4) were prevented by ozone pretreatment. The administration of ozone without CCl(4) (ozone control group) did not produce any changes in the evaluated parameters. Our results showed that ozone treatment, in our experimental conditions, was able to prevent anaerobic glycolysis and oxidative stress induced by CCl(4).


Subject(s)
Antioxidants/pharmacology , Carbon Tetrachloride Poisoning/prevention & control , Glycogen/deficiency , Liver/drug effects , Oxidative Stress/drug effects , Ozone/pharmacology , Animals , Body Weight/drug effects , Carbon Tetrachloride Poisoning/drug therapy , Catalase/analysis , Female , Free Radical Scavengers/antagonists & inhibitors , Glycolysis/drug effects , Injections, Intraperitoneal , Insufflation , Lactic Acid/analysis , Lipid Peroxidation/drug effects , Liver/metabolism , Liver/pathology , Organ Size/drug effects , Ozone/administration & dosage , Proteins/analysis , Rats , Rats, Sprague-Dawley , Superoxide Dismutase/analysis , Thiobarbituric Acid Reactive Substances/analysis , Uric Acid/analysis
8.
Obes Surg ; 10(4): 353-60, 2000 Aug.
Article in English | MEDLINE | ID: mdl-11007629

ABSTRACT

BACKGROUND: According to physical impairments of massive obesity, cardiac, respiratory and gastrointestinal physiology must be considered as much as pharmacokinetic behavior. Anesthetic management of morbidly obese patients has to be carefully planned, in order to minimize the increased risks of aspirative pneumonitis, hemodynamic instability and delay in recovery. The ideal anesthesia should provide a smooth and quick induction, allowing rapid airway control, prominent hemodynamic stability, and rapid emergence from anesthesia. To approach these ideal conditions, a Total Intravenous Anesthesia (TIVA) with midazolam, remifentanil, propofol and cisatracurium was designed and analyzed. METHODS: 10 consenting morbidly obese patients scheduled for elective Laparoscopic Adjustable Gastric Banding participated in the study. TIVA with midazolam, remifentanil, propofol and cisatracurium was used in all cases. Time to loss of consciousness, tracheal intubation, perianesthetic physiological parameters and complications, incidence of awareness with recall, recovery times, postoperative analgesia and costs of drugs were evaluated. RESULTS: The analyzed data showed adequate time and physiological conditions for induction and tracheal intubation, stable maintenance with easy handling of deepness, low incidence of perianesthetic complications, excellent recovery performance and institutional efficiency. CONCLUSIONS: TIVA with midazolam, remifentanil, propofol and cisatracurium was found to be effective, secure, predictable and economic for the anesthetic management of morbidly obese patients.


Subject(s)
Anesthesia, Intravenous , Anesthetics, Intravenous , Gastroplasty , Adult , Anesthesia Recovery Period , Atracurium/analogs & derivatives , Female , Humans , Male , Midazolam , Middle Aged , Neuromuscular Blocking Agents , Obesity, Morbid/surgery , Piperidines , Propofol , Remifentanil , Time Factors
9.
Mediators Inflamm ; 8(1): 37-41, 1999.
Article in English | MEDLINE | ID: mdl-10704088

ABSTRACT

On the basis that ozone (O3) can upregulate cellular antioxidant enzymes, a morphological, biochemical and functional renal study was performed in rats undergoing a prolonged treatment with O3 before renal ischaemia. Rats were divided into four groups: (1) control, a medial abdominal incision was performed to expose the kidneys; (2) ischaemia, in animals undergoing a bilateral renal ischaemia (30 min), with subsequent reperfusion (3 h); (3) O3 + ischaemia, as group 2, but with previous treatment with O3 (0.5 mg/kg per day given in 2.5 ml O2) via rectal administration for 15 treatments; (4) O2 + ischaemia, as group 3, but using oxygen (O2) alone. Biochemical parameters as fructosamine level, phospholipase A, and superoxide dismutases (SOD) activities, as well as renal plasma flow (RPF) and glomerular filtration rate (GFR), were measured by means of plasma clearance of p-amino-hippurate and inulin, respectively. In comparison with groups 1 and 3, the RPF and GFR were significantly decreased in groups 2 and 4. Interestingly, renal homogenates of the latter groups yielded significantly higher values of phospholipase A activity and fructosamine level in comparison with either the control (1) and the O3 (3) treated groups. Moreover renal SOD activity showed a significant increase in group 3 without significant differences among groups 1, 2 and 4. Morphological alterations of the kidney were present in 100%, 88% and 30% of the animals in groups 2, 4 and 3, respectively. It is proposed that the O3 protective effect can be ascribed to the substantial possibility of upregulating the antioxidant defence system capable of counteracting the damaging effect of ischaemia. These findings suggest that, whenever possible, ozone preconditioning may represent a prophylactic approach for minimizing renal damage before transplantation.


Subject(s)
Ischemia , Kidney/blood supply , Ozone/therapeutic use , Reperfusion Injury/prevention & control , Animals , Drug Tolerance , Fructosamine/metabolism , Inulin/pharmacokinetics , Kidney/drug effects , Kidney/physiology , Male , Phospholipases A/metabolism , Rats , Rats, Wistar , Reperfusion , Superoxide Dismutase/metabolism , Temperature , p-Aminohippuric Acid/pharmacokinetics
10.
Mediators Inflamm ; 7(4): 289-94, 1998.
Article in English | MEDLINE | ID: mdl-9792340

ABSTRACT

There is some anecdotal evidence that oxygen-ozone therapy may be beneficial in some human diseases. However so far only a few biochemical and pharmacodynamic mechanisms have been elucidated. On the basis of preliminary data we postulated that controlled ozone administration would promote an oxidative preconditioning preventing the hepatocellular damage mediated by free radicals. Six groups of rats were classified as follows: (1) negative control, using intraperitoneal sunflower oil; (2) positive control using carbon tetrachloride (CCl4) as an oxidative challenge; (3) oxygen-ozone, pretreatment via rectal insufflation (15 sessions) and after it, CCl4; (4) oxygen, as group 3 but using oxygen only; (5) control oxygen-ozone, as group 3, but without CCl4; group (6) control oxygen, as group 5, but using oxygen only. We have evaluated critical biochemical parameters such as levels of transaminase, cholinesterase, superoxide dismutase, catalase, phospholipase A, calcium dependent ATPase, reduced glutathione, glucose 6 phosphate dehydrogenase and lipid peroxidation. Interestingly, in spite of CCl4 administration, group 3 did not differ from group 1, while groups 2 and 4 showed significant differences from groups 1 and 3 and displayed hepatic damage. To our knowledge these are the first experimental results showing that repeated administration of ozone in atoxic doses is able to induce an adaptation to oxidative stress thus enabling the animals to maintain hepatocellular integrity after CCl4 poisoning.


Subject(s)
Ozone/pharmacology , Animals , Calcium/metabolism , Carbon Tetrachloride/toxicity , Female , Free Radicals , Liver/drug effects , Liver/pathology , Oxidative Stress , Ozone/therapeutic use , Rats , Rats, Sprague-Dawley
11.
Free Radic Biol Med ; 19(1): 115-9, 1995 Jul.
Article in English | MEDLINE | ID: mdl-7635353

ABSTRACT

Patients with cardiac infarction show a decrease in glutathione peroxidase and superoxide dismutase activities, which are beginners in the scavenger processes of lipid peroxide and superoxide radicals, respectively. In this study, we investigate the effects of endovenous ozone therapy on serum lipid pattern and on antioxidant defense system, such as te glutathione redox one, in the blood of patients with myocardial infarct. Twenty-two patients who had an infarction, between 3 months and 1 year before the study, were treated with ozone by autohemotherapy during 15 sessions. A statistically significant decrease in plasma total cholesterol and low density lipoprotein was observed. High biologically significant increases on erythrocyte glutathione peroxidase and glucose 6-phosphate dehydrogenase activities were found. There was no change in plasma lipid peroxidation level. It was concluded that endovenous ozone therapy in patients with myocardial infarction has a beneficial effect on blood lipid metabolism, provoking the activation of antioxidant protection system.


Subject(s)
Antioxidants/metabolism , Cholesterol/blood , Myocardial Infarction/drug therapy , Ozone/therapeutic use , Aged , Erythrocytes/enzymology , Glucosephosphate Dehydrogenase/blood , Glutathione Peroxidase/blood , Humans , Lipoproteins, HDL/blood , Lipoproteins, LDL/blood , Male , Middle Aged , Myocardial Infarction/blood , Ozone/administration & dosage , Triglycerides/blood
12.
In. Asociación de Facultades Ecuatorianas de Ciencias Médicas. Seminario nacional evaluación ciclo materno infantil del internado rotativo. Manta, AFEME, 1994. p.87-91.
Monography in Spanish | LILACS | ID: lil-330302
14.
Obstet. ginecol. latinoam ; 44(1/2): 2-13, 1986. ilus, tab
Article in Spanish | LILACS | ID: lil-46039

ABSTRACT

Los autores describen detalladamente la técnica utilizada y los resultados logrados en 142 ciclos monitorizados, desde enero de 1983 hasta mayo de 1985. Se destaca la minuciosidad con que explican las maniobras que realizan para jerarquizar a la laparoscopía como técnica de "recuperación ovocitaria" en un programa de fertilización in vitro, tema sobre el cual concentran su atención


Subject(s)
Humans , Female , In Vitro Techniques , Infertility, Female/therapy , Laparoscopy , Fertilization in Vitro/methods , Oocytes , Punctures
15.
Obstet. ginecol. latinoam ; 44(1/2): 2-13, 1986. ilus, Tab
Article in Spanish | BINACIS | ID: bin-31239

ABSTRACT

Los autores describen detalladamente la técnica utilizada y los resultados logrados en 142 ciclos monitorizados, desde enero de 1983 hasta mayo de 1985. Se destaca la minuciosidad con que explican las maniobras que realizan para jerarquizar a la laparoscopía como técnica de "recuperación ovocitaria" en un programa de fertilización in vitro, tema sobre el cual concentran su atención (AU)


Subject(s)
Humans , Female , In Vitro Techniques , Laparoscopy , Infertility, Female/therapy , Fertilization in Vitro/methods , Punctures , Oocytes
SELECTION OF CITATIONS
SEARCH DETAIL