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1.
Microb Drug Resist ; 27(3): 433-440, 2021 Mar.
Article in English | MEDLINE | ID: mdl-32706621

ABSTRACT

Increase in antimicrobial resistance to antibiotics is the product of the evolution and natural adaptation of microorganisms through mutations and genetic recombination caused by the indiscriminate use of antibiotics and the ineffective control and prevention of infection. The current study analyzes the profile of multiresistant hospital bacteria in two hospitals in Pelotas, state of Rio Grande do Sul, Brazil. Over the course of 4 months, patient's gender and age, hospital accommodation type, and sample site were evaluated. Two hundred and eighty-six microbiological culture antibiogram reports of hospitalized patients and outpatients of both sexes, between zero and 96 years of age, were analyzed. Bacterium Klebsiella pneumoniae was the most prevalent. The most resistant Gram-negative bacilli (GNB) were K. pneumoniae (27.5%); Acinetobacter baumannii (24.1%); Escherichia coli (14.7%); and Pseudomonas aeruginosa (14.5%). The most resistant Gram-positive cocci (GPC) were Enterococcus faecium (27.5%) and Staphylococcus aureus (25.5%). The classes of antibiotics with the greatest number of resistant GNB included penicillins (84.8%), quinolones (77.5%), and cephalosporins (75.7%). In the case of GPC, the most resistant were macrolides (95.4%); lincosamides (90.3%), and penicillins (77%). Among GNBs, polypeptides had the highest sensitivity rate (81.3%), whereas, among GPC, fusidanes, glycylcyclines, and lipopeptides had 100% sensitivity.


Subject(s)
Anti-Bacterial Agents/pharmacology , Bacteria/drug effects , Cross Infection/microbiology , Drug Resistance, Multiple, Bacterial/drug effects , Adolescent , Adult , Aged , Aged, 80 and over , Brazil/epidemiology , Child , Child, Preschool , Female , Hospitals , Humans , Infant , Infant, Newborn , Male , Microbial Sensitivity Tests , Middle Aged , Young Adult
2.
Arch Toxicol ; 85(1): 43-9, 2011 Jan.
Article in English | MEDLINE | ID: mdl-20490464

ABSTRACT

(S)-dimethyl 2-(3-(phenyltellanyl) propanamido) succinate, a new telluroamino acid derivative, showed remarkable glutathione peroxidase (GPx)-like activity, attesting to its antioxidant potential. However, the stability and toxicity of this compound has not yet been investigated. The present study was designed to investigate the pharmacological/toxicological properties of this compound in vitro and in vivo. In vitro, this telluroamino acid derivative significantly blocked spontaneous and Fe(II)-induced TBARS formation in rat brain homogenates, demonstrating high antioxidant activity. In addition, it exhibited GPx-like and thiol oxidase activities. However, when subcutaneously administered to mice, (S)-dimethyl 2-(3-(phenyltellanyl) propanamido) succinate indicated genotoxic and mutagenic effect in adult male mice. Considering the differential effects of (S)-dimethyl 2-(3-(phenyltellanyl) propanamido) succinate in vitro and in vivo, additional experiments are needed to elucidate the mechanism(s) by which this compound displays its antioxidant/toxicological effects.


Subject(s)
Antioxidants/pharmacology , Aspartic Acid/analogs & derivatives , Succinates/pharmacology , Administration, Oral , Analysis of Variance , Animals , Aspartic Acid/toxicity , Comet Assay , DNA Damage , Ferrous Compounds/metabolism , Glutathione Peroxidase/metabolism , Lethal Dose 50 , Male , Mice , Organometallic Compounds/metabolism , Organometallic Compounds/pharmacology , Organometallic Compounds/toxicity , Rats , Rats, Wistar , Succinates/toxicity , Tellurium/metabolism , Thiobarbituric Acid Reactive Substances/metabolism
3.
BMC Cancer ; 9: 138, 2009 May 08.
Article in English | MEDLINE | ID: mdl-19426494

ABSTRACT

BACKGROUND: Bone marrow transplantation (BMT) is often used in the treatment of various diseases. Before BMT, patients are submitted to a conditioning regimen (CR), which consists of the administration of high doses of chemotherapy. The action of many cytostatic drugs involves the overproduction of reactive oxygen species, which together with inadequate antioxidant protection can lead to oxidative stress and this has been implicated in the etiology of various diseases. The objectives of this study were to look for evidence of oxidative stress and also to analyze delta-Aminolevulinato dehydratase (delta-ALA-D) activity as a possible marker of oxidative stress in autologous and allogeneic BMT patients. METHODS: Lipid peroxidation, vitamin C and thiol group levels as well as catalase, superoxide dismutase and delta-ALA-D activity were determined in 37 healthy controls, 13 patients undergoing autologous peripheral blood stem cell transplantation and 24 patients undergoing allogeneic BMT. RESULTS: We found that patients presented signs of oxidative stress before they were submitted to BMT, during CR and up to 20 days after BMT. There was a decrease in enzymatic and non enzymatic antioxidant defenses, in delta-ALA-D activity, and an increase in lipoperoxidation in the blood of both patient groups. CONCLUSION: This study has indicated that autologous and allogeneic BMT are associated with oxidative stress. Moreover, blood delta-ALA-D activity seems to be an additional biomarker of oxidative stress in BMT patients.


Subject(s)
Bone Marrow Transplantation , Oxidative Stress , Porphobilinogen Synthase/blood , Adult , Ascorbic Acid/blood , Biomarkers/metabolism , Catalase/blood , Female , Hematopoietic Stem Cell Transplantation , Humans , Lipid Peroxidation , Male , Middle Aged , Superoxide Dismutase/blood , Transplantation Conditioning , Transplantation, Autologous , Transplantation, Homologous
4.
Pharmacol Res ; 59(4): 279-84, 2009 Apr.
Article in English | MEDLINE | ID: mdl-19162187

ABSTRACT

Severe toxicity is associated with cytotoxic drugs used during the conditioning regimen (CR) preceding bone marrow transplantation (BMT). The aim of this study was to evaluate the involvement of oxidative stress and possible use of delta-aminolevulinate dehydratase (delta-ALA-D) activity as a marker of oxidative stress in autologous BMT patients. We have also compared common drugs that are used during CR, namely, melphalan (M-200) and cyclophosphamide-BCNU-etoposide (CBV), in order to determine whether either of them could be less toxic to patients in terms of oxidative stress. The sample consisted of 10 patients admitted for autologous BMT, 5 with M-200 CR and 5 with CBV CR and 10 healthy controls. Lipid peroxidation (estimated as thiobarbituric acid-reactive substances, TBARS), vitamin C, thiol levels, catalase, superoxide dismutase and delta-ALA-D activity were determined before CR, during CR and on days 10 and 20 after BMT. Signs of exacerbated oxidative stress were minimal before CR, except for the CVB group (patients with lymphoma) where an increase in TBARS and a decrease in P-SH were detected. Indices of oxidative stress changed in both groups (CBV and M-200) during CR and up to 20 days after BMT. There was a decrease in enzymatic and non-enzymatic antioxidant defenses and in delta-ALA-D activity and an increase in lipoperoxidation in the blood of both patient groups. In conclusion, CBV and, principally, M-200 caused oxidative stress in patients undergoing autologous BMT and blood delta-ALA-D activity seems to be an additional biomarker of oxidative stress in BMT patients.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/adverse effects , Bone Marrow Transplantation/adverse effects , Melphalan/adverse effects , Oxidative Stress/drug effects , Porphobilinogen Synthase/blood , Transplantation Conditioning/adverse effects , Ascorbic Acid/blood , Biomarkers/analysis , Carmustine/adverse effects , Case-Control Studies , Cyclophosphamide/adverse effects , Etoposide/adverse effects , Humans , Lipid Peroxidation/drug effects , Male , Middle Aged , Reactive Oxygen Species/blood , Sulfhydryl Compounds/blood , Transplantation, Autologous
5.
Clin Biochem ; 42(7-8): 602-10, 2009 May.
Article in English | MEDLINE | ID: mdl-19109938

ABSTRACT

OBJECTIVES: To compare different conditioning regimens (CR), in order to determine whether either of them could be less toxic to allogeneic bone marrow transplantation (BMT) patients in terms of oxidative stress and also analyze delta-ALA-D activity as a possible marker of oxidative stress. DESIGN AND METHODS: Lipid peroxidation, vitamin C, thiol groups levels and catalase, superoxide dismutase and delta-ALA-D activity were determined in 21 healthy controls, 5 patients with fludarabine+cyclophosphamide (FluCy) CR, 12 with busulfan+cyclophosphamide (BuCy) and 4 with cyclophosphamide+total body irradiation (CyTBI). RESULTS: There were a decrease in enzymatic and non enzymatic antioxidants, in delta-ALA-D activity, and in all CRs and an increase in lipid peroxidation more pronounced in CyTBI CR. CONCLUSIONS: All CRs promoted oxidative stress in allogeneic BMT patients, but this was more pronounced with CyTBI and delta-ALA-D activity seemed to be an additional biomarker of oxidative stress in these patients.


Subject(s)
Bone Marrow Transplantation , Oxidative Stress/drug effects , Porphobilinogen Synthase/metabolism , Adult , Antioxidants/metabolism , Ascorbic Acid/metabolism , Catalase/metabolism , Cyclophosphamide/administration & dosage , Cyclophosphamide/pharmacology , Enzyme Activation/drug effects , Female , Humans , Lipid Peroxidation/drug effects , Male , Middle Aged , Superoxide Dismutase/metabolism , Vidarabine/administration & dosage , Vidarabine/analogs & derivatives , Vidarabine/pharmacology
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