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1.
Hum Exp Toxicol ; 34(7): 780-3, 2015 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-25352650

RESUMO

This study evaluated the protective potential of curcumin on the possible side effects of bortezomib (Bt) therapy on normal cells in mice. The mice were segregated into three groups (n = 10) that included normal control, Bt-treated, and Bt + curcumin-treated groups. The Bt treatment resulted in significant decrease in the enzyme activity of erythrocyte δ-aminolevulinic acid dehydratase (ALAD). Also a significant decrease in the hemoglobin (Hb) was also noticed. On the other hand, curcumin co-treatment improvised enzyme activity of erythrocyte ALAD as well as Hb values. The study, therefore, concludes that curcumin co-treatment with Bt has a potential to take care of possible side effects of Bt therapy on normal cells.


Assuntos
Antineoplásicos/efeitos adversos , Bortezomib/efeitos adversos , Curcumina/farmacologia , Substâncias Protetoras/farmacologia , Animais , Antineoplásicos/uso terapêutico , Bortezomib/uso terapêutico , Eritrócitos/efeitos dos fármacos , Eritrócitos/metabolismo , Hemoglobinas/análise , Masculino , Camundongos , Sintase do Porfobilinogênio/sangue
2.
Pain Med ; 16(6): 1073-6, 2015 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-24138673

RESUMO

BACKGROUND: The urine of a patient admitted for chest and epigastric pain tested positive for cocaine using an immunoassay-based drug screening method (positive/negative cutoff concentration 150 ng/mL). Despite the patient's denial of recent cocaine use, this positive cocaine screening result in conjunction with a remote history of drug misuse impacted the patient's recommended pain therapy. Specifically, these factors prompted the clinical team to question the appropriateness of opioids and other potentially addictive therapeutics during the treatment of cancer pain from previously undetected advanced pancreatic carcinoma. OBJECTIVE: After pain management and clinical pathology consultation, it was decided that the positive cocaine screening result should be confirmed by gas chromatography-mass spectrometry (GC-MS) testing. RESULTS: This more sensitive and specific analytical technique revealed that both cocaine and its primary metabolite benzoylecgonine were undetectable (i.e., less than the assay detection limit of 50 ng/mL), thus indicating that the positive urine screening result was falsely positive. With this confirmation, the pain management service team was reassured in offering intrathecal pump (ITP) therapy for pain control. ITP implantation was well tolerated, and the patient eventually achieved excellent pain relief. However, ITP therapy most likely would not have been utilized without the GC-MS confirmation testing unless alternative options failed and extensive vigilant monitoring was initiated. CONCLUSION: As exemplified in this case, confirmatory drug testing should be performed on specimens with unexpected immunoassay-based drug screening results. To our knowledge, this is the first report of a false-positive urine cocaine screening result and its impact on patient management.


Assuntos
Transtornos Relacionados ao Uso de Cocaína/urina , Cocaína/urina , Manejo da Dor/métodos , Dor/tratamento farmacológico , Dor/urina , Detecção do Abuso de Substâncias/normas , Analgésicos Opioides/administração & dosagem , Transtornos Relacionados ao Uso de Cocaína/diagnóstico , Reações Falso-Positivas , Humanos , Injeções Espinhais , Masculino , Pessoa de Meia-Idade , Dor/diagnóstico , Urinálise/normas
3.
Hum Exp Toxicol ; 33(6): 629-37, 2014 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-24064908

RESUMO

Photodynamic therapy (PDT) is a novel cancer treatment based on the tumor-specific accumulation of a photosensitizer followed by irradiation with visible light, which induces selective tumor cell death via production of reactive oxygen species. To elucidate the underlying mechanisms, microarray analysis was used to analyze the changes in gene expression patterns during PDT induced by various photosensitizers. Cancer cells were subjected to four different photosensitizer-mediated PDT and the resulting gene expression profiles were compared. We identified many differentially expressed genes reported previously as well as new genes for which the functionfunctions in PDT are still unclear. Our current results not only advance the general understanding of PDT but also suggest that distinct molecular mechanisms are involved in different photosensitizer-mediated PDT. Elucidating the signaling mechanisms in PDT will provide information to modulate the antitumor effectiveness of PDT using various photosensitizers.


Assuntos
Carcinoma de Células Escamosas/genética , Perfilação da Expressão Gênica/métodos , Regulação Neoplásica da Expressão Gênica/efeitos dos fármacos , Neoplasias de Cabeça e Pescoço/genética , Neoplasias Bucais/genética , Análise de Sequência com Séries de Oligonucleotídeos , Fotoquimioterapia , Fármacos Fotossensibilizantes/farmacologia , Carcinoma de Células Escamosas/patologia , Linhagem Celular Tumoral , Sobrevivência Celular/efeitos dos fármacos , Neoplasias de Cabeça e Pescoço/patologia , Humanos , Neoplasias Bucais/patologia , Reação em Cadeia da Polimerase em Tempo Real , Reprodutibilidade dos Testes , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Carcinoma de Células Escamosas de Cabeça e Pescoço , Fatores de Tempo
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