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Int J Radiat Oncol Biol Phys ; 82(5): e701-7, 2012 Apr 01.
Artigo em Inglês | MEDLINE | ID: mdl-22330992

RESUMO

PURPOSE: A new aminothiol, PrC-210, was tested for orally conferred radioprotection (rats, mice; 9.0 Gy whole-body, which was otherwise lethal to 100% of the animals) and presence of the debilitating side effects (nausea/vomiting, hypotension/fainting) that restrict use of the current aminothiol, amifostine (Ethyol, WR-2721). METHODS AND MATERIALS: PrC-210 in water was administered to rats and mice at times before irradiation, and percent-survival was recorded for 60 days. Subcutaneous (SC) amifostine (positive control) or SC PrC-210 was administered to ferrets (Mustela putorius furo) and retching/emesis responses were recorded. Intraperitoneal amifostine (positive control) or PrC-210 was administered to arterial cannulated rats to score drug-induced hypotension. RESULTS: Oral PrC-210 conferred 100% survival in rat and mouse models against an otherwise 100% lethal whole-body radiation dose (9.0 Gy). Oral PrC-210, administered by gavage 30-90 min before irradiation, conferred a broad window of radioprotection. The comparison of PrC-210 and amifostine side effects was striking because there was no retching or emesis in 10 ferrets treated with PrC-210 and no induced hypotension in arterial cannulated rats treated with PrC-210. The tested PrC-210 doses were the ferret and rat equivalent doses of the 0.5 maximum tolerated dose (MTD) PrC-210 dose in mice. The human equivalent of this mouse 0.5 MTD PrC-210 dose would likely be the highest PrC-210 dose used in humans. By comparison, the mouse 0.5 MTD amifostine dose, 400 µg/g body weight (equivalent to the human amifostine dose of 910 mg/m(2)), when tested at equivalent ferret and rat doses in the above models produced 100% retching/vomiting in ferrets and 100% incidence of significant, progressive hypotension in rats. CONCLUSIONS: The PrC-210 aminothiol, with no detectable nausea/vomiting or hypotension side effects in these preclinical models, is a logical candidate for human drug development to use in healthy humans in a wide variety of radioprotection settings, including medical radiation, space travel, and nuclear accidents.


Assuntos
Diaminas/administração & dosagem , Hipotensão/induzido quimicamente , Náusea/induzido quimicamente , Lesões Experimentais por Radiação/prevenção & controle , Protetores contra Radiação/administração & dosagem , Compostos de Sulfidrila/administração & dosagem , Vômito/induzido quimicamente , Administração Oral , Amifostina/administração & dosagem , Animais , Diaminas/efeitos adversos , Diaminas/química , Diaminas/farmacocinética , Avaliação Pré-Clínica de Medicamentos , Feminino , Furões , Infusões Intra-Arteriais , Infusões Parenterais , Injeções Subcutâneas , Masculino , Dose Máxima Tolerável , Camundongos , Camundongos Endogâmicos ICR , Protetores contra Radiação/efeitos adversos , Protetores contra Radiação/química , Protetores contra Radiação/farmacocinética , Ratos , Ratos Sprague-Dawley , Compostos de Sulfidrila/efeitos adversos , Compostos de Sulfidrila/química , Compostos de Sulfidrila/farmacocinética
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