Development of lisinopril for post-exposure mitigation of late effects from a rad

开发赖诺普利以减轻辐射后的迟发效应

• 批准号: 9066475
• 负责人: MEETHA M MEDHORA
• 金额: $ 64.13万
• 依托单位: MEDICAL COLLEGE OF WISCONSIN
• 依托单位国家: 美国
• 财政年份: 2013
• 资助国家: 美国
• 起止时间: 2013-06-01 至 2018-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9066475
• 关键词: Acute; Address; Adolescent; Angiotensin Receptor; Angiotensin-Converting Enzyme Inhibitors; Animal Model; Animals; Antibiotics; Attenuated; Award; Bone Marrow; Bone Marrow Cells; Bone Marrow Transplantation; CSF3 gene; Cancer Patient; Canis familiaris; Captopril; Cells; Childhood; Chronic; Clinic; Clinical Research; Clinical Trials; Development; Devices; Dose; Drug usage; Elderly; Enalapril; Energy Transfer; Event; Exposure to; Functional disorder; Gamma Rays; Goals; Granulocyte Colony-Stimulating Factor; Health; Hematopoietic; Hematopoietic Stem Cell Transplantation; Hour; Human; Human Resources; IACUC; Immune; Injury; Ionizing radiation; Kidney; Kidney Diseases; Knock-out; Late Effects; Lead; Licensure; Linear Energy Transfer; Lisinopril; Lung; Measures; Mediating; Modeling; Molecular; Morbidity - disease rate; Multiple Organ Failure; Mutate; Neutrons; Nuclear; Organ; Organ failure; Outcome; Patients; Peptidyl-Dipeptidase A; Pharmaceutical Preparations; Physiological; Plasma; Pulmonary Fibrosis; RNA; Radiation; Radiation Injuries; Radiation Pneumonitis; Radiation Toxicity; Rattus; Renin; Renin-Angiotensin System; Research; Retrospective Studies; Rodent Model; Roentgen Rays; Role; Skin; Supportive care; Survivors; Symptoms; Syndrome; Techniques; Terrorism; Testing; Therapeutic Agents; Thick; Training; Transplantation; Trauma; Whole-Body Irradiation; Work; Zinc Fingers; animal rule; base; improved; injured; irradiation; meetings; named group; next generation; novel; pre-clinical; prospective; radiation effect; radiation-induced injury; radiosensitive; transcriptome sequencing

DESCRIPTION (provided by applicant): Our research goal has been to mitigate radiation injuries to the lungs and kidneys. Mitigation is the use of a countermeasure after exposure to ionizing radiation but before symptoms develop. We have focused on a class of drugs, angiotensin converting enzyme (ACE) inhibitors, which have been used in the clinic for many indications. They have shown efficacy for mitigation of lethal radiation injuries to multiple organ in rats. We are now aiming to repurpose these drugs as mitigators for radiation-induced multiple organ failure, in survivors of acute hematological syndromes. Incidental use of these drugs by irradiated cancer patients decreased lung and kidney injuries. Since the ACE inhibitor lisinopril mitigates morbidity in rats when given 7 days after radiation, it fits the requirement of this U01 o be developed for post-exposure mitigation of injuries from a radiation or nuclear incident. We will address both purposes of this RFA. The first will be to further develop lisinopril by assessin efficacy post exposure in rats given total body irradiation. We will test lisinopril in combination with countermeasures proposed for the Strategic National Stockpile for use against acute radiation syndromes. We will also test lisinopril for mitigation after exposure to single low- and high-linear energy transfer irradiation (X-rays, neutron-gamma rays), and to radiation in combination with full thickness skin wounds that will occur from detonation of an improvised nuclear device. In addition we will evaluate efficacy in special populations (juvenile and geriatri rat models). For the second purpose of the U01, to elucidate the mechanism of action, we will use cutting-edge techniques to test a novel hypothesis to determine the molecular, cellular and physiological mechanism(s) of mitigation by lisinopril. These studies include next generation micro-ribonucleic acid sequencing (miRNA-Seq) and genetically altered (knock out) donor bone marrow transplantation in rats. Our results directly address the purposes of this RFA to advance lisinopril for licensure against radiation-induced multi-organ dysfunctions. We have organized an efficient as well as responsive research plan, team of experts and well trained personnel to meet our goals.

描述（由申请人提供）：我们的研究目标是减轻辐射对肺和肾脏的伤害。缓解是指在暴露于电离辐射之后，但在症状出现之前使用对抗措施。我们专注于一类药物，血管紧张素转换酶（ACE）抑制剂，它已在临床上用于许多适应症。它们已显示出减轻大鼠多器官致命辐射损伤的功效。我们现在的目标是将这些药物重新用作缓解急性血液学综合征幸存者中辐射诱导的多器官衰竭的药物。放疗癌症患者偶然使用这些药物可减少肺和肾损伤。由于ACE抑制剂赖诺普利在辐射后7天内可减轻大鼠的发病率，因此它符合本U01的要求，用于减轻辐射或核事件造成的暴露后损伤。我们将讨论RFA的两个目的。首先是通过评估全身照射大鼠暴露后的疗效来进一步开发赖诺普利。我们将测试赖诺普利联合用药