Restoring The Mechanical Properties of the Respiratory System as a Treatment of Fentanyl Overdose-Induced Hypoventilation using Kappa Agonists
使用 Kappa 激动剂恢复呼吸系统的机械特性来治疗芬太尼过量引起的通气不足
基本信息
- 批准号:10766378
- 负责人:
- 金额:$ 24.15万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2022
- 资助国家:美国
- 起止时间:2022-04-01 至 2025-03-31
- 项目状态:未结题
- 来源:
- 关键词:AbdomenAcuteAcute respiratory failureAgonistAirway ResistanceAlveolarAnimalsBolus InfusionBreathingCardiopulmonary ResuscitationCentral Sleep ApneaCessation of lifeChest wall structureChronicChronic Kidney FailureComplexDepressed moodDevelopment PlansDoseExposure toFatal OutcomeFentanylFormulationFrequenciesGoalsHourHumanHyperactive behaviorHypoventilationHypoxemiaHypoxiaIndividualInjectionsIntoxicationIntravenousJapanLifeLiteratureMammalsMechanical ventilationMetabolismModelingMorphineMovementMusMuscleMuscle ContractionMuscle RigidityNaloxoneNeuronsOpioidOpioid AntagonistOpioid agonistOverdoseOxygen ConsumptionPainPatientsPeriodicityPickwickian SyndromePontine structurePruritusPublishingPulmonary Gas ExchangeRattusRecoveryRespiratory FailureRespiratory MechanicsRespiratory SystemRiskRisk FactorsRodentRodent ModelRouteSecondary toSkeletal MuscleSpeedStimulantSurvival RateTestingTidal VolumeVentilatory DepressionWithdrawaladdictionchronic respiratory diseasedosageefficacy studyfentanyl overdoseimprovedkappa opioid receptorslocus ceruleus structuremass casualtymechanical propertiesmu opioid receptorsopioid overdosepreventrespiratoryrespiratory oxygenventilation
项目摘要
ABSTRACT
Mu-opioid agonist overdose is associated with immediate and prolonged tetanic and rhythmic contractions of the
inspiratory and expiratory muscles that impede respiratory movements for hours. This effect, referred to as opioid
induced chest wall rigidity, is a critical mechanism contributing to the lethality of opioid-induced hypoventilation.
Mu-opioid-induced muscle “rigidity” is produced by neurons in the locus coeruleus and can be suppressed by
kappa-opioid receptor agonists, but not by current ventilatory stimulants. The objective of our proposal is to
demonstrate, following an overdose by the mu-opioid receptor agonist fentanyl, that kappa-opioid receptor
agonists 1- restore the alteration of passive respiratory mechanics and suppress the hypermetabolism produced
by fentanyl induced muscle rigidity, 2- prevent a fatal outcome in unsedated rats. We will test nalfurafine, the
only commercially available kappa agonist, and show that it counteracts the ventilatory effects of a fentanyl
overdose. If efficacy is demonstrated in rodents, we will pursue these efficacy studies in non-anesthetized large
mammal models and will test intravenous as well as intranasal route. Our ultimate goal is to obtain FDA approval
for nalfurafine as a treatment of mu-opioid receptor agonist-induced hypoventilation, treatment that could be
used in indications ranging from mass casualty to individual victims of opioid intoxication.
抽象的
Mu-阿片受体激动剂过量与立即和长期的强直性和节律性收缩有关。
吸气和呼气肌肉会阻碍呼吸运动数小时,这种效应称为阿片类药物。
引起的胸壁僵硬是导致阿片类药物引起的通气不足致死的关键机制。
Mu-阿片类药物引起的肌肉“僵硬”是由蓝斑神经元产生的,可以通过以下方法抑制:
kappa-阿片受体激动剂,但不是目前的通气兴奋剂 我们建议的目标是
证明,在过量服用 mu-阿片受体激动剂芬太尼后,κ-阿片受体
激动剂 1- 恢复被动呼吸力学的改变并抑制产生的代谢亢进
通过芬太尼引起的肌肉僵硬,2-防止未镇静的大鼠出现致命结果。
唯一市售的 kappa 激动剂,并表明它可以抵消芬太尼的通气作用
如果在啮齿类动物中证实疗效,我们将在非麻醉大型动物中进行这些疗效研究。
我们的最终目标是获得 FDA 的批准。
对于纳芙拉芬作为 mu-阿片受体激动剂引起的通气不足的治疗,治疗可能是
用于从大规模伤亡到阿片类药物中毒个体受害者的适应症。
项目成果
期刊论文数量(1)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Revisiting the effects of the reciprocal function between alveolar ventilation and CO2 partial pressure (PACO2) on PACO2 homeostasis at rest and in exercise.
重新审视肺泡通气量和二氧化碳分压 (PACO2) 之间的倒数函数对静息和运动时 PACO2 稳态的影响。
- DOI:
- 发表时间:2022-10-01
- 期刊:
- 影响因子:0
- 作者:Haouzi; Philippe
- 通讯作者:Philippe
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Philippe A Haouzi其他文献
Philippe A Haouzi的其他文献
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{{ truncateString('Philippe A Haouzi', 18)}}的其他基金
Restoring The Mechanical Properties of the Respiratory System as a Treatment of Fentanyl Overdose-Induced Hypoventilation using Kappa Agonists
使用 Kappa 激动剂恢复呼吸系统的机械特性来治疗芬太尼过量引起的通气不足
- 批准号:
10410611 - 财政年份:2022
- 资助金额:
$ 24.15万 - 项目类别:
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10701905 - 财政年份:2020
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$ 24.15万 - 项目类别:
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小剂量右美托咪定治疗芬太尼过量所致呼吸衰竭
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10828679 - 财政年份:2020
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10223544 - 财政年份:2019
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