Evidence map›Paper›PMID 40181145›Full record

ArticlePediatric research2025

Dose-related systemic and cerebral hemodynamic effects of norepinephrine in newborn piglets with hypoxia-reoxygenation.

Po-Yin Cheung, Marwa Ramsie, Tze-Fun Lee, Megan O'Reilly, Georg M Schmölzer

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Article in Pediatric research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1 citing paper in PubMed.

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5 · Who and what money

Authors and funding

5 authors.

Po-Yin CheungCentre for the Studies of Asphyxia and Resuscitation, Neonatal Research Unit, Royal Alexandra Hospital, Edmonton, AB, Canada. poyin@ualberta.ca.
Marwa RamsieCentre for the Studies of Asphyxia and Resuscitation, Neonatal Research Unit, Royal Alexandra Hospital, Edmonton, AB, Canada.
Tze-Fun LeeCentre for the Studies of Asphyxia and Resuscitation, Neonatal Research Unit, Royal Alexandra Hospital, Edmonton, AB, Canada.
Megan O'ReillyCentre for the Studies of Asphyxia and Resuscitation, Neonatal Research Unit, Royal Alexandra Hospital, Edmonton, AB, Canada.
Georg M SchmölzerCentre for the Studies of Asphyxia and Resuscitation, Neonatal Research Unit, Royal Alexandra Hospital, Edmonton, AB, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLittle is known regarding systemic and regional hemodynamic effects of norepinephrine (NE) in hypotensive neonates after hypoxia-reoxygenation (H-R). We hypothesized that NE would improve cardiac function, systemic and cerebral hemodynamics without aggravating hyperlactatemia during H-R, compared with epinephrine (EPI).

methodsIn an established model of neonatal H-R, piglets were treated with either NE (0.05, 0.1 and 0.2 µg/kg/min), EPI (0.1 µg/kg/min) or saline for 2 h during reoxygenation in a blinded, randomized fashion (n = 8/group). Systemic hemodynamics, carotid blood flow, cerebral oxygenation, and cardiac contractile function were continuously measured. Myocardial, cerebral, renal and intestinal tissues were analyzed for lactate and oxidative stress levels.

resultsNorepinephrine (0.1 and 0.2 µg/kg/min) and EPI increased mean arterial pressure and cardiac output with corresponding changes in left ventricular systolic, but not diastolic, function. Norepinephrine at 0.1 µg/kg/min had the optimal systemic hemodynamic effects and cerebral perfusion with lower plasma lactate. Tissue lactate and oxidative stress levels were not different.

conclusionsIn newborn piglets with H-R, NE improved cardiac contractile function, cardiac output, blood pressure, and cerebral perfusion in a dose-related manner. Clinical studies of NE on systemic and regional hemodynamic effects in asphyxiated neonates are required to confirm the findings in this pre-clinical study. IMPACT: In an established model of neonatal hypoxia-reoxygenation, 2-h infusion of norepinephrine at 0.05-0.2 µg/kg/min has dose-related increases in cardiac systolic contractile function and systemic blood pressure with corresponding improvements in cerebral perfusion in newborn piglets, without significant changes in ischemic and oxidative stress markers in tissues. The hemodynamic effects of norepinephrine are comparable to those of epinephrine which causes increased plasma lactate. While norepinephrine is an effective inotropic vasopressor in the treatment of hypotensive shock in neonates with hypoxia-reoxygenation, studies are required to confirm its effects and safety in prolonged administration in clinical trials.

Indexed as

BrainCerebrovascular CirculationHemodynamicsHypoxiaNorepinephrineOxygenAnimalsAnimals, NewbornDisease Models, AnimalDose-Response Relationship, DrugEpinephrineHypotensionLactic AcidOxidative StressSwineEpinephrineLactic AcidNorepinephrineOxygen

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.