Development of a primate model to evaluate the effects of ketamine and surgical stress on the neonatal brain

dc.contributor.authorWang, Cheng
dc.contributor.authorBhutta, Adnan
dc.contributor.authorZhang, Xuan
dc.contributor.authorLiu, Fang
dc.contributor.authorLiu, Shuliang
dc.contributor.authorLatham, Leah E.
dc.contributor.authorTalpos, John C.
dc.contributor.authorPatterson, Tucker A.
dc.contributor.authorSlikker, William, Jr.
dc.contributor.departmentPediatrics, School of Medicine
dc.date.accessioned2024-04-11T12:25:45Z
dc.date.available2024-04-11T12:25:45Z
dc.date.issued2023
dc.description.abstractWith advances in pediatric and obstetric surgery, pediatric patients are subject to complex procedures under general anesthesia. The effects of anesthetic exposure on the developing brain may be confounded by several factors including pre-existing disorders and surgery-induced stress. Ketamine, a noncompetitive N-methyl-d-aspartate (NMDA) receptor antagonist, is routinely used as a pediatric general anesthetic. However, controversy remains about whether ketamine exposure may be neuroprotective or induce neuronal degeneration in the developing brain. Here, we report the effects of ketamine exposure on the neonatal nonhuman primate brain under surgical stress. Eight neonatal rhesus monkeys (postnatal days 5-7) were randomly assigned to each of two groups: Group A (n = 4) received 2 mg/kg ketamine via intravenous bolus prior to surgery and a 0.5 mg/kg/h ketamine infusion during surgery in the presence of a standardized pediatric anesthetic regimen; Group B (n = 4) received volumes of normal saline equivalent to those of ketamine given to Group A animals prior to and during surgery, also in the presence of a standardized pediatric anesthetic regimen. Under anesthesia, the surgery consisted of a thoracotomy followed by closing the pleural space and tissue in layers using standard surgical techniques. Vital signs were monitored to be within normal ranges throughout anesthesia. Elevated levels of cytokines interleukin (IL)-8, IL-15, monocyte chemoattractant protein-1 (MCP-1), and macrophage inflammatory protein (MIP)-1β at 6 and 24 h after surgery were detected in ketamine-exposed animals. Fluoro-Jade C staining revealed significantly higher neuronal degeneration in the frontal cortex of ketamine-exposed animals, compared with control animals. Intravenous ketamine administration prior to and throughout surgery in a clinically relevant neonatal primate model appears to elevate cytokine levels and increase neuronal degeneration. Consistent with previous data on the effects of ketamine on the developing brain, the results from the current randomized controlled study in neonatal monkeys undergoing simulated surgery show that ketamine does not provide neuroprotective or anti-inflammatory effects.
dc.eprint.versionFinal published version
dc.identifier.citationWang C, Bhutta A, Zhang X, et al. Development of a primate model to evaluate the effects of ketamine and surgical stress on the neonatal brain. Exp Biol Med (Maywood). 2023;248(7):624-632. doi:10.1177/15353702231168144
dc.identifier.urihttps://hdl.handle.net/1805/39910
dc.language.isoen_US
dc.publisherSage
dc.relation.isversionof10.1177/15353702231168144
dc.relation.journalExperimental Biology and Medicine
dc.rightsPublisher Policy
dc.sourcePMC
dc.subjectBrain
dc.subjectDevelopmental
dc.subjectAnesthesia
dc.subjectNeurotoxicology
dc.subjectNeuroscience
dc.subjectSurgery
dc.titleDevelopment of a primate model to evaluate the effects of ketamine and surgical stress on the neonatal brain
dc.typeArticle
ul.alternative.fulltexthttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10350805/
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