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Autor(en) / Beteiligte
Titel
The effect of N-acetylcysteine on the neurotoxicity of sevoflurane in developing hippocampus cells
Ist Teil von
  • Neurotoxicology (Park Forest South), 2024-07, Vol.103, p.96-104
Ort / Verlag
Elsevier B.V
Erscheinungsjahr
2024
Link zum Volltext
Quelle
ScienceDirect
Beschreibungen/Notizen
  • Sevoflurane, a common pediatric anesthetic, has been linked to neurodegeneration, raising safety concerns. This study explored N-acetylcysteine's protective potential against sevoflurane-induced neurotoxicity in rat hippocampi. Four groups were examined: Control: Received 6 hours of 3 l/min gas (air and 30 % O2) and intraperitoneal saline. NAC: Received 6 hours of 3 l/min gas and 150 mg/kg NAC intraperitoneally. Sev: Exposed to 6 hours of 3 l/min gas and 3 % sevoflurane. Sev+NAC: Received 6 hours of 3 l/min gas, 3 % sevoflurane, and 150 mg/kg NAC. Protein levels of NRF-2, NLRP3, IL-1β, caspase-1, Beclin 1, p62, LC3A, and apoptosis markers were assessed. Sevoflurane and NAC alone reduced autophagy, while Sev+NAC group maintained autophagy levels. Sev group had elevated NRF-2, NLRP3, pNRF2, Caspase-1, and IL-1β, which were reduced in Sev+NAC. Apoptosis was higher in Sev, but Sev+NAC showed reduced apoptosis compared to the control. In summary, sevoflurane induced neurotoxicity in developing hippocampus, which was mitigated by N-acetylcysteine administration. •Sevoflurane-induced neurotoxicity in developing brains involves disrupted autophagy, neuroinflammation, oxidative stress, and apoptosis, raising concerns for pediatric anesthesia.•N-acetylcysteine, with its antioxidant and anti-inflammatory properties, emerges as a potential protective agent against sevoflurane-induced neurotoxicity in a developing rat model.•The study shows that NAC preserves autophagy, suppresses neuroinflammation and oxidative stress, and mitigates apoptosis, offering a comprehensive approach to counter sevoflurane's harmful effects.•With its multifaceted protective effects, NAC shows promise in alleviating sevoflurane's neurotoxic impact on developing brain cells, providing valuable insights for clinical practice.
Sprache
Englisch
Identifikatoren
ISSN: 0161-813X
eISSN: 1872-9711
DOI: 10.1016/j.neuro.2024.05.006
Titel-ID: cdi_proquest_miscellaneous_3065983955

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