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Juvenile Rats Show Altered Gut Microbiota After Exposure to Isoflurane as Neonates
Likuan Wang1, Xudong Yang2, Haiyin Wu2
1Department of Anesthesiology, Peking University School and Hospital of Stomatology, #22 Zhongguancun South Avenue, Haidian District, Beijing, 100081, China. wanglikuan3@163.com.
Insights
Neonatal exposure to isoflurane altered gut microbiota composition in juvenile rats. This finding may explain neurocognitive dysfunction linked to anesthesia in early life.
Area of Science:
- Neuroscience
- Microbiology
- Anesthesiology
Background:
- Inhaled anesthetics like isoflurane may cause neurotoxicity in developing brains.
- Neonatal isoflurane exposure is linked to long-term neurocognitive deficits.
- Gut microbiota disruption is implicated in various neurological disorders.
Purpose of the Study:
- To investigate the impact of neonatal isoflurane exposure on gut microbiota composition in juvenile rats.
- To determine if isoflurane affects the balance of bacterial taxa in the gut microbiome.
Main Methods:
- Postnatal 7-day-old male rats were exposed to 1 minimum alveolar concentration (MAC) of isoflurane for 4 hours.
- Non-anesthetized rats served as controls.
- Fecal samples were analyzed using 16S rRNA sequencing on postnatal day 42.
Main Results:
- Isoflurane-exposed rats exhibited significant differences in gut microbiota composition compared to controls.
- Increased abundance of Firmicutes, Proteobacteria, Clostridia, Clostridiales, and Lachnospiraceae was observed.
- Decreased abundance of Bacteroidetes, Actinobacteria, Bacteroidia, and Bacteroidaceae was noted in exposed rats.
Conclusions:
- Neonatal isoflurane exposure significantly alters the gut microbiome in juvenile rats.
- These alterations in gut microbiota may contribute to isoflurane-induced neurotoxicity.
- Findings provide novel insights into the pathogenesis of neurodevelopmental issues following neonatal anesthesia.
Abstract:
Inhaled anesthetic agents may be neurotoxic to the developing brain of a neonatal rodent. Isoflurane is a commonly used volatile anesthetic agent for maintenance of general anesthesia in various types of surgery. Neonatal exposure to isoflurane has been implicated in long-term neurocognitive dysfunction in children. The mechanisms of isoflurane-induced neurotoxicity have not been fully elucidated. Disruption of gut microbiota is currently attracting considerable interest as a vital pathogeny of some neurologic disorders. In the rat model, it is unknown whether neonatal exposure to isoflurane impacts the gut microbiota composition of juvenile animals. In the present study, postnatal 7-day-old male rats were exposed to 1 minimum alveolar concentration isoflurane for 4 h. Non-anesthetized rats served as controls. The fecal microbiomes of rats were observed using 16S RNA sequencing technique on postnatal day 42. Results indicated that composition of gut microbiota of isoflurane-exposed rats was different from controls. Several bacteria taxa in isoflurane-exposed rats were different from those of controls at various taxonomic levels. In particular, the abundance of Firmicutes, Proteobacteria, Clostridia, Clostridiales, and Lachnospiraceae were significantly increased in exposed rats and the abundance of Bacteroidetes, Actinobacteria, Bacteroidia and Bacteroidaceae were significantly decreased compared to controls. These results may offer new insights into the pathogenesis of isoflurane-induced neurotoxicity.
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