Prenatal Isoflurane Exposure Induces Developmental Neurotoxicity in Rats: the Role of Gut Microbiota

被引:9
作者
Wang, Li-Kuan [1 ]
Yang, Xu-Dong [1 ]
Zhou, Dan [1 ]
Cheng, Tong [1 ]
Zhang, Xiang [1 ]
Wu, Hai-Yin [1 ]
机构
[1] Peking Univ Sch & Hosp Stomatol, Dept Anesthesiol, 22 Zhongguancun South Ave, Beijing 100081, Peoples R China
关键词
Isoflurane; Anesthetic neurotoxicity; Gut-brain axis; Gut microbiota; PARKINSONS-DISEASE; GENERAL-ANESTHESIA; BIFIDOBACTERIUM; DIVERSITY; PREGNANCY; BEHAVIOR; SYSTEM; IMMUNE; MICE;
D O I
10.1007/s12640-022-00487-6
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Fetal exposure to inhaled anesthetics, such as isoflurane, may lead to neurodevelopmental impairment in offspring. Yet, the mechanisms of prenatal isoflurane-induced developmental neurotoxicity have not been fully elucidated. Gut microbiota is a pivotal modulator of brain development and functions. While the antibiotic effect of isoflurane has been previously investigated, the relationship between prenatal isoflurane exposure and postnatal gut microbiota, brain biology, and behavior remains unknown. In the present study, we treated pregnant rats with 2% isoflurane for 4 h on gestational day 14. Their offspring were tested with novel object recognition task on postnatal day 28 (P28) to assess cognition. Fecal microbiome was assessed using 16S RNA sequencing. We also analyzed hippocampal expression of brain-derived neurotrophic factor (BDNF) in P28 rat brains. To further explore the role of gut microbiota on prenatal isoflurane-induced developmental neurotoxicity, we treated rats with mixed probiotics on P14 for 14 days and evaluated novel object recognition and hippocampal expression of BDNF on P28. Results indicate that prenatal exposure to isoflurane significantly decreased novel object recognition (novel object preference ratio: mean difference (MD) - 0.157; 95% confidence interval (CI) - 0.234 to - 0.080, P < 0.001) paralleled by diminished expression of hippocampal BDNF in juvenile rats. Prenatal exposure to isoflurane also significantly altered the diversity and composition of gut microbiota. Treatment with probiotics mitigated these changes in cognition (novel object preference ratio: isoflurane group vs. control group: MD - 0.177; 95% CI - 0.307 to - 0.047, P = 0.006; probiotic group vs. isoflurane group: MD 0.140; 95% CI 0.004 to 0.275, P = 0.042) and BDNF expression. Taken together, our findings suggest that gut dysbiosis may be involved in the pathogenesis of maternal isoflurane exposure-induced postnatal cognitive impairment. To determine the causal relationship between gut microbiota and cognition in prenatal anesthetic-induced developmental neurotoxicity, further studies are needed.
引用
收藏
页码:485 / 497
页数:13
相关论文
共 50 条
  • [31] Long-Term Effects of Developmental Exposure to Oxycodone on Gut Microbiota and Relationship to Adult Behaviors and Metabolism
    Lyu, Zhen
    Schmidt, Robert R.
    Martin, Rachel E.
    Green, Madison T.
    Kinkade, Jessica A.
    Mao, Jiude
    Bivens, Nathan J.
    Joshi, Trupti
    Rosenfeld, Cheryl S.
    MSYSTEMS, 2022, 7 (04)
  • [32] Prenatal amoxicillin exposure induces developmental toxicity in fetal mice and its characteristics
    Dai, Yongguo
    Peng, Yu
    Hu, Wen
    Liu, Yi
    Wang, Hui
    JOURNAL OF ENVIRONMENTAL SCIENCES, 2024, 137 : 287 - 301
  • [33] Modulation of gut microbiota in healthy rats after exposure to nutritional supplements
    Coklo, Mirna
    Maslov, Dina Resetar
    Kraljevic Pavelic, Sandra
    GUT MICROBES, 2020, 12 (01) : 1 - 28
  • [34] Gut microbiota perturbations and neurodevelopmental impacts in offspring rats concurrently exposure to inorganic arsenic and fluoride
    Qiu, Yulan
    Chen, Xushen
    Yan, Xiaoyan
    Wang, Jie
    Yu, Guan
    Ma, Wenyan
    Xiao, Bo
    Quinones, Sarah
    Tian, Xiaolin
    Ren, Xuefeng
    ENVIRONMENT INTERNATIONAL, 2020, 140
  • [35] Altered profile of gut microbiota after subchronic exposure to neochamaejasmin A in rats
    Yan, Lifeng
    Xu, Cheng
    Liu, Qian
    Gu, Aihua
    Jiang, Zhao-Yan
    ENVIRONMENTAL TOXICOLOGY AND PHARMACOLOGY, 2015, 39 (02) : 927 - 933
  • [36] Prenatal Nicotine Exposure Induces Low Birthweight and Hyperinsulinemia in Male Rats
    Nemoto, Takahiro
    Ando, Hisae
    Nagao, Mototsugu
    Kakinuma, Yoshihiko
    Sugihara, Hitoshi
    FRONTIERS IN ENDOCRINOLOGY, 2021, 12
  • [37] Dysregulation of immune system markers, gut microbiota and short-chain fatty acid production following prenatal alcohol exposure: A developmental perspective
    Vella, Victoria R.
    Ainsworth-Cruickshank, Garrett
    Luft, Carolina
    Wong, Kingston E.
    Parfrey, Laura W.
    Vogl, A. Wayne
    Holman, Parker J.
    Bodnar, Tamara S.
    Raineki, Charlis
    NEUROCHEMISTRY INTERNATIONAL, 2025, 185
  • [38] Fetal exposure to high isoflurane concentration induces postnatal memory and learning deficits in rats
    Kong, Fei-Juan
    Ma, Lei-Lei
    Hu, Wen-Wen
    Wang, Wen-Na
    Lu, Hui-Shun
    Chen, Shu-Ping
    BIOCHEMICAL PHARMACOLOGY, 2012, 84 (04) : 558 - 563
  • [39] Altered Gut Microbiota and Its Metabolites in Hypertension of Developmental Origins: Exploring Differences between Fructose and Antibiotics Exposure
    Hsu, Chien-Ning
    Chan, Julie Y. H.
    Wu, Kay L. H.
    Yu, Hong-Ren
    Lee, Wei-Chia
    Hou, Chih-Yao
    Tain, You-Lin
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2021, 22 (05) : 1 - 16
  • [40] Deciphering the Role of the Gut Microbiota in Exposure to Emerging Contaminants and Diabetes: A Review
    Li, Xueqing
    Niu, Huixia
    Huang, Zhengliang
    Zhang, Man
    Xing, Mingluan
    Chen, Zhijian
    Wu, Lizhi
    Xu, Peiwei
    METABOLITES, 2024, 14 (02)