Ginsenoside Rg1 attenuates isoflurane/surgery-induced cognitive disorders and sirtuin 3 dysfunction.

Biosci Rep

Department of Anesthesiology, Beijing Friendship Hospital, Capital Medical University, Beijing, People's Republic of China.

Published: October 2019

AI Article Synopsis

  • Isoflurane/surgery (I/S) can lead to neurocognitive disorders, but the exact mechanisms and treatments are not well understood.
  • Ginsenoside Rg1 was tested on male mice to see if it could reduce I/S-induced cognitive impairments and improve Sirtuin3 (Sirt3) function.
  • Results indicated that Rg1 treatment improved learning and memory by decreasing harmful reactive oxygen species (ROS) and enhancing mitochondrial function in the hippocampus.

Article Abstract

Isoflurane/surgery (I/S) may induce neurocognitive disorders, but detailed mechanisms and appropriate treatment remain largely unknown. This experiment was designed to determine whether ginsenoside Rg1 could attenuate I/S-induced neurocognitive disorders and Sirtuin3 (Sirt3) dysfunction. C57BL/6J male mice received 1.4% isoflurane plus abdominal surgery for 2 h. Ginsenoside Rg1 10 mg/kg was intraperitoneally given for 8 days before surgery. Neurocognitive function was assessed by the Barnes Maze test. Levels of reactive oxygen species (ROS), oxygen consumption rate (OCR), mitochondrial membrane potential (MMP), expression and deacetylation activity of Sirt3 in the hippocampus tissues were measured. Results showed that I/S induced hippocampus-dependent learning and memory impairments, with increased ROS levels, and reduced OCR, MMP, and expression and deacetylation activity of Sirt3 in hippocampus tissues. Ginsenoside Rg1 treatment before I/S intervention significantly ameliorated learning and memory performance, reduced ROS levels and improved the OCR, MMP, expression and deacetylation activity of Sirt3. In conclusion, this experiment demonstrates that ginsenoside Rg1 treatment can attenuate I/S-induced neurocognitive disorders and Sirt3 dysfunction.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6822512PMC
http://dx.doi.org/10.1042/BSR20190069DOI Listing

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