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Original Research Article | OPEN ACCESS

Mechanism of propofol-induced injury in hippocampal neurons in neonatal rats

Tao Zhang1, Jusheng Wu2

1Department of Anesthesiology, Jingling Hospital, Nanjing 210002, Jiangsu Province, China; 2Department of Anesthesiology, Zhuji People's Hospital, Zhuji 311800, Zhejiang Province, China.

For correspondence:-  Jusheng Wu   Email: wujusheng123123@126.com

Accepted: 4 March 2022        Published: 31 March 2022

Citation: Zhang T, Wu J. Mechanism of propofol-induced injury in hippocampal neurons in neonatal rats. Trop J Pharm Res 2022; 21(3):605-610 doi: 10.4314/tjpr.v21i3.21

© 2022 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..

Abstract

Purpose: To determine the deleterious effect of propofol on hippocampal neurons in developing rats, and the underlying mechanism.
Methods: Sixty Wistar rats were randomly assigned to fat emulsion group, low-dose propofol group and high-dose propofol group. Immunohistochemical staining of brain samples was used to detect BrdU-positive (+), nestin+ and GFAP+ cells. The influence of propofol on cellular multiplication, number of neurons in dentate gyrus, activation of astrocytes and microglial activation were determined. The expression levels of Sox2, Akt and ERK signal pathway-associated proteins were assayed by Western blotting.
Results: The population of BrdU-positive cells was significantly lower in propofol-exposed rats than in fat emulsion rats, while the levels of Sox2 protein were markedly and dose-dependably lower in propofol-exposed rats than the corresponding levels in fat emulsion rats (p < 0.05). The numbers of nestin+ cells, GFAP+ cells and Iba1+ cells in propofol-exposed rats were significantly and concentration-dependently reduced, relative to the corresponding numbers in fat emulsion rats, while p-Akt and p-ERK1/2 in propofol-exposed rats were and dose-dependently reduced, relative to fat emulsion rats (p < 0.05).
Conclusion: Propofol dose-dependently inhibits the proliferation of hippocampal dentate gyrus stem cells, and suppresses the activation of astrocytes and microglia through regulation of the expressions of Akt/ERK signal pathway-associated proteins. This provides a lead for research and development of new drugs for protecting hippocampal neurons.

Keywords: Propofol, Hippocampal neurons, Fat emulsion, Akt/ERK signal pathway, Astrocytes, Microglia, Dentate gyrus stem cell

Impact Factor
Thompson Reuters (ISI): 0.523 (2021)
H-5 index (Google Scholar): 39 (2021)

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