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Original Research Article | OPEN ACCESS

Anisodamine combined with lidocaine improves healing of myocardial ischemia-reperfusion injury in rats via PI3K/Akt signaling pathway

Shouyi Wang1, Jiahao Chen2, Jie Wang3, Hongbo Que3, Daming Wei3, Yanhao Zhu1, Qin Liu1, Yu Liu1, Chunyan Zhu4

1Department of Anesthesiology, The First Affiliated Hospital of Anhui University of Traditional Chinese Medicine, Hefei; 2Department of Cardiology, Wuxi Affiliated Hospital of Nanjing University of Traditional Chinese Medicine, Wuxi; 3Department of Anesthesiology, Anhui Integrated Traditional Chinese and Western Medicine Hospital, Hefei; 4Department of Anesthesiology and Pain Research Center, The First Hospital of Jiaxing, The Affiliated Hospital of Jiaxing University, Jiaxing, China.

For correspondence:-  Chunyan Zhu   Email: zhuchunyan308@163.com

Accepted: 11 November 2022        Published: 29 December 2022

Citation: Wang S, Chen J, Wang J, Que H, Wei D, Zhu Y, et al. Anisodamine combined with lidocaine improves healing of myocardial ischemia-reperfusion injury in rats via PI3K/Akt signaling pathway. Trop J Pharm Res 2022; 21(12):2561-2567 doi: 10.4314/tjpr.v21i12.9

© 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 study the effects of anisodamine (Ad) combined with lidocaine (Ldc) on myocardial ischemia-reperfusion injury (MIRI) in rats, and its correlation with PI3K/AKT signaling pathway.
Methods: A total of 70 healthy rats were randomly divided into S group, M group, Ad group, Ldc group, Ad + Ldc group, Ad + Ldc + LY group, and LY group. The cardiac hemodynamic indices in each group were determined, and the area of myocardial infarction measured. Serum biochemical indices were also determined. Furthermore, the protein expressions of p-Akt, T-Akt, Bcl-2, and Bax in myocardial cells were determined by Western blotting.
Results: Compared with those in M group, Ad group, Ldc group, Ad + Ldc + LY group, and LY group, cardiac hemodynamic indices significantly improved, while the area of myocardial infarction was significantly reduced (p < 0.01). Furthermore, serum malondialdehyde (MDA) concentration but the activities of CK, CK-MB, TNF-α, and IL-6 declined, while the activities of superoxide dismutase (SOD), CAT and GSH-Px rose in Ad + Ldc group (p < 0.01). In Ad + Ldc group, p-Akt, T-Akt, and Bcl-2 increased, while Bax significantly decreased. Through comparison LY294002 significantly inhibited the protective effect of Ad combined with Ldc against MIRI in rats (p < 0.01).
Conclusion: Anisodamine combination with lidocaine has a protective effect against MIRI in rats via PI3K/Akt signaling pathway, thus indicating that it is a potential therapeutic strategy for the management of myocardial ischemia-reperfusion.

Keywords: PI3K/Akt pathway, Anisodamine, Lidocaine, Myocardial ischemia-reperfusion

Impact Factor
Thompson Reuters (ISI): 0.6 (2023)
H-5 index (Google Scholar): 49 (2023)

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