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Original Research Article | OPEN ACCESS

Protective Effect of Modified Human Acidic Fibroblast Growth Factor against Actinomycin D-Induced NRK52E Cells Apoptotic Death

Hua XU1 , Hong XU2, Guang-fan HAI3, Qing HE1, Chang-e ZHANG4

1Jinan University College of Pharmacy, Guangzhou, Guangzhou 510632; 2United Front Work Department, Guangxi Medical University, Nanning, 530021; 3Department of Pharmacology, Xin-xiang Medical College, Xin-xiang 450031; 4Department of Pathophysiology, Guangzhou Medical College, Guangzhou 510182, China.

For correspondence:-  Hua XU   Email: huaxmail@126.com

Received: 17 July 2012        Accepted: 10 April 2013        Published: 12 June 2013

Citation: XU H, XU H, HAI G, HE Q, ZHANG C. Protective Effect of Modified Human Acidic Fibroblast Growth Factor against Actinomycin D-Induced NRK52E Cells Apoptotic Death. Trop J Pharm Res 2013; 12(3):343-349 doi: 10.4314/tjpr.v12i3.11

© 2013 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 investigate whether modified acidic fibroblast growth factor (MaFGF) can protect NRK52E cell against apoptotic death induced by actinomycin D (Act D) and the effect of MaFGF on PI3K/Akt signaling pathway.
Methods: NRK52E cell apoptotic death was measured by several methods including cell morphologic observation, Hoechst 33342 staining and flow cytometry. In addition, the levels of phosphorylated-Akt protein were analyzed by Western blotting method.
Results: The results showed that 0.75 mg/L Act D-treated NRK52E cell for 20 h was the optimal conditions for establishing NRK52E cell apoptotic model. Different doses of MaFGF (0.01, 0.03, 0.1, 0.3 and 1.0 mg/L) decreased apoptotic rate but enhanced the expression of phosphorylated Akt protein. However, MaFGF’s protection against Act D-induced apoptosis was significantly (p < 0.05) prevented when NRK52E cells were exposed to wortmannin.
Conclusion: These results reveal that MaFGF can reduce the level of ActD-induced apoptotic cell death in 20 h, and the protective mechanism of MaFGF may be associated with the activation of PI3K/Akt signaling pathway by up-regulation of expression of phosphorylated Akt protein.

Keywords: Modified acidic fibroblast growth factor (MaFGF), Renal injury, Apoptotic death, Actinomycin D (Act D)

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

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