›› 2011, Vol. 27 ›› Issue (6): 405-408,412.DOI: 10.3969/j.issn.1004-5619.2011.06.002

Previous Articles     Next Articles

Effects of Ketamine on Proliferation and Apoptosis of Pheochromocytoma Cell

ZUO YUAN-YI1,2,3, ZHAO YAN-BO4, JIANG XIAO-GANG3, GU ZHEN-LUN3, GUO CI-YI3, BIAN SHI-ZHONG1,2   

  1. (1. Department of Forensic Medicine, Medical College of Soochow University, Suzhou 215123, China; 2. Forensic Judicial Appraisal Institute, Soochow University, Suzhou 215000, China; 3. Suzhou Institute of Chinese Materia Medica, Suzhou 215006, China; 4. Department of Forensic Medicine, Criminal Police Brigade of Kunshan Public Security Bureau, Kunshan 215300, China)
  • Online:2011-12-25 Published:2011-12-28

Abstract: Objective To explore the effect of ketamine on adrenal pheochromocytoma(PC12) cell proliferation inhibition and induction of apoptosis and its mechanism. Methods PC12 cells of rats were models for dopaminergic neuron. PC12 cells were cultured with ketamine at concentrations of 0.9, 1.2, 1.5, 1.8 and 2.1 mmol/L, respectively. The cell viability was measured by MTT method after incubation at 12, 24, 48 and 72 h. Hoechst stain was used to observe the morphological changes of apoptosis. PC12 cells cultured after 48 h with different concentrations of ketamine were selected to detect apoptotic rate using flow cytometry and detect the expression of bax and bcl-2 proteins using Western blotting. Results For different concentrations of ketamine, vitality of PC12 cells significantly decreased with increase of the incubation time. Apoptosis was obviously observed using Hoechst staining. Flow cytometry showed that apoptosis rates significantly increased with increasing ketamine concentrations. Conclusion Ketamine can inhibit the proliferation of PC12 cell by inducing apoptosis of the PC12 cell in a concentrations-dependent manner. The underlying mechanism may be related to promoting the expression of bax and inhibiting the expression of bcl-2 in the cells.

Key words: forensic pathology, ketamine, PC12 cells, cell proliferation, apoptosis, rats

CLC Number: