TY - JOUR
T1 - Crocin inhibits glutamate-induced apoptosis of retinal ganglion cells
AU - Lü, Bo Chang
AU - Dang, Xiao Jie
AU - Xu, Zhi Guo
AU - Huo, Fu Quan
AU - Zhang, Ting
AU - Yang, Xin Guang
N1 - Publisher Copyright:
© 2017, Editorial Board of Journal of Xi'an Jiaotong University (Medical Sciences). All right reserved.
PY - 2017/5/5
Y1 - 2017/5/5
N2 - Objective: To evaluate the effects and underlying mechanisms of crocin on glutamate-induced apoptosis of retinal ganglion cells (RGCs) by affecting extracellular calcium influx. Methods: Primary rat retinal ganglion cells were isolated and stimulated with glutamate at concentrations of 0.1 mmol/L and 1 mmol/L for 24 h or 48 h, respectively, to establish apoptosis model of RGCs. Afterwards, crocin of different doses (0.1, 1.0 and 3.0 μmol/L) was used to treat the glutamate-induced RGCs for 12 h; then cell apoptosis was detected by Annexin V-FITC/PI staining. The intracellular calcium concentration was determined by Fluo-3/AM fluorescent labeling. Western blot was used to examine the effect of crocin on Ca2+-mediated apoptotic signal molecules calpain and CaMKII. The mitochondrial membrane potential was detected by JC-1 staining and mitochondrial apoptosis-related signaling molecules Caspase-3, Caspase-9 and Bcl-2/Bax were evaluated by Western blot, respectively. Results: In comparison with the untreated controls, the cell apoptosis of RGCs exposed to 0.1 mmol/L of glutamate for 24 h did not significantly change (P>0.05). However, apoptosis rate of the cells reached (43.050±2.616)% when the stimulation time lasted for 48 h and showed a significant increase (P<0.01). Treatment with higher-dose glutamate (1 mmol/L) significantly increased apoptosis of RGCs at 24 h (46.450±1.061)% and 48 h (45.500±3.253)% compared with the controls (P<0.01). RGCs were induced by 1 mmol/L of glutamate for 12 h, followed by the treatment with crocin at concentrations of 0.1, 1.0 and 3.0 μmol/L, respectively. Each dose of crocin could significantly inhibit cell apoptosis in the dose-dependent manner (P<0.01). In addition, crocin at 1.0 μmol/L blocked glutamate-induced extracellular calcium influx, inhibited the expression of calcium-dependent proteins Calpain1 and CaMKII. Moreover, crocin at the dose of 1.0 μmol/L also increased mitochondrial membrane potential, suppressed the expressions of Caspase-3 and Caspase-9, and elevated Bcl-2/Bax ratio. Conclusion: Crocin inhibits glutamate-induced apoptosis of retinal ganglion cells through suppressing extracellular calcium influx, thereby blocking calcium-dependent and mitochondria-dependent apoptosis signaling pathways.
AB - Objective: To evaluate the effects and underlying mechanisms of crocin on glutamate-induced apoptosis of retinal ganglion cells (RGCs) by affecting extracellular calcium influx. Methods: Primary rat retinal ganglion cells were isolated and stimulated with glutamate at concentrations of 0.1 mmol/L and 1 mmol/L for 24 h or 48 h, respectively, to establish apoptosis model of RGCs. Afterwards, crocin of different doses (0.1, 1.0 and 3.0 μmol/L) was used to treat the glutamate-induced RGCs for 12 h; then cell apoptosis was detected by Annexin V-FITC/PI staining. The intracellular calcium concentration was determined by Fluo-3/AM fluorescent labeling. Western blot was used to examine the effect of crocin on Ca2+-mediated apoptotic signal molecules calpain and CaMKII. The mitochondrial membrane potential was detected by JC-1 staining and mitochondrial apoptosis-related signaling molecules Caspase-3, Caspase-9 and Bcl-2/Bax were evaluated by Western blot, respectively. Results: In comparison with the untreated controls, the cell apoptosis of RGCs exposed to 0.1 mmol/L of glutamate for 24 h did not significantly change (P>0.05). However, apoptosis rate of the cells reached (43.050±2.616)% when the stimulation time lasted for 48 h and showed a significant increase (P<0.01). Treatment with higher-dose glutamate (1 mmol/L) significantly increased apoptosis of RGCs at 24 h (46.450±1.061)% and 48 h (45.500±3.253)% compared with the controls (P<0.01). RGCs were induced by 1 mmol/L of glutamate for 12 h, followed by the treatment with crocin at concentrations of 0.1, 1.0 and 3.0 μmol/L, respectively. Each dose of crocin could significantly inhibit cell apoptosis in the dose-dependent manner (P<0.01). In addition, crocin at 1.0 μmol/L blocked glutamate-induced extracellular calcium influx, inhibited the expression of calcium-dependent proteins Calpain1 and CaMKII. Moreover, crocin at the dose of 1.0 μmol/L also increased mitochondrial membrane potential, suppressed the expressions of Caspase-3 and Caspase-9, and elevated Bcl-2/Bax ratio. Conclusion: Crocin inhibits glutamate-induced apoptosis of retinal ganglion cells through suppressing extracellular calcium influx, thereby blocking calcium-dependent and mitochondria-dependent apoptosis signaling pathways.
KW - Bcl-2/Bax
KW - Calcium influx
KW - Caspase-3
KW - Caspase-9
KW - Crocin
KW - Glutamate
KW - Mitochondrial-dependent apoptosis
KW - Retinal ganglion cell
UR - https://www.scopus.com/pages/publications/85022189268
U2 - 10.7652/jdyxb201703023
DO - 10.7652/jdyxb201703023
M3 - 文章
AN - SCOPUS:85022189268
SN - 1671-8259
VL - 38
SP - 445
EP - 452
JO - Journal of Xi'an Jiaotong University (Medical Sciences)
JF - Journal of Xi'an Jiaotong University (Medical Sciences)
IS - 3
ER -