TY - JOUR
T1 - Effect of Emodin on intracellular calcium concentration ([Ca 2+]i) and apoptosis of hepatic cells after simulated cold ischemia-reperfusion
AU - Qi, Xiang
AU - Lü, Yi
AU - Shen, Nai Ying
AU - Liu, Chang
AU - Liu, Xue Min
AU - Wang, Bo
PY - 2009
Y1 - 2009
N2 - Objective: To investigate the effect of Emodin on intracellular calcium concentration ([Ca2+]i) and apoptosis of hepatic cells after simulated cold ischemia-reperfusion. Methods: Glucose-oxygen deprivation, low temperature, subsequent reoxygenation and rewarming were used to induce ischemia-reperfusion injury model in cultured hepatic cells which were divided into 4 groups: control group and Emodin-treated group (100, 10 and 1 μmol/L groups). The intracellular calcium concentration ([Ca2+]i) and apoptosis rate were determined by flow cytometry (FCM) respectively; the content of lactate dehydrogenase (LDH) in supernatant was tested. Results: Intracellular calcium fluorescence intensity in Emodin-treated groups of high, medium and low density was 24.12± 0.51, 26.35±1.34 and 39.12±1.94, respectively, which were significantly lower than 105.29±1.01 in control group(P<0.01). Apoptosis rate in Emodin-treated groups of high, medium and low density was 0.0546±0.0041, 0.1064±0.0064 and 0.1190±0.0050, respectively, which were significantly lower than 0.2540±0.0141 in control group(P<0.01). LDH was (198.83±14.22)u/L and (179.67±18.57)u/L in Emodin-treated groups of medium and high density respectively, which were significantly lower than (351.33±34.16) u/L in control group (P<0.01). Conclusion: Emodin could reduce [Ca2+]i and inhibit apoptosis of hepatic cells after simulated cold ischemia-reperfusion, thus protecting hepatic cells effectively.
AB - Objective: To investigate the effect of Emodin on intracellular calcium concentration ([Ca2+]i) and apoptosis of hepatic cells after simulated cold ischemia-reperfusion. Methods: Glucose-oxygen deprivation, low temperature, subsequent reoxygenation and rewarming were used to induce ischemia-reperfusion injury model in cultured hepatic cells which were divided into 4 groups: control group and Emodin-treated group (100, 10 and 1 μmol/L groups). The intracellular calcium concentration ([Ca2+]i) and apoptosis rate were determined by flow cytometry (FCM) respectively; the content of lactate dehydrogenase (LDH) in supernatant was tested. Results: Intracellular calcium fluorescence intensity in Emodin-treated groups of high, medium and low density was 24.12± 0.51, 26.35±1.34 and 39.12±1.94, respectively, which were significantly lower than 105.29±1.01 in control group(P<0.01). Apoptosis rate in Emodin-treated groups of high, medium and low density was 0.0546±0.0041, 0.1064±0.0064 and 0.1190±0.0050, respectively, which were significantly lower than 0.2540±0.0141 in control group(P<0.01). LDH was (198.83±14.22)u/L and (179.67±18.57)u/L in Emodin-treated groups of medium and high density respectively, which were significantly lower than (351.33±34.16) u/L in control group (P<0.01). Conclusion: Emodin could reduce [Ca2+]i and inhibit apoptosis of hepatic cells after simulated cold ischemia-reperfusion, thus protecting hepatic cells effectively.
KW - Apoptosis
KW - Emodin
KW - Hepatic cell
KW - Intracellular free calcium concentration
KW - Ischemia-reperfusion injury
UR - https://www.scopus.com/pages/publications/75149182783
M3 - 文章
AN - SCOPUS:75149182783
SN - 1671-8259
VL - 30
SP - 669-671+676
JO - Journal of Xi'an Jiaotong University (Medical Sciences)
JF - Journal of Xi'an Jiaotong University (Medical Sciences)
IS - 6
ER -