醫(yī)學(xué)論文范文:大黃素對(duì)模擬冷缺血再灌注后肝細(xì)胞內(nèi)鈣離子濃度及細(xì)胞凋亡的影響
【摘要】 目的 研究中藥大黃素對(duì)模擬冷缺血再灌注后肝細(xì)胞內(nèi)鈣離子濃度及細(xì)胞凋亡的影響。方法 體外培養(yǎng)肝細(xì)胞株HL7702,隨機(jī)分為對(duì)照組和大黃素處理組。對(duì)照組未予大黃素處理,大黃素處理組按100、10、1μmol/L分為高、中、低3個(gè)濃度組,建立模擬冷缺血再灌注模型,流式細(xì)胞技術(shù)檢測(cè)各組細(xì)胞內(nèi)鈣離子濃度及細(xì)胞凋亡水平,分別檢測(cè)各組細(xì)胞培養(yǎng)上清液乳酸脫氫酶水平。結(jié)果 冷缺血8h再灌注6h后,高、中、低濃度大黃素處理組鈣離子熒光強(qiáng)度分別為(24.12±0.51)、(26.35±1.34)、(39.12±1.94),均顯著低于對(duì)照組的105.29±1.01(P<0.01)。高、中、低濃度大黃素處理組細(xì)胞凋亡率分別為(5.46±0.41)%、(10.64±0.64)%、(11.90±0.50)%,均顯著低于對(duì)照組的(25.40±1.41)%(P<0.01)。高、中濃度大黃素處理組上清液LDH含量分別為(179.67±18.57)u/L、(198.83±14.22)u/L,顯著低于對(duì)照組的(351.33±34.16)u/L(P<0.01)。結(jié)論 大黃素可降低模擬冷缺血再灌注后的肝細(xì)胞內(nèi)鈣離子濃度,抑制細(xì)胞凋亡,減輕肝細(xì)胞損傷。
【關(guān)鍵詞】 大黃素;肝細(xì)胞;冷缺血再灌注;細(xì)胞內(nèi)鈣離子濃度;凋亡
Effect of Emodin on intracellular calcium concentration ([Ca2+]i) andapoptosis of hepatic cells after simulated cold ischemiareperfusion
QI Xiang, L Yi, SHEN Naiying, LIU Chang, LIU Xuemin, WANG Bo
Department of Hepatobiliary Surgery, the First Affiliated Hospital, Medical School ofXian Jiaotong University, Xian 710061, China
ABSTRACT: Objective To investigate the effect of Emodin on intracellular calcium concentration ([Ca2+]i) and apoptosis of hepatic cells after simulated cold ischemiareperfusion. Methods Glucoseoxygen deprivation, low temperature, subsequent reoxygenation and rewarming were used to induce ischemiareperfusion injury model in cultured hepatic cells which were divided into 4 groups: control group and Emodintreated group(100, 10 and 1μmol/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 Emodintreated 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 Emodintreated 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 Emodintreated 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 ischemiareperfusion, thus protecting hepatic cells effectively醫(yī).學(xué)全.在.線網(wǎng)站f1411.cn.
KEY WORDS: Emodin; hepatic cell; ischemiareperfusion injury; intracellular free calcium concentration; apoptosis
大黃素[12]化學(xué)結(jié)構(gòu)為1,3,8羥基6甲基蒽醌,具有抗炎、抗腫瘤、保護(hù)肝腎等多種生物學(xué)作用。有文獻(xiàn)報(bào)道[34],大黃素可對(duì)細(xì)胞內(nèi)鈣離子濃度及細(xì)胞凋亡產(chǎn)生影響。鈣超載及凋亡均為缺血再灌注損傷機(jī)制之一。本課題組前期研究發(fā)現(xiàn)[5],大黃素對(duì)肝細(xì)胞體外模擬冷缺血再灌注損傷具有保護(hù)作用。該保護(hù)作用是否與抑制肝細(xì)胞內(nèi)鈣超載及凋亡有關(guān)?大黃素對(duì)冷缺血再灌注后肝細(xì)胞內(nèi)鈣離子濃度及凋亡的影響未見(jiàn)相關(guān)報(bào)道。本研究擬通過(guò)觀察大黃素對(duì)模擬冷缺血再灌注后肝細(xì)胞內(nèi)鈣離子濃度及凋亡的影響,初步探討其對(duì)冷缺血再灌注損傷可能的保護(hù)機(jī)制,為其在臨床肝移植中的應(yīng)用提供一定的實(shí)驗(yàn)依據(jù)。