Cui Fei-fei, Pan Ying-ying, Dai Yan-li, Wang Zhou-guang, Xiao Jian, Jiang Li-ping
Nursing Department, Dongyang Hospital Affiliated to Wenzhou Medical University, Dongyang 322100, China.
Nursing Department, Dongyang Hospital Affiliated to Wenzhou Medical University, Dongyang 322100, China. Email:
Zhonghua Shao Shang Za Zhi. 2013 Oct;29(5):448-53.
To explore the effects of endoplasmic reticulum stress (ERS) related proteins and their mediated apoptosis in the formation of deep tissue injury of pressure ulcer in rats.
Forty male Sprague-Dawley rats were divided into normal control group and groups A, B, C, D according to the random number table, with 8 rats in each group. Rats in group A were loaded with 22.47 kPa pressure with a special pressure apparatus for 2.0 h in the region over gracilis, and then unloaded for 0.5 h. Rats in group B were treated with the same manoeuvre as that in group A for 3 times in one day. Rats in groups C and D were treated with the same manoeuvre as that in group B for 2 and 3 days. Rats in normal control group were free from pressure loading. Rats in groups A, B, C, and D were sacrificed after pressure loading, and then the central part of pressure loaded muscular tissues were harvested for observation of histomorphological change with HE staining; apoptotic nucleoli per millimeter pressure loaded muscular tissue were counted with Hoechst 33258 staining; the levels of binding protein (BIP), protein disulfide isomerase (PDI), C/EBP homologous protein (CHOP), and caspase-12 were assessed with Western blotting (denoted as gray level ratio of target protein to GAPDH). The same parts of gracilis of rats in normal control group were harvested for determination of all the indexes as above. Data were processed with one-way analysis of variance, LSD-t test was applied for paired comparison.
(1) Histomorphological observation. Some pathological changes, including inflammatory cell infiltration, myofibers lysis, and vacuolar degeneration, etc. were observed in pressure loaded muscular tissue of rats in groups A, B, C, and D, but not in the same parts of gracilis muscle of rats in normal control group. Compared with those in normal control group [(2.7 ± 1.4) per millimeter muscular tissue], the number of apoptotic nuclei was significantly increased in pressure loaded muscular tissue of rats in groups A, B, C, and D [(14.5 ± 4.4), (11.0 ± 2.9) , (13.8 ± 5.1), (21.3 ± 6.0) per millimeter pressure loaded muscular tissue, with t values from 4.223 to 6.000, P values all below 0.01). (2) Western blotting. The protein expressions of BIP and PDI in rats of normal control group and groups A, B, C, D were respectively 0.64 ± 0.12, 1.20 ± 0.34, 1.59 ± 0.24, 1.17 ± 0.28, 1.44 ± 0.33; 0.48 ± 0.15, 0.61 ± 0.19, 1.23 ± 0.38, 0.37 ± 0.19, 0.29 ± 0.15, and they showed significant statistical difference (with F values respectively 5.32, 7.95, P < 0.05 or P < 0.01). The protein expressions of CHOP and caspase-12 in rats of normal control group and groups A, B, C, D were respectively 0.58 ± 0.18, 1.48 ± 0.27, 1.03 ± 0.21, 0.95 ± 0.30, 1.69 ± 0.34; 0.55 ± 0.12, 1.08 ± 0.31, 0.69 ± 0.24, 1.79 ± 0.20, 2.06 ± 0.47, with significant statistical difference (with F values respectively 8.17, 15.48, P values all below 0.01).
ERS related proteins and their apoptotic pathway may play an important role in the formation of deep tissue injury of pressure ulcer in rats.
探讨内质网应激(ERS)相关蛋白及其介导的细胞凋亡在大鼠压疮深部组织损伤形成中的作用。
将40只雄性Sprague-Dawley大鼠按随机数字表分为正常对照组及A、B、C、D组,每组8只。A组大鼠用特制压力装置在股薄肌区施加22.47 kPa压力2.0 h,然后减压0.5 h。B组大鼠1天内按与A组相同方法处理3次。C组和D组大鼠分别按与B组相同方法处理2天和3天。正常对照组大鼠不施加压力。A、B、C、D组大鼠在压力加载后处死,取压力加载肌肉组织的中央部分,行HE染色观察组织形态学变化;用Hoechst 33258染色计数每毫米压力加载肌肉组织中的凋亡核仁;用蛋白质免疫印迹法检测结合蛋白(BIP)、蛋白二硫键异构酶(PDI)、C/EBP同源蛋白(CHOP)和半胱天冬酶-12的水平(以目标蛋白与甘油醛-3-磷酸脱氢酶的灰度比值表示)。取正常对照组大鼠股薄肌相同部位测定上述所有指标。数据采用单因素方差分析,组间两两比较采用LSD-t检验。
(1)组织形态学观察。A、B、C、D组大鼠压力加载肌肉组织出现一些病理改变,包括炎性细胞浸润、肌纤维溶解和空泡变性等,而正常对照组大鼠股薄肌相同部位未见上述改变。与正常对照组每毫米肌肉组织(2.7±1.4)相比,A、B、C、D组大鼠压力加载肌肉组织凋亡核数量显著增加[每毫米压力加载肌肉组织分别为(14.5±4.4)、(11.0±2.9)、(13.8±5.1)、(21.3±6.0),t值为4.223~6.000,P值均<0.01]。(2)蛋白质免疫印迹法。正常对照组及A、B、C、D组大鼠BIP和PDI蛋白表达分别为0.64±0.12、1.20±0.34、1.59±0.24、1.17±0.28、1.44±0.33;0.48±0.15、0.61±0.19、1.23±0.38、0.37±0.19、0.29±0.15,差异有统计学意义(F值分别为5.32、7.95,P<0.05或P<0.01)。正常对照组及A、B、C、D组大鼠CHOP和半胱天冬酶-12蛋白表达分别为0.58±0.18、1.48±0.27、1.03±0.21、0.95±0.30、1.69±0.34;0.55±0.12、1.08±0.31、0.69±0.24、1.79±0.20、2.06±0.47,差异有统计学意义(F值分别为8.17、15.48,P值均<0.01)。
ERS相关蛋白及其凋亡途径可能在大鼠压疮深部组织损伤形成中起重要作用。