Qing Guoping, Duan Xuanchu, Jiang Youqin
Department of Ophthalmology, the Second Xiangya Hospital, Central South University, Changsha, Hunan, 410011, China.
Yan Ke Xue Bao. 2005 Sep;21(3):163-8.
To investigate whether the induction of heat shock protein (HSP)72 by heat stress (HS) or zinc (Zn2+ ) administration can increase survival of retinal ganglion cells (RGC)in rat model of acute experimental glaucoma.
Acute glaucoma model was made by intracameral irrigation with BSS at 10(2) mmHg for two hours in right eyes of male Wistar rats. Glaucoma model rats were treated with HS once a week (six rats) or intraperitoneal injection of zinc sulfate (24.6 mg/kg) every two weeks (six rats), and were referred to as HS group and zinc group, respectively. Untreated model rats served as damage group (six rats). In control groups, quercetin (400 mg/kg) was intraperitoneally injected to inhibit the induction of heat shock proteins 6 hours before HS or zinc administration, and were referred to as HS+que group (six rats) and zinc+que group (six rats), respectively. Subsequent to 16 days of IOP elevation, the rats were sacrificed. Eyes were quickly enucleated, and the retinas were dissected. RGC were labeled with Nissl staining and counted under microscope.
The average RGC density in normal Wistar rats was (2504+/-181) cells/mm(2). In damage group, it decreased to (2015+/-1111) cells/mm(2). The RGC densities at 1, 2, and 3 mm from the center of the optic nerve head were (2716+/-215), (2496+/-168), and (2317+/-171) cells/mm(2), respectively, for normal rats and (2211+/-133), (1969+/-154), and (1872+/-68) cells/mm(2), respectively, for damage group. The latter was significantly lower at all locations compared with the former (P=0.027 for each, Mann-Whitney test). The average RGC densities were (2207+/-200) cells/mm(2) for HS group, (2272+/-155) cells/mm(2) for zinc group, (1964+/-188) cells/mm(2) for HS+que group, (2051+/-214) cells/mm(2 )for zinc+que group and (2015+/-111) cells/mm(2) for damage group. There were significant differences in density of labeled RGCs among the five groups (P=0.040, Kruskal-Wallis test). Both HS and zinc group had higher RGC densities than damage group (P =0.036 between HS and damage group, P=0.019 between zinc and damage group, Mann-Whitney test). There was no significant difference in RGC density between control groups and damage group(P=-0.260 between HS+que and damage group, P-0.748 between zinc+que and damage group, Mann-Whitney test).
The results demonstrated that the induction of HSP72 in RGCs by HS or zinc administration plays an important role in the survival of RGCs in rat model of acute glaucoma. A novel therapeutic approach to glaucoma through an enhanced induction of endogenous HSP72 could be possible.
研究热应激(HS)或给予锌(Zn2+)诱导热休克蛋白(HSP)72是否能提高急性实验性青光眼大鼠模型中视网膜神经节细胞(RGC)的存活率。
通过向雄性Wistar大鼠右眼前房内灌注平衡盐溶液(BSS)至眼压达10(2)mmHg并持续2小时制作急性青光眼模型。青光眼模型大鼠分别接受每周一次的热应激处理(6只大鼠)或每两周一次的腹腔注射硫酸锌(24.6 mg/kg)(6只大鼠),分别称为热应激组和锌组。未处理的模型大鼠作为损伤组(6只大鼠)。在对照组中,在热应激或给予锌前6小时腹腔注射槲皮素(400 mg/kg)以抑制热休克蛋白的诱导,分别称为热应激+槲皮素组(6只大鼠)和锌+槲皮素组(6只大鼠)。眼压升高16天后,处死大鼠。迅速摘除眼球,解剖视网膜。用尼氏染色法标记RGC并在显微镜下计数。
正常Wistar大鼠的平均RGC密度为(2504±181)个细胞/mm(2)。在损伤组中,其降至(2015±1111)个细胞/mm(2)。正常大鼠距视神经乳头中心1、2和3 mm处的RGC密度分别为(2716±215)、(2496±168)和(2317±171)个细胞/mm(2),损伤组分别为(2211±133)、(1969±154)和(1872±68)个细胞/mm(2)。损伤组各部位的RGC密度均显著低于正常组(每组P=0.027,曼-惠特尼检验)。热应激组的平均RGC密度为(2207±200)个细胞/mm(2),锌组为(2272±155)个细胞/mm(2),热应激+槲皮素组为(1964±188)个细胞/mm(2),锌+槲皮素组为(2051±214)个细胞/mm(2),损伤组为(2015±111)个细胞/mm(2)。五组中标记RGC的密度有显著差异(P=0.040,克鲁斯卡尔-沃利斯检验)。热应激组和锌组的RGC密度均高于损伤组(热应激组与损伤组之间P =0.036,锌组与损伤组之间P=0.019,曼-惠特尼检验)。对照组与损伤组的RGC密度无显著差异(热应激+槲皮素组与损伤组之间P=-0.260,锌+槲皮素组与损伤组之间P-0.748,曼-惠特尼检验)。
结果表明,热应激或给予锌诱导RGCs中的HSP72在急性青光眼大鼠模型中RGCs的存活中起重要作用。通过增强内源性HSP72的诱导来治疗青光眼的新方法可能是可行的。