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Inhibitory Effect of r-Hirudin Variant III on Streptozotocin-Induced Diabetic Cataracts in Rats

机译:r-水rud素变体Ⅲ对链脲佐菌素诱导的糖尿病性白内障的抑制作用

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摘要

The in vivo inhibitory effect of r-hirudin variant III (rHV3) on streptozotocin (STZ)-induced diabetic cataracts in rats was investigated. SD-rats were firstly made diabetic by a single intraperitoneal injection of 2% (W/V) STZ (65 mg/kg). Two weeks later, cataract formation was examined by slit lamp microscope, and the cataracted animals were randomly grouped. The animals in the treated groups received rHV3 drops administration to the eyes with various doses. After 4 weeks treatment, the animals were sacrificed to evaluate the biochemical changes of aldose reductase (AR), superoxide dismutase (SOD), glutathione peroxidase (GSH-Px), and malondialdehyde (MDA) levels in the eye lens. Meanwhile, the cataract progression was monitored by slit lamp microscope. As a result, rHV3 drops treatment significantly increased the activities of SOD and GSH-Px in the lens in a dose-dependent manner, whereas AR activity and MDA level in the lens were dramatically decreased. Also, the morphological observation further confirmed the inhibition of the development of STZ-induced diabetic cataracts by the rHV3 drops treatment. Thus, our data suggest that rHV3 drops are pharmacologically effective for the protection against STZ-induced diabetic cataracts in rats.
机译:研究了r-hirudin变体III(rHV3)对链脲佐菌素(STZ)诱导的大鼠糖尿病性白内障的体内抑制作用。首先通过单次腹膜内注射2%(W ​​/ V)STZ(65μmg/ kg)使SD大鼠成为糖尿病。两周后,通过裂隙灯显微镜检查白内障的形成,并将白内障动物随机分组。治疗组中的动物接受了rHV3滴剂以各种剂量向眼睛给药。治疗4周后,处死动物以评估其眼镜中醛糖还原酶(AR),超氧化物歧化酶(SOD),谷胱甘肽过氧化物酶(GSH-Px)和丙二醛(MDA)水平的生化变化。同时,通过裂隙灯显微镜监测白内障进展。结果,rHV3滴剂治疗以剂量依赖性方式显着增加了晶状体中SOD和GSH-Px的活性,而晶状体中AR活性和MDA水平则显着降低。而且,形态学观察进一步证实了rHV3滴剂治疗抑制STZ诱导的糖尿病性白内障的发展。因此,我们的数据表明,rHV3滴剂在保护大鼠免受STZ诱导的糖尿病性白内障方面具有药理作用。

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