He Tianqiong, Zhou Junkang, Wen Yixin, Liu Qian, Zhi Wenling, Yang Wenhao, He Shuangyan, Ouyang Lingxuan, Xia Xiaobo, Zhou Zhijun
Department of Laboratory Animal Science, Xiangya School of Medicine, Central South University; Changsha 410013.
Hunan Key Laboratory of Animal Models for Human Diseases, Central South University, Changsha 410013.
Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2024 Apr 28;49(4):553-561. doi: 10.11817/j.issn.1672-7347.2024.230534.
Age-related cataract is the most common type of adult cataract and a leading cause of blindness. Currently, there are few reports on the establishment of animal models for age-related cataract. During the experimental breeding of (), we first observed that aged 12 to 15 months could naturally develop cataracts. This study aims to explore the possibility of developing them as an animal model for age-related cataract via identifing and analyzing spontaneous cataract in .
The 12-month-old healthy were served as a control group and 12-month-old cataractous were served as an experimental group. The lens transparency was observed using the slit-lamp biomicroscope. Hematoxylin and eosin staining was used to detect pathological changes in the lens. Biochemical detection methods were applied to detect blood routine, blood glucose levels, the serum activities of superoxide dismutase (SOD), and glutathione peroxidase (GSH-Px) in both groups. Finally, real-time RT-PCR was used to detect the transcription levels of cataract-related genes in the lens of 2 groups.
Compared with the control group, the lens of cataract showed severely visible opacity, the structure of lens was destroyed seriously, and some pathological damage, such as swelling, degeneration/necrosis, calcification, hyperplasia, and fiber liquefaction were found in lens epithelial cells (LECs). The fibrous structure was disorganized and irregularly distributed with morgagnian globules (MGs) aggregated in the degenerated lens fibers. There was no statistically significant difference in blood glucose levels between the experimental and control groups (0.05). However, white blood cell (WBC) count (0.05), lymphocyte count (0.01), and lymphocyte ratio (0.05) were significantly decreased, while neutrophil percentage (0.05) and monocyte ratio (0.01) were significantly increased. The serum activities of SOD and GSH-Px (both 0.05) were both reduced. The mRNAs of cataract-related genes, including , , , , , , , and , were significantly downregultaed in the lenses of the experimental group (all 0.05).
There are significant differences in lens pathological changes, peroxidase levels, and cataract-related gene expression between cataract and healthy . The developed cataract spontaneously in is closely related to age, the cataract might be an ideal animal model for the research of age-related cataract.
年龄相关性白内障是成人白内障最常见的类型,也是导致失明的主要原因。目前,关于年龄相关性白内障动物模型建立的报道较少。在()的实验繁育过程中,我们首次观察到12至15月龄的()可自然发生白内障。本研究旨在通过识别和分析()中的自发性白内障,探讨将其开发为年龄相关性白内障动物模型的可能性。
将12月龄健康的()作为对照组,12月龄白内障的()作为实验组。使用裂隙灯生物显微镜观察晶状体透明度。采用苏木精-伊红染色检测晶状体的病理变化。应用生化检测方法检测两组的血常规、血糖水平、超氧化物歧化酶(SOD)和谷胱甘肽过氧化物酶(GSH-Px)的血清活性。最后,采用实时荧光定量PCR检测两组晶状体中白内障相关基因的转录水平。
与对照组相比,白内障()的晶状体出现严重可见的混浊,晶状体结构严重破坏,晶状体上皮细胞(LECs)出现一些病理损伤,如肿胀、变性/坏死、钙化、增生和纤维液化。纤维结构紊乱,分布不规则,变性的晶状体纤维中聚集有莫尔加尼小球(MGs)。实验组与对照组血糖水平差异无统计学意义(P>0.05)。然而,白细胞(WBC)计数(P<0.05)、淋巴细胞计数(P<0.01)和淋巴细胞比例(P<0.05)显著降低,而中性粒细胞百分比(P<0.05)和单核细胞比例(P<0.01)显著升高。SOD和GSH-Px的血清活性均降低(均P<0.05)。实验组晶状体中白内障相关基因,包括()、()、()、()、()、()、()、()和()的mRNA均显著下调(均P<0.05)。
白内障()与健康()在晶状体病理变化、过氧化物酶水平和白内障相关基因表达方面存在显著差异。()中自发形成的白内障与年龄密切相关,白内障()可能是研究年龄相关性白内障的理想动物模型。