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This protocol describes a procedure for rat retinal sampling and utilizing hematoxylin-eosin staining, TUNEL assay, and Western blot to detect pathological changes and apoptosis in the retina after intraperitoneal injection of N-Methyl-N-Nitrosourea.
Retinopathy can be observed in most ocular diseases and the late complications of diabetes mellitus. The specific pigment epithelial cells and optic cells' damage and degeneration are the main features of retinopathy. Many traditional medicines have shown substantial clinical efficacy in treating retinopathy. How to obtain a retina quickly and completely is a key step in traditional medicine research for the treatment of retinopathy. In this study, we aim to provide a standardized and exercisable procedure for sampling of N-methyl-N-nitrosourea (MNU)-induced rat's retina damage and multi-index evaluation of pathological changes. Rats were injected intraperitoneally with 60 mg/kg MNU once to induce retina damage, and retina samples were obtained after 7 days. Additionally, we performed hematoxylin-eosin staining to assess retinal pathological changes. Determination of the apoptosis rate and apoptosis protein by TUNEL and Western blot. These standardized protocols for retinal sampling and evaluation of pathological changes are helpful in promoting the exploration of the mechanism of retinopathy and the discovery of novel and effective traditional herbs.
Retinitis pigmentosa (RP) is a hereditary and blinding retinal disease1. The incidence of RP is between 1/3500 and 1/5000, affecting the visual function of about 2.5 million people in the world. It is one of the most well-known diseases leading to visual impairment in human beings, imposing a significant burden on the whole society2. The disease is characterized by the gradual loss of retinal pigment epithelial cell function and the progressive apoptosis of photoreceptors. In the early stage, patients experience night blindness, which manifests as peripheral visual field defects and eventually leads to the loss of centra....
All protocols and surgical procedures were approved by the Ethics Committee of Ningxia Medical University (Ethics number: NO. 2020-Q066). SPF Sprauge-Dawley (SD) male rats, aged 7-8 weeks and weighing 200-220 g, were purchased from Ningxia Medical University with the animal license number SCXK (Ning) 2020-0001. All the animals were raised in the Laboratory Animal Center of Ningxia Medical University. The temperature and humidity were suitable, the day-night light cycle was maintained, and the food and water were free and.......
After HE staining, all retinal layers of rats in the control group had clear tissue structure, orderly cell arrangement, and uniform staining, while the retinal structure of rats in the model group was significantly damaged, the outer retinal layer was thinner, the outer nuclear layer was almost completely integrated with the inner core layer, the arrangement of cells in the layer was extremely disordered, the number of cell layers was significantly reduced, and the thickness of the photosensitive cell layer and outer nu.......
RP is a common retinal disease in clinics. The onset, severity, and progression of RP are related to genes and genetic modes and are affected by the environment8,11. RP includes familial RP and occasional RP, of which familial RP accounts for about 60% of the patients. Through tracing the family genetic history, 83 genes related to RP have been identified so far, while occasional RP accounts for about 40%, which means this kind of patient lacks a family history a.......
This work was supported by the Scientific Research Project of the Higher Education Department of Ningxia (NYG2022029).
....Name | Company | Catalog Number | Comments |
Amersham Imager | GE | 680 | |
Ammonium persulfate | Boster Biological Technology Co.,Ltd | A8090 | |
Analytical Balance | Mettler Toledo | ME104E | |
BCA protein quantization kit | Ken Gen Biotech. Co. Ltd | KGP902 | |
cleaved caspase-3 antibody | Cell Signaling Technology | #9664 | |
cleaved caspase-7 antibody | Cell Signaling Technology | #8438 | |
cleaved caspase-9 antibody | Cell Signaling Technology | #9507 | |
DeadEnd Fluorometric TUNEL System | Promega | G3250 | |
Glycine | Boster Biological Technology Co.,Ltd | AR1200 | |
Goat Anti-Rabbit IgG H&L (HRP) | Bioss Antibodies | bs-80295G-HRP | |
Goat serum | Biosharp | BL210A | |
High speed crusher | Thermo Fisher Scientific | AG22331 | |
Immobilon-P SQ Transfer membranes | Merck Millipore. Ltd | ISEQ00010 | |
Isoflurane | RWD Life Science | R510-22-10 | |
Methanol | Chengdu Kelong Chemical Co., Ltd | 20230108 | |
Microplate Reader | Thermo Fisher Scientific | 1510 | |
Microscope | Olympus | IX73 | |
Microscope slide | Citotest Labware Manufacturing Co., Ltd | 7105P-G | |
Mini-PROTEAN Tetra | BIO-RAD | 1658001 | |
N-Methyl-N-Nitrosourea | sigma-Aldrich | N4766–100G | |
Oven | Shanghai Yuejin Medical Equipment Co., Ltd | DHG-8145 | |
Page Pre-solution (30% ) | Doublehelix Biology Science and Technology Co.,Ltd | L3202A | |
PageRuler Prestained Protein Ladder | Thermo Fisher Scientific | 26617 | |
PBS buffer | Biosharp | G4202 | |
SDS-PAGE Protein loading buffer (5×) | Beyotime Biotechnology | P0015 | |
Skim milk powder | BioFroxx | 1172GR500 | |
Sprague Dawley rats | Ningxia Medical University | SCXK (Ning) 2020-0001 | |
TEMED | Boster Biological Technology Co.,Ltd | AR1165 | |
Total protein extraction kit | Ken Gen Biotech. Co. Ltd | KGP2100 | |
Trans-Blot Module | BIO-RAD | 1703935 | |
Tris base | Boster Biological Technology Co.,Ltd | AR1162 | |
Tweezer | Changde BKMAM Biotechnology Co., Ltd | 130302027 | |
β-actin | Cell Signaling Technology | #4970 |
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