Skin type lupus erythematosus mouse model and construction method and application thereof
A construction method and technology for lupus erythematosus, which can be used in phototherapy, veterinary instruments, medical science, etc., can solve problems such as limitations, modeling success rate and efficiency limitations, and achieve the effect of accelerating clinical transformation.
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Embodiment 1
[0083] Embodiment 1: Construction method of experimental animal model of cutaneous lupus erythematosus
[0084] 1) Order SPF-grade female C57BL / 6 mice and Balb / c mice with animal quality certificates from formal production units. The age is 8W. Keep the outer packaging intact and spray disinfectant spray. After 30 minutes of ultraviolet sterilization, enter the SPF grade barrier environment, and then the experimental operations involved in the experiment of C57BL / 6 mice and Balb / c mice were carried out in this barrier environment;
[0085] All C57BL / 6 mice were weighed and recorded and arranged according to body weight from small to large, and the C57BL / 6 mice were randomly divided into Pristane i.c.+UVB group, PBS i.c.+UVB group, and Pristane i.c. group by random number table method; among them: Pristanei.c.+UVB group and Pristane i.c group were intradermally injected with Pristane 0.25ml at multiple points, PBS i.c.+UVB group was intradermally injected with PBS buffer 0.25ml...
Embodiment 2
[0090] Example 2: Verification experiment of the mouse model of cutaneous lupus erythematosus in Example 1
[0091] 2.1 Preparation of Paraffin Sections of Skin and Kidney Tissues of CLE Experimental Mice
[0092] 1) Euthanize the CLE experimental mice, cut a small piece of skin lesion tissue with a sharp blade, cut the whole kidney from the middle of the coronal plane, rinse with pre-cooled normal saline, and quickly put the skin tissue and kidney tissue in more than 4% Fix in POM at room temperature for 24 hours;
[0093] 2) Rinse the fixed skin lesions with running water;
[0094] 3) The washed specimens were soaked and dehydrated in sequence by 50% alcohol → 75% alcohol → 95% alcohol (I) → 95% alcohol (II) → absolute alcohol (I) → absolute alcohol (II). 2 hours;
[0095] 4) The dehydrated skin tissue was soaked in 1:1 absolute alcohol and xylene → xylene (I) → xylene (II) for 1 hour in sequence, and the tissue was visible in a transparent state;
[0096] 5) Melt three ...
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