Preparation system and preparation method of rat brain injury animal model
An animal model and preparation system technology, applied in medical science, veterinary instruments, veterinary surgery, etc., can solve the problems of short survival time of brain injury animal models, unstable production, and difficult removal of cushion balls, etc., to facilitate observation and manufacture Mold results, good stability, and long survival time
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Embodiment 1
[0044] This embodiment is a preparation system of a rat brain injury animal model, such as figure 1 As shown, the preparation system includes a cushion ball 1, a sleeve 2, a weight 3, and a plastic film 4. The plastic film 4 is arranged at the bottom of the sleeve 2, and the cushion ball 1 is arranged in the sleeve 2 and connected to the plastic film 4. , The weight 3 is set in the sleeve 2 and above the cushion ball 1;
[0045] Among them, the diameter of the cushion ball 1 is 2.2 mm; the inner diameter of the sleeve 2 is 1.6 cm; the weight 3 is spherical with a mass of 12 g and a diameter of 1.4 cm; the plastic film 4 is made of polyethylene; and the thickness is 0.9 dmm.
Embodiment 2
[0047] This embodiment is a preparation system of a rat brain injury animal model, such as figure 1 As shown, the preparation system includes a cushion ball 1, a sleeve 2, a weight 3, and a plastic film 4. The plastic film 4 is arranged at the bottom of the sleeve 2, and the cushion ball 1 is arranged in the sleeve 2 and connected to the plastic film 4. , The weight 3 is set in the sleeve 2 and above the cushion ball 1;
[0048] Among them, the diameter of the cushion ball 1 is 2mm; the inner diameter of the sleeve 2 is 1.7cm; the weight 3 is spherical with a mass of 14g and a diameter of 1.5cm; the plastic film 4 is made of polyethylene; and the thickness is 1dmm.
Embodiment 3
[0050] This example is a preparation method of a rat brain injury animal model. The preparation method adopts the preparation system of Example 1. The preparation method described above includes the following steps:
[0051] (a) The rats were anesthetized with 10% chloral hydrate by intraperitoneal injection, and then the rats were fixed and disinfected in the prone position, and then the scalp of the rats was incised along the median loss, at the top of the right side, bregma A bone window with a diameter of 4.5mm is opened at the rear 2mm and 2mm beside the midline;
[0052] (b) Cover the position of the bone window with plastic film, and place the cushion ball on the plastic film and face the bone window;
[0053] (c) Place the sleeve vertically above the bone window, and then put the weight into the sleeve and freely fall to hit the center of the cushion ball until the cushion ball sinks into the brain tissue 1.8mm;
[0054] (d) Take out the brain tissue from the cushion ball and ...
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