Method for establishing around vascellum endometrial hyperplasia animal model
A vascular intima, animal model technology, applied in the field of zoology, achieves important practical value and theoretical research value, good repeatability, and obvious clinical symptoms.
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Embodiment 1
[0025] 1.1 To establish a rabbit animal model of peripheral vascular intimal hyperplasia (Intima hyperplasia, IH), the steps are:
[0026] (1). Select 10 male healthy New Zealand white rabbits weighing 1.2-1.8kg, ordinary grade, provided by the Rabbit Breeding Factory of Shandong Academy of Agricultural Sciences, production license number "SCXK (Lu) 20040013", and randomly divided into control group and the test group, each with 5 rats. Oridonin A for injection was injected into the experimental group by auricular vein injection once a day at a dose of 7.2mg / kg·d -1 , continuous injection for 10 days; the control group was fed normally for 10 days. The experimental group and the control group maintained the same feeding conditions and feeding environment.
[0027] (2). The animals in the experimental group and the control group were sacrificed, and the auricular artery was isolated, fixed in situ with 10% formalin solution, dehydrated, embedded, sectioned, and stained with V...
Embodiment 2
[0040] 2.1 To establish a rat animal model of intima hyperplasia (IH), the steps are as follows:
[0041] (1). Take 10 healthy male SD rats, weighing 310-350g, provided by the Experimental Animal Center of Shandong University, production license number "SCXK (Lu) 20040004", and randomly divide them into control group and test group (five rats each) ). Oridonin for injection was injected into the experimental group by tail vein injection once a day at a dose of 12mg / kg·d -1 , continuous injection for 10 days; the control group was fed normally for 10 days. The experimental group and the control group maintained the same feeding conditions and feeding environment.
[0042](2). SD rats were killed, and blood vessels of 0.5 cm were taken from the same position of the peripheral arterioles of each rat, fixed in formalin, dehydrated, embedded in paraffin, and sliced 8 to 10 pieces evenly in each section of blood vessels. For HE staining, 6 slices were randomly selected in each ...
Embodiment 3
[0054] 3.1 To establish a canine animal model of intimal hyperplasia in peripheral blood vessels, the steps are as follows:
[0055] (1). Take 10 healthy Beagle dogs, male or female, weighing 15-20kg. They were raised routinely and provided by the Experimental Animal Center of Shandong University. The production license number is "SCXK (Lu) 20040004". Group (5 each). For the test group, subcutaneous cephalic vein injection of oridonin for injection was performed once a day at a dose of 4.2 mg / kg·d -1 , continuous injection for 10 days; the control group was fed normally for 10 days. The experimental group and the control group maintained the same feeding conditions and feeding environment.
[0056] (2). All the animals in the two groups were killed, and 0.5 cm blood vessels were taken from the same part of the peripheral arterioles, and the fixed peripheral arterioles were embedded in paraffin, sliced serially at a thickness of 5 μm, stained with hematoxylin-eosin (HE), an...
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