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Preparation method of mouse chronic atrophic gastritis model

A technology for atrophic gastritis and mice, applied in the field of medicine, can solve the problems of high infection volume, difficult colonization, short cycle, etc., and achieve the effects of stable pathological changes, low experimental cost and simple operation.

Active Publication Date: 2019-05-17
右江民族医学院
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  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The main methods for constructing animal models of chronic atrophic gastritis include chemical carcinogenesis and Helicobacter pylori infection, etc., but so far, the construction of the model is not ideal, and there are still many areas worth exploring, such as the selection of experimental animals, the combination of drugs and The size of the dose, the length of modeling time, the ease of operation, etc.
N-methyl-N-nitro-nitrosoguanidine, ammonia water, sodium deoxycholate, sodium salicylate, etc. are currently commonly used chemical modeling materials, and rats or Mongolian gerbils are basically used for modeling , mice are rarely used to establish models of chronic atrophic gastritis, the reason may be that mice are not easy to control the dose of intervention, and are prone to other complications or side effects; Helicobacter pylori is the main cause of gastritis and gastric ulcer, It is the only pathogenic bacterium for constructing CAG animals. The animal model it constructs is closer to the CAG caused by human infection, which is more conducive to the study of the pathogenesis of CAG. However, Helicobacter pylori is easier to colonize in rats and Mongolian gerbils, and the incidence is relatively high , but it is difficult to colonize in mice. The clinically isolated strains can only be colonized after adaptive domestication, and the colonization period is relatively short. Generally, the colonization amount reaches the maximum in the first month after infection, and the colonization amount will decrease in the second and third months. decreased, and could not maintain a relatively high infection rate; Zeng Zhirong, the First Affiliated Hospital of Sun Yat-sen Medical University, infected C57BL / 6 mice and BALB / c mice with the Sydney strain of Helicobacter pylori (SS1), although the strain maintained in the body for a long time High colonization rate, but the strain is CagA-negative, so that chronic atrophic gastritis has not yet appeared 24 weeks after the last inoculation; Wang Jian, Zhongshan Hospital Affiliated to Fudan University, et al. Nitrosourea (MNU)" joint modeling, chronic atrophic gastritis in mice at 36 weeks is 23.1%, which requires a long period and the success rate is low; we used mice in the preliminary experiment, using "Helicobacter pylori group +N-Methyl-N-nitro-nitrosoguanidine group" method, the mice did not appear chronic atrophic gastritis in the 4th month after the last infection
It can be seen that it is very difficult to prepare chronic atrophic gastritis in mice infected with Helicobacter pylori in a short period of time.

Method used

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  • Preparation method of mouse chronic atrophic gastritis model
  • Preparation method of mouse chronic atrophic gastritis model
  • Preparation method of mouse chronic atrophic gastritis model

Examples

Experimental program
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Effect test

Embodiment 1

[0016] 1. Animal grouping: 280 6-week-old Kunming mice were randomly selected and divided into PBS control group, Helicobacter pylori group, N-methyl-N-nitro-nitrosoguanidine group, ammonia water group, and "Helicobacter pylori group". Bacteria group + N-methyl-N-nitro-nitrosoguanidine" two-factor combined model group, "Helicobacter pylori group + base-N-nitro-nitrosoguanidine group + ammonia water" three-factor combined model group Modules, male and female.

[0017] 2. Immune intervention and chemical injury: The experimental group was fed with 120 μg / mL N-methyl-N-nitroso-nitrosoguanidine according to the body weight of the mice at 5 mL / kg, once a day, 7 consecutive interventions, feeding and drinking water 0.02wt.% ammonia water. Control group: without any intervention, normal feeding.

[0018] 3. Bacterial infection: use clinically isolated Helicobacter pylori strains, which are identified as Helicobacter pylori by Gram staining, urease test, oxidase test, catalase test ...

Embodiment 2

[0027] Adopt the method of above-mentioned embodiment 1, Helicobacter pylori is poured 1 * 10 per mouse 8 CFU, N-methyl-N-nitro-nitrosoguanidine was administered to mice at a concentration of 100 μg / mL at a concentration of 5 mL / kg, once a day, for 7 consecutive interventions, and 0.04wt.% ammonia water was used for feeding and drinking water. The experimental results are shown in Table 2.

[0028] Table 2 Modeling results of chronic atrophic gastritis

[0029]

Embodiment 3

[0031] Adopt the method of above-mentioned embodiment 1, Helicobacter pylori is poured 1 * 10 per mouse 9 CFU, N-methyl-N-nitroso-nitrosoguanidine was administered orally with a concentration of 110 μg / mL according to the body weight of the mice at 5 mL / kg, once a day, for 7 consecutive interventions, and 0.03wt.% ammonia water was used for feeding and drinking water. The experimental results are shown in Table 3.

[0032] Table 3 Modeling results of chronic atrophic gastritis

[0033]

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Abstract

The invention relates to a preparation method of a mouse chronic atrophic gastritis model, which comprises the following steps: filling N-methyl-N-nitro-nitrosoguanidine according to the weights of the mice, using low-content ammonia water as feeding and drinking water; after the intervention by using the N-methyl-N-nitro-nitrosoguanidine, filling helicobacter pylori with positive CagA and VagA; wherein the mice are fasted before gastric administration and fasted and fasted with water after gastric administration; extracting male and female mice, carrying out gastric mucosa histopathological examination, and isolating and culturing the helicobacter pylori from the gastric mucosa to confirm the establishment of the helicobacter pylori and the formation of inflammation. The method uses miceto construct chronic atrophic gastritis, has simple operation, low cost, short period, high success rate, stable pathological change and strong repeatability, has outstanding substantive advantages, and provides a good animal model for studying chronic atrophic gastritis, gastric cancer and other diseases caused by helicobacter pylori infection.

Description

technical field [0001] The invention belongs to the field of medicine, and in particular relates to a preparation method of a mouse chronic atrophic gastritis model. Background technique [0002] Chronic atrophic gastritis (CAG) is a precancerous disease of the stomach. Its onset is slow, lingering, protracted, and difficult to treat. If it is not well controlled, it may develop into intestinal metaplasia or atypical hyperplasia, and finally form stomach cancer. The research and treatment of CAG have attracted much attention. The modeling of CAG animal models is the key material for the basic and clinical research of the disease. A good animal model will provide direct in vivo evidence for the prevention and treatment of the disease. The main methods for constructing animal models of chronic atrophic gastritis include chemical carcinogenesis and Helicobacter pylori infection, etc., but so far, the construction of the model is not ideal, and there are still many areas worth ...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): A61K35/74A61K31/155A61K33/02A01K67/02
CPCA01K67/02A61K31/155A61K33/02A61K35/74A61K2300/00
Inventor 黄衍强黄干荣王露瑶梁凌玲赵丽娟周滢龙
Owner 右江民族医学院
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