Method for constructing an animal model of complex inflammation in middle-aged and elderly type and related application thereof
By injecting D-galactose and using sodium dextran sulfate solution in an animal model, a complex inflammatory animal model of middle-aged and elderly people was constructed. This solved the problem that existing models could not simulate the intestinal-hepatic axis dysfunction in middle-aged and elderly people, and achieved a realistic simulation of the pathological characteristics of middle-aged and elderly people and an evaluation of intervention substances.
Patent Information
- Application Number
- CN202610428759.2
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- Filing Date
- 2026-04-02
- Publication Date
- 2026-06-09
AI Technical Summary
Existing animal models of colitis are insufficient to simulate the complex pathological state of intestinal inflammation, liver oxidative stress, and gut-liver axis dysfunction in middle-aged and elderly individuals, and cannot truly reflect the chronic inflammatory characteristics of this population.
By subcutaneously injecting D-galactose into adult animals after adaptive feeding, combined with drinking of sodium dextran sulfate solution, intestinal inflammatory damage and liver oxidative stress were induced, thus constructing a middle-aged and elderly complex inflammatory animal model to simulate the intestinal-liver axis dysfunction under relevant physiological conditions in middle-aged and elderly individuals.
A stable and reproducible complex inflammation model for middle-aged and elderly individuals was successfully constructed, which can simultaneously reflect intestinal inflammation, intestinal barrier damage, and abnormal liver oxidative stress, realistically simulating the pathological characteristics of middle-aged and elderly populations, and is suitable for the evaluation and research of intervention substances.
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Figure CN122162751A_ABST
Abstract
Claims
1. A method for constructing a middle-aged and elderly animal model of complex inflammation based on gut-liver axis dysfunction, characterized in that, The construction method includes the following steps: (1) Select adult animals as model animals; (2) Adaptive feeding for 1-2 weeks to prepare for modeling; (3) D-galactose was injected subcutaneously daily during the modeling period; (4) On the 8th to 10th day of modeling, the model animals were given free access to a 3% to 5% sodium dextran sulfate solution every day; (5) On the 11th day of modeling, replace the sodium dextran sulfate solution with sterile drinking water; (6) On the 12th to 13th day of modeling, replace the sterile drinking water with a 2% to 5% sodium dextran sulfate solution; (7) A middle-aged and elderly complex inflammation animal model was obtained on the 14th day of modeling.
2. The construction method according to claim 1, characterized in that, The injection dose of D-galactose is 0.1~0.4 mL / 10 g body weight, and the molecular weight of the DSS solution is 30,000~50,000 Da.
3. The construction method according to claim 1, characterized in that, The animals were 6-week-old male BALB / c mice.
4. An animal model of complex inflammation in middle-aged and elderly individuals based on gut-liver axis dysfunction, characterized in that, The animal model is obtained by the construction method described in any one of claims 1 to 3.
5. The animal model according to claim 4, characterized in that, The animal model possesses the following characteristics: DAI A score ≥4; colon length shortening ≥20%; impaired intestinal barrier function; crypt structure destruction and inflammatory cell infiltration; significantly elevated TNF-α and IL-6 expression; decreased ZO-1 and Occludin expression; and abnormal liver oxidative stress indicators.
6. The use of the animal model described in claim 4 or 5 in screening and preparing drugs, medical nutrition products and functional foods that improve diseases related to gut-liver axis dysfunction.
