阅读说明：本技术 脑组织特异性pltp过表达模型构建方法及测定方法 (Method for constructing brain tissue specificity PLTP overexpression model and determination method ) 是由 王浩 王文芝 陈莹 李明伟 于 2020-05-11 设计创作，主要内容包括：本发明属于PLTP过表达模型构建技术领域,公开了一种脑组织特异性PLTP过表达模型构建方法及测定方法,10月龄3×Tg-AD雄鼠,随机分为模型组,实验组,以同月龄具有相同遗传背景的雄性C57BL/6J作为对照组；AD模型注射携带PLTP基因增强型绿色荧光蛋白报告基因的腺相关病毒AAV-PLTP-EGFP,诱导PLTP的高表达；对照组与模型组均注射不携带PLTP基因只携带增强型绿色荧光蛋白报告基因的腺相关病毒AAV-EGFP。本发明的PLTP过表达可改善3×Tg-AD小鼠的学习记忆能力、对3×Tg-AD小鼠学习记忆能力的改善；通过促进GSK-3β失活进而减少Aβ产生和Tau蛋白磷酸化有关。(The invention belongs to the technical field of PLTP overexpression model construction, and discloses a method for constructing a brain tissue specificity PLTP overexpression model and a determination method, wherein a 10-month-old 3 x Tg-AD male mouse is randomly divided into a model group and an experimental group, and male C57BL/6J with the same genetic background at the same month age is used as a control group; injecting adeno-associated virus AAV-PLTP-EGFP carrying PLTP gene enhanced green fluorescent protein reporter gene into the AD model to induce high expression of PLTP; both the control group and the model group are injected with adeno-associated virus AAV-EGFP which does not carry PLTP gene and only carries enhanced green fluorescent protein reporter gene. The PLTP overexpression can improve the learning and memory ability of a 3 × Tg-AD mouse and improve the learning and memory ability of the 3 × Tg-AD mouse; the reduction of A beta production by promoting GSK-3 beta inactivation is related to Tau protein phosphorylation.)

1. A method for constructing a brain tissue specific PLTP overexpression model is characterized by comprising the following steps:

step one, 3 × Tg-AD mice are taken as an AD model, 3 × Tg-AD male mice at the age of 10 months are randomly divided into a model group and an experimental group, and male C57BL/6J with the same genetic background at the age of the same month is taken as a control group;

secondly, injecting AAV-PLTP-EGFP carrying PLTP gene enhanced green fluorescent protein reporter gene into the AD model to induce high expression of PLTP;

thirdly, injecting AAV-EGFP which does not carry PLTP gene and only carries enhanced green fluorescent protein reporter gene into the control group and the model group.

2. The method for constructing a brain tissue specific PLTP overexpression model according to claim 1, wherein 24 male mice 3 x Tg-AD at 10 months of age are randomly divided into 12 models and 12 experiments.

3. The method of claim 1, wherein male C57BL/6J having the same genetic background at the same age is used as the control group of 12 subjects.

4. A brain tissue specific PLTP overexpression model constructed by the method for constructing a brain tissue specific PLTP overexpression model according to any one of claims 1 to 3.

5. Use of the brain tissue specific PLTP overexpression model of claim 4 for the treatment of a target of alzheimer's disease.

6. A method for determining the brain tissue specific PLTP overexpression model according to claim 4, wherein the method for determining the brain tissue specific PLTP overexpression model comprises:

step one, a 3 × Tg-AD mouse is used as an AD model to construct a brain tissue specificity PLTP overexpression model;

secondly, observing the influence of the PLTP overexpression on the learning and memory capacity of the 3 × Tg-AD mice;

thirdly, pathologically observing the protective effect of the PLTP overexpression on 3 × Tg-AD mice;

fourthly, observing the influence of the PLTP overexpression on the Abeta and the generation of related proteins thereof;

fifthly, observing the influence of the PLTP overexpression on the total Tau protein and the pTau protein thereof;

sixthly, observing the influence of the PLTP overexpression on the GSK-3 beta and the GSK-3 beta; and (3) detecting the protein expression level of the GSK-3 beta and the GSK-3 beta by adopting western blot.

7. The method of determining a brain tissue specific PLTP overexpression model according to claim 6, wherein said second step observes the effect of PLTP overexpression on learning and memory ability of 3 x Tg-AD mice; after injecting AAV-PLTP-EGFP virus into lateral ventricle of mouse for 2 weeks, testing learning and memory ability of mouse by water maze experiment and shuttle passive avoidance experiment; the water maze experiment is divided into a positioning navigation experiment and a space exploration experiment, and the cognitive function is evaluated by taking the latency of a mouse searching platform and the frequency of entering the platform as indexes; the shuttle passive avoidance experiment is carried out in a light and dark shuttle box, and the learning and memory ability is evaluated by taking the latency of the mouse entering the dark box and the residence time of the mouse in the dark box as indexes.

8. The method of claim 6, wherein the third step of pathology is performed by observing the protective effect of PLTP overexpression on 3 × Tg-AD mice, and the pathological lesions of each group are detected by HE staining and Nie's staining, and A β is performed₁-42 changes in senile plaques SP of each group were observed by immunohistochemical staining and changes in neurofibrillary tangles NFT of each group were observed by Bielschowsky silver staining.

9. The method for determining the brain tissue specific PLTP overexpression model of claim 6, wherein the fourth step is to observe the effect of PLTP overexpression on A β and its related protein production, after behavioral experiments, mice are sacrificed, the cerebral cortex and hippocampus of the mice are separated to prepare tissue homogenate, the expression levels of APP, PS1 and BACE1 related proteins generated by A β are detected by Western blotting technique, and the ELISA method is used to detect A β_1-40And A β_1-42And (4) horizontal.

10. The method of determining a brain tissue specific PLTP overexpression model according to claim 6, wherein the fifth step observes the effect of PLTP overexpression on total Tau protein and pTau protein thereof; detecting the expression of total Tau protein and pTau protein of cerebral cortex and hippocampus in pSer199, pSer214, pThr231 and pSer404 phosphorylation sites by using western blot;

the data of the determination method of the brain tissue specificity PLTP overexpression model are counted by SPSS16.0 software, a one-way analysis of variance ANOVO is adopted for comparison among a plurality of groups of samples, and statistical difference exists when P is less than 0.05.

Technical Field

The invention belongs to the technical field of PLTP overexpression model construction, and particularly relates to a method for constructing a brain tissue specificity PLTP overexpression model and a determination method.

Background

Alzheimer's Disease (AD) is a degenerative disease of the central nervous system and is the most common type of dementia. At present, the study on AD by scholars at home and abroad draws attention, a plurality of pathogenic mechanism theories are put forward, and a targeted drug with a certain treatment effect is developed, but the pathogenic mechanism is not completely clarified, and an effective treatment drug is not provided yet. The phospholipid transport protein (PLTP) is a glycoprotein widely expressed in the central nervous system, and in recent years, in vivo and in vitro studies have found that PLTP is closely related to AD. PLTP deficiency can promote the decline of cognitive functions of aged mice, so whether the high expression of PLTP has the effect of improving AD or not is not reported in domestic and foreign research. A plurality of modes can be used for researching the influence of the PLTP overexpression on AD, for example, the recombinant PLTP protein is given, but the price of the recombinant protein is high, and animal administration also needs to consider whether the medicine can be absorbed into an organism and can enter into brain tissues to play a role through a blood brain barrier, so that the technology that the PLTP gene is induced to be highly expressed after brain positioning injection by using the virus as a carrier and further the expression of the PLTP protein is up-regulated is ideal, and by using the technology, the AD mouse combined with APP/PS1/Tau three transgenes can define the protection effect of the PLTP high expression on AD in an overall level. Although AD is an important disease harmful to human, at present, no animal model which can completely simulate human AD exists, which brings difficulty to the research of AD mechanism and drug development. The AD mouse with three transgenes of APP/PS1/Tau is a relatively better AD model in a plurality of models at present, and the anti-AD effect of PLTP can be more confirmed through the research on the AD protection effect of the model on the high expression of PLTP. In addition, both A beta and Tau are key molecules in the pathogenesis of AD, and the high expression of PLTP has a regulation function on both the molecules, thereby also indicating that the A beta and Tau are expected to become one of the components or targets of clinical AD resistance. While gene therapy mediated by viruses has been used in the treatment of tumors, the treatment of AD through virus-mediated gene expression has certain possibilities.

Through the above analysis, the problems and defects of the prior art are as follows: PLTP deficiency can promote the decline of cognitive functions of aged mice, and whether PLTP high expression has an effect of improving AD or not is not reported in domestic and foreign research.

The difficulty in solving the above problems and defects is: injecting the lateral ventricle in a positioning way, and constructing the high expression gene of the adeno-associated virus PLTP.

The significance of solving the problems and the defects is as follows: provides basis for the clinical AD treatment taking PLTP as a target.

Disclosure of Invention

Aiming at the problems in the prior art, the invention provides a method for constructing a brain tissue specificity PLTP overexpression model and a determination method.

The invention is realized in such a way, and the method for constructing the brain tissue specificity PLTP overexpression model comprises the following steps:

step one, 3 × Tg-AD mice are taken as an AD model, 3 × Tg-AD male mice at the age of 10 months are randomly divided into a model group and an experimental group, and male C57BL/6J with the same genetic background at the age of the same month is taken as a control group;

secondly, injecting AAV-PLTP-EGFP carrying PLTP gene enhanced green fluorescent protein reporter gene into the AD model to induce high expression of PLTP;

thirdly, injecting AAV-EGFP which does not carry PLTP gene and only carries enhanced green fluorescent protein reporter gene into the control group and the model group.

Furthermore, the brain tissue specificity PLTP overexpression model construction method is that 24 male mice of 3 × Tg-AD with the age of 10 months are randomly divided into 12 model groups and 12 experimental groups.

Further, the brain tissue specific PLTP overexpression model construction method uses male C57BL/6J with the same genetic background at the same age as the control group 12.

The invention also aims to provide a brain tissue specific PLTP overexpression model constructed by the construction method of the brain tissue specific PLTP overexpression model.

Another object of the present invention is to provide a method for measuring the brain tissue-specific PLTP overexpression model, comprising:

step one, a 3 × Tg-AD mouse is used as an AD model to construct a brain tissue specificity PLTP overexpression model; induce high expression of PLTP gene.

Secondly, observing the influence of the PLTP overexpression on the learning and memory capacity of the 3 × Tg-AD mice; the main clinical manifestations of AD are cognitive function decline, and the water maze and other methods can detect the cognitive function of animals to evaluate the anti-AD effect of PLTP high expression.

Thirdly, pathologically observing the protective effect of the PLTP overexpression on 3 × Tg-AD mice; pathological changes characteristic of AD at age spots and neurofibrillary tangles, so pathological observations can confirm the anti-AD effect of high PLTP expression.

Fourthly, observing the influence of the PLTP overexpression on the Abeta and the generation of related proteins thereof; a beta and Tau are key molecules for the pathogenesis of AD, and the detection of two pathway proteins confirms the possible pathway of improving AD by PLTP.

Fifthly, observing the influence of the PLTP overexpression on the total Tau protein and the pTau protein thereof; a beta and Tau are key molecules for the pathogenesis of AD, and the detection of two pathway proteins confirms the possible pathway of improving AD by PLTP.

Sixthly, observing the influence of the PLTP overexpression on the GSK-3 beta and the GSK-3 beta; and (3) detecting the protein expression level of the GSK-3 beta and the GSK-3 beta by adopting western blot. GSK3 beta can regulate A beta and Tau, and the activity of PLTP in regulating GSK3 beta is reported in documents, and the mechanism of the anti-AD action of PLTP is determined by detecting GSK3 beta.

Further, the second step observes the influence of the overexpression of PLTP on the learning and memory ability of 3 × Tg-AD mice; after injecting AAV-PLTP-EGFP virus into lateral ventricle of mouse for 2 weeks, testing learning and memory ability of mouse by water maze experiment and shuttle passive avoidance experiment; the water maze experiment is divided into a positioning navigation experiment and a space exploration experiment, and the cognitive function is evaluated by taking the latency of a mouse searching platform and the frequency of entering the platform as indexes; the shuttle passive avoidance experiment is carried out in a light and dark shuttle box, and the learning and memory ability is evaluated by taking the latency of the mouse entering the dark box and the residence time of the mouse in the dark box as indexes.

Further, the third step of pathology observation is carried out on the protective effect of PLTP overexpression on 3 × Tg-AD mice, and pathological injuries of each group are detected through HE staining and Nie staining and A β₁-42 changes in senile plaques SP of each group were observed by immunohistochemical staining and changes in neurofibrillary tangles NFT of each group were observed by Bielschowsky silver staining.

Further, the fourth step is to observe the influence of PLTP overexpression on A β and the related protein generated by the same, after behavioral experiments, mice are sacrificed, the cerebral cortex and the hippocampus of the mice are separated, tissue homogenate is prepared, the expression levels of APP, PS1 and BACE1 which are related to the generation of A β proteins are detected by adopting a protein immunoblotting technology, and A β and the expression levels of A1 are detected by an ELISA method₁-40 and A β₁42 levels.

Further, the fifth step is to observe the influence of PLTP overexpression on total Tau protein and its pTau protein; western blot was used to examine the expression of total Tau protein and pTau protein of cerebral cortex and hippocampus at the four phosphorylation sites of pSer199, pSer214, pThr231 and pSer 404.

Furthermore, the data of the determination method of the brain tissue specificity PLTP overexpression model are counted by SPSS16.0 software, a one-way analysis of variance ANOVO is adopted for comparison among multiple groups of samples, and the statistical difference exists when P is less than 0.05.

By combining all the technical schemes, the invention has the advantages and positive effects that: the invention takes a 3 × Tg-AD (namely an APPSwe/PS1dE91/TauP301L triple transgenic) mouse as an AD model, constructs a brain tissue specific PLTP overexpression model by adenovirus-mediated PLTP gene lateral intracerebroventricular transfection, and discusses the prevention and treatment effect and possible mechanism of the PLTP overexpression on AD by learning memory capacity, senile plaques, A beta-related proteins, total Tau proteins, pTau proteins and GSK-3 beta pathway-related proteins through the detection of technologies and methods such as water maze, shuttle passive avoidance experiments, pathological staining, western blot and the like, so as to provide important basis for searching new targets and new ideas of AD treatment through PLTP.

The PLTP overexpression of the invention can improve the learning and memory ability of a 3 × Tg-AD mouse; the improvement of learning and memory ability of 3 × Tg-AD mice by PLTP overexpression is probably related to the reduction of A beta generation and Tau protein phosphorylation by promoting GSK-3 beta inactivation. The invention shows that PLTP high expression can obviously improve the learning ability of AD mice, the mechanism of the PLTP high expression can regulate and control GSK3B expression, further the formation of A beta and phosphorylation tau is influenced, further the anti-AD effect is generated, the invention is expected to become a new target point for AD treatment, and the invention can become a new method through virus-mediated PLTP gene high expression.

Drawings

FIG. 1 is a flow chart of a method for constructing a brain tissue specific PLTP overexpression model according to an embodiment of the present invention.

FIG. 2 is a flowchart of a method for determining a brain tissue-specific PLTP overexpression model according to an embodiment of the present invention.

FIG. 3 is a graph showing the expression of PLTP in the cerebral cortex and hippocampus of each group of mice (n 4, # P <0.05, # P <0.01vs. WT; # P <0.05, # P <0.01vs.3 × Tg-AD) according to the example of the present invention;

in the figure: a: expression of the PLTP protein bands in the hippocampus and cortex of model and 3 × Tg-AD mice; and B: expression of PLTP in hippocampus and cortex of model and 3 × Tg-AD mice.

FIG. 4 is a graph showing that overexpression of PLTP according to the present invention can improve learning and memory ability of 3 × Tg-AD mice (n 12, # P <0.05, # P <0.01vs. WT; # P <0.05, # P <0.01vs.3 × Tg-AD);

in the figure: a: the water maze positioning navigation experiment mouse escapes from the incubation period; b: positioning the running track of a sailing experimental mouse; c: the water maze space exploration experiment shows that the number of times of passing through the platform is 60 seconds and the latency period of the mouse entering the area where the platform is located; d: shuttling the latency period for passively avoiding the experimental mice to enter the dark box and the residence time in the dark box.

Detailed Description

In order to make the objects, technical solutions and advantages of the present invention more apparent, the present invention is further described in detail with reference to the following embodiments. It should be understood that the specific embodiments described herein are merely illustrative of the invention and are not intended to limit the invention.

Aiming at the problems in the prior art, the invention provides a method for constructing a brain tissue specific PLTP overexpression model and a method for measuring the brain tissue specific PLTP overexpression model, and the invention is described in detail with reference to the attached drawings.

As shown in fig. 1, the method for constructing a brain tissue specific PLTP overexpression model provided by the embodiment of the present invention includes the following steps:

s101: 3 × Tg-AD mice were used as AD model, 24 male mice 3 × Tg-AD at 10 months of age were randomly divided into model group (12), experimental group (12), and male C57BL/6J (Wild Type, WT) having the same genetic background at the same month of age were used as control group (12).

S102: the AD model is injected with adeno-associated virus (AAV-PLTP-EGFP) carrying PLTP gene enhanced green fluorescent protein reporter gene to induce the high expression of PLTP.

S103: both the control group and the model group were injected with adeno-associated virus (AAV-EGFP) carrying no PLTP gene and only the reporter gene of enhanced green fluorescent protein.

As shown in fig. 2, the method for determining a brain tissue specific PLTP overexpression model provided in the embodiment of the present invention includes the following steps:

s201: a brain tissue-specific PLTP overexpression model was constructed using a 3 × Tg-AD mouse as an AD model.

S202: the effect of PLTP overexpression on learning and memory ability of 3 × Tg-AD mice was observed.

S203: pathology observations the protective effect of PLTP overexpression in 3 × Tg-AD mice.

S204: the effect of PLTP overexpression on Α β and its production-related proteins was observed.

S205: the effect of PLTP overexpression on total Tau protein and its pTau protein was observed.

S206: observing the effect of PLTP overexpression on GSK-3 beta and GSK-3 beta (pSer 9); the protein expression levels of GSK-3. beta. and GSK-3. beta. (pSer9) were determined using western blots.

The technical solution of the present invention is further described with reference to the following specific examples.

Method and device

1. Constructing a brain tissue specificity PLTP overexpression model by taking a 3 × Tg-AD mouse as an AD model; 24 male mice 3 × Tg-AD at 10 months of age were randomly divided into a model group (12) and an experimental group (12), and male C57BL/6J (Wild Type, WT) having the same genetic background at the same month was used as a control group (12). Adeno-associated virus (AAV-PLTP-EGFP) carrying PLTP gene-enhanced green fluorescent protein reporter gene was injected into the lateral ventricle (0.6 mm posterior from bregma and 1.2mm lateral to the sagittal suture) to induce high expression of PLTP. Both the control group and the model group were injected with adeno-associated virus (AAV-EGFP) carrying no PLTP gene and only the reporter gene of enhanced green fluorescent protein.

2. Observing the influence of the PLTP overexpression on the learning and memory capacity of 3 × Tg-AD mice; after injecting AAV-PLTP-EGFP virus into lateral ventricle of mouse for 2 weeks, the learning and memory ability of mouse is tested by water maze experiment and shuttle passive avoidance experiment. The water maze experiment is divided into a positioning navigation experiment and a space exploration experiment, and the cognitive function of the mouse is evaluated by taking the latency of searching the platform and the frequency of entering the platform as indexes. The shuttle passive avoidance experiment is carried out in a light and dark shuttle box, and the learning and memory ability of the mouse is evaluated by taking the latency of the mouse entering the dark box and the residence time of the mouse in the dark box as indexes.

3. Pathology observation of the protective effect of PLTP overexpression on 3 × Tg-AD mice, detection of pathological lesions in each group by HE staining and Nie's staining, A β₁42 immunohistochemical staining to observe changes in Senile Plaques (SP) and by Bielschowsky silver staining to observe changes in neurofibrillary tangles (NFT) in each group.

4. Observing the influence of PLTP overexpression on A β and its related protein production, killing mouse after behavioral experiment, separating cerebral cortex and hippocampus of mouse, preparing its tissue homogenate, detecting the expression level of APP, PS1 and BACE1 related proteins produced by A β by western blot technique, and detecting A β by ELISA method₁-40 and A β₁42 levels.

5. Observing the influence of PLTP overexpression on total Tau protein and pTau protein thereof; western blot was used to examine the expression of total Tau protein and pTau protein of cerebral cortex and hippocampus at the four phosphorylation sites of pSer199, pSer214, pThr231 and pSer 404.

6. Observing the effect of PLTP overexpression on GSK-3 beta and GSK-3 beta (pSer 9); the protein expression levels of GSK-3. beta. and GSK-3. beta. (pSer9) were determined using western blots.

7. The experimental data were statistically analyzed using SPSS16.0 software, and the comparison between the multiple groups of samples was performed using one-way analysis of variance (ANOVO), with statistical differences at P < 0.05.

Second, result in

1. The learning and memory ability of 3 × Tg-AD mice can be improved by the overexpression of PLTP; the water maze results show: in a positioning navigation experiment and a space exploration experiment, compared with a WT mouse, a 3 multiplied by Tg-AD mouse has obviously prolonged escape latency, the frequency of entering a region where a platform is located in the exploration experiment is obviously reduced, and the latency of entering the region where the platform is located is obviously increased; and the escape latency of the PLTP high-expression 3 x Tg-AD mouse is obviously shortened, the times of entering the region of the platform in the exploration experiment are obviously increased, and the latency of entering the region of the platform is obviously shortened. The differences are statistically significant. The shuttle passive avoidance experiment results show that: compared with WT mice, the latency period of the 3 × Tg-AD mice entering the dark box is obviously shortened, and the residence time of the dark box is obviously prolonged; the incubation period of PLTP-highly expressed 3 × Tg-AD mice entering a dark box is obviously prolonged, the retention time is obviously shortened, and the difference has statistical significance. Thus, the PLTP overexpression can obviously improve the learning and memory ability of 3 × Tg-AD mice.

2. The PLTP overexpression can improve the pathological damage, senile plaque and neurofibrillary tangle formation of 3 × Tg-AD mice, and the HE staining and the Nie staining show that the 3 × Tg-AD mice have reduced cortical nerve cells, concentrated cell nucleus and apoptosis, A β₁42 immunohistochemical staining revealed distinct SP, whereas silver staining revealed distinct NFT; after over-expression of PLTP, cortical neuronal cells are increased, SP is reduced, and NFT is also obviously reduced.

3. The overexpression of PLTP can reduce the formation of A β, and ELISA results show that 3 × Tg-AD mice hippocampus andskin zone, A β_1-40And A β_1-42The protein expression is increased, A β is obtained after the overexpression of PLTP_1-40And A β_1-42Protein expression was reduced.

4. PLTP overexpression reduces the expression of proteins associated with a β production; western blot results show that: 3 × Tg-AD mice have increased expression of the related markers of A beta generation, namely APP, PS1 and BACE1 in hippocampal and cortical regions; after the PLTP is over-expressed, the expression of APP, PS1 and BACE1 is reduced.

5. The over-expression of PLTP can inhibit the expression of Tau protein and pTau protein thereof; western blot results show that: 3 × Tg-AD mouse hippocampal and cortical regions, total Tau and pTau protein thereof are all increased in the expression of pSer199, pSer214, pThr231 and pSer404 sites; the expression of total Tau and pTau protein thereof after the overexpression of PLTP is reduced at four sites of pSer199, pSer214, pThr231 and pSer 404.

6. The overexpression of PLTP can promote the phosphorylation of serine at the 9 th site of GSK-3 beta to inactivate the GSK-3 beta; western blot results show that: increased GSK-3 β expression in hippocampal and cortical regions of 3 × Tg-AD mice, with decreased expression of GSK3 β (pSer9) phosphorylated at the 9 th threonine residue; after overexpression of PLTP, GSK-3. beta. expression decreased, and GSK 3. beta. (pSer9) was increased by phosphorylation of threonine residue at position 9.

The PLTP overexpression of the invention can improve the learning and memory ability of a 3 × Tg-AD mouse; the improvement of learning and memory ability of 3 × Tg-AD mice by PLTP overexpression is probably related to the reduction of A beta generation and Tau protein phosphorylation by promoting GSK-3 beta inactivation.

The technical effects of the present invention will be described in detail below with reference to the accompanying drawings.

FIG. 3 shows the expression of PLTP in the cerebral cortex and hippocampus of each group of mice (n: 4, # P <0.05, # P <0.01vs. WT; # P <0.05, # P <0.01vs.3 × Tg-AD) according to the example of the present invention; in the figure: a: expression of the PLTP protein bands in the hippocampus and cortex of model and 3 × Tg-AD mice; and B: expression of PLTP in hippocampus and cortex of model and 3 × Tg-AD mice.

FIG. 4 shows that overexpression of PLTP provided by the examples of the present invention can improve learning and memory ability of 3 × Tg-AD mice (n is 12, # P <0.05, # P <0.01vs. WT; # P <0.05, # P <0.01vs.3 × Tg-AD); in the figure: a: the water maze positioning navigation experiment mouse escapes from the incubation period; b: positioning the running track of a sailing experimental mouse; c: the water maze space exploration experiment shows that the number of times of passing through the platform is 60 seconds and the latency period of the mouse entering the area where the platform is located; d: shuttling the latency period for passively avoiding the experimental mice to enter the dark box and the residence time in the dark box.

The above description is only for the purpose of illustrating the present invention and the appended claims are not to be construed as limiting the scope of the invention, which is intended to cover all modifications, equivalents and improvements that are within the spirit and scope of the invention as defined by the appended claims.