This protocol presents a modified mouse model of repetitive mild traumatic brain injury (rmTBI) induced via a closed-head injury (CHI) method. The approach features a thinned-skull window and fluid percussion to reduce the inflammation commonly caused by meninges exposure, along with improved reproducibility and accuracy in modeling rmTBI in rodents.
Mild traumatic brain injury is a clinically highly heterogeneous neurological disorder. Highly reproducible traumatic brain injury (TBI) animal models with well-defined pathologies are urgently needed for studying the mechanisms of neuropathology after mild TBI and testing therapeutics. Replicating the entire sequelae of TBI in animal models has proven to be a challenge. Therefore, the availability of multiple animal models of TBI is necessary to account for the diverse aspects and severities seen in TBI patients. CHI is one of the most common methods for fabricating rodent models of rmTBI. However, this method is susceptible to many factors, including the impact method used, the thickness and shape of the skull bone, animal apnea, and the type of head support and immobilization utilized. The aim of this protocol is to demonstrate a combination of the thinned-skull window and fluid percussion injury (FPI) methods to produce a precise mouse model of CHI-associated rmTBI. The primary objective of this protocol is to minimize factors that could impact the accuracy and consistency of CHI and FPI modeling, including skull bone thickness, shape, and head support. By utilizing a thinned-skull window method, potential inflammation due to craniotomy and FPI is minimized, resulting in an improved mouse model that replicates the clinical features observed in patients with mild TBI. Results from behavior and histological analysis using hematoxylin and eosin (HE) staining suggest that rmTBI can lead to a cumulative injury that produces changes in both behavior and gross morphology of the brain. Overall, the modified CHI-associated rmTBI presents a useful tool for researchers to explore the underlying mechanisms that contribute to focal and diffuse pathophysiological changes in rmTBI.
Mild TBI, including concussion and sub-concussion, account for the majority of all TBI cases (>80% of all TBI)1. Mild TBI commonly results from falls, traffic accidents, acts of violence, contact sports (e.g., football, boxing, hockey), and military combat2,3. Mild TBI can lead to neurobiological events that affect neurobehavioral functions throughout the patient's lifetime and increase the risk of neurodegenerative diseases4,5,6. Animal models provide an efficient and controlled means to study mild TBI, with the hope of further enhancing the diagnosis and treatment of mild TBI. Various models for mild TBI have been developed, such as the controlled cortical impact (CCI), weight drop (WD), fluid percussion injury (FPI), and blast-TBI models7,8. No single experimental model can mimic the entire complexity of TBI-induced pathology9,10. The heterogeneity of these models is advantageous for addressing the diverse features associated with mild TBI patients and investigating the corresponding cellular and molecular mechanisms. However, each animal model of TBI has its limitations3, limiting our current knowledge concerning animal mild TBI and their clinical relevance.
The WD and CCI models are utilized to replicate clinical conditions such as cerebral tissue loss, acute subdural hematoma, axonal injury, brain concussion, blood-brain barrier dysfunction, and even coma following TBI3,11,12. The WD model involves inducing brain damage by striking either the dura mater or skull with freely falling weights. The impact of a weighted object upon an intact skull can replicate mixed focal/diffuse injuries; however, this method is associated with poor accuracy and repeatability of the injury site, rebound injury, and a higher mortality rate due to skull fractures3,11,12. The CCI model involves applying air-driven metal to impact the exposed dura mater directly. Compared to the WD model, the CCI model is more accurate and reproducible, but it does not produce diffuse injury due to the small diameter of the impacting tip11. During FPI modelling, the brain tissue is briefly displaced and deformed by percussion. FPI can induce mixed focal/diffuse injury and replicate intracranial hemorrhage, brain swelling and progressive gray matter damage after TBI. However, FPI has a high mortality rate due to brainstem damage and prolonged apnea3,12. The craniotomy involved in conventional WD, CCI, and FPI models can lead to cortical contusion, hemorrhagic lesions, the damage of the blood-brain barrier, immune cell infiltration, glial cell activation, prolonged modeling time, and possible fatal outcomes3,12.
Mild TBI is characterized by a GCS (Glasgow coma scale, GCS) score within the range of 13 to 152. Mild TBI can be either focal or diffuse and is associated with both acute injuries, such as breakdown of cellular homeostasis, excitotoxicity, glucose depletion, mitochondrial dysfunction, blood flow disturbance, and axonal damage, as well as subacute injuries, including axonal damage, neuroinflammation, and gliosis2,3. Despite significant progress in delineating the intricate pathophysiology of TBI, the underlying mechanisms of mild TBI/rmTBI remain elusive and require further investigation9. Given that CHI is the most common type of TBI12, this protocol presents a novel approach to creating a more precisely controlled mouse model of rmTBI using a modified FPI device to perform impact in a thinned-skull window13. By avoiding craniotomy-induced injuries, variable skull thickness and shape-induced inaccuracies, and rebound injury, this approach aims to overcome the main disadvantages associated with the WD, CCI, and FPI models. Applying FPI impact on the thinned-skull window is convenient for evaluating cerebral vessel damage following rmTBI and helps minimize high mortality rates in some models, resulting in a closer resemblance to the clinical features of TBI patients.
All procedures involved in this protocol were performed under the Institutional Animal Care and Use Committee approval (Zhejiang Normal University, Permit Number, dw2019005) and in compliance with the ARRIVE and the NIH Guide for the Care and Use of Laboratory Animals. Technical specifications can be found in the Table of Materials.
1. Animal handling procedure
2. Preparation of TBI device
3. Thinned-skull preparation
NOTE: The animal surgery and thinned-skull preparation should not be performed in view of other mice. The thinned-skull window is useful for evaluating cerebral vessel damage following an FPI procedure.
4. CHI associated rmTBI modeling procedure
5. Morris water maze (MWM) test
NOTE: The MWM (see Table of Materials) is a widely recognized method for evaluating spatial learning and memory deficits in mice following TBI.
The protocol described in this study outlines a method for inducing rmTBI through a thinned-skull window, which offers a solution to the brain injury caused by craniotomy preparation during conventional percussion TBI modeling. By utilizing this modified fluid percussion procedure with the modified device, improved precision and reproducibility of FPI impact were achieved13. The modified impactor has the versatility to be used for both CHI and FPI modeling, with or without a skull craniotomy. Furthermore, the severity of the injury is modulated by adjusting injury parameters, such as the falling angle of the impact pendulum, or by adding additional closed-cell ethylene-vinyl acetate foam pads of varying hardness to the end plate of the piston pole.
The modified rmTBI model provides significant advantages, such as producing focal and diffuse pathology without exposing the cortical dural, which minimizes inflammation from meningeal exposure and/or direct FPI on parenchyma. Moreover, this model reduces variations in skull bone thickness and shape to produce reliable injury outcomes. Therefore, the modified rmTBI model is effective and reliable in simulating clinically relevant post-concussive symptoms (PCS)-related neuropathological and behavioral deficits across different injury degrees. Particularly, this model is useful for investigating TBI pathological mechanisms that rely on animal TBI models' accuracy and reproducibility, especially for investigating mild TBI-related mechanisms.
The frontal lateral branch of the mouse middle cerebral artery and caudal rhinal vein19, situated beneath the thinned-skull, allowed for clear visualization under the camera. Following two rmTBI percussions, each at a pressure of approximately 2.0 atm, all mice exhibited subdural hematomas at 0 DPI. Although the integrity of the thinned-skull did not appear to be compromised; however, a reduction in the number of microvessels was observed alongside changes in microvasculature morphology (Figure 2H), as previously reported15. By 2 DPI, the hematomas largely resolved. Mortality primarily results from impact while the mouse is under deep anesthesia, which may significantly prolong apnea. Regularly assessing the depth of anesthesia before impact through the palpebral and paw withdrawal reflexes can substantially reduce mortality. Additional factors that can impact mortality rates after fluid percussion include mouse strain, skull hardness, sex, and age. In a previous study using the same rmTBI protocol, one C57BL/6J mouse had died15. In this protocol, only male ICR mice were utilized to introduce the whole procedures.
Both human and animal studies have shown that even repetitive subconcussive head impacts can cause widespread microstructural white matter injuries20,21,22, which are associated with worse cognitive performance21,22. At 7-12 DPI, rmTBI can produce impairments in spatial learning and memory, which were examined using the MWM paradigm. Figure 4 illustrates the results obtained from this assessment.
Analysis of the last acquisition trial in the MWM demonstrated a significant increase (p< 0.05) in the latency by rmTBI mice to reach the submerged platform, compared to the control group. In the probe trial, the analysis of the percentage of time spent in the original platform quadrant demonstrated a significant reduction (p<0.01) in the rmTBI group relative to the control group, indicating a decline in spatial reference learning and memory capabilities in mice with rmTBI.
The method described here was utilized in an earlier publication15 using the C57BL/6J mice. Apart from the MWM three additional analyses were conducted as described below.
The OFT was utilized to assess locomotion and exploration capabilities by measuring the mean travel speed, total distance traveled, and percentage of distance traveled in the center zones. Conduct an Open-field test (OFT) at 6 DPI to evaluate locomotion, exploration, and anxiety in mice. The test device measuring 40 x 40 x 40 cm, which was divided into 16 zones (each measuring 18 x 18 cm). The mouse was placed in the center of the device and allowed to freely explore for 5 min. Recording the distance traveled in the center 4 zones, total distance traveled, mean moving speed, and time spent in the border zones was done. Anxiety levels were evaluated based on the percentage of distance traveled in the central zones and the time spent by rodents in the bordering zones during a 5 min observation period. At 6 DPI, rmTBI may not have a significant impact on the mice's general locomotive abilities, it can induce significant anxiety and alter exploratory behavior, as shown in Figure 415. Moreover, the modified rmTBI model induces diffuse axonal injuries, which can be evaluated through additional behavioral tests, such as the cognitive ability test described in this protocol.
RmTBI has been shown to impair spatial working and reference memory in mice, as illustrated in Figure 515. These cognitive functions were assessed using the Y-maze test. The test was performed at 8 DPI to measure short-term working memory deficits in mice. For spontaneous alternation behavior: an acrylic Y-maze device (20 cm high, 50 cm long, and 10 cm in width at the bottom) was used. After placing the mouse in the center of the device and allowing it to explore for 8 min, the arm entries were recorded. Spontaneous alternation behavior is defined as the successive entry of the mouse into the three arms on triplet sets. Calculate the spontaneous alternation rate (%) as (successive triplet sets / total number of arm entries minus 2) x 100. For spatial reference memory, during the 8 min training, randomly close off one arm of the Y-maze device. After 1 h after the initial exposure, the mouse is reintroduced into the maze with all three arms open and allow it to explore freely for 3 min. The time spent exploring the novel arm versus the other two arms is recorded. Calculate the preference index as time spent in the novel arm versus time spent in all three arms.
Furthermore, we suggest evaluating gross structural lesions in the brain using simple HE staining (Figure 6)15 upon completing all behavioral tests. Use cortical region coronally sectioned from 1 mm anterior to the lesion site to the posterior margin of the lesion, and the hippocampal region coronally sectioned at the typical crescent-shaped zone (Bregma: -1.7 to -2.2 mm). Counting neurons in each slide from six randomized fields using an ocular grid (magnification 400x) and averaging the neuronal number provided the numeral density per visual field (numeral density). The brain regions affected by rmTBI were found to exhibit varying degrees of neuron injuries15. Specifically, the motor cortex demonstrated a more potent and varied extent of such injuries than the hippocampus. HE staining showed a considerable shift towards pyknotic morphology from normal neurons (Figure 6A,B,E,F). Furthermore, the extracellular matrix was observed to become loosened specifically in the region of the lesion (Figure 6F). Besides the observed matrix-loosened areas, rmTBI mice also showed a significant increase in hyperchromic staining, seen as a darker red color, in a significant number of subgranular neurons in the dentate gyrus and some cortical and CA1 neurons. Intriguingly, these staining patterns did not present any accompanying signs of cytoplasmic shrinkage or pyknotic nucleus (Figure 6C,D,G,H,K)15. The behavioral (except for WMM test) and HE staining methods mentioned above were detailed in a recent publication, which introduced the modified rmTBI model15.
Figure 1: The modified FPI device and the software screenshot. (A) The modified FPI device. (B) The screenshot displays the FPI pressure waveform and the automatic measurement and exportation of real-time impact pressure parameters such as rise time, fall time, and half width duration. Please click here to view a larger version of this figure.
Figure 2: The modified mouse model of rmTBI in ICR mice. (A) A midline incision is made to expose the surgical area. (B) A thinned-skull window was fabricated on the motor cortex. The clarity of the exposed cortical micro-vessels is used to determine the thickness of the skull. (C) The thickness of the skull can also be verified by gently probing the thinned-skull with the flattened tip of a fine syringe needle and assessing its softness. (D) The female Luer Lock was glued to the thinned-skull window. (E) The attached female Luer Lock was secured by applying the dental cement. (F) The depth of the anesthesia was monitored by checking the palpebral and paw withdrawal reflexes. (G) The FPI impact was delivered after the return of a withdrawal reflex to a paw pinch. (H) Post-rmTBI image of thinned-skull window at 0 DPI. (I) The scalp was sutured with tissue adhesive. Please click here to view a larger version of this figure.
Figure 3: The effects of rmTBI on spatial reference learning and memory in ICR mice. (A) The navigation trace for mice during the last acquisition trial recorded at 11 DPI, (B) the spatial probe route in the probe trial recorded at 12 DPI, and (C) the escape time it took mice to locate the platform during the last acquisition trial. The results revealed that the rmTBI group took significantly longer to reach the hidden platform than the control group (p<0.05). (D) The percentage of time mice spent in the original platform quadrant relative to the total navigation time during the probe trial was significantly lower in the rmTBI group than in the control group (p<0.01). n=8. *p<0.05, **p<0.01 vs. control by unpaired t-test. Please click here to view a larger version of this figure.
Figure 4: The effects of rmTBI on locomotion, exploration, and anxiety in C57BL/6J mice. (A) Representative traces of control and rmTBI mice movement during 5 min OFT. (B-E) Summarized data show distance traveled in the center zones, total traveled distance, mean travel speed and time spent in the periphery zones, respectively. Control, n=13; rmTBI, n =12. ***p<. 01 vs. control by unpaired t-test. This figure has been modified from15. Please click here to view a larger version of this figure.
Figure 5: The effects of rmTBI on spatial working and reference memory in C57BL/6J mice. (A, B) Representative traces of control and rmTBI mice movement during the spatial working and reference memory assessments in Y maze. The Y maze spontaneous alternation test is a commonly used method for assessing short-term memory in rodent models15. (C) Summary of spontaneous alternation rates of control and rmTBI mice during spatial working assessment. Rodents usually prefer exploring a new arm of the maze rather than revisiting one they have already explored. A preference index is calculated based on the time rodent spend in the novel arm compared to the time spent in all three arms, and this index is then analyzed. (D) Summary of preference index of control and rmTBI mice during the spatial working assessment. Control, n=13; rmTBI, n=12. ***p<. 01 vs. control by unpaired t-test. This figure has been modified from15. Please click here to view a larger version of this figure.
Figure 6: Comparison of HE staining of the ipsilateral injured motor cortex and hippocampal dentate gyrus subregion between control and rmTBI in C57BL/6J mice. (A, B) Normal motor cortex; and (C, D) the hippocampal region of control mice in different magnifications. (E, F) Injured motor cortex and (G, H) hippocampal regions of rmTBI mice. Hyperchromic neurons in the cortex and CA1 may have been slightly affected by either surgery preparation or sustained rmTBI; however, hypochromic (possibly intermediate injured) and pyknotic (apoptotic neurons) neurons were observed in the motor cortex of rmTBI mice when compared to normal neurons in the control mice. These neuronal apoptosis features included neuronal cytoplasmic and nucleus shrinkage, accompanied by apparent vacuolation. Notably, the demarcation white line in (E) represents the boundary between the lesioned and the surrounding tissue. Additionally, the hyperchromic neurons in the DG subregion (H) possibly referred to newly generated immature and mature granular neurons. The bar graphs below show the distribution of normal and rmTBI-affected neurons in the (I) motor cortex and hippocampal (J) CA1 and (K) DG subregions. Control, n=13; rmTBI, n=12, ***p<. 001 vs. control by unpaired t-test. This figure has been modified from15. Please click here to view a larger version of this figure.
TBI refers to two primary types, closed and penetrating, with the latter characterized by a disruption of the skull and dura mater. Clinical data suggest that CHIs are more prevalent than penetrating injuries1,2. After a single mild TBI, most patients experience PCS symptoms that typically resolve in a short period of time, and there is controversy regarding the proportion of patients whose PCS develop into long-term sequelae23,24. Consequently, researchers have shifted their focus to repetitive CHI models to better understand the cumulative effects of multiple concussions25, which commonly occur in falls, traffic accidents, and contact sports. These repeated impacts may lead to more severe and long-term effects26,27. By using repetitive CHI models, researchers can explore the potential additive or synergistic effects of multiple concussions and gain a better understanding of the underlying mechanisms that contribute to PCS. Such models may facilitate the development of targeted therapeutic interventions to mitigate the long-term consequences of repeated head impacts.
Although some CHI models attempt to simulate both focal single and rmTBI by incorporating both linear and rotational forces, these models can result in rebound injury and inaccuracies in injury severity due to factors such as skull fracture, skull morphology and thickness, extended animal apnea10, and variability in mechanical input parameters, particularly when rotational head movement is incorporated9. Piston-controlled impact and weight-drop methods are commonly used to induce rmTBI in animal models of CHI25. Piston-controlled impact allows for precise and adjustable setting of impact parameters through the use of electromagnetic or pneumatic driven impactor devices, thereby enabling high impact reproducibility. However, the use of piston-controlled impact, whether onto the exposed cortex as in CCI or onto the closed-skull, still requires stringent immobilization of the animal's head in a stereotaxic frame during impact. Conversely, weight-drop methods require simple and cost-effective materials that are easy to set up, but the trade-off is a somewhat high variability in the severity of the injury25.
The FPI model typically induces mixed focal and diffuse injuries, allowing for fabrication of TBI of varying severities. Despite its advantages, the FPI model also has potential limitations. Like the CCI model, FPI still requires craniotomy, a surgical procedure that may induce inflammation in the brain tissue17. Moreover, even mild FPI frequently penetrates the dura at varying depths, which can introduce confounds in the interpretation of data. Thus, CCI and FPI models have limitations in replicating the clinical features observed in mild TBI patients9. Hence, we present a protocol that combines the thinned-skull window and FPI methods, which can be utilized to produce a more precise mouse model of CHI associated rmTBI. The objective of this protocol is to closely mirror the clinical features of mild TBI patients. A highly reproducible model would be an invaluable tool for investigating the mechanisms underlying the pathophysiology of mild TBI and evaluating potential therapeutic interventions.
Our research findings on rmTBI align with previous publications that utilized thinned-skull windows for mild TBI investigations28,29. For example, Ren et al. created a thinned-skull window with a thickness of approximately 30 µm in the left parietal association cortex, inducing mild TBI by gently pressing the window using a blunt end with a diameter of 1 mm from a surgical stereotaxic instrument29. Their study showed a notable expansion of cell death and reactive oxidative species (ROS) expression in the injured cortex29. To investigate rmTBI, Nguyen et al. applied three CCIs with a modified impactor tip (3-mm-diameter round silicone tip of 1.5 mm thickness) on a mouse thinned-skull window (20-40 µm in thickness) in the parietal association cortex28. To protect and maintain the transparency of the thinned-skull area for long-term imaging, they covered the thinned-skull window with a thin layer of cyanoacrylate glue. The three CCIs were performed once a week for 3 weeks, with impact parameters of 4 m/s in speed and 2 mm in depth. As a result of the three CCIs, the mice showed evident astrogliosis and microglial activation28. Given that the usage of thinned-skull window as a model for mild TBI/rmTBI is relatively recent, further research is required to examine the relationship between injury severity/progression and different impact techniques. For example, in a previous study, we were able to observe obvious changes in cell morphology after two FPIs that were administered with a 2 day interval15. Meanwhile, in other studies, a single gentle compression to the thinned-skull window induced mild TBI with evident cell death and reactive oxidative species expression29, and three weekly-CCIs resulted in robust astrogliosis and microglial activation28.
Several steps should be cautiously proceeded to fabricate a consistent injury model using the described method. During the thinned-skull window operation, based on different target area (e.g., we focused on motor cortex), the mouse head should be fixed in a stereotactic frame at horizonal level or at a slight lateral angle toward opposite side of the thinned-skull window in this protocol. This specific positioning can facilitate the creation of the thinned-skull window in the area corresponding to the motor cortex. Accurately placing the ear bars is one of the most challenging aspects of this procedure, and it can take time and practice to master. Before attempting the thinned-skull window operation or inducing CHI, it is essential to ensure that the skull is level. If the skull is not positioned correctly, the head should be adjusted accordingly. Due to the uneven shape and thickness of the skull bone, skull growth is variable even within a specific bone30, it is critical to adjust the head positioning before undertaking the thinned-skull window procedure or CHI. Failure to do so increases the risk of skull fractures, which can significantly impact the CHI accuracy and reliability. For more comprehensive guidance on the thinned-skull window procedure, refer to the protocol outlined by Guang et al.14.
The choice of TBI modeling area varies among researchers based on their research focus. Given the significant variability in the actual location of the injury in CHI, despite most studies reporting the impact site to be centrally located between bregma and lambda, it is recommended to vary the impact location in future experimental studies, as noted in a review of CHI animal models25. To validate the modified CHI thinned-skull injury model, we recommend starting with the motor cortex, as outlined in this protocol. The rmTBI can cause focal motor cortex injuries, which can be easily evaluated using locomotor assessment approaches such as the OFT in this protocol. The incision made during this procedure requires time to heal, and this can potentially trigger a peripheral immune response, ultimately introducing variability into the experiment. To minimize the risk of inflammation, infection, and post-surgical pain and discomfort, we recommend applying a topical ointment containing a combination of erythromycin and sodium diclofenac to the wound. This approach has been shown to be effective in reducing inflammation and pain associated with surgical procedures in animals.
The thinned-skull-based fluid percussion protocol is a promising method for modeling rmTBI in rodents since it reduces the inflammation commonly caused by exposing the meninges to FPI. This technique, featured in the thinned-skull window, can effectively generate clinically relevant PCS at varying degrees, providing a potential alternative for researchers studying rmTBI. Moreover, the thinned-skull window facilitates the observation of Ca2+ homeostasis and neuronal hyperexcitability in the cortex in vivo15. Using this technique can improve our understanding of the underlying mechanisms of PCS progression in the short/moderate/long terms, thereby enhancing the ability to predict its development and develop more effective therapeutic treatments.
The authors have nothing to disclose.
This work was supported by the Key Social Development Foundation of Jinhua Municipality (No. 2020-3-071), Zhejiang College Student Innovation and Entrepreneurship Training Program (No: S202310345087, S202310345088) and Zhejiang Provincial College Students' Science and Technology Innovation Activity Plan Project (2023R404044). The authors thank Miss Emma Ouyang (first-year student of Johns Hopkins University, Bachelor of Science, Baltimore, USA) for language editing the article.
75% ethanol | Shandong XieKang Medical Technology Co., Ltd. | 220502 | |
Buprenorphine hydrochloride | Tianjin Pharmaceutical Research Institute Pharmaceutical Co., Ltd | H12020272 | Solution, Analgesic |
Carprofen | Shanghai Guchen Biotechnology Co., Ltd | 53716-49-7 | Powder, Analgesic |
Chlorhexidine digluconate | Shanghai Macklin Biochemical Co.,Ltd. | 18472-51-0 | 19%-21% aqueous solution, Antimicrobial |
Dental cement and solvent kit | Shanghai New Century Dental Materials Co., Ltd. | 20220405, 3# | Powder reconsituted in matching solvent |
Dissecting microscope | Shenzhen RWD Life Science Inc. | 77019 | |
Erythromycin ointment | Wuhan Mayinglong Pharmaceutical Group Co.,Ltd. | 220412 | Antibiotic |
Fiber Optic Cold Light Source | Shenzhen RWD Life Science Inc. | F-150C | |
Flat-tipped micro-drill bit | Shenzhen RWD Life Science Inc. | HM31008 | 2 mm, steel |
FPI device software | Jiaxing Bocom Biotech Inc. | Biocom Animal Brain Impactor V1.0 | |
ICR mice | Jinhua Laboratory Animal Center | Stock#2023091 | 25 Male mice, 25-30g, 8 weeks old |
Isoflurane | Shandong Ante Animal Husbandry Technology Co., Ltd. | 2023090501 | |
Isothermal heating pad | Wenzhou Repshop Pet Products Co., Ltd. | ||
Luer Loc hup | Custom made using a 19G needle hub | ||
Micro hand-held skull drill | Shenzhen RWD Life Science Inc. | 78001 | Max: 38,000rpm |
Modified FPI device | Jiaxing Bocom Biotech Inc. | ||
Morris water maze | Shenzhen RWD Life Science Inc. | 63031 | Evaluate mouse spatial learning and memory abilities |
Open field | Shenzhen RWD Life Science Inc. | 63008 | Evaluate mouse locomoation and anxiety |
Ophthalmic lubricant | Suzhou Tianlong Pharmaceutical Co., Ltd. | SC230724B | |
Sodium diclofenac ointment | Wuhan Mayinglong Pharmaceutical Group Co.,Ltd. | 221207 | nonsteroidal anti-inflammatory drug |
Small animal anesthesia system-Enhanced | Shenzhen RWD Life Science Inc. | R530IP | |
Smart video-tracking system | Panlab Harvard Apparatus Inc., MA, USA | V3.0 | Animal tracking and analysis |
Stereotactic frame | Shenzhen RWD Life Science Inc. | 68043 | |
Vetbond Tissue Adhesive | 3M, St Paul, MN, USA | 202402AX | Suture the animal wound |
Y maze | Shenzhen RWD Life Science Inc. | 63005 | Evaluate mouse spatial working memory |