|Spring Scissors (Triangular)||S/S Str/5*0.1mm/8.5cm|
|Spring Scissors (Triangular)||S/S Cvd/5*0.1mm/8.5cmm|
|IRIS-Fine Scissors (Round Type)||S/S Str/10.5cm|
|IRIS-Fine Scissors (Round Type)||S/S Cvd/10.5cm|
|O’BRIEN Stitch Scissors||S/S Angled/9.5cm|
|Dressing Forceps w/o Serrations||45°Cvd, S/S, 10cm|
|ADSON 1×2 Teeth Tissue Forceps||1.5mm, 12cm|
|IRIS Dissecting Forceps||Str, 0.8mm Tips, 10cm|
|IRIS Dissecting Forceps Light||Cvd 0.8mm Tips, 10cm|
|Forceps w/5mm Platform||Str, 0.4mm Tips, 9cm|
|HEGAR Needle Holders with Scissors||Str, 12cm|
|STEVENS Hooks 1 Angled Tooth (5mm long)||12.5cm|
|Colibri Eye Specula||1.5cm spread, 4cm|
Ophthalmic surgery, also known as ocular surgery, is performed on the eye specifically upon the external surface of the cornea. A thorough and detailed ophthalmic examination provides a rapid and accurate diagnosis of many ophthalmic diseases. Research in vision and ophthalmology improves treatment and quality of life in humans as well as in animals. This improvement stems from advancement in diagnosis and treatment of human and animal diseases and disability. As vision research is aiming at revealing and understanding the morphology and physiology of complex and interconnected biological systems, research on living animals is essential to continue progress in many areas of clinical and basic ophthalmic research.
Earlier animal models of ophthalmic surgery included dogs and cats due to their large eye sizes. However, these models have their shortcomings which include the husbandry cost, handling difficulties and lack of availability of transgenic animals. These disadvantages led to the popularity of rodents as the new model organisms in ophthalmic research. Among rats and mice, the latter has seen more popularity due to the availability of a range of genetically modified mice and the existence of an extensive array of reagents that can be used to further define responses in this species. Rodents, as opposed to the previously used animal models, have shorter breeding cycles and faster regeneration. These qualities combined with their lower costs and smooth handling make them ideal for ophthalmic research.Before any surgical procedure, it is necessary to ensure that the apparatus and the equipment used are thoroughly cleaned and sterilized. The instruments can be sterilized by using heat (e.g., autoclave or bead sterilizer), gas (ethylene oxide), or chemical methods (limited to 2% glutaraldehyde). Also, the operation area should be cleaned and sterilized properly.
Record the subject’s identification details such as strain and gender, most importantly note the weight of the subject. Also, make a physical assessment of the subject for its health status and activeness. Ensure that the subject has been appropriately acclimated to the facility. Acclimation process can last from a few days to a couple of weeks.
Anesthesia is induced in the subject via inhalant agents with the help of anesthetic systems that use a face mask or an anesthetic chamber. The dose of the anesthetic agent and the duration of induction are dependent on the weight of the subject among other factors. Once the anesthesia is induced, the depth of anesthesia can be assessed using the toe pinch test. Additionally, physiological parameters can be monitored throughout the procedures to ensure that the anesthesia is effective.
- Measure the thickness of the Inner Plexiform (IPL), Inner Nuclear (INL), Outer Plexiform (OPL), and Outer Nuclear (ONL) layers, and the total thickness by taking the mean value of five different measurements at three points per section.
In Vivo Ocular Enucleation Protocol (Aerts et al., 2014)
- Anesthetize the animal by giving an intraperitoneal injection of a mixture of ketamine hydrochloride (75 mg/ml) and medetomidine hydrochloride (1 mg/kg) in saline.
- Assess the depth of the anesthesia by toe pinching.
- Disinfect the eyelids by applying 70% ethanol using a cotton tip.
- Place the animal on a flat, dry, and smooth surface.
- Sterilize the forceps with the help of a curved, serrated tip (preferred tip size: 0.5 x 0.4 mm).
- Press the corner of the eye (canthus) gently with the help of forceps until the eyeball is displaced out from the socket and the optic nerve is accessible.
- Approach the eye from behind with the forceps. Push and grasp the optic nerve firmly, with the beginning of the curve and not the very tip of the forceps. The grip will help to lift the globe from the socket and to clamp the optic nerve completely.
- Move the forceps with least resistance in a circular motion and the mouse swings along the surface according to the direction of the hand movement.
- Perform this action with gradually increasing speed until the optic nerve is constricted in two (usually between 7 to 15 circular movements, approximately a half to one full turn per second). The detached eyeball is removed.
Ex-orbital and Intra-orbital Lacrimal Gland Excision Protocol (Shinomiya et al., 2018)
- Anesthetize the animals by intraperitoneal administration of ketamine hydrochloride 100 mg/kg and xylazine hydrochloride 10 mg/kg.
- Carefully make an incision close to the temporal lid margin to expose the ILG.
- Excise the ILG from the orbit using ophthalmic forceps with the aid of a stereoscopic microscope.
- Make an additional incision anterior to the ear, and then expose and excise the ELG.
- Suture the surgical incisions using 6-0 ophthalmic nylon thread and apply the ointment containing Ofloxacin.
Murine Corneal Transplantation Protocol (Yin et al., 2014)
- Induce general anesthesia in the animal by IP injections of ketamine (86.98 mg/kg) and xylazine (13.04 mg/kg).
- Apply Puralube ointment on the eye not undergoing surgery to prevent dryness.
Obtaining the donor corneal button
- After achieving full anesthesia, obtain adequate mydriasis by administering 1% tropicamide and 2.5% phenylephrine hydrochloride eye drops.
- Place the head of the donor animal horizontally on a board placed on a robust, movable support. With a strip of tape, fix the head of the animal across the neck to ensure the horizontal eye position throughout the entire procedure.
- With the help of a 2 mm diameter trephine, whose tip is dyed with methyl blue, sketch the central cornea graft site.
- Using a sharp blade, infiltrate the cornea and inject sodium hyaluronate into the anterior chamber to deepen it reducing the chance of damage to the donor endothelium and the underlying lens.
- Excise the donor graft with vannas scissors and place into a dish containing Hanks’ balanced salt solution until use.
- After the donor graft has been the removed, euthanize the donor animal via CO2 inhalation.
Graft bed preparation
- Repeat the first two steps mentioned above for the recipient animal.
- With the help of a 1.5 mm diameter trephine, outline the recipient graft site.
- Using a sharp blade, infiltrate the cornea and inject sodium hyaluronate into the anterior chamber to deepen it to reduce the chance of damage to the underlying lens.
- Remove the outlined central corneal button from the recipient using vannas scissors and discard.
- Set the donor cornea over the graft bed in the recipient’s cornea. Make sure that adequate sodium hyaluronate is present under the donor cornea to protect the donor endothelial cells from damage by direct contact with the lens.
- Using super-fine tipped micro-forceps, place the first bite of 11-0 nylon suture into the donor side, through the donor with 90% depth of full thickness to recipient’s side, then tie off.
- Once the cornea is anchored in place, perform mid-cardinal interrupted sutures such that the cornea has 8 to 10 total sutures and the donor cornea is securely lined up with and attached to the recipient corneal graft bed.
Deepening the anterior chamber
- Penetrate the anterior chamber by injecting HBSS or air bubble into the anterior chamber and assess the strength and integrity of the corneal graft for leakage with a cellulose sponge gently.
- Anesthetize the animals as mentioned above and remove the lid suture after 48 hours or prescribed time.
- Anesthetize the animals on day 7 postoperatively. Carefully remove the sutures while securing the cornea. Return the animal to its cage after suture removal and consciousness regain.
Composite Orbital and Periorbital Allotransplantation Protocol (Zor & Karagoz, 2015)
- Anesthetize the animals by intraperitoneal injection of xylazine (2 % solution) and ketamine (30 mg/kg).
- Excise the sternocleidomastoid muscle via an anterior incision on the neck and then expose the external jugular vein and two main branches of the common carotid artery.
- Excise the anterior and posterior bellies of the digastric muscle, omohyoid muscle, and greater horn of the hyoid to get better exposure of the external carotid artery and its branches.
- Ligate and cut the internal carotid artery and all branches of the external carotid artery except the superficial temporal artery.
- Prepare the flap containing orbital tissues, external ear and a part of the facial skin.
- Cut the optic nerve at its most possible proximal end to the eyeball and include it in the flap.
- Raise the composite tissue flap based on the common carotid artery and external jugular vein.
- Expose and anastomose the external jugular vein and the common carotid artery via an anterior incision on the neck.
- Cut the great auricular nerve with fine dissection scissors, and use the proximal stump of the nerve for coaptation.
- Anastomose the vein of the flap to the external jugular vein of the recipient animal in end-to-end fashion using No. 10-0 interrupted monofilament nylon sutures.
- Anastomose the artery of the flap to the common carotid artery of the recipient animal in end-to-side fashion using the same suture material.
- Obtain the perfusion of the graft, and then coapt the optic nerve of the flap to the distal stump of the great auricular nerve of the recipient animal in end-to-end fashion with four epineural sutures.
- Finally, perform the complete tarsorrhaphy on the eye of the allograft using 8/0 monofilament nylon sutures.
The variable bypass vaporizers are the most commonly used vaporizes. Their working principle involves splitting the fresh gas flow and saturating a small portion completely with the volatile anesthetic before recombining into the main gas flow. This process is achieved by setting of the anesthetic concentration using the control dial and the pressurized chamber of the plenum vaporizers. These devices are also equipped with thermo-compensation capabilities for a steady vaporizer output.Preventive measures for post-operative pain in the subject can be done by the administration of opioids such as buprenorphine before incision. After the surgery, the subject must be kept warm in a recovery unit using hot water blankets, hot water bottle, heat pads and warm sterile saline before returning it to its home cage. Recovery from anesthesia should be monitored closely and respiratory support, if needed, should be provided. Analgesic should be maintained post-operatively for up to 48 hours in increments of 24 hours or as required. The subject can be returned to its home cage once it has recovered.
Check the wound redness, swelling or purulent discharge for at least 5 days. Also, monitor the body weights of the subjects daily. Rarely, postoperative prophylactic antibiotics can be administered to prevent infections. Euthanize the subject in case of an infection.Study of Retinal Ganglion Cell Survival in an Optic Nerve Crush Injury Murine Model
Zhongshu Tang et al. conducted a detailed study on retinal ganglion cell survival using an optic nerve crush injury murine model. In the experiment, axonal degeneration followed by the progressive death of retinal ganglion cells (RGCs) resulted after optic injury, consequently lead to an irreversible vision loss. Traumatic optic neuropathy and optic nerve degeneration in glaucoma are the examples of such diseases in humans. It is distinguished by regular transformations in the optic nerve head, progressive optic nerve degeneration, and loss of retinal ganglion cells.
The ophthalmic surgery kit is utilized to create the optic nerve crush (ONC) injury mouse model, which is an essential experimental disease model for traumatic optic neuropathy, and glaucoma. In this model, the crush injury to the optic nerve leads to progressive apoptosis of retinal ganglion cells. This disease model is widely used to investigate the general processes and mechanisms of neuronal death and survival, which is vital to the development of therapeutic measures.
Performing In Vivo Ocular Enucleation in the Mouse after Eye Opening
In the experiment, a more comfortable and straightforward technique for the removal of one or both eyes is designed and validated for mice older than 20 days. Summarily expressed, curved forceps were used to clamp the optic nerve behind the eye. Then circular movements were performed to limit the optic nerve, and the eyeball was removed. The strength of this technique is high reproducibility, minimal to no bleeding, rapid postoperative recovery and a very low learning threshold for the researcher.
Eye enucleation in rodents and many species are widely performed using different methods, which often involve the removal of the eyelids and cutting the optic nerve. These methods are more invasive and have a higher learning curve than the technique used in the experiment. Without removing or suturing the eyelids, the post-surgery recovery time is depreciated, resulting in higher animal welfare and more reproducible results. The in vivo enucleation technique employed in the research has been successfully applied with minor modifications in rats and appears useful to study the afferent visual pathway of rodents in general.
Development of a Dry Eye Mouse Model Produced by Ex-orbital and Intra-orbital Lacrimal Gland Excision
Katsuhiko Shinomiya et al. created a new dry eye model by exorbital and intraorbital lacrimal gland excision. The chronic dry eye is an increasingly prevalent condition worldwide, causing loss of vision and adversely affecting the quality of life. They have developed an improved surgical mouse model for the dry eye based on severe aqueous fluid deficiency, by excising both the exorbital and intraorbital lacrimal glands (ELG and ILG, respectively) of mice. After ELG plus ILG excision, dry eye symptoms were assessed using fluorescein infiltration observation, tear production measurement, and histological analysis of ocular surface. Tear production in the model mice was significantly diminished compared with the controls. Histological examination revealed significant severe inflammatory changes in the cornea, conjunctiva or meibomian glands of the model mice after surgery. The rodent ophthalmic model is useful for investigating both pathophysiologies as well as new therapies for the tear-volume-reduction type dry eye.
Evaluation of Ocular Ischemic Syndrome
The ocular ischemic model was designed to characterize the functional and morphologic changes caused by Bilateral Internal Carotid Artery Occlusion (BICAO). In the experiment, adult mice underwent BICAO or sham surgery. Variations in ocular blood flow and retinal circulation after surgery were investigated by MRA to verify the retinal blood flow occlusion. The images were taken to measure the thicknesses of the various retinal layers, and then the nucleus from the eyes was removed, and the enucleated eyes were embedded in paraffin for morphological and histological studies. The MRA images suggested that the ligation of both internal carotid arteries significantly diminished ocular blood flow and narrowed the blood vessels. Sham surgery or BICAO for seven days was evaluated by both ocular fundus photography and fluorescein angiography finding. The total retinal thickness and retinal ganglion cell density were reduced as compared with the sham group. However, no such variations were evident in the IPL layer in BICAO group, which was according to the results obtained from OCT images. The researchers successfully visualized the occlusion of blood flow after the BICAO by MRA, and angiography could also demonstrate that BICAO for 7 d was sufficient to maintain the retinal ischemia and induce the morphological changes. The protocol might be used as a mouse model for OIS in the future (Ling et al., 2017).
Designing Composite Orbital and Periorbital Allotransplantation Model
Vascularized composite allotransplantation has opened new avenues in reconstructive surgery and provided the researchers to reconstruct the defective tissue with the same tissue. The anatomic and histologic features of the eyeball are unique, and it is impossible to reconstruct the globe. The advancement in allotransplantation provided an option for the transplantation of eyeball. In the experiment, an orbital composite tissue allotransplantation model is designed. The results were encouraging and suggested that periorbital tissues together with the globe could be transplanted to another animal, even if they are not functional. However, a functional repair of the optic nerve might be possible in the future, given the significant advances in the field of neuro-ophthalmic, namely on the survival of the retinal ganglion cells and regeneration of the optic nerve. The allotransplantation model designed is providing essential hints about the issues that need to be studied before eye transplantation. Periorbital tissues with the globe can be transplanted from one individual to another, and the flap can survive, but the regeneration of the optic nerve regeneration and the survival of retinal ganglion cells are still the challenges that need to be overcome.
Evaluating Solid Organ Transplantation in Murine Corneal Transplantation Model
Several animal models exist for corneal transplantation and mice are the commonly used species. The strengths of using mice are the relative cost, the existence of various strains (genetically defined) that enable the researchers to study the immune responses, and the occurrence of an extensive array of reagents that can be used to define responses in this species further. The model created by ophthalmic surgery has defined factors in the cornea that are responsible for the relative immune privilege status of the ophthalmic tissues enabling corneal allografts to survive acute rejection in the absence of immunosuppressive therapy. The murine corneal transplantation model has also been used to define those factors that are most important in rejection of such allografts. Consequently, concerning mechanisms of both corneal allograft acceptance and rejection are understood studying murine models of corneal transplantation. The model allows the understudies to test various therapeutic strategies concerning eye diseases in an animal which have an immune system similar to that of humans. To that end, the existence of many reagents that react with murine factors as well as transgenic and gene-targeted mice permits evaluation of many more factors that would be the case with other species. This ability to evaluate numerous different factors, essential to both the success and failure of corneal allografts, is an added benefit of using the murine model as compared to other animal models in which surgery is more comfortable to perform due to the increased size of the eyes of the species.
Antifibrotic Drug Evaluation in Glaucoma Filtration Surgical Mouse Model
Glaucoma is an optic neuropathy, which leads to blindness if left untreated. The most common risk factor in glaucoma is elevated intraocular pressure (IOP), which can be counteracted surgically by filtration surgery. The postoperative subconjunctival scarring response, however, remains the primary obstacle to achieving long-term surgical success. Anti-tumor agents such as mitomycin C is widely used to avoid postoperative subconjunctival scarring. The model of glaucoma filtration surgery in the mouse has shown that the mouse model typically scarred within 14 d, but when augmented with mitomycin C, animals maintained lower IOP for a more extended period. The blebs following mitomycin C treatment resembled morphologically well-documented clinical observations confirming the validity and clinical relevance of this model. The anti-scarring action of mitomycin C is likely to be due to its effects on conjunctival fibroblast proliferation, apoptosis and collagen deposition and the suppression of inflammation. The data supported the suitability of the glaucoma filtration surgery mouse model for studying the wound healing response in glaucoma filtration surgery, and as a potentially useful tool for the in vivo evaluation of anti-fibrotic therapeutics in the eye (Seet et al., 2011).The eye is a delicate organ, and requires extreme care before, during, and after a surgical procedure. An expert surgeon should select the appropriate surgical procedure and perform effective eye care. Complete understanding of the eye functioning and ocular diseases is necessary to perform ophthalmological operations. The researcher needs to address three critical issues: First, ocular pain and blindness may endanger animal welfare. Second, several ocular diseases are vital signs of systemic disease with significant implications both for pets and laboratory animals. Third, eye diseases may complicate research efforts.
An appropriate strain and breed of the laboratory animal must be selected depending on the requirements of the investigation since the subject’s strain affects the ophthalmic manipulations. Other factors to be considered when selecting the subject are the age and the gender. Both these aspects influence the eye physiology and morphology. Prepare a separate area from the surgical area for pre-operative preparations such as fur removal or hair trimming from the surgical site. The separate preoperative area is vital to eliminate contamination of the operative area. Before beginning the surgical procedure, ensure that all the equipment and the instruments are thoroughly cleaned and sterilized. Make sure that the subject is adequately anesthetized before beginning surgery. During surgery take care not to damage the surrounding tissues and muscles. Prepare an appropriate post-operative recovery area for the subject. Home cages that are to be used after the subject has recovered from surgery should be clean to avoid infecting the surgery area.
Topical application of the drugs may cause systemic absorption more relative to the size of the animal. Systemic absorption of the drugs may interfere with both the treatment of ocular disease and potential side effects, as the drug could act through circulating blood levels as well as by direct ocular penetration. The orbital vascular plexus, present in rodents and lagomorphs, differs substantially between species and understanding its anatomy is essential in orbital surgery and enucleation. Also, when evaluating ocular findings in experimental species derived from laboratory strains, the prevalence of inherited disease must be seen as a background against which other ocular diseases are noted. Background disease prevalence is particularly crucial among inbred strains, in which recessive genes may occur in a given strain not being used to study that specific trait.
Also, look out for the opening of sutures and displacement of pins after the surgery. Follow appropriate pain management protocols to avoid unnecessary discomfort for the subject. Care must be taken when translating results from rodent models of ophthalmic surgery to humans given their small size and skeletal differences.Rodent models for ophthalmic surgery offer many advantages as compared to the larger animals like cats and dogs. Despite the advantage of larger size, the handling and maintenance of large animals outweigh their strengths for being used as models in research. Additionally, the cost of husbandry is high in comparison to rodents. Also, the transgenic animals are not readily available for the larger animals. Rodents, on the other hand, are economical since they are inexpensive and have shorter breeding cycles. Further, rodents are well-researched animals, and their biological processes and responses to diet modifications and drug administration are well-documented. The availability of athymic, transgenic and knock-out rodents also makes them a viable choice for biomedical investigations.
However, there are significant anatomical, physiological and pathobiological differences between the eyes of the dog and cat and those of the rabbit, guinea pig, mouse and rat which have substantial implications for the investigation of ophthalmic conditions in these animals. For pathological studies, the precorneal tear film glands in rodents may prolapse. Similarly, the orbital vascular plexus, present in rodents and lagomorphs, differs substantially between species and the knowledge of its anatomy is essential in orbital surgery and enucleation. Also, the small size of the globe in many species may complicate the procedures. Investigating conjunctivitis in rodents requires a full and thorough history and clinical examination of individual animals as well as of the group since the conjunctivitis is common in rodents and may be influenced by the environmental conditions, which may interfere with the undergoing ophthalmic research. Many laboratory rodents possess red crusting around their eyes in cases of ocular irritation, upper respiratory tract infection, and stress. Porphyrin pigmented tears in normal amounts are produced by the Harderian glands in several rodent species but mainly by the rat, also some other rodent species. Diseases such as mycoplasmosis and sialodacryoadentitis (SDA), nutritional deficiencies, and other physiologic stresses are the factors that may cause chromodacryorrhea in rodent models for ophthalmic research (Williams, 2007). Appropriate remedial action to remove the stressors (infections, environmental or management conditions) should be taken.
- Ophthalmic research involves the improvement of treatments of ocular diseases and conditions.
- Rodent models have significant advantages over large animal models such as low maintenance and cost, shorter breeding cycles and faster regeneration.
- Athymic, transgenic, and knock-out rodent models availability makes them ideal for various research requirements.
- The precorneal tear film glands in rodents may prolapse in pathological conditions.
- The orbital vascular plexus, present in rodents and lagomorphs, differs substantially between species and the understanding of its anatomy is essential in orbital surgery and enucleation.
- Rodent strain, breed, and allergic history among other factors may influence the ophthalmic investigations.
- Anesthesia induction can be done using inhalant or injectable agents. The depth of anesthesia should be verified before beginning surgical procedures.
- During surgical procedures, care must be taken not to damage surrounding tissues or muscles.
- A recovery area should be set-up and fluids should be replaced by subcutaneous or intraperitoneal injection of warm sterile saline.
- Infections may influence the results of the investigation, hence, euthanizing the subject is recommended should it occur.
- Appropriate pain management techniques should be followed.
Aerts, J., Nys, J., & Arckens, L. (2014). A Highly Reproducible and Straightforward Method to Perform In Vivo Ocular Enucleation in the Mouse after Eye Opening. J Vis Exp, 92.
Ling, Y., Fu, Z., & Wang, Y. (2017). Surgical model for ocular ischemic syndrome in mice. Biomedical Research, 28(14).
Seet, L.-F., Lee, W. S., Su, R., Finger, S. N., Crowston, J. G., & Wong, T. T. (2011) Validation of the Glaucoma Filtration Surgical Mouse Model for Antifibrotic Drug Evaluation. Mol Med, 17(5-6), 557-567.
Shinomiya, K., Ueta, M., & Kinoshita, S. (2018). A new dry eye mouse model produced by exorbital and intraorbital lacrimal gland excision. Scientific reports, 8.
Tang, Z., Zhang, S., Lee, C., Kumar, A., Arjunan, P., Li, Y., . . . Li, X. (2011). An Optic Nerve Crush Injury Murine Model to Study Retinal Ganglion Cell Survival. J Vis Exp, 50.
Williams, D. (2007). Rabbit and rodent ophthalmic. EJCAP, 17(3).
Yin, X.-T., Tajfirouz, D. A., & Stuart, P. M. (2014). Murine Corneal Transplantation: A Model to Study the Most Common Form of Solid Organ Transplantation. J Vis Exp, 93.
Zor, F., & Karagoz, H. (2015). Composite Orbital and Periorbital Allotransplantation Model. In M. Z. Siemionow, Plastic and Reconstructive Surgery (pp. 369-372). Chicago: Springer.