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PURPOSE: To report a new surgical method for intracorneal hematoma removal using combination of keratocentesis and gas tamponade in the anterior chamber. METHODS: We reviewed the clinical course and outcomes of surgical intervention. RESULTS: An 82-year-old woman visited our department because of a sudden decline in visual acuity (20/800 on the Snellen chart) in her left eye. We observed neovascularization from the superior corneal limbus and a hematoma near the Descemet membrane, deep in the stroma of the corneal center. Filtered air was injected into the anterior chamber, keratocentesis was performed at four locations from the corneal epithelium through the stroma, and the hematoma was removed from the puncture sites. The corneal hematoma disappeared, and the best-corrected visual acuity reached 20/20 at postoperative month 4. DISCUSSION: Combination of keratocentesis and gas tamponade in the anterior chamber is a simple and effective method for removing intracorneal hematomas.
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Doenças da Córnea , Humanos , Feminino , Idoso de 80 Anos ou mais , Doenças da Córnea/cirurgia , Córnea , Procedimentos Cirúrgicos Oftalmológicos , Câmara Anterior/cirurgia , Hematoma/cirurgia , Hematoma/complicações , Lâmina Limitante Posterior/cirurgiaRESUMO
The first product in the world for ex vivo cultivated oral mucosal epithelial cell transplantation (COMET) to treat limbal stem cell deficiency (LSCD), named Ocural®, was launched in June 2021 in Japan. COMET was performed on two patients, including the first case in the post-marketing phase of Ocural®. Pathological and immunohistochemical examinations were also carried out using specimens obtained before and after COMET and the spare cell sheet. In case 1, the ocular surface remained free from epithelial defects for approximately six months. In case 2, although defect of the cornea-like epithelia was observed after COMET for one month, it was resolved after the insertion of lacrimal punctal plugs. In case 1, adjuvant treatment was interrupted due to an accident during the second month after COMET, resulting in conjunctival ingrowth and corneal opacity. Eventually, a lamellar keratoplasty was required at six months after COMET. Immunohistochemistry revealed the presence of markers for stem cells (p63, p75), proliferation (Ki-67), and differentiation (Keratin-3, -4, and -13) in both the cornea-like tissue after COMET and a cultivated oral mucosal epithelial cell sheet. In conclusion, Ocural® can be accomplished without major complications, and the stem cells derived from oral mucosa might be successfully engrafted.
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Doenças da Córnea , Mucosa Bucal , Humanos , Mucosa Bucal/patologia , Doenças da Córnea/metabolismo , Células-Tronco do Limbo , Transplante de Células , Células Epiteliais/metabolismo , Transplante Autólogo , Transplante de Células-Tronco/métodos , Células CultivadasRESUMO
Tear film instability is a major cause of dry eye disease. In order to treat patients with short tear film breakup time (TBUT)-type dry eye, the development of tear film stabilizing agents is essential. However, the lack of an appropriate animal model of tear film instability has made drug development difficult. Although rabbit dry eye models have been reported in the past, there are only a few reports that focus on tear film instability. Herein, we assessed the tear film stability of a rabbit dry eye model induced by dacryoadenectomy. A clinical evaluation of the ocular surface, interferometry, and histological assessments of the cornea and conjunctiva were performed. Following the removal of the lacrimal glands, TBUT was shortened significantly, with dimple and random breakup patterns prominently observed. Furthermore, the blink rate in this model increased after dacryoadenectomy, suggesting that this model partially captured the phenotypes of human short TBUT-type dry eye and may be useful as an animal model for investigating potential drug candidates.
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Síndromes do Olho Seco , Aparelho Lacrimal , Animais , Humanos , Coelhos , Aparelho Lacrimal/cirurgia , Lágrimas , Síndromes do Olho Seco/tratamento farmacológico , Córnea , Túnica ConjuntivaRESUMO
OBJECTIVES: To examine the severe ocular complications associated with contact lens wearing in Japan. METHOD: A questionnaire was sent to 964 ophthalmologist training facilities inquiring for cases of contact lens-associated complications from April 2016 to March 2018. The inclusion criteria were as follows: (1) corrected distance visual acuity ≤0.1 decimal after treatment for 3 months, (2) corneal perforation observed during follow-up, and (3) requiring surgery. A secondary analysis was conducted, inquiring for further information on the type of contact lens, clinical manifestations, and course of treatment. RESULTS: Forty-two patients with infectious keratitis met the inclusion criteria. Eight patients were users of rigid gas-permeable contact lens, and 34 were users of soft contact lens. Microbiological tests were positive in 73.0%. The organisms isolated in microbiological culture were bacteria in 11 patients (Pseudomonas aeruginosa in 9 patients), fungi in 2 patients, and Acanthamoeba in 14 patients. Ten patients were treated with local antibiotics, 11 with a combination of systemic antibiotics, and 21 with a combination of surgical approaches, including 13 with corneal transplantation. CONCLUSIONS: The major cause of serious contact lens-associated ocular complications was microbial keratitis, and P. aeruginosa and Acanthamoeba were the major pathogens in Japan.
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Acanthamoeba , Lentes de Contato Hidrofílicas , Ceratite , Olho , Humanos , Japão/epidemiologia , Ceratite/epidemiologia , Ceratite/etiologiaRESUMO
Ex vivo cultivated oral mucosal epithelial cell transplantation (COMET) was first introduced in Japan in June 2021. This technique is used to treat limbal stem cell deficiency (LSCD). This article provides a detailed description of one of the most critical steps in COMET, which is the harvesting of oral mucosa, along with accompanying videos. The samples harvested using this method were successfully cultured into cell sheets, which were then used in surgical procedures without complications.
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Background: Sudden volcanic eruptions can lead to volcanic ash entering the eyes, causing severe discomfort and complicating evacuation efforts. The specific effects of volcanic ash on ocular tissues, especially when wearing soft contact lenses (SCLs), are not well documented, prompting this experimental investigation. Methods: White rabbits with normal eyes were randomly divided into three groups: (1) a bare eye group: bare eye + volcanic ash exposure + eye washing, (2) an SCL group: SCL-wearing eye + volcanic ash exposure + eye washing, and (3) a control group: eye washing only. In groups 1 and 2, volcanic ash was applied to one eye under topical anesthesia, followed by immediate saline rinsing. Slit-lamp microscopy and histopathological analysis were conducted after euthanasia. Results: Slit-lamp and histopathological examinations revealed more significant corneal and conjunctival erosion in the bare eye group compared to the SCL group, which showed limited damage. The control group displayed no ocular damage. Conclusions: Guidelines from the "Volcanic Ash Health Effects: A Guide for the Public" by the National Research Institute for Earth Science and Disaster Resilience recommend removing SCLs during ashfall. Our findings suggest that the damage to the corneal and conjunctival epithelium is less severe in SCL-wearing eyes than in bare eyes, recommending that SCL wearers prioritize evacuation over lens removal during sudden ashfall.
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A 63-year-old male with high myopia developed sudden visual loss, eyelid swelling, eye pain, discharge, and tearing in his left eye while wearing soft contact lenses (CLs) during the day and orthokeratology lenses at night. At the initial visit, his corrected visual acuity in the left eye was 20/1000, with a ring-shaped ulcer in the central cornea, corneal infiltration across the entire cornea, and conjunctival hyperemia. Pseudomonas aeruginosa was detected from corneal scrapings, and after antibiotic treatment, the ulcer healed with corneal opacity remaining. On the 60th day, corrected visual acuity of 20/20 was achieved with rigid gas-permeable CLs. To prevent CL-related ocular complications, eye care professionals must carefully evaluate the suitability of all CLs, including orthokeratology.
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Purpose: This study aimed to compare subjective allergic conjunctivitis symptoms and anti-allergic eye drop use patterns between antihistamine-releasing contact lens users and daily disposable soft contact lens users during Japan's hay fever season. Methods: This web-based retrospective cohort study included daily disposable soft contact lens or antihistamine-releasing contact lens users with a history of seasonal allergic conjunctivitis who regularly used daily disposable soft contact lenses since the previous year. The total ocular symptom score (range 0-20) based on 5-item questionnaire scores and time from the start of the hay fever season to the initiation of anti-allergic eye drop treatment were compared between antihistamine-releasing contact lens users and daily disposable soft contact lens users. Results: The study included 24 participants: 17 using daily disposable soft contact lenses and 7 using antihistamine-releasing contact lenses. Antihistamine-releasing contact lens users experienced a greater reduction in total ocular symptom score from 2021 to 2022 compared with daily disposable soft contact lens users (mean total ocular symptom score [standard deviation]: daily disposable soft contact lens: -0.65 [1.4], antihistamine-releasing contact lens: -4.7 [3.6]; n = 24; Mann-Whitney U test, P = 0.010). Fourteen daily disposable soft contact lens users and five antihistamine-releasing contact lens users eventually required anti-allergic eye drops. Kaplan-Meier analysis revealed a significant delay in the initiation of anti-allergic eye drop treatment among those using antihistamine-releasing contact lenses compared with those using daily disposable soft contact lenses (median days, daily disposable soft contact lenses: 19 days, antihistamine-releasing contact lens: 57 days; n = 24; log-rank test, P = 0.045). Conclusions: Antihistamine-releasing contact lenses can potentially mitigate worsening ocular allergic responses during the hay fever season when used appropriately as a preventive measure.
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Purpose: To evaluate the treatment outcome of surgical punctal occlusion with combined canaliculi ablation and punctal suturing in patients with severe dry eye. Methods: Eleven eyes of seven patients were diagnosed with severe dry eye with decreased lacrimal secretion and were refractory to treatment with various eye drops and/or had repeatedly experienced loss of punctal plugs, and continued to experience subjective symptoms received surgical punctal occlusion. In 20 puncta, lacrimal canaliculi ablation was performed along the entire length of the lacrimal canaliculus where a diathermy needle could be inserted. After resection of the annulus fibrosus in the peri-punctal area, tight cross-stitch suturing of the puncta was performed with 8-0 absorbent thread. Visual acuity, corneal staining score according to the area (A) and density (D) classification, and Schirmer tear test (STT); tear break up time (tBUT); and subjective symptoms assessed by the University of North Carolina (UNC) and Dry Eye Management Scale were compared before and one year after surgery. Results: Recanalization occurred in 1/20 puncta (5.0% at month 5) in 1/11 eyes. Student's t-test showed significant improvement at one year compared with preoperative values for LogMAR value (P = 0.019), corneal staining score A (P = 0.00003) and D (P = 0.0003), STT (P = 0.004), and subjective symptoms (P = 0.015). No change was shown in tBUT and no serious adverse event occurred. Conclusion: This improved, minimally invasive surgical procedure has a low recanalization rate and achieves both objective and subjective improvements at one year.
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We present two cases in which the drug-eluting daily disposable soft contact lens (DDSCL) Acuvue® TheravisionTM with Ketotifen (Johnson & Johnson Vision Care, Inc., Jacksonville, Florida, USA) (ATK), which contains the anti-allergic drug ketotifen fumarate, alleviated ocular allergic symptoms. Case 1 was a 57-year-old woman with a history of allergic conjunctivitis in the spring and fall. In the summer and winter, the patient used frequent replacement soft contact lenses, but in the allergy seasons, she used DDSCLs in combination with anti-allergic eye drops. She agreed to start wearing ATK lenses from before the next fall season. The lenses suppressed her allergic signs and symptoms, and she felt comfortable wearing them and continued their use throughout the season. Her symptoms were suppressed, providing her comforts that enabled uses of the CLs for some time. She successfully used the lenses again from the beginning of the next spring season. Case 2 was a 31-year-old woman with a history of cedar pollinosis. The patient previously used DDSCLs and was prescribed ATK lenses at her regular clinic. About one month later, she was referred to our department. With ATK lenses, she did not experience any subjective symptoms during the pollinosis season. At a subsequent visit, hyperemia had decreased compared with the initial visit. In these two cases, the use of ATK lenses from before until the end of both the spring and fall allergy seasons suppressed the symptoms of allergic conjunctivitis, allowing the patients to continue to wear contact lenses.
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We report a case of herpetic keratitis in an orthokeratology lens wearer. A 17-year-old man who wore an overnight orthokeratology lens for correction of myopia presented to our hospital with pain, lacrimation, and blurred vision affecting the left eye. His corrected visual acuity decreased to 18/20, and he showed dendrites and decreased corneal sensitivity in the left eye. The herpes simplex virus (HSV) immunochromatographic assay kit for the diagnosis of herpes epithelial keratitis was positive. As these findings were suggestive of HSV keratitis, topical acyclovir ointment was administered five times daily. All findings disappeared and visual acuity recovered to 20/20 at 14 days after the first visit. Herpetic keratitis rarely develops in orthokeratology lens wearers as well as contact lens (CL) wearers, although Acanthamoeba keratitis is sometimes erroneously diagnosed as herpetic keratitis in CL wearers with dendrites.
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In this report, we present a case of ââââââBurkholderia cepacia (B. cepacia)-induced bilateral microbial keratitis in a patient who wore colored contact lenses (CLs) on both eyes. The patient was a 19-year-old woman who presented to our hospital with pain, discharge, and photophobia affecting both eyes while she was wearing colored cosmetic CLs. There were corneal ulcers in both of her eyes without refractive correction. Although impairment of vision was not detected at the first visit, both eyes showed neovascularization of the upper part of the cornea and had relatively well-demarcated corneal ulcers associated with corneal stromal opacity. Cultures of cornea grew B. cepacia in both eyes. She received antimicrobial agents to which this organism was sensitive, resulting in the healing of the corneal ulcers with scarring after approximately one month. Improper fitting of colored cosmetic CLs, contamination of lenses or solutions, and inadequate lens care can be risk factors for developing this condition.
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YOUSOFT is a new soft contact lens (CL) specifically designed for the correction of astigmatism. It is a conventional FDA Group II soft contact lens (SCL) and the optical zone in its centre is thick, and on its rear surface it has a prism ballast structure to prevent rotation. This lens was prescribed for a 59-year-old male on the eye with irregular corneal astigmatism after receiving penetrating keratoplasty (PKP) for refractive correction, whose eye was difficult to wear hard CLs (HCLs). After following the directions in the fitting manual provided by the manufacturer, fitting was good in the right eye and corrected visual acuity was 20/25 in Snellen Chart. He could continue wearing without CL discomfortable YOUSOFT may be useful in patients who have received PKP.
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This study evaluated the distribution of goblet cells and the expression of MUC5AC mRNA in the canine nictitating membrane. The distribution of goblet cells in the nictitating membrane and temporal bulbar conjunctiva of beagle dogs was examined by histochemical analysis of impression cytology specimens and frozen sections. MUC5AC mRNA was detected by the reverse transcription polymerase chain reaction (RT-PCR). The distribution of MUC5AC mRNA was also examined by in situ hybridization using digoxigenin-labeled antisense and sense RNA probes. Histochemical analysis showed that the canine nictitating membrane epithelium contained many more periodic acid-Schiff positive goblet cells, particularly on the palpebral side, compared with the temporal bulbar conjunctiva. RT-PCR revealed that MUC5AC was expressed in both the nictitating membrane and in conjunctival tissue. When the distribution of MUC5AC mRNA was assessed by in situ hybridization, its expression was high on the palpebral side of the nictitating membrane and low in the temporal bulbar conjunctiva. MUC5AC mRNA expression corresponded with the distribution of goblet cells by histochemical examination. In conclusion, there were numerous goblet cells in the canine nictitating membrane epithelium, particularly on the palpebral side, and MUC5AC mRNA was expressed in the nictitating membrane epithelium at locations corresponding to the goblet cells.
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Células Caliciformes/citologia , Mucina-5AC/genética , Membrana Nictitante/citologia , Membrana Nictitante/metabolismo , RNA Mensageiro/metabolismo , Animais , Contagem de Células , Túnica Conjuntiva/citologia , Túnica Conjuntiva/metabolismo , Cães , Hibridização In Situ , Sondas RNA , Reação em Cadeia da Polimerase Via Transcriptase ReversaRESUMO
With development of the contact lens sensor (CLS), it has become possible to monitor the intraocular pressure (IOP) for 24 hrs continuously. Wearing of CLS often brings blurred vision with transient aggravation of myopia and changes in corneal shape. The author, a 51-year-old man with myopic astigmatism, wore a CLS for 24 hrs on the right eye, and the fellow eye served as a contra-lateral control eye. After wearing, his corrected visual acuity on the right eye decreased from 20/16 to 20/25 with blurred vision, and subjective spherical power and cylindrical power aggravated. Topographical analysis revealed that the instantaneous power increased on the central cornea but decreased on the mid-peripheral cornea. Differential instantaneous map of pre- and post-wearing CLS showed a specific pattern similar to the central island pattern, which is known as the results of steeper fitting of the orthokeratology lens. A surface imprint was observed on the bulbar conjunctiva, corresponding to the edge of the contact lens. These findings seemed due to orthokeratological effects by the steeper fitting of CLS. All of them resolved within 24 hrs after the removal of the CLS.
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PURPOSE: To report a case of microcysts in the cornea of a female who wore silicone hydrogel contact lenses (CLs) including observation by an in vivo confocal laser microscope. METHODS: A 31-year-old woman who wore Acuvue Oasys CLs was referred to our hospital because of reduced visual acuity, eye pain, and photophobia in both eyes. The patient's history and clinical presentation were reviewed. In vivo investigation was also performed by using HRT II Rostock Cornea Module. RESULTS: Slitlamp microscopy revealed corneal haze and a number of microcysts in both eyes. The cysts were less obvious on fluorescein staining than on corneal observation. Observation with the HRT II Rostock Cornea Module showed a number of irregular oval-shaped cysts in the basal layer of the corneal epithelium. The cysts were much larger than those induced by infection with Acanthamoeba, so the possibility of Acanthamoeba keratitis was ruled out. Based on these findings, treatment with betamethasone phosphate eye drops and levofloxacin eye drops (both five times daily) were started for the microcysts. After about 10 days of treatment, all of the cysts resolved. CONCLUSIONS: Microcysts may occur in persons who wear silicone hydrogel CLs caused by inflammatory, mechanical etiology, or a toxic reaction from the solution/lens interaction that the patient was using. In vivo Confocal laser microscope is useful for making a definite diagnosis of microcysts.
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Lentes de Contato Hidrofílicas/efeitos adversos , Doenças da Córnea/etiologia , Doenças da Córnea/patologia , Cistos/etiologia , Cistos/patologia , Microscopia Confocal , Adulto , Betametasona/administração & dosagem , Betametasona/análogos & derivados , Doenças da Córnea/tratamento farmacológico , Doenças da Córnea/fisiopatologia , Cistos/tratamento farmacológico , Cistos/fisiopatologia , Quimioterapia Combinada , Feminino , Glucocorticoides/administração & dosagem , Humanos , Hidrogel de Polietilenoglicol-Dimetacrilato , Levofloxacino , Ofloxacino/administração & dosagem , Soluções Oftálmicas , Silicones , Resultado do Tratamento , Acuidade VisualRESUMO
PURPOSE: Fragments of a rigid gas-permeable contact lens embedded in the corneal subepithelial superficial stroma were observed with an in vivo confocal laser microscope. CASE REPORT: A 22-year-old man suffered damage to the contact lens in his left eye by the strap of his bag during baggage inspection at airport. Although he developed ocular pain, simply treated it with an artificial tears. He was then referred to and examined at our clinic. RESULTS: Slitlamp microscopy revealed many bright particles in the subepithelial superficial stroma, but no conjunctival injection or positive vital staining of the keratoconjunctival epithelium. In vivo Confocal laser microscopy revealed a large number of very fine bright particles in the corneal subepithelial superficial stroma, which showed an arrangement like the Milky Way. Because there were no inflammatory cells and no evidence of infection and no influence of these fragments on his vision, it was decided that he would be followed up without removal of the particles. CONCLUSIONS: In vivo Confocal laser microscope visualized contact lens fragments embedded the subepithelial superficial stroma as very bright particles. Since the presence of inflammatory cells and pathogen could also be denied, microscopy was useful for selecting the treatment.
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Lentes de Contato/efeitos adversos , Substância Própria , Corpos Estranhos no Olho/diagnóstico , Corpos Estranhos no Olho/etiologia , Microscopia Confocal , Humanos , Masculino , Adulto JovemRESUMO
PURPOSE: To assess the influence of topical application of ibudilast for seasonal allergic conjunctivitis in patients wearing soft contact lenses (SCLs). MATERIALS AND METHODS: There were 16 SCL wearers (32 eyes) with allergic conjunctivitis due to cedar pollen, who were studied from February to April 2007. Before enrollment, informed consent to participation in this study was obtained from all subjects. A frequent replacement SCL (2 Week Pure) was worn for 2 weeks, and ibudilast was applied topically four times daily during this period. The severity of allergic symptoms and the severity of SCL-related symptoms were assessed by scoring using two questionnaires, and before and after topical application of ibudilast results were compared. The severity of objective ocular findings was also scored and compared in the same way. After the final examination, the SCLs were collected and immersed in physiologic saline. Then morphologic changes and drug adsorption were investigated. RESULTS: Among the allergic symptoms, itching and a dry sensation improved after topical application of ibudilast ophthalmic solution (both P<0.05). Phlyctenular conjunctivitis was noted in one eye after topical application, but there were no significant differences of SCL-related symptoms and objective ocular findings between before and after application. There were also no morphologic changes of the contact lenses, and the ibudilast concentration in the lenses was below the detection limit. CONCLUSIONS: These results suggest that topical application of ibudilast while using 2 Week Pure lenses can improve subjective symptoms without influencing drug adsorption or lens morphology.
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Antialérgicos/administração & dosagem , Conjuntivite Alérgica/tratamento farmacológico , Lentes de Contato Hidrofílicas , Prurido/etiologia , Piridinas/administração & dosagem , Administração Tópica , Cedrus/imunologia , Conjuntivite Alérgica/complicações , Conjuntivite Alérgica/imunologia , Conjuntivite Alérgica/fisiopatologia , Humanos , Pólen/imunologia , Prurido/fisiopatologia , Estações do Ano , Resultado do Tratamento , Xeroftalmia/etiologia , Xeroftalmia/fisiopatologiaRESUMO
PURPOSE: To investigate ability of vitamin A (VA, retinol palmitate) to promote wound healing after injury in rabbit eye. METHODS: After keratoconjunctival injury by 20 microL of n-heptanol, VA eye drops at 500, 1000, or 1500 IU/mL were started 6 times a day for 11 days. Fluorescein and rose bengal staining and histological analysis were performed. RESULTS: Fluorescein staining was significantly reduced by 1000 and 1500 IU/mL of VA and rose bengal staining by all concentrations. Histological examination revealed acceleration of wound healing after 7 days (1500 IU/mL). CONCLUSIONS: VA may be useful in treatment of keratoconjunctival injury.
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Queimaduras Químicas/tratamento farmacológico , Doenças da Túnica Conjuntiva/tratamento farmacológico , Doenças da Córnea/tratamento farmacológico , Queimaduras Oculares/induzido quimicamente , Soluções Oftálmicas/administração & dosagem , Vitamina A/análogos & derivados , Cicatrização/efeitos dos fármacos , Animais , Doenças da Túnica Conjuntiva/induzido quimicamente , Doenças da Túnica Conjuntiva/patologia , Doenças da Córnea/induzido quimicamente , Doenças da Córnea/patologia , Modelos Animais de Doenças , Diterpenos , Células Epiteliais/efeitos dos fármacos , Células Epiteliais/patologia , Proteínas do Olho/metabolismo , Fluoresceína , Corantes Fluorescentes , Heptanol/toxicidade , Masculino , Mucinas/metabolismo , Soluções Oftálmicas/uso terapêutico , Coelhos , Ésteres de Retinil , Rosa Bengala , Lágrimas/metabolismo , Vitamina A/administração & dosagem , Vitamina A/uso terapêuticoRESUMO
PURPOSE: Tear secretion from the main lacrimal gland (LG) is mainly regulated by parasympathetic nerves. We performed several innervation studies to investigate lacrimation. METHODS: In male rabbits, we performed a retrograde dye-tracing study of LG innervation, evaluated preganglionic parasympathetic denervation, and administered glial cell-derived neurotrophic factor (GDNF) in the surgical area after parasympathetic denervation. RESULTS: Accumulation of fluorescent dye was observed in the pterygopalatine ganglion cells on the same side as the dye injection into the main LG. Fewer stained cells were observed in the cervical and trigeminal ganglia. After parasympathetic denervation surgery, tear secretion was decreased, and fluorescein and rose bengal staining scores were increased at day 1 after surgery and remained increased for 3 months on the denervated side only. Most of the effects in rabbits with parasympathetic denervation were not recovered by administration of GDNF. CONCLUSIONS: The main LG is primarily innervated by parasympathetic nerves to stimulate tear secretion. After preganglionic parasympathetic denervation, lacrimation was decreased, resulting in dry eyes, and this was maintained for at least 3 months. Administration of GDNF only minimally altered the effects of denervation.