Assessment of retinal atrophy in mixed breed dogs using spectral domain optical coherence tomography (SD-OCT) and electroretinography.

The aim of the study was to characterize retinal atrophy (RA) with progressive retinal atrophy symptoms in mixed breed dogs using ophthalmoscopy, spectral domain optical coherence tomography (SD-OCT) and electroretinography (ERG).The study was performed on 13 mixed breed dogs affected by retinal atrophy (11 males and 2 females that were 1.5-14 years old). Depending on the advancement of RA, SD-OCT examinations identified retinal abnormalities ranging from layer disorganisation to advanced atrophy. The most advanced RA occurred ventral to the optic disc. Total retinal thickness in both eyes (mean ± SD) was lower in dogs with RA compared to controls dorsally (77.7 ± 39.5 µm vs 173.5 ± 13.3 µm), ventrally (33.4 ± 29.9 µm vs 139.5 ± 10.8 µm), nasally (65.0 ± 34.5 µm vs 163.9 ± 11.0 µm) and temporally (61.8 ± 41.7 µm vs 171.9 ± 11.1 µm) to the optic disc. In dogs with locally normal architecture of inner retina, loss of definition of outer retinal layers occurred in many regions. Dark and light-adapted ERGs were reduced in 2 dogs with RA and were unrecordable in 11 dogs. Lesions evident in SD-OCT scans of mixed breed dogs affected with retinal atrophy initially appear ventrally to the optic disc and ventro-dorsally in advanced RA. In all mixed breed dogs with retinal atrophy, clinical signs and SD-OCT results correlate with ERG findings.

Morphological and Morphometric Analysis of Canine Choroidal Layers Using Spectral Domain Optical Coherence Tomography.

The choroid, a multifunctional tissue, has been the focus of research interest for many scientists. Its morphology and morphometry facilitate an understanding of pathological processes within both the choroid and retina. This study aimed to determine the choroidal layer thicknesses in healthy, mixed-breed mesocephalic dogs, both male (M) and female (F), using spectral domain optical coherence tomography (SD-OCT) with radial, cross-sectional, and linear scans. The dogs were divided into two groups based on age: middle-aged (MA) and senior (SN). Thicknesses of choroidal layers, namely RPE-Bruch's membrane-choriocapillaris complex (RPE-BmCc) with tapetum lucidum in the tapetal fundus, the medium-sized vessel layer (MSVL), and the large vessel layer with lamina suprachoroidea (LVLS), as well as whole choroidal thickness (WCT), were measured manually using the caliper function integrated into the OCT software. Measurement was performed dorsally and ventrally at a distance of 5000-6000 µm temporally and nasally at a distance of 4000-7000 µm to the optic disc on enhanced depth scans. The measurements were conducted temporally and nasally in both the tapetal (temporal tapetal: TempT, nasal tapetal: NasT) and nontapetal (temporal nontapetal: TempNT, nasal nontapetal: NasNT) fundus. The ratio of the MSVL thickness to the LVLS thickness for each region was calculated. In all examined dogs, the RPE-BmCc in the dorsal (D) region and MSVL in the Tt region were significantly thicker than those in the other regions. The MSVL was thinner in the ventral (V) region than in the D, TempT, TempNT and NasT regions. The MSVL was significantly thinner in the NasNT region than in the D region. LVLS thickness and WCT were significantly greater in the D and TempT regions than those in the other regions and significantly lesser in the V region than those in the other regions. The MSVL-to-LVLS thickness ratio did not differ between the age groups. Our results reveal that the choroidal thickness profile does not depend on age. Our findings can be used to document the emergence and development of various choroidal diseases in dogs in the future.

Refractive errors in mixed breed dogs of different ages.

The purpose of the study was to evaluate the occurrence and range of refractive errors in dogs of different ages. A total of 99 clinically healthy, mixed-breed mesocephalic dogs were included in the study and divided into three different age groups according to the current human/pet analogy chart: 40 adults (23 males, 17 females, 1-8 years old, 3-70 kg), 21 seniors (14 males, 7 females, 6-11 years old, 7-42 kg), and 38 geriatrics (22 males, 16 females, 8-13 years old, 5-45 kg). All the dogs underwent an ophthalmic examination, including Schirmer tear test, tonometry, biomicroscopy, and ophthalmoscopy. Neither eye drops nor pharmacological sedatives were administered before the autorefractometry. The refractive states were assessed bilaterally using a hand-held Retinomax 3 (Righton) autorefractor. The results underwent statistical analysis using Statistica v12 software (ANOVA and t-test). A P-value < 0.05 was considered as significant. Emmetropia, defined as a refractive state > -0.5 D and < +0.5 D, was found in 36% of the adult, 43% of the senior, and 38% of the geriatric patients. Anisometropia was found in 1% of the adult, 9.5% of the senior and 5.5% of the geriatric dogs when the refractive power of the two eyes differed ≥ 1.0 myopia ≤ -0.5 D and hyperopia ≥ +0.5 D were found in 23% and 41% of the adult eye globes as well as 24% and 33% in the senior dogs and 15% and 47% in the geriatric dogs, respectively. The maximal values of the myopia in the adult and geriatric dogs were -2.5 D and -2.75 D, respectively. The maximal values of the hyperopia in the adult and geriatric dogs were 1.75 D and 2.5 D, respectively. No statistically significant correlation was found between the groups. Ametropia is a common refractive state for dogs of different ages. The most frequent refractive state in ametropic mixed-bed dogs in all age groups is hyperopia.

The use of optical coherence tomography for skin evaluation in healthy rats.

BACKGROUND: Noninvasive diagnostic techniques allow for morphological and morphometric in vivo evaluation of the skin. Optical coherence tomography (OCT) is a method that allows visualization of dermal structures up to several 100 µm with a resolution of 3-7.5 µm. OBJECTIVES: The aim of the study was the morphological and morphometric assessment of rats' skin using SD-OCT. ANIMALS: Fifteen male Wistar rats, aged 3 and 8 months, weighing 350-450 g. MATERIALS AND METHODS: The skin of the plantar metatarsal area of the right pelvic limb was assessed. The measurements were performed using Spectral Domain Optical Coherence Tomography (SD-OCT) scans and histological images. RESULTS: Spectral Domain Optical Coherence Tomography could determine the boundary between the epidermis and the dermis. Apart from the stratum corneum (SC), it did not allow for the differentiation of the individual epidermal layers. In the SD-OCT and in the histological examination, the mean thicknesses of the layers (µm ± SD) were (respectively): SC 33.053 ± µm(SD 5.85, 29.675 ± 5.54; epidermis 88.2 ± 7.97, 65.126 ± 13.23; dermis 259.86 ± 18.29, 166.05 ± 31.88 µm. There was a correlation between the total epidermal SD-OCT and histological measurements (r = 0.43, p = 0.05). Bland-Altman plots revealed a bias of -19.18 (95% confidence interval) -39.21 to 0.84 µm) in the case of live epidermis (stratum granulosum, stratum spinous, stratum basale). CONCLUSIONS AND CLINICAL RELEVANCE: Spectral Domain Optical Coherence Tomography can be used to evaluate rat epidermis and dermis. The method enables the differentiation of the SC, as well as the epidermis and the dermis. SD-OCT and histological thickness dimensions of the epidermis and skin differ.

Contexte - Les techniques de diagnostic non invasives permettent une évaluation morphologique et morphométrique in vivo de la peau. La tomographie par cohérence optique (OCT) est une méthode qui permet de visualiser les structures dermiques jusqu'à plusieurs centaines de micromètres avec une résolution de 3 à 7,5 µm. Objectifs - Le but de l'étude était l'évaluation morphologique et morphométrique de la peau des rats par SD-OCT. Animaux - Quinze rats Wistar mâles, âgés de 3 et 8 mois, pesant 350-450 g. Matériels et méthodes - La peau de la zone métatarsienne plantaire du membre pelvien droit a été évaluée. Les mesures ont été réalisées à l'aide de scaners SD-OCT (Spectral Domain Optical Coherence Tomography) et d'images histologiques Résultats - Le SD-OCT a pu déterminer la frontière entre l'épiderme et le derme. En dehors de la couche cornée (SC), il n'a pas permis la différenciation des couches épidermiques individuelles. Au SD-OCT et à l'examen histologique, les épaisseurs moyennes des couches (µm ± SD) étaient (respectivement) : SC 33,053 ± µm (SD 5,85, 29,675 ± 5,54 ; épiderme 88,2 ± 7,97, 65,126 ± 13,23 ; derme 259,86 ± 18,29, 166,05 ± 31,88 µm). Il y avait une corrélation entre le SD-OCT épidermique total et les mesures histologiques (r = 0,43, P = 0,05) Les tracés de Bland-Altman ont révélé un biais de -19,18 (intervalle de confiance à 95 %) -39,21 à 0,84 µm) dans le cas d'épiderme vivant (stratum granulosum, stratum spinous, stratum basale). Conclusions et pertinence clinique - Le SD-OCT peut être utilisé pour évaluer l'épiderme et le derme de rat. La méthode permet de différencier le SC, ainsi que l'épiderme et le derme. Le SD-OCT et les dimensions d'épaisseur histologiques de l'épiderme et de la peau diffèrent.

Introducción - las técnicas de diagnóstico no invasivas permiten la evaluación morfológica y morfométrica in vivo de la piel. La tomografía de coherencia óptica (OCT) es un método que permite la visualización de estructuras dérmicas de hasta varios cientos de micrómetros con una resolución de 3 a 7,5 µm. Objetivos - El objetivo del estudio fue la evaluación morfológica y morfométrica de la piel de ratas mediante SD-OCT. Animales - Quince ratas Wistar macho, de 3 y 8 meses de edad, con un peso de 350 a 450 g. Materiales y métodos - Se evaluó la piel de la zona metatarsiana plantar del miembro pélvico derecho. Las mediciones se realizaron utilizando escaneos SD-OCT (Tomografía de Coherencia Óptica de Dominio Espectral) e imágenes histológicas. Resultados - SD-OCT pudo determinar el límite entre la epidermis y la dermis. Aparte del estrato córneo (SC), no permitía la diferenciación de las capas epidérmicas individuales. En la SD-OCT y en el examen histológico, los espesores medios de las capas (µm ± SD) fueron (respectivamente): SC 33.053 ± µm (SD 5.85, 29.675 ± 5.54; epidermis 88.2 ± 7.97, 65.126 ± 13.23; dermis 259.86 ± 18,29, 166,05 ± 31,88 µm. Hubo una correlación entre el SD-OCT epidérmico total y las mediciones histológicas (r = 0,43, P = 0,05). Las gráficas de Bland-Altman revelaron un sesgo de -19,18 (intervalo de confianza del 95 %) -39,21 a 0,84 µm) en el caso de epidermis viva (estrato granuloso, estrato espinoso, estrato basal). Conclusiones y relevancia clínica- SD-OCT se puede utilizar para evaluar la epidermis y la dermis de rata. El método permite diferenciar el SC, así como la epidermis y la dermis. Las dimensiones de grosor de la epidermis y la piel difieren entre SD-OCT y la histología.

Contexto - Técnicas diagnósticas não invasivas permitem a avaliação morfológica e morfométrica in vivo da pele. A tomografia de coerência óptica (OCT) é um método que possibilita a visualização de estruturas dérmicas de até centenas de micrômetros com uma resolução de 3-7,5 µm. Objetivos - O objetivo do estudo foi a avaliação morfométrica e morfológica da pele de ratos utilizando SD-OCT. Animais - Quinze ratos Wistar machos, de três a oito meses de idade, pesando de 350 a 450 g. Materiais e métodos - A pele da região metatársica plantar do membro pélvico direito foi avaliada. As mensurações foram realizadas utilizando o SD-OCT (Spectral Domain Optical Coherence Tomography) e imagens histológicas. Resultados - A SD-OCT foi capaz de determinar o limite entre derme e epiderme. A exceção do estrato córneo (SC), não foi possível a diferenciação das camadas da epiderme individualmente. Na SD-OCT e na avaliação histológica, as espessuras médias das camadas fora, (µm ± DP), respectivamente: SC 33,053 ± 5,85; 29,675 ± 5,54; epiderme 88,2 ± 7,97; 65,126 ± 13,23; derme 259,86 ± 18,29; 166,05 ± 31,88 µm. Houve correlação entre SD-OCT e avaliação histológica nas mensurações da epiderme total (r = 0,43, P = 0,05). Os gráficos de Bland-Altman revelaram um viés de -19,8% (95% de intervalo de confiança) - 39,21 a 0,84 µm) no caso da epiderme viva (estrato espinhoso, estrato granuloso e estrato basal). Conclusões e relevância clínica - SD-OCT pode ser utilizada para avaliar a derme e a epiderme de ratos. Este método permite a diferenciação do SC, bem como da derme e epiderme. Pode haver discrepância na espessura da epiderme e da pele na SD-OCT e análise histológica.

Proteomic Analysis of Tear Film in Canine Diabetic Patients with And Without Retinopathy.

Introduction: Diabetic retinopathy (DR) is the leading cause of blindness in human and animal patients. Early detection and treatment of the disease are important and can be facilitated by proteomic approaches providing biomarkers. Material and Methods: Tear films were collected on Schirmer strips from 32 canine patients (12 diabetic dogs without changes in the retina, 8 diabetic dogs with signs of DR, and 12 control dogs). Two-dimensional electrophoresis was used to separate tear film proteins prior to their identification with matrix-assisted laser desorption/ionisation-tandem time-of-flight mass spectrometry and interrogation of protein function databases to find matches. Results: Five significantly differentially expressed proteins were identified; of those, one was downregulated (2'-5'-oligoadenylate synthase 3) and four were upregulated in the tear film of two diabetic groups (Ras-related protein RAB-13; aldo-keto-reductase family 1 member C3; 28S ribosomal protein S31, mitochondrial; and 60S ribosomal protein L5). The differentially expressed proteins identified in the tear film were involved in signalling pathways associated with impaired protein clearance, persistent inflammation and oxidative stress. Conclusion: The results of our study confirm that the pathological process in the retina in the course of diabetes mellitus causes changes in the tear film proteome.

Ocular abnormalities in Polish Hunting Dogs.

This study aimed to describe and determine the prevalence of ocular abnormalities in Polish Hunting Dogs. The study was conducted with 193 Polish Hunting Dogs: 101 female and 92 male animals, aged between 3 months and 12 years. Ophthalmic examinations were performed using slit lamp biomicroscopy, ophthalmoscopy, and tonometry based on the ophthalmological protocol for the examination of hereditary eye diseases. Spectral-domain optical coherence tomography (SD-OCT) was performed for dogs with sudden acquired retinal degeneration syndrome (SARDS) and progressive retinal atrophy (PRA), while electroretinography was also performed in dogs with SARDS. Five dogs (2.6%) were diagnosed with cataract, iris coloboma in 3 dogs (1.6%), ocular dermoid in 1 dog (0.5%), and retinal dysplasia, distichiasis and entropion in 1 dog (1%). Three dogs (1.6%) were diagnosed with PRA and SARDS occurred in 1 dog. Retinal lesions was observed in 16 dogs (8.3%). The clinical signs of retinopathy observed in Polish Hunting Dogs included discoloration of the tapetal fundus, patchy increased reflectivity in the region of discoloration, focus of hyperpigmentation and an area of tapetal hyper-reflectivity with a pigmented center. SD-OCT performed in the 3 dogs with PRA revealed alteration in the retinal layers, which was most advanced in the non-tapetal fundus. Although SD-OCT revealed retinal layers with normal architecture only in some parts of the dorsal, nasal and temporal regions in dogs with SARDS, areas of disorganized external limiting membrane, myeloid zone, ellipsoid zone, outer photoreceptor segment and interdigitation zone were also observed. Polish Hunting Dogs should undergo periodic ophthalmological examination for the evaluation of other hereditary eye diseases. The prevalence of retinal lesions in Polish Hunting Dogs requires further research.

Morphometrical analysis of the canine choroid in relation to age and sex using spectral domain optical coherence tomography.

This study determined the choroidal thickness of senior (SN, n = 24) and middle-aged (MA, n = 17) healthy, mixed-breed mesocephalic dogs, both males (M) and females (F), using spectral domain optical coherence tomography (SD-OCT). The dogs were divided into two groups for examination: MA dogs (4-7 years old; 6 M, 11 F) and SN dogs (8-13 years old; 12 M, 12 F). Choroidal thickness of the dogs was investigated using SD-OCT radial and linear scans. The software of the device allowed determination of the exact measurement location on the choroid. Measurements of the choroid were taken manually using the SD-OCT calliper function at distances of 5,000-6,000 µm (dorsal and ventral) and 4,000-7,000 µm (nasal and temporal) from the optic disc. Mean (µm ± SD) (MA, SN) dorsal (188 ± 28, 184 ± 33), ventral (116 ± 23, 111 ± 16), temporal (152 ± 31, 151 ± 26), and nasal (135 ± 27, 132 ± 18) choroidal thicknesses demonstrated significant differences (P < 0.02-0.001) between all areas within each group. The choroid was thickest in the dorsal region and thinnest in the ventral region. There were no significant differences based on age. Mean (µm ± SD) (M, F) dorsal (181 ± 32, 190 ± 30), ventral (117 ± 16, 11 ± 21), temporal (150 ± 26, 153 ± 30), and nasal (128 ± 20, 138 ± 23) choroidal thicknesses demonstrated significant differences (P < 0.05) between dorsal and nasal regions. The choroidal thickness in dogs depends on the area assessed independently of their age and sex.

Pedigree and Molecular Analyses in the Assessment of Genetic Variability of the Polish Greyhound.

The aim of the study was to assess the genetic variability of the Polish Greyhound population based on pedigree analysis and molecular DNA testing and to determine the degree of relatedness among individuals in the population. Pedigree data of 912 Polish Greyhounds recorded in pedigree books since they were opened for this breed were analyzed. For molecular testing, DNA was obtained from cheek swabs taken from 235 dogs of the tested breed. A panel of 21 markers (Short Tandem Repeat-STR) was used. The mean inbreeding determined for the Polish Greyhound population based on pedigree analyses was low and amounted to 11.8%, but as many as 872 individuals of the 912 dogs in the studied population were inbred. A total of 83 founders (at least one unknown parent) were identified, among which 27 founders had both unknown parents. Full-sibling groups consisted of 130 individuals, with a minimum and maximum litter size of 2 and 16, respectively. The average litter size was 5.969. Gene diversity calculated based on the mean kinship matrix was 0.862 and the population mean kinship was 0.138. The founder genome equivalent based on the mean kinship matrix was 3.61; the founder genome surviving level was 12.34; the mean Ne was estimated at 21.76; and the Ne/N ratio was 0.135. The FIS inbreeding coefficient for 21 STR was negative, and the mean FIS value for all loci had a low negative value (-0.018). These values suggest a low level of inbreeding in the examined breed as well as the avoidance of mating related animals.

The in vitro efficacy of eye drops containing a bacteriophage solution specific for Staphylococcus spp. isolated from dogs with bacterial conjunctivitis.

BACKGROUND: The purpose of the study was to evaluate the in vitro antibacterial effect of experimental eye drops with bacteriophages in elimination of Staphylococcus spp. isolated from dogs with bacterial conjunctivitis.. The bacterial material was collected from dogs with independent clinical signs of bacterial conjunctivitis. Staphylococcus spp. were identified by phenotypic and genotypic methods (MALDI-TOF MS mass spectrometry). Antibiotic resistance was determined by the disc-diffusion method. Phage activity (Plaque forming units, PFU) was determined on double-layer agar plates. Phages with lytic titres > 108 PFU were used to prepare eye drops. The stability of the antibacterial titre was evaluated for preparations stored in sealed bottles as well as after opening and reclosing. RESULTS: The tests confirmed the occurrence of Staphylococcus spp. strains as etiological agents of bacterial conjunctivitis in dogs. A high percentage of strains were resistant to more than three antibiotics. The experimental phage eye drops used in the study exhibited 100% efficacy in vitro against the tested Staphylococcus isolates. Particularly noteworthy is the long duration of activity and constant antibacterial lytic titre of ≥108 PFU/mL of two eye drop solutions, nos. 7 and 12, after the bottle had been opened (21 days) and after hermetically sealed packaging (28 days) at 4-8 °C. CONCLUSIONS: The results represent the first stage of research and require continuation in vivo. If positive effects are obtained in animals, the results can be used in applied research in humans and animals.

DNA Adduct Assessment During Antihormonal Treatment of Perianal Gland Tumors With Tamoxifen in Male Dogs.

BACKGROUND/AIM: Determination of DNA adduct count was performed in mononuclear cells during antihormonal treatment of perianal gland tumors. MATERIALS AND METHODS: Eight- to fifteen-year-old dogs with carcinoma (CAR Group; N=5), epithelioma (EPI Group; N=16) or adenoma (ADE Group; N=24) were used. The control group suffered from perineal hernia or rectal diverticulum (CTR Group; N=25). Blood was collected at baseline, and at one and six months after the beginning of the anti-hormonal treatment with tamoxifen (1 mg/kg of body weight). DNA adduct count was determined using autoradiography. RESULTS: At baseline, DNA adduct count reached the highest value in the CTR Group, and the lowest in the EPI Group (p<0.05). Six-month-long therapy with tamoxifen resulted in a significant increase in the DNA adduct count by 78.7%, 221.5% and 198.3% in the ADE, EPI and CAR groups, respectively (p<0.05). CONCLUSION: Increased DNA adduct formation after long-term administration of tamoxifen shows its genotoxicity.

Assessment of corneal and conjunctival metaplasia by impression cytology during the treatment of canine keratoconjunctivitis sicca.

The purpose of this study was to assess the condition of cells in the conjunctiva and corneal epithelium prior to and during cyclosporine- or tacrolimusbased treatment of keratoconjunctivitis sicca (KCS). The study was performed on 40 dogs with KCS. The dogs were divided into two groups of 20 animals each. In Group I, 0.75% cyclosporine eye drops were administered three times a day, while in Group II 0.02% tacrolimus eye drops were administered twice daily. Additionally, each group was subdivided into three subgroups based on the results of the Schirmer I tear test (STT I). Evaluation of cellular metaplasia in the cornea and the palpebral and bulbar conjunctiva based on the Nelson-Adams scale was performed by impression cytology using Millipore round filters (Millipore VSWP 01300 DA) of 25 µm pore diameter applied to the studied area. Ophthalmological and cytological examinations were performed prior to the treatment as well as after one and two months of therapy. In both groups, a decrease in Nelson-Adams values was observed, corresponding to the increasing STT values [Rxy Spearman statistically significant correlation coefficient values between -0.75 (P < 0.001) and -0.45 (P < 0.01)]. The absence of goblet cells was observed in all dogs, regardless of the KCS stage. Goblet cells reappeared following both tacrolimus- and cyclosporine-based treatment in impression cytology specimens classified as 0 in the Nelson-Adams scale. The extent of corneal and conjunctival metaplasia in the course of tacrolimus- and cyclosporine-based treatment of KCS decreases with increasing STT values.

Heat Shock Proteins 70kDa, Eosinophil Cationic Protein, and Nitric Oxide During Chronic Superficial Keratitis in Dogs.

The objective of the study is to determine the levels of eosinophil cationic protein (ECP), heat shock proteins 70, and nitric oxide ions measured as nitrite ions (Griess reaction) in dogs with chronic superficial keratitis (CSK). The study was conducted on 24 dogs with CSK. Blood sera from the animals were tested for concentrations of heat shock proteins 70, ECP, and nitrite ions before treatment and again 5 weeks and 6 months after treatment. Dogs with CSK were treated for 6 months with various regimes involving the use of ophthalmic drops containing dexamethasone, dimethyl sulfoxide, and cyclosporine. The control group consisted of 16 clinically healthy German Shepherds. The results obtained indicated a significant (P ≤ 0.05) elevation in the concentrations of heat shock proteins 70 and nitrite ions in dogs with CSK in comparison to healthy dogs and dogs after 5 weeks of therapy. After 6 months of treatment, concentrations of heat shock proteins 70, ECP, and nitrite ions had fallen below pretreatment values. Significant correlations were found between concentrations of heat shock proteins 70, ECP, and nitrite ions in healthy animals and animals with CSK. The elevated concentrations of heat shock proteins 70, ECP, and nitrite ions in dogs with CSK may indicate that the disease was both localized and systemic. The significant correlation between levels of heat shock proteins 70 and nitrite ions suggests that these parameters may be used as indirect indicators of CSK.

Comparative clinical evaluation of tacrolimus and cyclosporine eye drops for the treatment of canine keratoconjunctivitis sicca.

The aim of this study was to evaluate the efficacy of tacrolimus eye drops in alleviating the clinical symptoms of canine keratoconjunctivitis sicca (KCS) and to compare this efficacy with that of cyclosporine. The clinical study was conducted on 40 dogs diagnosed with idiopathic KCS. The dogs were divided into two groups of 20 animals each. In Group I, 0.75% cyclosporine eye drops were administered three times a day, while in Group II 0.02% tacrolimus eye drops were given twice daily. In addition, each group was subdivided into three subgroups based on the results of Schirmer tear test I (STT I). Clinical and ophthalmologic examinations were performed prior to the treatment as well as after one and two months of therapy. The application of both tacrolimus and cyclosporine resulted in a significant reduction of neovascularisation after the first and second month of treatment (P < 0.05, P < 0.001); however, in moderate and advanced stages, the observed efficacy of tacrolimus was higher. Across all patients, a significant increase in STT I values was observed after both the first and second month of treatment with tacrolimus (P < 0.01), as well as after two months of treatment with cyclosporine (P < 0.05). In both groups, some patients were observed to exhibit inhibited development of pigmentation, but an analysis of particular clinical cases and statistical data revealed no statistically significant discrepancies in the course of the study. In cases of advanced canine KCS, the efficacy of tacrolimus may be higher than that of cyclosporine.

Serum vascular endothelial growth factor concentration in dogs diagnosed with chronic superficial keratitis.

The objective of this study was to measure the vascular endothelial growth factor (VEGF) levels in dogs diagnosed with chronic superficial keratitis (CSK). The study was performed on 25 German shepherds (14 males and 11 females, aged between 3 and 11 years). The VEGF levels were determined in blood serum using commercially available enzyme-linked immunosorbent assay (ELISA; Quantikine Canine VEGF Immunoassay, R&D Systems). The test group of affected German shepherds was subdivided into two subgroups, based on the area of corneal neovascularisation. The first subgroup (9 patients) comprised dogs with neovascularisation observed in 1 to 2 quadrants of the right and left cornea, while the second subgroup (16 patients) comprised dogs with neovascularisation observed in 3 to 4 quadrants of the right and left cornea. The control group comprised 12 clinically healthy German shepherds (7 males and 5 females, aged between 3 and 9 years). The results were then statistically analysed by the Mann-Whitney test. The study indicated that the median serum VEGF concentration in healthy dogs was 14.9 pg/mL. The VEGF level observed in sick German shepherds was elevated (19.5 pg/mL) as compared to the values found in healthy dogs; however, a statistically significant increase in VEGF concentration, as compared to the values observed in healthy dogs, was only noted in the first subgroup, where the median VEGF concentration was 22.0 pg/mL. Elevated serum VEGF concentration was observed in German shepherds diagnosed with CSK. A statistically significant increase in VEGF levels was observed in dogs in the first stage of the disease, i.e. the early stage of neovascularisation.

Three clinical cases of Anaplasma phagocytophilum infection in cats in Poland.

The purpose of this study was to describe Anaplasma phagocytophilum infection of three cats in Poland showing signs of fever, swollen and painful joints, pale mucous membranes and epistaxis. Morulae consistent with A phagocytophilum were present within the neutrophils of two of the cats. A polymerase chain reaction (PCR) was found targeting the 16S rRNA gene amplified DNA consistent with A phagocytophilum in the blood of all three cats. The sequence of the PCR product obtained showed 99.6-100% homology with the sequence of A phagocytophilum, gene number EU 090186 from Genbank. Applied therapy (including administration of tetracyclines for 3 weeks) resulted in a gradual clinical recovery.

Funduscopic abnormalities and electroretinography in cases of retinopathy in German Shepherd dogs.

OBJECTIVE: To perform a clinical, ophthalmological, and electroretinographic assessment of retinopathic lesions in German Shepherd dogs. ANIMALS: The study was conducted on 14 German Shepherds diagnosed with retinopathy during the course of an ophthalmological checkup. The animals were systemically healthy police dogs used for patrolling and tracking duties and which were, at times, exposed to considerable physical strain and stress. PROCEDURE: Periodic ophthalmological examinations using slit-lamp biomicroscopy, direct and indirect ophthalmoscopy, and photography, as well as maze testing, were performed on all dogs. Electroretinography (ERG) was performed on 10 affected German Shepherds and eight control dogs. RESULTS: Ophthalmological examination revealed areas of tapetal hyper-reflectivity with pigmented centers, which were characteristic of inactive chorioretinitis. Most of the lesions were in proximity to blood vessels, and in a number of eyes, progression was observed during repeated examinations. Transition from active to inactive lesions, as well as onset in previously unaffected eyes, was also recorded. The ERG recordings showed impaired cone function, with significantly lower b-wave amplitudes and prolonged implicit times, in the mixed rod-cone, photopic, and flicker tests of affected dogs (P < 0.05). CONCLUSIONS: Retinopathy observed in German Shepherd dogs is characterized by areas of tapetal hyper-reflectivity with pigmented centers. The underlying causes of retinopathy in German Shepherd dogs remain unknown, although husbandry conditions and proximity of the lesions to blood vessels may suggest an association with physical exertion or circulatory disorders, respectively.