The evaluation of the effect of tafluprost on the intraocular pressure of healthy male guinea pigs under different light‐and‐darkness regimes
Abstract Background Ocular hypertension is one of the most underdiagnosed ocular abnormalities among guinea pigs around the world. Objectives The current study investigates the effect of 0.0015% preservative‐free tafluprost ophthalmic solution (Zioptan) on the intraocular pressure of 16 healthy male...
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Wiley
2023-05-01
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Series: | Veterinary Medicine and Science |
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Online Access: | https://doi.org/10.1002/vms3.1082 |
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author | Arghavan Armin Farnoosh Arfaee Saeed Ozmaie Ahmad Asghari |
author_facet | Arghavan Armin Farnoosh Arfaee Saeed Ozmaie Ahmad Asghari |
author_sort | Arghavan Armin |
collection | DOAJ |
description | Abstract Background Ocular hypertension is one of the most underdiagnosed ocular abnormalities among guinea pigs around the world. Objectives The current study investigates the effect of 0.0015% preservative‐free tafluprost ophthalmic solution (Zioptan) on the intraocular pressure of 16 healthy male guinea pigs (Cavia porcellus) under different light/darkness regimes. Methods All guinea pigs received a single drop of tafluprost at 5:30 in the right eye, whereas the contralateral eyes served as control to receive a placebo. Then, the animals were randomly divided into two groups; group A was exposed to light, whereas group B was placed in darkness from 5:30 to 18:00. Rebound tonometry (TonoVet) was instrumented to measure IOP values at 5:30 (baseline), 6:00, 7:00, 8:00, 9:00 and then every 3 h until 18:00. Results The maximum IOP reduction associated with tafluprost was observed at 6:00 by −1.4 ± 1.1 mmHg (p‐value = 0.026) and −2.5 ± 1.2 mmHg (p‐value = 0.011) in group A and B, respectively (repeated measure ANOVA test). There was a significant difference between the mean right and left eye IOP values in both groups at 5:30, 6:00, 7:00 and 8:00 (p‐value <0.05), which was greater in amount in group B compared to group A due to the effect of darkness on IOP reduction. Conclusions It is suggested that the variations of IOP in different light/dark conditions be taken into consideration when applying ocular hypotensive agents on guinea pigs’ eyes. |
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language | English |
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spelling | doaj.art-99f7433a817944359b29410a4b04e6452023-05-16T19:51:19ZengWileyVeterinary Medicine and Science2053-10952023-05-01931172117810.1002/vms3.1082The evaluation of the effect of tafluprost on the intraocular pressure of healthy male guinea pigs under different light‐and‐darkness regimesArghavan Armin0Farnoosh Arfaee1Saeed Ozmaie2Ahmad Asghari3Department of Clinical Sciences, Faculty of Specialized Veterinary Sciences The Science and Research Branch of Islamic Azad University Tehran IranDepartment of Clinical Sciences, Faculty of Specialized Veterinary Sciences The Science and Research Branch of Islamic Azad University Tehran IranDepartment of Clinical Sciences, Faculty of Specialized Veterinary Sciences The Science and Research Branch of Islamic Azad University Tehran IranDepartment of Clinical Sciences, Faculty of Specialized Veterinary Sciences The Science and Research Branch of Islamic Azad University Tehran IranAbstract Background Ocular hypertension is one of the most underdiagnosed ocular abnormalities among guinea pigs around the world. Objectives The current study investigates the effect of 0.0015% preservative‐free tafluprost ophthalmic solution (Zioptan) on the intraocular pressure of 16 healthy male guinea pigs (Cavia porcellus) under different light/darkness regimes. Methods All guinea pigs received a single drop of tafluprost at 5:30 in the right eye, whereas the contralateral eyes served as control to receive a placebo. Then, the animals were randomly divided into two groups; group A was exposed to light, whereas group B was placed in darkness from 5:30 to 18:00. Rebound tonometry (TonoVet) was instrumented to measure IOP values at 5:30 (baseline), 6:00, 7:00, 8:00, 9:00 and then every 3 h until 18:00. Results The maximum IOP reduction associated with tafluprost was observed at 6:00 by −1.4 ± 1.1 mmHg (p‐value = 0.026) and −2.5 ± 1.2 mmHg (p‐value = 0.011) in group A and B, respectively (repeated measure ANOVA test). There was a significant difference between the mean right and left eye IOP values in both groups at 5:30, 6:00, 7:00 and 8:00 (p‐value <0.05), which was greater in amount in group B compared to group A due to the effect of darkness on IOP reduction. Conclusions It is suggested that the variations of IOP in different light/dark conditions be taken into consideration when applying ocular hypotensive agents on guinea pigs’ eyes.https://doi.org/10.1002/vms3.1082glaucomaguinea pigintraocular pressurelightocular hypertensiontafluprost |
spellingShingle | Arghavan Armin Farnoosh Arfaee Saeed Ozmaie Ahmad Asghari The evaluation of the effect of tafluprost on the intraocular pressure of healthy male guinea pigs under different light‐and‐darkness regimes Veterinary Medicine and Science glaucoma guinea pig intraocular pressure light ocular hypertension tafluprost |
title | The evaluation of the effect of tafluprost on the intraocular pressure of healthy male guinea pigs under different light‐and‐darkness regimes |
title_full | The evaluation of the effect of tafluprost on the intraocular pressure of healthy male guinea pigs under different light‐and‐darkness regimes |
title_fullStr | The evaluation of the effect of tafluprost on the intraocular pressure of healthy male guinea pigs under different light‐and‐darkness regimes |
title_full_unstemmed | The evaluation of the effect of tafluprost on the intraocular pressure of healthy male guinea pigs under different light‐and‐darkness regimes |
title_short | The evaluation of the effect of tafluprost on the intraocular pressure of healthy male guinea pigs under different light‐and‐darkness regimes |
title_sort | evaluation of the effect of tafluprost on the intraocular pressure of healthy male guinea pigs under different light and darkness regimes |
topic | glaucoma guinea pig intraocular pressure light ocular hypertension tafluprost |
url | https://doi.org/10.1002/vms3.1082 |
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