Comparison of Topical and Intravenous Administration of WIN 55-212-2 in Normotensive Rabbits

Objective: This study compares the effect of topical versus intravenous (IV) administration of synthetic WIN 55-212-2 (WIN) or timolol on intraocular pressure (IOP). Methods: WIN or timolol were administered either topically or by IV in normotensive New Zealand white rabbits. IOP was measured at bas...

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Published inCurrent eye research Vol. 33; no. 10; pp. 857 - 863
Main Authors Samudre, Sandeep S., Schneider, Jennifer L., Oltmanns, Matthew H., Hosseini, Alireza, Pratap, Kiran, Loose-Thurman, Patricia, Allen, Robert C., Williams, Patricia B., Lattanzio, Frank A., Sheppard, John D.
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Published England Informa UK Ltd 01.01.2008
Taylor & Francis
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Abstract Objective: This study compares the effect of topical versus intravenous (IV) administration of synthetic WIN 55-212-2 (WIN) or timolol on intraocular pressure (IOP). Methods: WIN or timolol were administered either topically or by IV in normotensive New Zealand white rabbits. IOP was measured at baseline and 30, 60, and 120 min after administration (n = 4 per group). Blood pressure (BP) and heart rate (HR) were measured concomitantly with IOP. Results: IV administration of 0.1 mg/kg WIN reduced IOP by 30% after 30 min, which continued to decline for up to 120 min. Timolol injection (25 μ g/kg) also reduced IOP by 25% after 30 min but was not sustained. In comparison, both topical WIN (1.0%) and timolol (0.5%) reduced IOP by 20% from baseline after 30 min. IV injection of either WIN or timolol significantly reduced HR to 155.4 ± 11.4 bpm and 165.9 ± 11.1 bpm, respectively, from a baseline of 256.3 ± 9.9 bpm. Topical administration was well tolerated and did not affect behavior, BP, or HR. Conclusion: Topical administration of either WIN or timolol did not decrease IOP as much as IV administration, but the lack of systemic or local toxicity could make it the safer alternative.
AbstractList This study compares the effect of topical versus intravenous (IV) administration of synthetic WIN 55-212-2 (WIN) or timolol on intraocular pressure (IOP). WIN or timolol were administered either topically or by IV in normotensive New Zealand white rabbits. IOP was measured at baseline and 30, 60, and 120 min after administration (n = 4 per group). Blood pressure (BP) and heart rate (HR) were measured concomitantly with IOP. IV administration of 0.1 mg/kg WIN reduced IOP by 30% after 30 min, which continued to decline for up to 120 min. Timolol injection (25 mu g/kg) also reduced IOP by 25% after 30 min but was not sustained. In comparison, both topical WIN (1.0%) and timolol (0.5%) reduced IOP by 20% from baseline after 30 min. IV injection of either WIN or timolol significantly reduced HR to 155.4 +/- 11.4 bpm and 165.9 +/- 11.1 bpm, respectively, from a baseline of 256.3 +/- 9.9 bpm. Topical administration was well tolerated and did not affect behavior, BP, or HR. Topical administration of either WIN or timolol did not decrease IOP as much as IV administration, but the lack of systemic or local toxicity could make it the safer alternative.
Objective: This study compares the effect of topical versus intravenous (IV) administration of synthetic WIN 55-212-2 (WIN) or timolol on intraocular pressure (IOP). Methods: WIN or timolol were administered either topically or by IV in normotensive New Zealand white rabbits. IOP was measured at baseline and 30, 60, and 120 min after administration (n = 4 per group). Blood pressure (BP) and heart rate (HR) were measured concomitantly with IOP. Results: IV administration of 0.1 mg/kg WIN reduced IOP by 30% after 30 min, which continued to decline for up to 120 min. Timolol injection (25 μ g/kg) also reduced IOP by 25% after 30 min but was not sustained. In comparison, both topical WIN (1.0%) and timolol (0.5%) reduced IOP by 20% from baseline after 30 min. IV injection of either WIN or timolol significantly reduced HR to 155.4 ± 11.4 bpm and 165.9 ± 11.1 bpm, respectively, from a baseline of 256.3 ± 9.9 bpm. Topical administration was well tolerated and did not affect behavior, BP, or HR. Conclusion: Topical administration of either WIN or timolol did not decrease IOP as much as IV administration, but the lack of systemic or local toxicity could make it the safer alternative.
Author Samudre, Sandeep S.
Lattanzio, Frank A.
Pratap, Kiran
Schneider, Jennifer L.
Sheppard, John D.
Loose-Thurman, Patricia
Oltmanns, Matthew H.
Hosseini, Alireza
Allen, Robert C.
Williams, Patricia B.
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  givenname: Sandeep S.
  surname: Samudre
  fullname: Samudre, Sandeep S.
  organization: 1Eastern Virginia Medical School, Norfolk, Virginia, USA
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  givenname: Jennifer L.
  surname: Schneider
  fullname: Schneider, Jennifer L.
  organization: 1Eastern Virginia Medical School, Norfolk, Virginia, USA
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Snippet Objective: This study compares the effect of topical versus intravenous (IV) administration of synthetic WIN 55-212-2 (WIN) or timolol on intraocular pressure...
This study compares the effect of topical versus intravenous (IV) administration of synthetic WIN 55-212-2 (WIN) or timolol on intraocular pressure (IOP). WIN...
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SubjectTerms Administration, Topical
Animals
Benzoxazines - administration & dosage
Benzoxazines - adverse effects
Blood Pressure - drug effects
Cannabinoids - administration & dosage
Cannabinoids - adverse effects
Dose-Response Relationship, Drug
Female
Heart Rate - drug effects
Injections, Intravenous
Intraocular Pressure - drug effects
intravenous
Morpholines - administration & dosage
Morpholines - adverse effects
Naphthalenes - administration & dosage
Naphthalenes - adverse effects
Rabbits
Timolol - administration & dosage
Tocrisolve
Tonometry, Ocular
topical
WIN 55-212-2
Title Comparison of Topical and Intravenous Administration of WIN 55-212-2 in Normotensive Rabbits
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https://www.ncbi.nlm.nih.gov/pubmed/18853319
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