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Vol. 292, Issue 1, 136-139, January 2000
Department of Pharmacology and Toxicology, University of Louisville
School of Medicine, Louisville, Kentucky (Z.H.S.); and Department of
Medical Pharmacology and Toxicology, Texas A&M University Health
Science Center, College Station, Texas (Z.H.S., C.-A.S.)
It is known that marijuana smoking and administration of natural
cannabinoids reduce intraocular pressure. However, it has not been
established whether the intraocular pressure-lowering effects of
cannabinoids are mediated by cannabinoid receptors. Aminoalkylindoles
are a new class of cannabimimetics with structures entirely different
from those of natural cannabinoids. WIN55212-2, a prototypic
aminoalkylindole, has been shown to bind cannabinoid receptors and to
exhibit cannabinoid-like activities. The objective of this study was to
determine whether aminoalkylindoles lower intraocular pressure and
whether the effects of aminoalkylindoles are mediated by ocular
cannabinoid receptors. The intraocular pressure of New Zealand White
rabbits was measured with the use of applanation pneumatonography.
After the measurement of baseline intraocular pressure, drugs were
applied topically and the intraocular pressure was monitored. The
topical application of WIN55212-2 significantly reduced intraocular
pressure in the treated eyes. The intraocular pressure-lowering effects
of WIN55212-2 were time and dose dependent, and the maximal reduction
was 4.7 ± 0.5 mm Hg at a dose of 100 µg. In contrast to treated
eyes, the intraocular pressure on the contralateral eyes was not
significantly affected. The topical application of WIN55212-3, the
enantiomer of WIN55212-2, had no effect on intraocular pressure.
Furthermore, the intraocular pressure-lowering effects of WIN55212-2
were significantly reduced by topically administered SR141716A, a
selective antagonist for the CB1 cannabinoid receptor. The
dose-response curve of WIN55212-2 is shifted parallel to the right by
SR141716A. These data demonstrate that like natural cannabinoids,
WIN55212-2 also reduces intraocular pressure, and the effects of
WIN55212-2 are mediated at least in part by the CB1 cannabinoid
receptors in the eye.
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