Br J Ophthalmol 2000;84:1411-1414
( December )
Mechanism related to reduction of intraocular pressure by
melanocortins in rabbits
N Naveha, A Kaplan-Messasa, J Marshallb
a Goldschleger
Eye Research Institute, Tel Aviv University School of Medicine, Sheba
Medical Center, Israel, b Rayne's Institute, St Thomas's Hospital,
London, UK
Correspondence to: Professor N Naveh, 15 Rav Ashi St, Tel Aviv 69395, Israel
hnave{at}zahav.net.il
Accepted for publication 23 June 2000
AIM
To investigate
whether the ocular hypotensive effect of alpha melanocyte stimulating
hormone (MSH) is related to eicosanoids or cyclic AMP (cAMP).
METHODS
Intraocular
pressure (IOP) readings were taken at a similar time on the day before
and after a single dose of topical MSH. Changes in the levels of
prostaglandin E2 (PGE2) and prostacyclin in
incubated iris ciliary body (ICB) explants were measured by specific
radioimmunoassay (RIA). Incubated ICB explants were exposed to MSH or
adrenaline (epinephrine) for a week. In addition, cAMP levels in the
medium were determined following short term incubation using RIA.
RESULTS
A significant
dose related reduction in IOP was noted with topical MSH (mean (SD)
maximal effect 4.5 (0.1) mm Hg (21%); p<0.001 v appropriate baseline) which persisted up
to 6 hours (p=0.05). MSH treated ICB explants showed a 1.5-fold
increase in PGE2 and prostacyclin levels (p<0.001 for each
parameter) while cAMP levels were increased twofold (p<0.001).
CONCLUSIONS
A single
application of MSH caused a sustained dose related ocular hypotensive
effect with no side effects. An increase in eicosanoid and cAMP levels
following ICB exposure to MSH indicated their involvement in MSH
induced ocular hypotension. MSH and its analogues might have clinical
relevance as antiglaucoma drugs with fewer side effects because of
their antiallergic and anti-inflammatory properties.
© 2000 by British Journal of Ophthalmology