Pharmacological studies of 8-OH-DPAT-induced pupillary dilation in anesthetized rats

Y. Yu, M.C. Koss, A.G. Ramage

Research output: Contribution to journalArticle

18 Citations (Scopus)

Abstract

Serotonin (5-HT) receptor agonists have been reported to produce mydriasis in mice, and miosis in rabbits and humans. However, the underlying mechanisms for this action are unclear. This study was undertaken in an attempt to explore the mechanism by which 5-HT receptors are involved in the modulation of pupillary size in pentobarbital-anesthetized rats. Intravenous administration of the 5-HT receptor agonist, (2R)-(+)-8-hydroxy-2-(di-n-propylamino)tetralin hydrobromide (8-OH-DPAT; 0.003-3 mg/kg), elicited dose-dependent pupillary dilation, which was not affected by section of the preganglionic cervical sympathetic nerve. 8-OH-DPAT-elicited mydriatic responses were attenuated by the selective 5-HT receptor antagonist, N-[2-[4-(2-methoxyphenyl)-1-piperazinyl]ethyl]-N-2- pyridinylcyclohexanecarboxamide maleate (WAY 100635; 0.3-1 mg/kg, i.v.), as well as by the selective a -adrenoceptor antagonist, (8aR,12aS,13aS)-5,8,8a,9,10,11,12,12a,13,13a-dechydro-3-methoxy-12- (ethylsulfonyl)-6H-isoquino[2,1-g][1,6]naphthyridine hydrochloride (RS 79948; 0.3 mg/kg, i.v.), but not by the selective a -adrenoceptor antagonist, prazosin (0.3 mg/kg, i.v.). Mydriatic responses elicited by the a -adrenoceptor agonist, guanabenz (0.003-0.3 mg/kg, i.v.), were not antagonized by WAY 100635 (0.3-1 mg/kg, i.v.). To determine whether central nervous system (CNS) 5-HT receptors, like a -adrenoceptors, are involved in reflex mydriasis, voltage response curves of pupillary dilation were constructed by stimulation of the sciatic nerve in anesthetized rats. WAY 100635 (1 mg/kg, i.v.) did not antagonize the evoked reflex mydriasis, which, however, was blocked by RS 79948 (0.3 mg/kg, i.v.). Taken together, these results suggest that 8-OH-DPAT produces pupillary dilation in anesthetized rats by stimulating CNS 5-HT receptors, which in turn trigger the release of norepinephrine, presumably from the locus coeruleus. The latter reduces parasympathetic neuronal tone to the iris sphincter muscle by stimulation of postsynaptic a - adrenoceptors within the Edinger-Westphal nucleus. Unlike a - adrenoceptors, 5-HT receptors in the CNS do not mediate reflex mydriasis evoked by sciatic nerve stimulation.
Original languageEnglish
Pages (from-to)207-213
Number of pages7
JournalEuropean Journal of Pharmacology
Volume489
Issue number3
DOIs
Publication statusPublished - 12 Apr 2004

Fingerprint

8-Hydroxy-2-(di-n-propylamino)tetralin
Serotonin Receptors
Dilatation
Adrenergic Receptors
Mydriasis
Pharmacology
Mydriatics
Reflex
Serotonin Receptor Agonists
Central Nervous System
Sciatic Nerve
Guanabenz
Naphthyridines
Miosis
Serotonin Antagonists
Locus Coeruleus
Prazosin
Iris
Pentobarbital
hydroxide ion

Cite this

Yu, Y. ; Koss, M.C. ; Ramage, A.G. / Pharmacological studies of 8-OH-DPAT-induced pupillary dilation in anesthetized rats. In: European Journal of Pharmacology. 2004 ; Vol. 489, No. 3. pp. 207-213.
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Pharmacological studies of 8-OH-DPAT-induced pupillary dilation in anesthetized rats. / Yu, Y.; Koss, M.C.; Ramage, A.G.

In: European Journal of Pharmacology, Vol. 489, No. 3, 12.04.2004, p. 207-213.

Research output: Contribution to journalArticle

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