Skip to main content

Advertisement

Log in

In vivo studies on the effects of α1-adrenoceptor antagonists on pupil diameter and urethral tone in rabbits

  • Original Article
  • Published:
Naunyn-Schmiedeberg's Archives of Pharmacology Aims and scope Submit manuscript

Abstract

α1-Adrenoceptors mediate contraction of iris dilator smooth muscle and hence pupil dilatation. We compared the ability of i.v. bolus injections of alfuzosin, doxazosin, naftopidil, prazosin, tamsulosin and terazosin to antagonise phenylephrine-induced mydriasis relative to their potency for inhibiting phenylephrine-induced elevations of intraurethral pressure (IUP) in rabbits. Moreover, we compared the ability of these drugs to induce miosis in conscious rabbits in the absence of phenylephrine. All antagonists inhibited the effects of phenylephrine on pupil size and IUP, and the ratio of the respective ED50 values was close to unity in all cases. The doses required to induce statistically significant miosis in the absence of phenylephrine were 30- to 100-fold higher than those inhibiting phenylephrine-induced mydriasis for all antagonists, except for naftopidil. Moreover, the miotic effects of all α1-adrenoceptor antagonists were fully reversible within 8 h. We conclude that alfuzosin, doxazosin, naftopidil, prazosin, tamsulosin and terazosin inhibit phenylephrine-induced mydriasis in the same dose range as they inhibit elevations in IUP. Higher doses of all antagonists are required to induce miosis in the absence of an exogenous agonist, and such miosis is always reversible within hours.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4

Similar content being viewed by others

References

  • Chang DF, Campbell JR (2005) Intraoperative floppy iris syndrome associated with tamsulosin. J Cataract Refract Surg 31:664–673

    Article  PubMed  Google Scholar 

  • Chidlow G, Cupido A, Melena J, Osborne NN (2001) Flesinoxan, a 5-HT1A receptor agonist/α1-adrenoceptor antagonist, lower intraocular pressure in NZW rabbits. Curr Eye Res 23:144–153

    Article  PubMed  CAS  Google Scholar 

  • Churchill GC, Louis CF (1997) Stimulation of P2U purinergic or α1A adrenergic receptors mobilizes Ca2+ in lens cells. Invest Ophthalmol Vis Sci 38:855–865

    PubMed  CAS  Google Scholar 

  • Clarke RJ, Zhang H, Gamlin PDR (2003) Characteristics of the pupillary light reflex in the alert rhesus monkey. J Neurophysiol 89:3179–3189

    Article  PubMed  Google Scholar 

  • Foglar R, Shibata K, Horie K, Hirasawa A, Tsujimoto G (1995) Use of recombinant α1-adrenoceptors to characterize subtype selectivity of drugs for the treatment of prostatic hypertrophy. Eur J Pharmacol 288:201–207

    Article  PubMed  CAS  Google Scholar 

  • Grayson TH, Ellis JM, Chen S, Graham RM, Brown RD, Hill CE (1998) Immunohistochemical localisation of α1B-adrenergic receptors in the rat iris. Cell Tissue Res 293:435–444

    Article  PubMed  CAS  Google Scholar 

  • Gurbaxani A, Packard R (2005) Intracameral phenylephrine to prevent floppy iris syndrome during cataract surgery in patients on tamsulosin. Eye http://dx.doi.org/10.1038/sj.eye.6702172

  • Haddad NJ, Moyer NJ, Riley FC Jr (1970) Mydriatic effect of phenylephrine hydrochloride. Am J Ophthalmol 70:729–733

    PubMed  CAS  Google Scholar 

  • Hey JA, Koss MC (1988) α1- and α2-adrenoceptor antagonists produce opposing mydriatic effects by a central action. J Auton Pharmacol 8:229–239

    Article  PubMed  CAS  Google Scholar 

  • Hill CE, Klemm M, Edwards FR, Hirst GDS (1993) Sympathetic transmission to the dilator muscle of the rat iris. J Auton Nerv Syst 45:107–123

    Article  PubMed  CAS  Google Scholar 

  • Hodges RR, Shatos MA, Tarko RS, Vrouvlianis J, Gu J, Dartt DA (2005) Nitric oxide and cGMP mediate α1D-adrenergic receptor-stimulated protein secretion and p42/p44 MAPK activation in rat lacrimal gland. Invest Ophthalmol Vis Sci 46:2781–2789

    Article  PubMed  Google Scholar 

  • Ishikawa H, Miller DD, Patil PN (1996) Comparison of post-junctional α-adrenoceptors in iris dilator muscle of humans, and albino and pigmented rabbits. Naunyn-Schmiedebergs Arch Pharmacol 354:765–772

    Article  PubMed  CAS  Google Scholar 

  • Ichikawa M, Okada Y, Asai Y, Hara H, Ishii K, Araie M (2004) Effects of topically instilled bunazosin, an α1-adrenoceptor antagonist, on constrictions induced by phenylephrine and ET-1 in rabbit retinal arteries. Invest Ophthalmol Vis Sci 45:4041–4048

    Article  PubMed  Google Scholar 

  • Koike T, Kitazumi H, Mukai H (2001) Tissue distribution of NS-49, a phenylethylamine class α1A-adrenoceptor agonist, in pigmented rats. Arzneimittelforschung 51:402–407

    PubMed  CAS  Google Scholar 

  • Kokubu N, Satoh M, Takayanagi I (1993) Contractile responses and calcium movements induced by α1-adrenoceptor stimulant, norepinephrine, in rabbit iris dilator muscle. Gen Pharmacol 24:1541–1545

    PubMed  CAS  Google Scholar 

  • Michel MC, Vrydag W (2006) α1-, α2- and b-adrenoceptors in the urinary bladder, urethra and prostate. Br J Pharmacol (in press)

  • Michel MC, Grübbel B, Taguchi K, Verfürth F, Otto T, Kröpfl D (1996) Drugs for treatment of benign prostatic hyperplasia: affinity comparison at cloned α1-adrenoceptor subtypes and in human prostate. J Auton Pharmacol 16:21–28

    Article  PubMed  CAS  Google Scholar 

  • Muramatsu I, Tanaka T, Suzuki F, Li Z, Hiraizumi-Hiraoka Y, Anisuzzaman AS, Yamamoto H, Horinouchi T, Morishima S (2005) Quantifying receptor properties: the tissue segment binding method—a powerful tool for the pharmacome analysis of native receptors. J Pharmacol Sci 98:331–339

    Article  PubMed  CAS  Google Scholar 

  • Nakamura S, Taniguchi T, Suzuki F, Akagi Y, Muramatsu I (1999) Evaluation of α1-adrenoceptors in the rabbit iris: pharmacological characterization and expression of mRNA. Br J Pharmacol 127:1367–1374

    Article  PubMed  CAS  Google Scholar 

  • Okada K, Gregory DS (2001) Hydroxyamphetamine increases intraocular pressure in rabbits. Arch Ophthalmol 119:235–239

    PubMed  CAS  Google Scholar 

  • Okuda T, Tokutomi N, Tokutomi Y, Murai Y, Negi A, Nishi K (2001) Noradrenaline receptor-mediated potentiation of caffeine-induced Ca2+-activated K+ currents in bovine ciliary muscle cells. Curr Eye Res 23:455–462

    Article  PubMed  CAS  Google Scholar 

  • Ostrin LA, Glasser A (2004) The effects of phenylephrine on pupil diameter and accommodation in rhesus monkeys. Invest Ophthalmol Vis Sci 45:215–221

    Article  PubMed  Google Scholar 

  • Paggiarino DA, Brancato LJ, Newton RE (1993) The effect on pupil size and accommodation of sympathetic and parasympatholytic agents. Ann Ophthalmol 25:244–253

    PubMed  CAS  Google Scholar 

  • Pärssinen O (2005) The use of tamsulosin and iris hypotony during cataract surgery. Acta Ophthalmol Scand 83:624–626

    Article  PubMed  Google Scholar 

  • Quinn RH, Quong JN, Miller SS (2001) Adrenergic receptor activated ion transport in human fetal retinal pigment epithelium. Invest Ophthalmol Vis Sci 42:255–264

    PubMed  CAS  Google Scholar 

  • Rouquier I, Claustre Y, Benavides J (1994) α1-Adrenoceptor antagonists differentially control serotonin release in the hippocampus and striatum: a microdialysis study. Eur J Pharmacol 261:59–64

    Article  PubMed  CAS  Google Scholar 

  • Rymer J, Miller SS, Edelman JL (2001) Epinephrine-induced increases in [Ca2+]in and KCl-coupled fluid absorption in bovine RPE. Invest Ophthalmol Vis Sci 42:1921–1929

    PubMed  CAS  Google Scholar 

  • Salazar-Bookaman MM, Wainer I, Patil PN (1994) Relevance of drug-melanin interactions to ocular pharmacology and toxicology. J Ocul Pharmacol 10:217–239

    Article  PubMed  CAS  Google Scholar 

  • Soldati L, Gianesello V, Galbiati I, Gazzaniga A, Virno M (1993) Ocular pharmacokinetics and pharmacodynamics in rabbits of ibopamine, a new mydriatic agent. Exp Eye Res 56:247–254

    Article  PubMed  CAS  Google Scholar 

  • Suzuki F, Taniguchi T, Nakamura S, Akagi Y, Kubota C, Satoh M, Muramatsu I (2002) Distribution of alpha-1 adrenoceptor subtypes in RNA and protein in rabbit eyes. Br J Pharmacol 135:600–608

    Article  PubMed  CAS  Google Scholar 

  • Takayanagi I, Konno F, Kameda H, Kubo H, Furukawa A, Toyoda T (1986) A difference in mode of antagonism between optical isomers of a potent selective alpha1-adrenoceptor blocker (YM-12617) and norepinephrine in isolated rabbit iris dilator and aorta. Jpn J Pharmacol 42:579–582

    Article  PubMed  CAS  Google Scholar 

  • Takei R, Ikegaki I, Shibata K, Tsujimoto G, Asano T (1999) Naftopidil, a novel α1-adrenoceptor antagonist, displays selective inhibition of canine prostatic pressure and high affinity binding to cloned human α1-adrenoceptors. Jpn J Pharmacol 79:447–454

    Article  PubMed  CAS  Google Scholar 

  • Vidovic M, Hill CE (1995) Alpha adrenoceptor gene expression in the rat iris during development and maturity. Dev Brain Res 89:309–313

    Article  CAS  Google Scholar 

  • Wikberg-Matsson A, Uhlen S, Wikberg JES (2000) Characterization of α1-adrenoceptor subtypes in the eye. Exp Eye Res 70:51–60

    Article  PubMed  CAS  Google Scholar 

  • Yokota T (1990) Urodynamic characteristics during animal hypnosis in the rabbit. Nippon Hinyokika Gakkai Zasshi 81:1659–1666

    PubMed  CAS  Google Scholar 

  • Yousufzai SY, Abdel-Latif AA (1984) The effects of alpha1-adrenergic and muscarinic cholinergic stimulation on prostaglandin release by rabbit iris. Prostaglandins 28:399–415

    Article  PubMed  CAS  Google Scholar 

  • Yousufzai SY, Abdel-Latif AA (1987) α1-Adrenergic receptor induced subsensitivity and supersensitivity in rabbit iris-ciliary body. Effects on myo-inositol trisphosphate accumulation, arachidonate release, and prostaglandin synthesis. Invest Ophthalmol Vis Sci 28:409–419

    PubMed  CAS  Google Scholar 

  • Yousufzai SY, Gracy RA, Aboul-Khair HS, Abdel-Latif AA (1988) In vivo electrical stimulation of the sympathetic nerve of the eye increases inositol phosphate production and prostaglandin release in the rabbit iris muscle. J Neurochem 50:752–758

    Article  PubMed  CAS  Google Scholar 

  • Yu Y, Koss MC (2002) α1A-Adrenoceptors mediate sympathetically evoked pupillary dilation in rats. J Pharmacol Exp Ther 300:521–525

    Article  PubMed  CAS  Google Scholar 

  • Yu Y, Koss MC (2003a) Functional characterization of α-adrenoceptors mediating pupillary dilation in rats. Eur J Pharmacol 471:135–140

    Article  PubMed  CAS  Google Scholar 

  • Yu Y, Koss MC (2003b) Studies of α-adrenoceptor antagonists on sympathetic mydriasis in rabbits. J Ocul Pharmacol Ther 19:255–263

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Martin C. Michel.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Michel, M.C., Okutsu, H., Noguchi, Y. et al. In vivo studies on the effects of α1-adrenoceptor antagonists on pupil diameter and urethral tone in rabbits. Naunyn Schmied Arch Pharmacol 372, 346–353 (2006). https://doi.org/10.1007/s00210-006-0034-9

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00210-006-0034-9

Keywords

Navigation