Skip to main content
Log in

Role of β3-adrenoceptors in regulation of retinal vascular tone in rats

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

Abstract

The aim of this study was to determine the role of β3-adrenoceptors in the action of endogenous catecholamines (adrenaline and noradrenaline) on rat retinal arterioles in vivo. Using an original high-resolution digital fundus camera, the rat ocular fundus images were captured. The diameter of retinal arterioles contained in the images was measured. Both systemic blood pressure and heart rate were recorded continuously. Adrenaline (0.3–5.0 μg/kg/min, i.v.) increased the diameter of retinal arterioles, mean blood pressure and heart rate in a dose-dependent manner. Under blockade of β12-adrenoceptors with propranolol (2 mg/kg, i.v. bolus followed by 100 μg/kg/min infusion), adrenaline decreased the diameter of retinal arterioles. Similar observation was made under treatment with the β3-adrenoceptor antagonist L-748337 (50 μg/kg, i.v.). The pressor response to adrenaline was enhanced by propranolol, but not by L-748337. The positive chronotropic action of adrenaline was markedly prevented by propranolol, whereas it was unaffected by L-748337. Noradrenaline (0.03–1.0 μg/kg/min, i.v.) decreased the diameter of retinal arterioles but increased the mean blood pressure and heart rate. The effects of noradrenaline on retinal arteriolar diameter and blood pressure were unaffected by propranolol or L-748337. The positive chronotropic action of noradrenaline was almost completely abolished by propranolol. These results suggest that β3-adrenoceptors play crucial roles in vasodilator responses to adrenaline of retinal arterioles but have minor or no effect on noradrenaline-induced responses. The results also indicate that the functional role of β3-adrenoceptors may be more important than that in peripheral resistance vessels.

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

Access this article

We’re sorry, something doesn't seem to be working properly.

Please try refreshing the page. If that doesn't work, please contact support so we can address the problem.

Fig. 1
Fig. 2

References

  • Abdelrahman A, Tabrizchi R, Pang CC (1990) Effects of β1- and β2-adrenoceptor stimulation on hemodynamics in the anesthetized rat. J Cardiovasc Pharmacol 15:720–728

    Article  PubMed  CAS  Google Scholar 

  • Benedito S, Prieto D, Nielsen PJ, Nyborg NC (1991) Role of the endothelium in acetylcholine-induced relaxation and spontaneous tone of bovine isolated retinal small arteries. Exp Eye Res 52:575–579

    Article  PubMed  CAS  Google Scholar 

  • Boussery K, Delaey C, Van de Voorde J (2002) Rat retinal tissue releases a vasorelaxing factor. Invest Ophthalmol Vis Sci 43:3279–3286

    PubMed  Google Scholar 

  • Dawes M, Chowienczyk PJ, Ritter JM (1997) Effects of inhibition of the L-arginine/nitric oxide pathway on vasodilation caused by β-adrenergic agonists in human forearm. Circulation 95:2293–2297

    PubMed  CAS  Google Scholar 

  • Delaey C, Van de Voorde J (1998) Retinal arterial tone is controlled by a retinal-derived relaxing factor. Circ Res 83:714–720

    PubMed  CAS  Google Scholar 

  • Delaey C, Van De Voorde J (2000) Regulatory mechanisms in the retinal and choroidal circulation. Ophthalmic Res 32:249–256

    Article  PubMed  CAS  Google Scholar 

  • De La Cruz JP, Gonzalez-Correa JA, Guerrero A, de la Cuesta FS (2004) Pharmacological approach to diabetic retinopathy. Diabetes Metab Res Rev 20:91–113

    Article  Google Scholar 

  • Flammer J, Orgul S, Costa VP, Orzalesi N, Krieglstein GK, Serra LM, Renard JP, Stefansson E (2002) The impact of ocular blood flow in glaucoma. Prog Retin Eye Res 21:359–393

    Article  PubMed  Google Scholar 

  • Grieshaber MC, Flammer J (2005) Blood flow in glaucoma. Curr Opin Ophthalmol 16:79–83

    Article  PubMed  Google Scholar 

  • Haefliger IO, Flammer J, Luscher TF (1992) Nitric oxide and endothelin-1 are important regulators of human ophthalmic artery. Invest Ophthalmol Vis Sci 33:2340–2343

    PubMed  CAS  Google Scholar 

  • Ikezono K, Zerkowski HR, Beckeringh JJ, Michel MC, Brodde OE (1987) β2-adrenoceptor-mediated relaxation of the isolated human saphenous vein. J Pharmacol Exp Ther 241:294–299

    PubMed  CAS  Google Scholar 

  • Lurie KG, Tsujimoto G, Hoffman BB (1985) Desensitization of α1-adrenergic receptor-mediated vascular smooth muscle contraction. J Pharmacol Exp Ther 234:147–152

    PubMed  CAS  Google Scholar 

  • Monopoli A, Conti A, Forlani A, Ongini E (1993) β1 and β2 adrenoceptors are involved in mediating vasodilation in the human coronary artery. Pharmacol Res 27:273–279

    Article  PubMed  CAS  Google Scholar 

  • Mori A, Saito M, Sakamoto K, Narita M, Nakahara T, Ishii K (2007) Stimulation of prostanoid IP and EP2 receptors dilates retinal arterioles and increases retinal and choroidal blood flow in rats. Eur J Pharmacol 570:135–141

    Article  PubMed  CAS  Google Scholar 

  • Mori A, Saigo O, Hanada M, Nakahara T, Ishii K (2009) Hyperglycemia accelerates impairment of vasodilator responses to acetylcholine of retinal blood vessels in rats. J Pharmacol Sci 110:160–168

    Article  PubMed  CAS  Google Scholar 

  • Mori A, Miwa T, Sakamoto K, Nakahara T, Ishii K (2010) Pharmacological evidence for the presence of functional β3-adrenoceptors in rat retinal blood vessels. Naunyn-Schmiedeberg’s Arch Pharmacol 382:119–126

    Article  CAS  Google Scholar 

  • Nakane T, Tsujimoto G, Hashimoto K, Chiba S (1988) Beta adrenoceptors in the canine large coronary arteries: beta-1 adrenoceptors predominate in vasodilation. J Pharmacol Exp Ther 245:936–943

    PubMed  CAS  Google Scholar 

  • Nakazawa T, Kaneko Y, Mori A, Saito M, Sakamoto K, Nakahara T, Ishii K (2007) Attenuation of nitric oxide- and prostaglandin-independent vasodilation of retinal arterioles induced by acetylcholine in streptozotocin-treated rats. Vasc Pharmacol 46:153–159

    Article  CAS  Google Scholar 

  • Nakazawa T, Sato A, Mori A, Saito M, Sakamoto K, Nakahara T, Ishii K (2008) β-Adrenoceptor-mediated vasodilation of retinal blood vessels is reduced in streptozotocin-induced diabetic rats. Vascular Pharmacol 49:77–83

    Article  CAS  Google Scholar 

  • Ogawa N, Mori A, Hasebe M, Hoshino M, Saito M, Sakamoto K, Nakahara T, Ishii K (2009) Nitric oxide dilates rat retinal blood vessels by cyclooxygenase-dependent mechanisms. Am J Physiol Regul Integr Comp Physiol 297:R968–R977

    Article  PubMed  CAS  Google Scholar 

  • Pelosi GG, Tavares RF, Fernandes KBP, Corrêa FMA (2009) Cardiovascular effects of noradrenaline microinjection into the medial part of the superior colliculus of unanesthetized rats. Brain Res 1290:21–27

    Article  CAS  Google Scholar 

  • Saiki C, Miura A, Furuya H, Matsumoto S (2007) MK-801 alters diaphragmatic activities in unanesthetized rats differently between normoxia and hypoxia. Life Sci 80:1206–1212

    Article  PubMed  CAS  Google Scholar 

  • Schmetterer L, Wolzt M (1999) Ocular blood flow and associated functional deviations in diabetic retinopathy. Diabetologia 42:387–405

    Article  PubMed  CAS  Google Scholar 

  • Seasholtz TM, Gurdal H, Wang HY, Johnson MD, Friedman E (1997) Desensitization of norepinephrine receptor function is associated with G protein uncoupling in the rat aorta. Am J Physiol 273:H279–H285

    PubMed  CAS  Google Scholar 

  • Vatner SF, Knight DR, Hintze TH (1985) Norepinephrine-induced β1-adrenergic peripheral vasodilation in conscious dogs. Am J Physiol 249:H49–H56

    PubMed  CAS  Google Scholar 

Download references

Acknowledgements

This study was supported in part by a Grant-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology, Japan (No. 21590102 K.I.) and by a Kitasato University Research Grant for Young Researchers (A.M.).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Tsutomu Nakahara.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Mori, A., Nakahara, T., Sakamoto, K. et al. Role of β3-adrenoceptors in regulation of retinal vascular tone in rats. Naunyn-Schmiedeberg's Arch Pharmacol 384, 603–608 (2011). https://doi.org/10.1007/s00210-011-0682-2

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00210-011-0682-2

Keywords

Navigation