Do low-affinity states of beta-adrenoceptors have roles in physiology and medicine?
- PMID: 15514247
- PMCID: PMC1575436
- DOI: 10.1038/sj.bjp.0705991
Do low-affinity states of beta-adrenoceptors have roles in physiology and medicine?
Abstract
The pharmacology once ascribed to the 'beta4-adrenoceptor' is now believed to be that of a low-affinity state of the beta1-adrenoceptor. The beta2-adrenoceptor may also have a low-affinity state or site, while the beta3-adrenoceptor--the original low-affinity beta-adrenoceptor--can display more than one pharmacology. In this issue, Mallem et al. show that CGP-12177 relaxes thoracic aorta rings from normal rats by stimulating vascular smooth muscle low-affinity beta1-adrenoceptors, apparently linked in part to Gi protein. By contrast, in rings from hypertensive rats, CGP-12177 acts mainly via endothelial beta3-adrenoceptors. This work raises the possibility that low-affinity states of beta-adrenoceptors have physiological roles, and suggests that they might be drug targets.
Comment on
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Impairment of the low-affinity state beta1-adrenoceptor-induced relaxation in spontaneously hypertensive rats.Br J Pharmacol. 2004 Nov;143(5):599-605. doi: 10.1038/sj.bjp.0705990. Epub 2004 Oct 4. Br J Pharmacol. 2004. PMID: 15466443 Free PMC article.
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References
-
- ARCH J.R. β3-Adrenoceptor agonists: potential, pitfalls and progress. Eur. J. Pharmacol. 2002;440:99–107. - PubMed
-
- COHEN M.L., BLOOMQUIST W., ITO M., LOWELL B.B. β3 receptors mediate relaxation in stomach fundus whereas a fourth beta receptor mediates tachycardia in atria from transgenic β3 receptor knockout mice. Receptors Channels. 2000;7:17–23. - PubMed
-
- HEUBACH J.F., RAVENS U., KAUMANN A.J. Epinephrine activates both Gs and Gi pathways, but norepinephrine activates only the Gs pathway through human beta2-adrenoceptors overexpressed in mouse heart. Mol. Pharmacol. 2004;65:1313–1322. - PubMed
-
- KAUMANN A.J., ENGELHARDT S., HEIN L., MOLENAAR P., LOHSE M. Abolition of (−)-CGP 12177-evoked cardiostimulation in double β1/β2-adrenoceptor knockout mice. Obligatory role of β1-adrenoceptors for putative β4-adrenoceptor pharmacology. Naunyn-Schmiedeberg's Arch. Pharmacol. 2001;363:87–93. - PubMed
-
- KAUMANN A.J., PREITNER F., SARSERO D., MOLENAAR P., REVELLI J.P., GLACOBINO J.P. (−)- CGP 12177 causes cardiostimulation and binds to cardiac putative β4-adrenoceptors in both wild-type and β3-adrenoceptor knockout mice. Mol. Pharmacol. 1998;53:670–675. - PubMed
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