Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2006 Oct-Dec;31(2-3):119-30.
doi: 10.1385/CRIAI:31:2:119.

Current issues with beta2-adrenoceptor agonists: pharmacology and molecular and cellular mechanisms

Affiliations
Review

Current issues with beta2-adrenoceptor agonists: pharmacology and molecular and cellular mechanisms

Gary P Anderson. Clin Rev Allergy Immunol. 2006 Oct-Dec.

Abstract

Beta2-adrenoceptors are widely, almost ubiquitously, expressed. Activation of these receptors on bronchial smooth muscle by short- and long-acting beta2-adrenoceptor agonists causes bronchodilation. Here, the beta2-adrenoceptor is linked by the G protein, Gs, to adenylyl cyclase, which increases cyclic adenosine monophosphate (cAMP), thus activating protein kinase A, which affects calcium levels and reduces the efficiency of myosin light-chain kinase, causing relaxation. Activation also entrains numerous acute and longer term downregulation responses affecting the number, location, and net efficiency of signaling of the receptor. Synthetic beta2-agonists are all "partial agonists," incompletely able to optimally stimulate cAMP signal transduction. However, compared with some cells (such as mast cells) involved in exercise- induced asthma induction, airway smooth muscle is privileged in that transduction efficiency is intrinsically high and the tissue is very resistant to complete downregulation. Glucocorticosteroids have broadly beneficial interactions with beta2-adrenoceptors. Researchers have recently discovered that the beta2-adrenoceptor may function as a homodimer and that it can form heterodimers with both the beta1- and beta3-adrenoceptors, and possibly other receptors. This further complicates interpretation of the effect of beta2-adrenoceptor polymorphisms, but it is unknown whether this occurs in humans in vivo. Researchers have known for some time that strong contraction involving receptors coupled to the Gq G protein (e.g., cholinergic and leukotriene receptors via negative biochemical crosstalk), virus infection (via uncoupling), and inflammation (via kinases) can impair relaxation. Most recently, researchers have discovered that the beta2-adrenoceptor can also send potentially adverse signals after "atypical coupling" to Gq rather than Gs. The clinical implications of these uncouplings, crosstalk, and atypical coupling possibilities are not well-understood.

PubMed Disclaimer

References

    1. Life Sci. 1993;52(26):2145-60 - PubMed
    1. Br J Clin Pharmacol. 2004 Jan;57(1):68-75 - PubMed
    1. J Allergy Clin Immunol. 2006 Jan;117(1):3-16; quiz 17 - PubMed
    1. J Biol Chem. 2004 Aug 6;279(32):33390-7 - PubMed
    1. Am J Respir Crit Care Med. 2000 Mar;161(3 Pt 1):996-1001 - PubMed

MeSH terms

Substances

LinkOut - more resources