Receptors, Adrenergic, beta-2
"Receptors, Adrenergic, beta-2" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A subclass of beta-adrenergic receptors (RECEPTORS, ADRENERGIC, BETA). The adrenergic beta-2 receptors are more sensitive to EPINEPHRINE than to NOREPINEPHRINE and have a high affinity for the agonist TERBUTALINE. They are widespread, with clinically important roles in SKELETAL MUSCLE; LIVER; and vascular, bronchial, gastrointestinal, and genitourinary SMOOTH MUSCLE.
MeSH Number(s)
D12.776.543.750.070.300.300.340.725
D12.776.543.750.100.150.300.340.725
D12.776.543.750.720.300.300.300.340.200
Concept/Terms
Receptors, Adrenergic, beta-2- Receptors, Adrenergic, beta-2
- Adrenergic beta-2 Receptors
- Adrenergic beta 2 Receptors
- Receptors, Adrenergic beta-2
- beta-2 Receptors, Adrenergic
- Receptor, Adrenergic, beta-2
- beta 2 Adrenergic Receptors
- beta-2 Adrenergic Receptors
- Adrenergic Receptors, beta-2
- Receptors, beta-2 Adrenergic
- Receptors, beta 2 Adrenergic
- Adrenergic Receptor, beta-2
- Adrenergic Receptor, beta 2
- Receptor, beta-2 Adrenergic
- beta-2 Adrenergic Receptor
Below are MeSH descriptors whose meaning is more general than "Receptors, Adrenergic, beta-2".
- Chemicals and Drugs [D]
- Amino Acids, Peptides, and Proteins [D12]
- Proteins [D12.776]
- Membrane Proteins [D12.776.543]
- Receptors, Cell Surface [D12.776.543.750]
- Receptors, Biogenic Amine [D12.776.543.750.070]
- Receptors, Catecholamine [D12.776.543.750.070.300]
- Receptors, Adrenergic [D12.776.543.750.070.300.300]
- Receptors, Adrenergic, beta [D12.776.543.750.070.300.300.340]
- Receptors, Adrenergic, beta-2 [D12.776.543.750.070.300.300.340.725]
- Receptors, G-Protein-Coupled [D12.776.543.750.100]
- Receptors, Catecholamine [D12.776.543.750.100.150]
- Receptors, Adrenergic [D12.776.543.750.100.150.300]
- Receptors, Adrenergic, beta [D12.776.543.750.100.150.300.340]
- Receptors, Adrenergic, beta-2 [D12.776.543.750.100.150.300.340.725]
- Receptors, Neurotransmitter [D12.776.543.750.720]
- Receptors, Biogenic Amine [D12.776.543.750.720.300]
- Receptors, Catecholamine [D12.776.543.750.720.300.300]
- Receptors, Adrenergic [D12.776.543.750.720.300.300.300]
- Receptors, Adrenergic, beta [D12.776.543.750.720.300.300.300.340]
- Receptors, Adrenergic, beta-2 [D12.776.543.750.720.300.300.300.340.200]
Below are MeSH descriptors whose meaning is more specific than "Receptors, Adrenergic, beta-2".
This graph shows the total number of publications written about "Receptors, Adrenergic, beta-2" by people in Harvard Catalyst Profiles by year, and whether "Receptors, Adrenergic, beta-2" was a major or minor topic of these publication.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1995 | 1 | 1 | 2 |
| 1996 | 2 | 0 | 2 |
| 1997 | 2 | 0 | 2 |
| 1998 | 1 | 0 | 1 |
| 2000 | 4 | 0 | 4 |
| 2001 | 5 | 2 | 7 |
| 2002 | 2 | 2 | 4 |
| 2003 | 2 | 3 | 5 |
| 2004 | 5 | 1 | 6 |
| 2005 | 1 | 2 | 3 |
| 2006 | 6 | 1 | 7 |
| 2007 | 4 | 1 | 5 |
| 2008 | 3 | 0 | 3 |
| 2009 | 4 | 4 | 8 |
| 2010 | 4 | 1 | 5 |
| 2011 | 3 | 1 | 4 |
| 2012 | 7 | 0 | 7 |
| 2013 | 4 | 3 | 7 |
| 2014 | 5 | 4 | 9 |
| 2015 | 3 | 5 | 8 |
| 2016 | 4 | 1 | 5 |
| 2017 | 3 | 2 | 5 |
| 2018 | 1 | 1 | 2 |
| 2019 | 5 | 0 | 5 |
| 2020 | 2 | 3 | 5 |
| 2021 | 2 | 1 | 3 |
| 2024 | 0 | 1 | 1 |
Below are the most recent publications written about "Receptors, Adrenergic, beta-2" by people in Profiles.
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Probing Activation and Conformational Dynamics of the Vesicle-Reconstituted ß2 Adrenergic Receptor at the Single-Molecule Level. J Phys Chem B. 2024 Mar 07; 128(9):2124-2133.
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ß2-adrenergic receptor regulates ER-mitochondria contacts. Sci Rep. 2021 11 02; 11(1):21477.
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Unique Positive Cooperativity Between the ß-Arrestin-Biased ß-Blocker Carvedilol and a Small Molecule Positive Allosteric Modulator of the ß2-Adrenergic Receptor. Mol Pharmacol. 2021 11; 100(5):513-525.
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Roadmap for the use of base editors to decipher drug mechanism of action. PLoS One. 2021; 16(9):e0257537.
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ß2-Adrenoceptor Agonists Promote Extracellular Signal-Regulated Kinase 1/2 Dephosphorylation in Human Airway Epithelial Cells by Canonical, cAMP-Driven Signaling Independently of ß-Arrestin 2. Mol Pharmacol. 2021 10; 100(4):388-405.
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Design and rationale of a clinical trial to increase cardiomyocyte division in infants with tetralogy of Fallot. Int J Cardiol. 2021 09 15; 339:36-42.
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ß3-Adrenergic receptors regulate human brown/beige adipocyte lipolysis and thermogenesis. JCI Insight. 2021 06 08; 6(11).
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ß2-adrenergic receptor agonist counteracts skeletal muscle atrophy and oxidative stress in uremic mice. Sci Rep. 2021 04 28; 11(1):9130.
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ß2-Adrenergic Signaling Modulates Mitochondrial Function and Morphology in Skeletal Muscle in Response to Aerobic Exercise. Cells. 2021 01 13; 10(1).
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The Arg/N-degron pathway targets transcription factors and regulates specific genes. Proc Natl Acad Sci U S A. 2020 12 08; 117(49):31094-31104.