Bitter Taste Receptors as Regulators of Abdominal Muscles Contraction
Jazyk angličtina Země Česko Médium print-electronic
Typ dokumentu časopisecké články
Grantová podpora
R01 DK106964
NIDDK NIH HHS - United States
PubMed
31647294
PubMed Central
PMC7521620
DOI
10.33549/physiolres.934156
PII: 934156
Knihovny.cz E-zdroje
- MeSH
- břišní svaly účinky léků fyziologie MeSH
- chuť účinky léků fyziologie MeSH
- gentamiciny farmakologie MeSH
- krysa rodu Rattus MeSH
- orgánové kultury - kultivační techniky MeSH
- potkani Wistar MeSH
- receptory spřažené s G-proteiny antagonisté a inhibitory fyziologie MeSH
- svalová kontrakce účinky léků fyziologie MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- gentamiciny MeSH
- receptory spřažené s G-proteiny MeSH
- Taste Receptors, Type 2 MeSH
Bitter taste receptors (TAS2R) are expressed in many non-sensor tissues including skeletal muscles but their function remains unexplored. The aim of this study is to investigate the role of TAS2R in rat abdominal skeletal muscles contractions using denatonium, a TAS2R agonist. Low concentration of denatonium (0.01 mmol/l) caused a significant decrease of amplitudes of the electrical field stimulation (EFS)-induced contractions in abdominal skeletal muscles preparations in vitro. This inhibitory effect was significantly reduced when the preparations were pre-incubated with gentamicin (0.02 mmol/l) used as a non-specific inhibitor of IP3 formation or with BaCl(2) (0.03 mmol/l) applied to block the inward-rectifier potassium current. All experiments were performed in the presence of pipecuronium in order to block the nerve stimulation of the contractions. The data obtained suggest that denatonium decreases the force of rat abdominal muscles contractions mainly via activation of TAS2R, phosphatidylinositol 4,5-biphosphate and its downstream signal metabolites.
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