Literature DB >> 8384826

Activation of Ca2+ release from sarcoplasmic reticulum vesicles by 4-alkylphenols.

T J Beeler1, K S Gable.   

Abstract

4-Alkylphenols induce Ca2+ release from junctional (terminal cisternae) sarcoplasmic reticulum vesicles, but not from nonjunctional sarcoplasmic reticulum vesicles. The 4-alkylphenol concentration required to induce Ca2+ release decreases about threefold for every methylene carbon increase in the alkyl chain length, indicating that the Ca(2+)-releasing potency of 4-alkylphenols is related to their ability to partition into the membrane. The rate and amount of Ca2+ release induced by relatively low 4-octylphenol concentrations (25 nmol/mg protein) are altered by the sarcoplasmic reticulum Ca2+ channel activators, Ca2+ and ATP, and the Ca2+ channel inhibitors, Mg2+ and ruthenium red. Ca2+ release induced by 250 nmol 4-octylphenol/mg protein is much less influenced by Ca2+ channel activators and inhibitors; however, even at this high 4-octylphenol concentration, Ca2+ release is not induced from nonjunctional sarcoplasmic reticulum vesicles. The data indicate that 4-alkylphenols induce Ca2+ release by activating the sarcoplasmic reticulum Ca2+ channel.

Entities:  

Mesh:

Substances:

Year:  1993        PMID: 8384826     DOI: 10.1006/abbi.1993.1136

Source DB:  PubMed          Journal:  Arch Biochem Biophys        ISSN: 0003-9861            Impact factor:   4.013


  1 in total

1.  The ryanodine receptor agonist 4-chloro-3-ethylphenol blocks ORAI store-operated channels.

Authors:  Bo Zeng; Gui-Lan Chen; Nikoleta Daskoulidou; Shang-Zhong Xu
Journal:  Br J Pharmacol       Date:  2014-03       Impact factor: 8.739

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.