@article {Zorzato1192, author = {F Zorzato and E Scutari and V Tegazzin and E Clementi and S Treves}, title = {Chlorocresol: an activator of ryanodine receptor-mediated Ca2+ release.}, volume = {44}, number = {6}, pages = {1192--1201}, year = {1993}, publisher = {American Society for Pharmacology and Experimental Therapeutics}, abstract = {In the present study we investigated the effect of the compound chlorocresol on intracellular Ca2+ homeostasis. Three different systems that have been shown to express the ryanodine receptor Ca2+ channel were chosen, i.e., skeletal muscle sarcoplasmic reticulum, cerebellar microsomes, and PC12 cells. In skeletal muscle sarcoplasmic reticulum, 4-chloro-m-cresol was found to be a potent activator of Ca2+ release mediated by a ruthenium red/caffeine-sensitive Ca2+ release channel. In cerebellar microsomes, this compound released Ca2+ from an inositol-1,4,5-trisphosphate-insensitive store, suggesting that there too it was acting at the ryanodine receptor level. When tested on PC12 cells, chlorocresol released Ca2+ from a caffeine- and thapsigargin-sensitive intracellular store. In addition, the compound was capable of releasing Ca2+ after pretreatment of PC12 cells with bradykinin, suggesting that it acts on a channel contained within an intracellular Ca2+ store that is distinct from that sensitive to inositol-1,4,5-trisphosphate. Structure-activity relationship analyses suggest that the chloro and methyl groups in chlorocresols are important for the activation of the ryanodine receptor Ca2+ release channel.}, issn = {0026-895X}, URL = {https://molpharm.aspetjournals.org/content/44/6/1192}, eprint = {https://molpharm.aspetjournals.org/content/44/6/1192.full.pdf}, journal = {Molecular Pharmacology} }