Abstract
In permcabilized rat hepatocytcs a maximal concentration (25 μM) of 2,5-di-(tert-butyl)-1,4-benzohydroquinone (tBuBHQ) mobilized 70% of sequestered Ca2+ and a half-maximal effect was produced by 1.7 μM tBuBHQ. Inositol 1,4,5-trisphosphate (Ins(1,4,5)P3) stimulated release of about 40% of the intracellular Ca2+ stores. Combined applications of a range of tBuBHQ concentrations with a maximal concentration of Ins(1,4,5)P3 demonstrated that tBuBHQ has slight selectivity for the Ca2+ transport process of the Ins(1,4,5)P3-sensitive stores. We conclude that the Ins(1,4,5)P3-sensitive stores arc a subset of those sensitive to tBuBHQ and that the latter is therefore unlikely to prove useful as a tool to discriminate Ins(1,4,5)P3-sensitive and -insensitive Ca2+ stores though it may provide opportunities to design more selective agents. © 1990.
Original language | English |
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Pages (from-to) | 214-216 |
Number of pages | 2 |
Journal | FEBS Letters |
Volume | 274 |
Issue number | 1-2 |
Publication status | Published - 12 Nov 1990 |
Keywords
- 4
- 5-Di-(tert-butyl)-1.4-benzohydroquinone
- 5-trisphosphate: Intracellular Ca2+ store: 2
- Inositol 1