Why the study?
Does K+ stimulation induce Ca2+-dependent release of ANG II-like peptide in cultured fetal rat brain cells?
Does K+ stimulation induce Ca2+-dependent release of ANG II-like peptide in cultured fetal rat brain cells?
The study provides evidence supporting the role of ANG II as a chemical transmitter in the brain by demonstrating its Ca2+-dependent release upon K+ stimulation in cultured fetal rat brain cells.
Supports ANG II neurotransmission in developing rodent brain; leaves open human relevance and any clinical translation.
Recent evidence has demonstrated that dissociated fetal rat brain cells in culture synthesize an angiotensin II (ANG II)-like peptide that shares common properties with authentic ANG II, suggesting that brain has a complete renin angiotensin system that is independent of peripheral substrates. Although ANG II has been postulated to function as a neurotransmitter/neuromodulator, the release of ANG II from presynaptic nerve terminals has not been established. To investigate the mechanism of ANG II release, brain cells from 20-day gestational age Sprague-Dawley rats were dissociated by mild trypsinization and grown in culture. The cells were maintained in serum-free medium for 5 days prior to experimental analysis. Cultured brain cells were challenged with 59 mM KCl in the presence or absence of 5 mM CaCl2, and the incubation medium was measured for the release of ANG II by radioimmunoassay and high-performance liquid chromatography. The data demonstrate that K+ stimulation results in a rapid and time-dependent release of ANG II-like peptide that is Ca2+ dependent. We have concluded that these findings are consistent with those for other neurotransmitter/neurohormone systems and therefore provide further support for the role of ANG II as a chemical transmitter in the brain.
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Meyer et al. (1986) studied this question.
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