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Caffeine stores and dopamine differentially require Ca(2+) channels in goldfish somatotropes
C J Wong1, J D Johnson, W K Yunker
1Department of Biological Sciences, University of Alberta, Edmonton, Alberta T6G 2E9, Canada.
Summary
Growth hormone (GH) secretion involves intracellular calcium stores. Caffeine-activated stores, modulated by ryanodine receptors and calcium channels, regulate GH release in goldfish.
Area of Science:
- Endocrinology
- Neuroendocrinology
- Cellular Signaling
Background:
- Intracellular calcium (Ca2+) stores play a critical role in regulating hormone secretion.
- Previous studies indicated that gonadotropin-releasing hormone (GnRH) stimulates GH release via intracellular Ca2+ stores.
- The specific mechanisms and temporal dynamics of these stores in neuroendocrine regulation require further elucidation.
Purpose of the Study:
- To investigate the role of intracellular Ca2+ stores in regulating growth hormone (GH) secretion in goldfish somatotropes.
- To characterize the caffeine-activated intracellular Ca2+ store and its modulation by ryanodine receptors.
- To compare the temporal requirements of Ca2+ channels in dopamine- and caffeine-evoked GH release.
Main Methods:
- Dissociation of goldfish pituitary cells to isolate somatotropes.
- Stimulation with caffeine and dopamine to evoke GH release.
- Application of ryanodine and blockade of Cd2+-sensitive Ca2+ channels to assess the involvement of specific pathways.
Main Results:
- Caffeine-stimulated GH release was partially mediated by caffeine-activated ryanodine receptors, with a ~28% reduction by ryanodine.
- The initial phase of dopamine-evoked GH release depended on Ca2+ channel activity.
- The initial phase of caffeine-evoked GH release was sensitive to prior blockade, suggesting Ca2+ influx is required for store maintenance.
Conclusions:
- Intracellular Ca2+ stores, particularly caffeine-activated ones involving ryanodine receptors, are crucial for GH secretion.
- Differential temporal requirements for Ca2+ channels in caffeine- and dopamine-evoked signaling suggest distinct regulatory mechanisms.
- This segregation of signaling pathways may allow for precise control of neuroendocrine regulation in teleosts.