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Endothelin‐Mediated Calcium Responses in Supraoptic Nucleus Astrocytes Influence Magnocellular Neurosecretory Firing Activity
Author(s) -
Filosa J. A.,
Naskar K.,
Perfume G.,
Iddings J. A.,
Biancardi V. C.,
Vatta M. S.,
Stern J. E.
Publication year - 2012
Publication title -
journal of neuroendocrinology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.062
H-Index - 116
eISSN - 1365-2826
pISSN - 0953-8194
DOI - 10.1111/j.1365-2826.2011.02243.x
Subject(s) - supraoptic nucleus , medicine , vasopressin , endocrinology , thapsigargin , magnocellular cell , glutamate receptor , bapta , oxytocin , chemistry , biology , receptor , hypothalamus , astrocyte , endothelin receptor , calcium , central nervous system
In addition to their peripheral vasoactive effects, accumulating evidence supports an important role for endothelins (ETs) in the regulation of the hypothalamic magnocellular neurosecretory system, which produces and releases the neurohormones vasopressin (VP) and oxytocin (OT). Still, the precise cellular substrates, loci and mechanisms underlying the actions of ETs on the magnocellular system are poorly understood. In the present study, we combined patch‐clamp electrophysiology, confocal Ca 2+ imaging and immunohistochemistry to study the actions of ETs on supraoptic nucleus (SON) magnocellular neurosecretory neurones and astrocytes. Our studies show that ET‐1 evoked rises in [Ca 2+ ] i levels in SON astrocytes (but not neurones), an effect largely mediated by the activation of ET B receptors and mobilisation of thapsigargin‐sensitive Ca 2+ stores. The presence of ET B receptors in SON astrocytes was also verified immunohistochemically. ET B receptor activation either increased (75%) or decreased (25%) SON firing activity, both in VP and putative OT neurones, and these effects were prevented when slices were preincubated in glutamate receptor blockers or nitric oxide synthase blockers, respectively. Moreover, ET B ‐mediated effects in SON neurones were also prevented by a gliotoxin compound, and when changes in [Ca 2+ ] i were prevented with bath‐applied BAPTA‐AM or thapsigargin. Conversely, intracellular Ca 2+ chelation in the recorded SON neurones failed to block ET B ‐mediated effects. In summary, our results indicate that ET B receptor activation in SON astrocytes induces the mobilisation of [Ca 2+ ] i , likely resulting in the activation of glutamate and nitric oxide signalling pathways, evoking in turn excitatory and inhibitory SON neuronal responses, respectively. Taken together, our study supports an important role for astrocytes in mediating the actions of ETs on the magnocellular neurosecretory system.