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Neurohypophyseal Hormones:From Genomics and Physiology to Disease
Department of Physiology and Biophysics, University of Colorado at Denver and Health Sciences Center, Aurora, Colorado
Submitted 11 October 2005 ; accepted in final form 23 January 2006
Vasopressin (VP) release from the hypothalamo-neurohypophyseal system (HNS) is stimulated by ATP activation of P2X purinergic receptors and by activation of
1-adrenergic receptors by phenylephrine (PE). These responses are potentiated by simultaneous exposure to ATP+PE. Potentiation was blocked by depleting intracellular calcium stores with thapsigargin. To test the hypothesis that the synergistic response to ATP+PE reflects alterations in the intracellular calcium concentration ([Ca2+]i), [Ca2+]i was monitored in supraoptic neurons in HNS explants loaded with fura 2-AM. Both ATP and PE induced rapid, but transient, elevations in [Ca2+]i. In 0.3 mM Ca2+, the peak response to ATP was greater than to PE but did not differ from the peak response to ATP+PE. A sustained elevation in [Ca2+]i was induced by ATP+PE, that was greater than ATP or PE alone. In 2 mM Ca2+, the peak response to ATP+PE was significantly greater than to either ATP or PE alone, and the sustained response to ATP+PE was greater than to either agent alone. Responses were comparable in the presence of TTX. The sustained elevation in [Ca2+]i was also observed when ATP+PE was removed after 1 min, but it was eliminated by either thapsigargin or removing external calcium, indicating that both calcium influx and calcium release from internal stores are required. Some cells were vasopressinergic based on a VP-induced increase in [Ca2+]i. These observations support the hypothesis that simultaneous exposure to ATP+PE induces a different pattern of [Ca2+]i than either agent alone that may initiate events leading to synergistic stimulation of VP release.
vasopressin; oxytocin; norepinephrine; posterior pituitary; fura-2AM
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Z. Song, S. Vijayaraghavan, and C. D. Sladek ATP increases intracellular calcium in supraoptic neurons by activation of both P2X and P2Y purinergic receptors Am J Physiol Regulatory Integrative Comp Physiol, January 1, 2007; 292(1): R423 - R431. [Abstract] [Full Text] [PDF] |
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