1992
DOI: 10.1016/0006-8993(92)91378-r
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Endothelin acts at the subfornical organ to influence the activity of putative vasopressin and oxytocin-secreting neurons

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Cited by 44 publications
(27 citation statements)
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“…Although the present experiment does not identify the locus of the presynaptic excitatory neurons, most likely targets are the local glutamatergic interneurons around the SON (Boudaba et al, 1997). An excitatory action would be consistent with observations of excitatory actions of endothelin in the anteroventral third ventricular region (Yamamoto et al, 1993) and in the subfornical organ (Wall and Ferguson, 1992). The different responses of OT and VP neurons to ET-1 thus appear to be due to the fact that they activate different receptors (ET A vs ET B ) and the fact that these receptors are on different cells.…”
Section: Discussionsupporting
confidence: 86%
See 1 more Smart Citation
“…Although the present experiment does not identify the locus of the presynaptic excitatory neurons, most likely targets are the local glutamatergic interneurons around the SON (Boudaba et al, 1997). An excitatory action would be consistent with observations of excitatory actions of endothelin in the anteroventral third ventricular region (Yamamoto et al, 1993) and in the subfornical organ (Wall and Ferguson, 1992). The different responses of OT and VP neurons to ET-1 thus appear to be due to the fact that they activate different receptors (ET A vs ET B ) and the fact that these receptors are on different cells.…”
Section: Discussionsupporting
confidence: 86%
“…Studies examining the link between endothelin and neuroendocrine output have revealed that ET-1 induces VP secretion both in vitro (Shichiri et al, 1989;Ritz et al, 1992;Chen, 2002, 2006;Rossi, 2004) and in vivo (Rossi et al, 1997a(Rossi et al, ,b, 2008, while intracerebroventricular administration of endothelin stimulates the release of OT (Samson et al, 1991). Furthermore, ET-1 activates both OT and VP MNCs through an action at the subfornical organ (Wall and Ferguson, 1992).…”
Section: Introductionmentioning
confidence: 98%
“…ET-1 may stimulate the release of VP by acting indirectly via stimulation of the catecholaminergic or renin-angiotensinergic system, as was suggested by Yamamoto et al [21], or via activation of neurons of the subfornical organ [23]. It is noteworthy that ET can interact with VP also at the level of the kidney: both peptides increase [Na]+i in the glomerular mesangial cells in the rat [24], whereas ET-1 inhibits VP-dependent cyclic adenosine monophosphate accumulation [25] and VP-stimulated osmotic water permeability [26] in rat collecting ducts.…”
Section: Discussionmentioning
confidence: 90%
“…Moreover, the origin of endogenous ET binding at these regions cannot be distinguished as to whether it is a peripherally circulating or central nervous one. Wall and Ferguson [21] reported that intravenously administered (i.e. peripherally circulating) ET acted on subfornical organ to influence the vasopressin and oxytocin neurons, but not on their neurons directly.…”
Section: And Cholecystokininmentioning
confidence: 99%