1999
DOI: 10.1016/s0306-4522(99)00477-7
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Magnocellular neurons of the rat supraoptic nucleus are endowed with functional nicotinic acetylcholine receptors

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Cited by 26 publications
(22 citation statements)
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“…In addition to influencing specific cortical areas, the adrenergic/cholinergic link in the BF may participate in autonomic control by modulating hypothalamic neuroendocrine and autonomic networks. Several experiments in the rat have provided evidence for cholinergic influence on osmosensitive neurons and vasopressin release in the hypothalamic paraventricular and supraoptic nuclei (Akaishi and Negoro, 1983; Mason, 1985; Michels et al, 1986; Ota et al, 1992; Okuda et al, 1993; Shioda et al, 1997; Qadri et al, 1998; Zaninetti et al, 2000) and on body temperature and water intake regulation in the preoptic‐anterior hypothalamic areas (Takahashi et al, 2001) and in the lateral hypothalamus (Puig de Parada et al, 1997). Although the source of cholinergic input to these neuroendocrine and autonomic networks remains to be elucidated (Sawchenko and Swanson, 1983; Rao et al, 1987; Grove, 1988; Jhamandas et al, 1989; Ruggiero et al, 1990), it is likely that at least a proportion of this input originates as collaterals of BF cholinergic neurons that receive PNMT innervation.…”
Section: Discussionmentioning
confidence: 99%
“…In addition to influencing specific cortical areas, the adrenergic/cholinergic link in the BF may participate in autonomic control by modulating hypothalamic neuroendocrine and autonomic networks. Several experiments in the rat have provided evidence for cholinergic influence on osmosensitive neurons and vasopressin release in the hypothalamic paraventricular and supraoptic nuclei (Akaishi and Negoro, 1983; Mason, 1985; Michels et al, 1986; Ota et al, 1992; Okuda et al, 1993; Shioda et al, 1997; Qadri et al, 1998; Zaninetti et al, 2000) and on body temperature and water intake regulation in the preoptic‐anterior hypothalamic areas (Takahashi et al, 2001) and in the lateral hypothalamus (Puig de Parada et al, 1997). Although the source of cholinergic input to these neuroendocrine and autonomic networks remains to be elucidated (Sawchenko and Swanson, 1983; Rao et al, 1987; Grove, 1988; Jhamandas et al, 1989; Ruggiero et al, 1990), it is likely that at least a proportion of this input originates as collaterals of BF cholinergic neurons that receive PNMT innervation.…”
Section: Discussionmentioning
confidence: 99%
“…Central cholinergic pathways have profound effects on rhythmic neuronal activity in a number of systems. For example, in the mammalian hippocampus (Cobb et al, 1999), supraoptic nucleus (Zaninetti et al, 1999), somatosensory cortex (Buhl et al, 1998) and entorhinal cortex (Klink and Alonso, 1997), ACh can initiate burst-mode activity and promote synchrony within neuronal populations. Furthermore, mammalian osmoregulatory vasopressin neurons, which have comparable activity patterns to bursting Dahlgren cells (Armstrong et al, 1994), are stimulated via both nicotinic and muscarinic pathways.…”
Section: Discussionmentioning
confidence: 99%
“…Although perinuclear inputs are generally regarded as being principally glutamatergic or GABAergic, a large proportion of neurones in the perinuclear zone of the SON also synthesise acetylcholine . SON MNCs express nicotinic receptors that mediate synaptic activation by perinuclear zone stimulation in vitro and central administration of the muscarinic receptor agonist, carbachol, markedly increases the firing rate of both oxytocin and vasopressin MNCs in the SON . It is likely that PVN MNCs are similarly innervated because they are directly excited via nicotinic receptors in vitro .…”
Section: Afferent Inputs To Mncsmentioning
confidence: 99%