Elsevier

Neuroscience

Volume 28, Issue 3, 1989, Pages 573-584
Neuroscience

The supraoptic nucleus: Afferents from areas involved in control of body fluid homeostasis

https://doi.org/10.1016/0306-4522(89)90006-7Get rights and content

Abstract

Physiological evidence indicates that the supraoptic nucleus may be an important integrating region for information relating to body fluid homeostasis. It is known that the supraoptic nucleus receives neural influences from brain receptive zones for plasma osmolality and angiotensin II, as well as from relay centers for blood pressure and blood volume. It is also known that these influences interact to modulate vasopressin release from the supraoptic nucleus. Therefore, a detailed investigation of the neurochemical afferents to the supraoptic nucleus from regions of the lamina terminalis and the brainstem was undertaken.

Injection of a fluorescent retrograde tracer, doxorubicin, into the supraoptic nucleus was combined with histochemistry of angiotensin II and catecholamines. Following supraoptic nucleus injection, retrograde label was found in forebrain neurons of the subfornical organ, median preoptic nucleus, and organum vasculosum of the lamina terminals. Some labeled cells in the subfornical organ and organum vasculosum of the lamina terminalis were also found to contain angiotensin II immunoreactivity. In the brainstem, retrograde label was found in neurons of the A1, A2 and A6 cell groups. Many of these cells were also found to contain catecholamine fluorescence or tyrosine hydroxylase immunoreactivity. Corroboration of the A2 projection was obtained by lesions of this nucleus, which reduced catecholamine fluorescence in the supraoptic nucleus.

These findings provide an anatomical basis for the functional observations that the supraoptic nucleus plays a key integrative role in the maintenance of body fluid homeostasis.

References (61)

  • KodaL.Y. et al.

    Doxorubicin: a fluorescent neurotoxin retrogradely transported in the central nervous system

    Neurosci. Lett.

    (1983)
  • LindR.W. et al.

    Angiotensin II immunoreactivity in the neural afferents of the subfornical organ of the rat

    Brain Res.

    (1984)
  • LoizouL.A.

    Projections of the nucleus locus coeruleus in the albino rat

    Brain Res.

    (1969)
  • McKellarS. et al.

    Efferent projections of the A1 catecholamine cell group in the rat: an autoradiographic study

    Brain Res.

    (1982)
  • MiselisR.R.

    The efferent projections of the subfornical organ of the rat: a circumventricular organ within a neural network subserving water balance

    Brain Res.

    (1981)
  • MitchellL.D. et al.

    Two possible actions for circulating angiotensin II in the control of vasopressin release

    Peptides

    (1982)
  • MitchellL.D. et al.

    Systemic angiotensin II, blood pressure and supraoptic neuronal activity

    Peptides

    (1985)
  • PhillipsM.L et al.

    An angiotensin-like peptide in the brain

    Life Sci.

    (1980)
  • RamsayD.J. et al.

    The organum vasculosum laminae terminalis: a critical area for osmoreception

    Prog. Brain Res.

    (1983)
  • RenaudL.P. et al.

    Terminal degeneration in supraoptic nucleus following subfornical organ lesions: ultrastructural observations in the rat

    Brain Res.

    (1983)
  • RicardoJ.A. et al.

    Anatomical evidence of direct projections from the nucleus of the solitary tract to the hypothalamus, amygdala, and other forebrain structures in the rat

    Brain Res.

    (1978)
  • SawchenkoP.E. et al.

    The organization and biochemical specificity of afferent projections to the paraventricular and supraoptic nuclei

    Prog. Brain Res.

    (1983)
  • SawchenkoP.E. et al.

    The organization of noradrenergic pathways from the brainstem to paraventricular and supraoptic nuclei in the rat

    Brain Res. Rev.

    (1982)
  • SgroS. et al.

    Subfornical organ-supraoptic nucleus connections: an electro-physiological study

    Brain Res.

    (1984)
  • TheodosisD.T. et al.

    Immunocytochemical analysis of the GABAergic innervation of oxytocin- and vasopressin-secreting neurons in the rat supraoptic nucleus

    Neuroscience

    (1986)
  • TribolletE. et al.

    Extrahypothalamic afferent inputs to the supraoptic nucleus area of the rat as determined by retrograde and anterograde tracing techniques

    Neuroscience

    (1985)
  • Van HoutenM. et al.

    Radioautographic localization of specific binding sites for blood-borne angiotensin II in the rat brain

    Brain Res.

    (1980)
  • ChangarisD.G. et al.

    Angiotensin II immunohistochemistry of the rat brain

    Neuroendocrinology

    (1978)
  • CoonsA.H.

    Fluorescent antibody methods

  • EverittB.J. et al.

    Brainstem noradrenergic pathways modulate vasopressin secretion in the rat

    J. Physiol.

    (1983)
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