Literature DB >> 4137106

Physiological and morphological identification of hypothalamic magnocellular neuroendocrine cells in goldfish preoptic nucleus.

J N Hayward.   

Abstract

1. Intracellular recordings were made from antidromically identified neurones in the goldfish preoptic nucleus and Procion Yellow was ejected from the recording pipette, marking these magnocellular neuroendocrine cells diffusely, for histological identification.2. In confirmation of earlier studies these preoptic neuroendocrine cells showed resting membrane potentials of 47 mV, action potentials up to 85 mV, action potentials of long duration (3.9 msec) occurring in two steps, long-lasting hyperpolarizing after-potentials and orthodromic driving from olfactory input.3. Magnocellular neuroendocrine cells exhibited all-or-none jumps to shorter antidromic latencies as pituitary stimulus strength increased, suggesting multiple branching of the ;axones' either near the preoptic nucleus or within the neural lobe.4. I find three morphological types of neuroendocrine cells throughout the magnocellular part of the preoptic nucleus. Cell Type I is a large (37 mum), multipolar neurone, 48 mum from the ependyma, with fine ;dendrites' projecting into the lateral hypothalamus and within the preoptic nucleus, with multiple branched ;axones'. Cell Type II is a large (31 mum), multipolar neurone, 24 mum from the ependyma, with a coarse ;dendrite' to the ependyma and fine ;dendrites' within the preoptic nucleus, with limited ;axonal' branching. Cell Type III is a small (18 mum), multipolar neurone, 46 mum from the ependyma, with fine ;dendritic' processes distributed within the preoptic nucleus, with limited ;axonal' branching.5. I conclude that magnocellular neuroendocrine cells show electrical membrane properties of other central neurones with both physiological and morphological evidence for multiple ;axonal' branching. The three identifiable neuroendocrine cell types (I, II, III) are distributed widely within the anatomical limits of the preoptic nucleus, pars magnocellularis, with each type receiving ;specific' input connexions and with unique output pathways. I suggest that these three types of neuroendocrine cells may be related to the ;cellular' secretion of ;specific' neurohypophysial hormones and neurophysins.

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Year:  1974        PMID: 4137106      PMCID: PMC1330940          DOI: 10.1113/jphysiol.1974.sp010558

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  50 in total

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3.  Influence of sleep-waking and nociceptor-induced behavior on the activity of supraoptic neurons in the hypothalamus of the monkey.

Authors:  J N Hayward; D P Jennings
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4.  Respiratory neurones of the ventrolateral nucleus of the solitary tract of cat: vagal input, spinal connections and morphological identification.

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5.  Hypothalamic input to supraoptic neurons.

Authors:  J N Hayward
Journal:  Prog Brain Res       Date:  1972       Impact factor: 2.453

6.  Osmosensitive single neurones in the hypothalamus of unanaesthetized monkeys.

Authors:  J N Hayward; J D Vincent
Journal:  J Physiol       Date:  1970-11       Impact factor: 5.182

7.  Spontaneous activity of single neurones in the hypothalamus of rabbits during sleep and waking.

Authors:  A L Findlay; J N Hayward
Journal:  J Physiol       Date:  1969-03       Impact factor: 5.182

8.  THE LOCALIZATION OF CHOLINESTERASE ACTIVITY IN RAT CARDIAC MUSCLE BY ELECTRON MICROSCOPY.

Authors:  M J KARNOVSKY
Journal:  J Cell Biol       Date:  1964-11       Impact factor: 10.539

9.  The role of sodium current in the radial spread of contraction in frog muscle fibers.

Authors:  L L Costantin
Journal:  J Gen Physiol       Date:  1970-06       Impact factor: 4.086

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  9 in total

1.  Reversal of the action of amino acid antagonists by barbiturates and other hypnotic drugs.

Authors:  N G Bowery; A Dray
Journal:  Br J Pharmacol       Date:  1978-05       Impact factor: 8.739

2.  Hypophysiotropic neurons in the goldfish hypothalamus demonstrated by retrograde transport of horseradish peroxidase.

Authors:  J N Fryer; L Maler
Journal:  Cell Tissue Res       Date:  1981       Impact factor: 5.249

3.  Intracellular dye-marked enkephalin neurons in the magnocellular preoptic nucleus of the goldfish hypothalamus.

Authors:  T A Reaves; J N Hayward
Journal:  Proc Natl Acad Sci U S A       Date:  1979-11       Impact factor: 11.205

4.  Intracellular recordings from the paraventricular nucleus in slices of rat hypothalamus.

Authors:  F E Dudek; G I Hatton; B A Macvicar
Journal:  J Physiol       Date:  1980-04       Impact factor: 5.182

5.  Isotocinergic neurons in the goldfish hypothalamus: physiological and morphological studies on chemically identified cells.

Authors:  T A Reaves; J N Hayward
Journal:  Cell Tissue Res       Date:  1979-10-02       Impact factor: 5.249

6.  Morphological features of physiologically identified hypothalamic neurons as revealed by intracellular marking.

Authors:  M J Kelly; U Kuhnt; W Wuttke
Journal:  Exp Brain Res       Date:  1979-01-02       Impact factor: 1.972

7.  Immunocytochemical identification of enkephalinergic neurons in the hypothalamic magnocellular preoptic nucleus of the goldfish, Carassius auratus.

Authors:  T A Reaves; J N Hayward
Journal:  Cell Tissue Res       Date:  1979-08-03       Impact factor: 5.249

8.  Cytoarchitecture of the rat's supraoptic nucleus.

Authors:  J E Bruni; P M Perumal
Journal:  Anat Embryol (Berl)       Date:  1984

9.  Osmoreceptors or sodium receptors: an investigation into ADH release in the rhesus monkey.

Authors:  S Swaminathan
Journal:  J Physiol       Date:  1980-10       Impact factor: 5.182

  9 in total

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