Literature DB >> 3644888

Pinealocyte dense-cored vesicles and synaptic ribbons: a correlative ultrastructural-biochemical investigation in rats and mice.

J A McNulty, L M Fox, S J Lisco.   

Abstract

Dense-cored vesicles (DCV) and synaptic ribbons (SR) were quantified in the pineal gland of the rat (Sprague-Dawley) and mouse (Sasco/ICR strain), and day/night differences in frequency of these organelles correlated with levels of indoles determined by high performance liquid chromatography (HPLC). There were significant day/night differences in levels of serotonin (5HT), 5-hydroxyindole acetic acid (5HIAA), N-acetyl-5HT, and melatonin in the rat gland. Melatonin and N-acetyl-5HT were not detectable in the mouse gland sampled every 4 h over the light:dark cycle. The concentrations of 5HT and 5HIAA (ng/microgram protein) were similar in light-adapted rats and mice, but these indoles did not exhibit a circadian rhythm in the mouse gland. Correlative ultrastructural/biochemical results suggest that DCV do not contain physiologically important stores of 5HT since 1) the mouse gland contains the same number of DCV as the rat during the daytime, but only one-tenth the levels of 5HT, 2) day/night 5HT levels do not vary in the mouse gland, but there is a significant nocturnal decline in DCV numbers, and 3) 5HT levels in the rat gland decline at night when DCV numbers increase. Numbers of SR were significantly elevated at night in the rat and mouse, and the frequency of this organelle was similar in both species. However, ribbon-type SR predominated in rat pinealocytes, whereas SR in the mouse were almost exclusively spherical in shape. Day/night differences in SR numbers in the mouse gland suggest that cellular mechanisms regulating the frequency of this organelle do not involve factors related to indole metabolism. Because of the lack of photoperiodic effects on indole metabolism in the mouse pineal gland, this species is a potentially important model to study the functional relationship of pinealocyte organelles to cyclical changes in pineal products other than indoles (e.g., peptide/protein factors).

Entities:  

Mesh:

Substances:

Year:  1987        PMID: 3644888     DOI: 10.1111/j.1600-079x.1987.tb00840.x

Source DB:  PubMed          Journal:  J Pineal Res        ISSN: 0742-3098            Impact factor:   13.007


  6 in total

1.  Effects of electrical stimulation of the superior cervical ganglia on the number of "synaptic" ribbons and the activity of melatonin-forming enzymes in the rat pineal gland.

Authors:  S Reuss; W Concemius; J Stehle; A Seidel; H Schröder; L Vollrath
Journal:  Anat Embryol (Berl)       Date:  1989

2.  Circadian changes in synaptic ribbons and spherules in pinealocytes of the Syrian hamster (Mesocricetus auratus).

Authors:  C Díaz; M Alvarez-Uría; J Tolivia; J M López
Journal:  Cell Tissue Res       Date:  1990-10       Impact factor: 5.249

3.  Sympathetic denervation and chronic serotonin uptake blockade by fluoxetine do not affect pineal gland 5-hydroxyindole acetic acid: evidence that oxidative deamination of pineal serotonin is a property of the pinealocyte.

Authors:  J A McNulty; V Colin
Journal:  J Neural Transm Gen Sect       Date:  1992

4.  Twenty-four-hour changes in pinealocytes, capillary endothelial cells and pericapillary and intercellular spaces in the pineal gland of the mouse. Semiquantitative electron-microscopic observations.

Authors:  S Matsushima; Y Sakai; Y Hira
Journal:  Cell Tissue Res       Date:  1989-02       Impact factor: 5.249

Review 5.  Molecular Assembly and Structural Plasticity of Sensory Ribbon Synapses-A Presynaptic Perspective.

Authors:  Roos Anouk Voorn; Christian Vogl
Journal:  Int J Mol Sci       Date:  2020-11-19       Impact factor: 5.923

Review 6.  Melatonin Uptake by Cells: An Answer to Its Relationship with Glucose?

Authors:  Juan C Mayo; Arturo Aguado; Rafael Cernuda-Cernuda; Alejandro Álvarez-Artime; Vanesa Cepas; Isabel Quirós-González; David Hevia; Rosa M Sáinz
Journal:  Molecules       Date:  2018-08-10       Impact factor: 4.411

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.